Enzyme ResearchVolume 2011 (2011), Article ID 327923, 20 pagesdoi:10.4061/2011/327923

Review Article

Therapeutic Implications of Targeting AKT Signaling in Melanoma

SubbaRao V. Madhunapantula1,2 and Gavin P. Robertson1,2,3,4,5,6

¹Department of Pharmacology, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA²Penn State Melanoma Center, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA³Department of Pathology, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA⁴Department of Dermatology, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA⁵Penn State Melanoma Therapeutics Program, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA⁶The Foreman Foundation for Melanoma Research, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA

Received 26 October 2010; Accepted 1 January 2011

Academic Editor: Yong-Doo Park

Copyright © 2011 SubbaRao V. Madhunapantula and Gavin P. Robertson. SubbaRao V. Madhunapantula and . This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Identification of key enzymes regulating melanoma progression and drug resistance has the potential to lead to the development of novel, more effective targeted agents for inhibiting this deadly form of skin cancer. The Akt3, also known as protein kinase B gamma, pathway enzymes regulate diverse cellular processes including proliferation, survival, and invasion thereby promoting the development of melanoma. Accumulating preclinical evidence demonstrates that therapeutic agents targeting these kinases alone or in combination with other pathway members could be effective for the long-term treatment of advanced-stage disease. However, currently, no selective and effective therapeutic agent targeting these kinases has been identified for clinical use. This paper provides an overview of the key enzymes of the PI3K pathway with emphasis placed on Akt3 and the negative regulator of this kinase called PTEN (phosphatase and tensin homolog deleted on chromosome 10). Mechanisms regulating these enzymes, their substrates and therapeutic implications of targeting these proteins to treat melanoma are also discussed. Finally, key issues that remain to be answered and future directions for interested researchers pertaining to this signaling cascade are highlighted.

1. Introduction

Kinases and phosphatases are the key components of signaling cascades regulating metabolic processes such as cell survival, proliferation, apoptosis, differentiation, and cell motility [1–4]. Aberrant expression and activities of these enzymes have been reported to lead to the development of several cancers including melanoma [4–10]. Due to genetic and epigenetic modifications, deregulating oncogenic kinases and tumor inhibitory proteins, melanocytes acquire transformed characteristics leading to malignant melanoma [4–10]. Members of the PI3K and Akt3 signaling cascades have been implicated in initiation, progression, invasive, and drug resistance phenotypes of melanomas [1–4]. Enzymes in this signaling cascade are therefore attractive targets for treating or preventing melanoma development [11–13]. This paper provides an overview of enzymes involved in PI3K-Akt signaling pathway focusing specifically on the tumor suppressor phosphatase PTEN, lipid kinase PI3K, and the oncogenic survival kinase Akt3. Key structural features, mechanisms regulating the expressionm and activities of these proteins as well as therapeutic implications of targeting this pathway to treat melanoma are reviewed.

1.1. Tumor Suppressor PTEN Is a Key Phosphatase Regulating PI3K-Akt3 Signaling and Thereby Melanoma Development

The PTEN (phosphatase and tensin homolog deleted on chromosome 10) gene, which is also known as MMAC1 (mutated in multiple advanced cancers), and TEP1 (TGF-β regulated and epithelial cell-enriched phosphatase) is a unique 55 kDa dual specificity phosphatase located on the long arm of chromosome 10 at 10q23 [14, 15]. PTEN dephosphorylates proteins [16–18] and hydrolyzes the secondary messenger inositol trisphosphates (PIP₃s) [17, 19] thereby inhibiting the activities of several proteins or pathways, which regulate cell proliferation, survival, and apoptosis [14, 20].

Preclinical and clinical evidence has demonstrated the inactivation of PTEN in 29 to 43% of melanoma cell lines or tumors from patients. For example, a recent study showed decreased PTEN expression in 43% melanoma cases and demonstrated a significant correlation between alterations in PTEN expression and primary tumor ulceration [20]. However, only a few studies, although controversial, demonstrated the clinical implications of PTEN as a prognostic marker in melanoma. Addressing this aspect, a recent study concluded that the utility of PTEN status as a prognostic marker is limited despite decreased PTEN expression observed commonly in primary melanomas associated with aggressive tumor behavior [20]. This clinical study analyzed 127 primary melanomas and found no significant association between PTEN expression and patient survival.

Key experiments demonstrating the tumor suppressor function of PTEN in melanomas include (a) triggering and sensitization of melanoma cells to apoptosis following introduction of PTEN (Figure 1) [8, 22] as demonstrated by increased cleaved caspase-3 only when wild-type PTEN is expressed compared to inactive G129R mutant in UACC 903 cells [8]; (b) enhanced phosphorylation of Akt3 in melanocytes and early melanoma WM35 cells expressing wild-type PTEN protein only upon PTEN inhibition [23]; (c) loss of cell viability, decreased activity of Akt3, and downstream pPRAS40 following the introduction of PTEN in melanoma cells lacking functional protein (Figure 2) [8, 9, 21]; (d) appearance of spontaneous melanoma tumors in mice lacking PTEN−/− and expressing conditionally induced V600EB-Raf. B-Raf, one of the key regulators of proliferation, has been shown to be mutated in ~60% melanomas [4, 24]. The most common mutation T1799A, which results in the substitution of valine to glutamic acid, has been identified in >90% of melanoma patient tumors harboring a mutant B-Raf protein [4, 24]. Furthermore, targeted deletion of PTEN in melanomas induced BCl₂, which resulted in enhanced resistance to growth factor receptor inhibitors and chemotherapeutic agents [8, 9, 20, 21].

Figure 1: PTEN (EC number: 3.1.3.67) regulates Akt signaling in melanomas. Isogenic UACC 903 cell lines expressing (29A, 36A, 37A) or not expressing (parental UACC 903, revertant 36A-R1, 36A-R2) PTEN were treated with 1 μM staurosporine for 4 h and cell lysates analyzed for the expression of pAkt, pPRAS40, and cleaved caspase-3. The data demonstrates that PTEN null cell lines express high pAkt, pPRAS40, and decreased cleaved caspase-3 fragments compared to cells harboring PTEN, indicating that PTEN sensitizes melanoma cells to chemotherapeutic agents [21].

(a)

(b)

Figure 2: Targeting Akt3 signaling inhibits melanoma cell survival. SiRNA-mediated targeting of Akt3 or downstream PRAS40 inhibited anchorage independent growth and induces caspase-3/7 activity in melanomas compared to control buffer or scrambled siRNA transfected cells [21].

PTEN expression has been shown to inhibit melanoma cell proliferation and survival. Mechanistically, decreased PTEN activity alters cell cycle progression, migration, and adhesion of melanoma cells [14]. Recently, PTEN loss and V600EB-Raf have been shown to cooperate to promote metastatic melanoma development [24]. Furthermore, PTEN loss increased melanoma cell and nontransformed melanocytes invasion and migration by increasing Akt2 activity and by E-cadherin downregulation [25]. It is interesting that targeting PTEN differentially regulates Akt3-mediated cell survival and Akt2-mediated metastasis in melanomas.

In addition to PI3K-Akt pathway regulation, PTEN also regulates the synthesis of proteins in melanoma cells. Mechanistically, PTEN controls phosphorylation of eukaryotic initiation factor-2α (eIF2α), independent of its phosphatase activity, thereby inducing the antiproliferation and apoptotic signals [26]. Isogenic melanoma cells lacking PTEN had low phosphorylated eIF2 compared to cells expressing wild-type PTEN. Furthermore, reconstitution of wild-type or phosphatase-defective PTEN in PTEN-null human glioblastoma cells enhanced phosphorylation of eIF2α via binding to PTEN’s PDZ domain [26]. Phosphorylated eIF2α inhibits eIF2B and blocks the initiation of translation and overall protein synthesis [26].

PTEN also regulates several key processes such as inhibition of cell proliferation by altering cell cycle progression through G1 to S phase and control of apoptosis by modulating Akt activity [20, 27–29]. Furthermore, PTEN expression using a variety of vectors or from an introduced chromosome in melanoma cell lines lacking PTEN induced apoptosis and inhibited tumor development [8, 20, 22]. Cells containing functionally active PTEN protein exhibited elevated p27 expression, decreased cyclin-D1 and cyclin-D2 protein levels [14, 29, 30].

1.2. Mechanisms Regulating the Expression and Activity of PTEN in Melanomas

PTEN expression and activity are regulated at transcriptional and posttranslational levels [15, 19, 31] by positive regulators EGR-1 (early growth regulated transcription factor), PPARγ (peroxisome proliferator-activated receptors), and p53 [19] as well as negative regulators MKK-4 (mitogen-activated protein kinase kinase 4), NFκB (nuclear factor kappa-light-chain-enhancer of activated B cells), TGF-β (transforming growth factor beta), and c-JUN [14, 19, 32]. At a posttranslational level, phosphorylation, oxidation, acetylation, and ubiquitination are key factors regulating PTEN activity [19, 33, 34]. For example, oxidation of cysteine residues C71 and C124 by reactive oxygen radicals inhibits PTEN phosphatase activity. Similarly, acetylation of PTEN catalytic domain lysine residues 125 and 128 by histone acetyltransferase PCAF (p300/CBP-associated factor) decreases affinity towards PIP₃’s thereby regulating melanoma development [35]. Other posttranslational modifications such as phosphorylation of the C-terminal tail serine and threonine residues (S362, T366, S370, S380, T382, T383, S385) by CK2 (casein kinase 2), LKB1, Src, GSK3β have been shown to play critical roles regulating PTEN activity by altering protein stability [19, 33]. Phosphorylated PTEN is stable but less active compared to unphosphorylated PTEN [19, 36]. For example, PTEN proteins either lacking the C-tail or harboring mutations in C-tail are short lived [33, 36, 37]. However, it is not known whether such posttranslational modifications contribute to human melanoma development.

The subcellular localization of PTEN also plays a key role in melanoma development [14, 19] as PTEN has intrinsic membrane translocation signals in the phosphatase and C2 domains. Mutations in these regions and interactions with other proteins impair ability of PTEN to translocate to the plasma membrane. For example, ubiquitination of PTEN catalyzed by NEDD4-1 (neural precursor cell expressed, developmentally downregulated 4) influences its cellular localization, as monoubiquitination promotes nuclear localization while polyubiquitination causes PTEN protein to remain in the cytosol [38, 39]. It would be interesting to determine whether similar ubiquitination patterns occur in melanomas.

Genetic and epigenetic mechanisms such as loss of a whole chromosome, mutations, and epigenetic miRNAs also modulate the expression as well as activity of PTEN [18, 19]. For example, loss of chromosome 10 (the site of PTEN gene), occurs in 30%–60% of noninherited melanomas [8]. Similarly, screening of melanoma cell lines and paired uncultured metastatic melanoma to peripheral blood specimens for PTEN loss and/or alterations, found homozygous deletions in ~20% melanoma cell lines, while 9% had nonsense, frame shift, or intronic mutations. However, only ~12% of uncultured melanoma specimens contained nonsense mutations or homozygous deletions [40, 41]. Intragenic polymorphisms in introns have also been reported to regulate PTEN expression in melanomas. Furthermore, ~12% of melanomas have mutations in the PTEN gene [40, 41].

Early melanocytic lesions frequently have undergone loss of one allele of PTEN or haploinsufficiency occurring due to loss of the entire chromosome 10 [14, 42–45]. Allelic loss or mutations of PTEN have been reported in 5%–15% of uncultured melanoma specimens and in 30%–40% of established melanoma cell lines [40, 41]. Decreased PTEN levels due to haploinsufficiency plays an important role in early melanomas by specifically increasing Akt3 activity in these cells, thereby protecting these cells from apoptosis as well as releasing quiescent melanocytes from V600EB-Raf induced cell senescence [25, 46–48]. Loss or inactivation of PTEN also induces phosphorylation and monoubiquitination of DNA damage checkpoint kinase, Chk1, which then causes genomic instability, double-stranded DNA breaks, culminating in cancer development [41]. Amino acid altering mutations (P95S, F154L, L325F) induced by UV radiation have also been shown to impair PTEN function and thereby promote the development of early melanomas [49].

Epigenetic modifications such as methylation of CpG islands or microRNAs also regulate PTEN activity. For example, CpG islands methylation has been reported in melanomas [14, 50, 51]. Recently, PTEN promoter methylation leading to inactivation of transcription was found to occur in ~62% of metastatic melanoma patients [52–60]. However, contradictory to this observation, the most recent studies by Liu et al., 2008, and Bonazzi et al., in 2009, found no DNA methylation of the PTEN promoter [61, 62]. Therefore, although regulation of PTEN expression by DNA methylation appears to be important, further studies are warranted to measure its contribution to melanoma development. If mutational and epigenetic silencing studies of PTEN are combined together, functional inactivation might occur in ~77% of nonfamilial melanomas [54, 63–65].

1.3. PI3K Is a Key Regulator of Melanoma Development

Phosphatidyl inositol 3 kinases (PI3Ks) are a family of intracellular lipid kinases that phosphorylate the 3′ hydroxyl group of phosphatidylinositols (Pis) and phosphoinositides [66, 67]. Activation of PI3K affects cell growth, proliferation and survival thereby influencing the tumorigenic potential of melanoma cells [66, 67]. PI3Ks are classified based on substrate specificity and structure, into class-I, class-II, and class-III kinases [66, 68] (Figure 3). Whereas class-I PI3Ks convert PIP2 into PIP3, class-II, and class-III PI3Ks use PIs to generate PI-3-P. Class-I PI3Ks are further subdivided into class-Ia and class-Ib [66, 67]. Activity of class-Ia PI3K is triggered by growth factor receptor tyrosine kinases, whereas class-Ib is activated by G protein-coupled receptors. Class-Ia PI3K is a heterodimer comprising of p85 regulatory and p110 catalytic subunits [66, 68]. At the plasma membrane class-Ia PI3Ks phosphorylate PIP2 at the 3′ position and convert it into PIP3 upon growth factor stimulation. PIP3 binds to the PH domain containing PDK1 and Akt proteins leading to recruitment to the plasma membrane. In addition to lipid kinase activity, class-I PI3Ks also exhibit protein kinase activity. The physiological relevance of this activity differs between the members of class I PI3Ks. For example, class-Ia PI3K phosphorylates insulin receptor substrate-1 (IRS-1), whereas class-Ib PI3K activates the MAPK signaling cascade [66, 68].

Figure 3: Schematic representation of PI3 kinase enzymes. PI3 kinases are a group of enzymes involved in regulating cell growth, proliferation, differentiation, motility, and survival. Based on structure and substrate specificity PI3 kinases have been divided into Class I (EC number: 2.7.1.153), Class II (EC number: 2.7.1.154), and Class III (2.7.1.137) enzymes. Class I and II PI3Ks are composed of regulatory and catalytic subunits, whereas Class III contains only catalytic subunit. Depending on the type of subunits, heteromeric Class I PI3Ks are further subdivided into Class IA and Class IB. Whereas Class IA PI3K consists of p85 regulatory subunit and p110 catalytic subunit, the Class IB PI3K is made up of p101 regulatory subunit and p110γ catalytic subunit. Class IA PI3K is the most common PI3Ks implicated in the development of cancers.

PI3K-mediated activation of Akt occurs as a result of ligand-dependent activation of tyrosine kinase receptors, G-protein-coupled receptors, or integrins [69]. Many of theses ligands are overexpressed in cancers, making this a route for Akt activation in melanomas [70, 71]. Receptor-independent activation of PI3K also occurs in 10%–20% melanomas expressing constitutively active Ras proteins [72–74]. Elevated PI3K activity itself can also cause Akt activation. Chromosome 3q26 containing the p110 catalytic subunit of PI3K, which is frequently amplified in cancer of the ovary [75] and cervix [76], leads to increased PI3K catalytic activity. The importance of PI3K signaling in melanoma was demonstrated by overexpressing a deleted subunit of PI3K (Deltap85) to reduce PI3K signaling [77]. In this manner, Delta p85 functioned as a dominant-negative disrupting p85/p110 subunit interaction, consequently inducing apoptosis in the melanoma cell line G361.

PI3K is a critical regulator of melanoma progression. Targeting this kinase using siRNAs or pharmacological agents such as ZSTK474, which binds to ATP-binding pocket of PI3K, reduced melanoma tumor development [66, 68]. In addition, preclinical studies have shown that therapeutic agents inhibiting PI3K activity synergizes with MAPK inhibitors. Although PI3K appears to be a critical regulator of melanoma development, to date, not many studies have shown its expression in patient tumor samples. Furthermore, results of publications are controversial, as some studies found no or low expression of PI3K in patient samples, while others have reported high level of expression [66, 68]. Addressing this aspect a recent study quantitatively assessed the expression of PI3K in 523-melanoma and 540-nevi samples, and showed that p85 and p110 subunit expression is high in melanomas compared to nevi [66, 68]. However, neither subunit served as prognostic marker in either primary or metastatic patients.

1.4. Akt3 Is Central to the Development of Melanomas

Akt, also known as protein kinase B, is a member of AGC family kinases and has three isoforms Akt1 (PKBα), Akt2 (PKBβ), and Akt3 (PKBγ) [71, 78] (Figure 4). These three isoforms share >80% homology and contain pleckstrin homology (PH), catalytic and regulatory domains [70, 71, 78–84]. The N-terminal PH domain spans amino acids 1 to 107, mediating protein-protein and protein-lipid interactions [85, 86], whereas the central catalytic domain (CD) contains a key phosphorylation residue T³⁰⁵ [87, 88]. The carboxy terminal regulatory domain (RD), also referred as hydrophobic motif (HM), contains a second phosphorylation site serine (S⁴⁷²), whose phosphorylation is required for complete activation of this kinase. Other possible phosphorylation sites may also be important, and research in this area continues [89]. In one study it has been shown that the E40K mutation enhances the enzymatic activity of Akt3 in melanomas [21, 46]. Splice variants of Akt3 lacking serine 472 have been identified but the significance of this form of the protein remains unknown [90, 91].

Figure 4: Schematic representation of Akt kinases (EC number: 2.7.11.1). Akt, also known as protein kinase B, is a serine, threonine protein kinase implicated in the development and chemotherapeutic resistance of cancers. Although the three isoforms, Akt1, Akt2, and Akt3, share high degree of structural homology in terms or domain (PH, catalytic, and regulatory) architecture, they exhibit variations in some of the key amino acid residues and cellular functions. Domain organization and key phosphorylation site are represented.

Akt is a positive regulator of cell proliferation and survival, which are controlled by various growth factors and extracellular stimuli (Figure 5) [10]. Despite sharing high degree of homology and some cellular activities, Akt1, Akt2, and Akt3 also exhibit isoform-specific functions [92, 93]. Studies using isoform-specific knockout mice have demonstrated that Akt1 has a key role in maintaining cell survival [93]. Akt1 knockout mice are smaller compared to wild-type mice, and cells lacking Akt1 undergo apoptotic cell death [93, 94]. Likewise, Akt2 knockout mice developed type-2 diabetes, whereas mice lacking Akt3 displayed impaired brain growth [95, 96]. However, not much is known about how these isoform-specific functions are regulated. Some of the key factors regulating isoform-specific functions of Akt include (a) differential tissue distribution [93], (b) differences in the Akt responses to extracellular stimuli [97, 98], (c) structural variations in the key domains regulating translocation, substrate binding, and catalytic activity [10, 99], and finally (d) intracellular compartmentalization [93, 97].

Figure 5: Akt is the key regulator of cell survival and proliferation. Growth factors and hormones trigger the Akt pathway by a series of phosphorylation and dephosphorylation events. Shown are some of the substrates of Akt implicated in cell survival, proliferation, and migration.

Aberrant activation of Akt kinases has been reported in several malignancies including melanoma. Mechanisms leading to Akt activation can involve (a) mutations in the upstream regulators PI3K and PTEN; (b) overexpression of the gene due to increased copy number or activating point mutations in Akt itself, (c) deletion of negative regulators such as PTEN; (d) altered expression of interacting proteins such as TCL1, HSP90, APPL1, and RasGAP [5, 6, 8, 67]. Akt activity is also regulated by posttranslational modifications such as phosphorylation, ubiquitination and also by physical interactions with effector proteins such as Hsp90 and Pin1 [92, 100, 101]. Although physiological functions of Akt isoforms are regulated through similar mechanisms, the activity of a particular isoform is cell type dependent [70, 71, 78–84].

Translocation to the cell membrane followed by phosphorylation of key amino acid residues activates Akt signaling. In normal cells, Akt is cytoplasmic and inactive. Upon growth factors binding to a cell surface receptor or through G-protein-coupled receptors, PI3K gets activated, which, then phosphorylates phosphatidylinositol-4,5-bisphosphate (PIP₂) on the 3-OH group, generating second messenger phosphatidylinositol-3,4,5-trisphosphate (PIP₃) [102]. PIP₃ binds to the PH domain of Akt thereby facilitating translocation to the plasma membrane. Akt activation is initiated when the translocated Akt is phosphorylated on T308 residue by membrane-localized phosphoinositide-dependent kinase-1 (PDK-1). However, complete activation is achieved only when a PDK2 phosphorylates the second phosphorylation site S473. Recent studies have shown that serine 473 phosphorylation is mediated by rapamycin-insensitive mTORC2 [103, 104]. PDK2 activity of the mTOR complex has been recently established but in melanomas its role in maintaining Akt3 phosphorylation has not been studied [103, 104]. Akt autophosphorylation might also play a role in the activation process [70, 71, 78–84]. Furthermore, it has been shown that prior phosphorylation of tyrosine 315 (Y315) and 326 (Y326) residues is a prerequisite for the activation of Akt kinases (Figure 4).

Preferential activation of a specific Akt isoform has been reported in cancers of breast, ovarian, pancreas, and skin [93]. For example, Akt2 gene amplification has been observed in ovarian and pancreatic cancers. Similarly, Akt3 found to be selectively activated in melanomas [5, 6, 9]. Therefore, selective activation of a speficic Akt isoform appears to regulate the development of a particular cancer. But, to date, the mechanistic basis for this isoform-specific regulation is not known and slowly starting to emerge [93].

Akt activity is also regulated by dephosphorylation of phosphorylated Thr308 and Ser473. Phosphatases are the key enzymes controlling phosphorylation status of Akt. Whereas PTEN dephosphorylates secondary messenger PIP3 into PIP2, the protein phosphatase 2A (PP2A) and PH domain leucine-rich repeat protein phosphatase (PHLPP) remove phosphate groups from T308 and S473, respectively, to deactivate Akt kinases [92, 105, 106]. Okadaic acid, a strong inhibitor of PP2A, promotes phosphorylation of Akt, whereas ceramide, an activator of PP2A, reduces Akt activity [92, 107, 108]. Although extensive studies have been reported on the critical role of PTEN phosphatase, not much is known about the status of PP2A and PHLPP in melanomas.

Another posttranslational modification that has been shown to regulate Akt activity is ubiquitination. Ubiquitination-dependent upregulation of Akt activity has been reported in various cancers [92, 100]. Studies have demonstrated that TRAF6 E3 ligase is required for Akt ubiquitination [109]. Cells overexpressing TRAF6 exhibit high Akt kinase activity, whereas TRAF6 null cells had negligible phosphorylated active Akt [109]. Experiments measuring the effect of TRAF6 expression on Akt activity before and after translocation revealed that TRAF6 is essential for membrane translocation of Akt, but once the Akt is bound to cell membranes, TRAF6 has no effect on regulating Akt activity [100, 109].

Primary structure of Akt also influences its activity. Since the constituent amino acid sequences, especially ubiquitination sites, are involved in regulating protein stability, mutations in these key sites might influence the protein stability thereby enzyme activity. For example, site-directed mutagenesis analysis showed that ubiquitination of Akt occurs at K8 and K14 residues located in the PH domain [100]. Growth-promoting somatic mutations in the PH domain of Akt have been reported in several cancers [92, 100, 110]. For example, E17K mutation in Akt is found in cancers of breast (8%), colon (6%), skin (1.5%), and ovaries (2%) [92, 99, 100, 110, 111]. Similarly, E49K mutation is identified in a subset of bladder cancer patients [112]. However, the abundance of E17K mutation is either too low, or, in some instances, no such mutations were found making it difficult to consider this as a biomarker of tumor progression. For example, in nonsmall cell lung cancers and acute myelogenous leukaemias no such mutations in Akt1 were identified [113, 114]. Moreover, no differences in the ability to translocate to the plasma membrane were observed in experiments where the PH domain of Akt1 was switched with Akt2 PH domain indicating that it is not just the PH domain mediating translocation of the protein but other factors such as posttranslational modification, which might also play a role [93]. Thus, basal Akt activity in a cell primarily depends upon several factors regulating subcellular localization, specifically a balance between positive and negative regulators controlling Akt phosphorylation status and proteins that interact with the kinase itself.

2. Functional Characterization of Akt3 Signaling in Human Melanomas

2.1. Akt3 Is a Key Protein Kinase Regulating Melanoma Development and Chemotherapeutic Resistance

Increased Akt3 expression/activity occur in 60%–70% of sporadic melanomas demonstrating a key role in melanoma development [23, 115]. Activated Akt3 phosphorylates several substrate proteins containing Arg-X-Arg-X-X-[Ser/Thr]-Hyd (where X is any amino acid and Hyd is a bulky hydrophobic amino acid) consensus sequences thereby regulating cellular survival and chemotherapeutic resistance (Figure 5). For example, phosphorylation of (a) GSK3β inhibits its activity thereby promoting cell cycle progression through increased cyclin D levels [116, 117]; (b) PRAS40 at threonine 246 (T²⁴⁶) inhibits the interactions with mTORC1 thereby increasing the nutrient status of the cells [21, 118, 119]; (c) V600EB-Raf decreases its activity to levels that promote rather than inhibit cell proliferation [46, 120]; (d) osteopontin, a glyco-phosphoprotein, promotes melanoma progression levels to a highly metastatic state [121]. Furthermore, Akt3 inhibits cellular apoptosis by decreasing caspase-3/7 activity and increasing the expression of cleaved caspase-3 and cleaved PARP levels [9, 122]. Decreased apoptosis makes melanoma cells less sensitive to chemotherapeutic agents functioning through this mechanism.

Increased Akt3 activity also plays a significant role in progression to more advanced aggressive tumors [6, 21, 23]. For example, expression of Akt3 has been elevated in cell lines derived from primary melanoma tumors at the radial and vertical stages of cell growth compared to normal human melanocytes (Figure 6). No significant changes were observed in the levels of Akt1 and Akt2 in the same lysates, indicating that Akt3 activation performs critical functions in melanoma development [6, 23]. Consistent with this observation, a recent report also showed elevated Akt3 expression in melanoma cell lines having high pAkt [123]. Analysis of a panel of 58 melanoma cell lines and 96 melanoma metastases showed elevated pAkt in cells harboring a mutant V600EB-Raf compared to cells containing N-Ras [123]. However, it is unknown why Akt3 and not the other isoforms is activated in melanomas. Various explanations with experimental evidence have provided some clues by demonstrating (a) increased copy numbers of the Akt3 gene compared to other isoforms in melanomas, which might contribute to some extent for the preferential Akt3 activation [14, 23] and (b) selective activation of Akt3 by preferentially interacting with PIP₃ and/or accessory proteins that bind to PH domain of Akt3 but not to Akt2 or Akt1. Structurally Akt3 has different phosphorylation sites within the PH domain compared to other Akt isoforms [70, 71, 78–84]. For example, TCL1 selectively binds to the Akt3 PH domain, thereby promoting hetero-oligomerization of Akt1 with Akt3, causing transphosphorylation of Akt in leukemias [124–126]. Thus, factors interacting preferentially with Akt3 may lead to selective activation in melanomas.

Figure 6: Akt3 but not Akt2 or Akt1 is upregulated in the majority of melanoma cells. Protein lysates were harvested from melanocytes and melanoma cell lines representing radial (WM35, WM3211), vertical (WM115, WM98.1, and WM278), and metastatic (UACC 903) stages and analyzed by western blotting. Arrows indicate the cell lines expressing high Akt3 and pAkt. Note. Expression of Akt1 and Akt2 is not changed in majority of advanced melanomas, indicating that Akt3 is the key regulator of cell survival in melanomas [9].

Recent studies have identified another mechanism for isoform-specific regulation of Akt signaling. These studies have shown that the phosphatidylinositol 3-phosphate binding FYVE domain-containing protein WDFY2, localizes to a distinct subset of early endosomes that are close to the plasma membrane thereby serves as a molecular scaffold to regulate the phosphorylation of Akt kinases in an isoform-specific manner [127]. For example, WDFY2-depleted cells expressed very low levels of Akt2 and pAkt compared to control cells containing WDFY2. Similarly another study also demonstrated the endosome mediated, isoform-specific regulation of Akt activity and substrate selectivity [127]. Rab5 effector endosomal protein Appl1 interacts with transmembrane receptors and Akt thereby influencing Akt activity and substrate selectivity [128]. Human adaptor protein containing PH domain, PTB domain, and leucine zipper (Appl1) is an Akt-interacting protein involved in the regulation of cell survival and proliferation [128]. Targeted depletion of Appl1 decreased phosphorylation of GSK3 but not TSC2 indicating the substrate selectivity induced by this endosomal protein [128]. However, it is not known whether similar regulatory mechanisms also occur in melanoma. We now know that GSK3 regulates cell survival and proliferation rates of melanoma cells but whether Appl1 regulates GSK3 activity in melanoma is not known. Addressing this might open up new avenues for understanding the mechanistic basis of Akt-mediated cell survival regulation and help designing potent therapeutic agents to inhibit this signaling cascade in melanomas.

A central role of the Akt3 isoform in melanoma development is well established; however, a recent report using human melanoma biopsy samples found Akt2 as a predominantly activated isoform in melanomas [129]. In addition, a different study demonstrated that loss of PTEN promoted melanoma cell metastasis via activating Akt2 but not Akt1 or Akt3 [25]. Interestingly, this study also demonstrated that expression of myrAkt3 inhibited invasion of melanoma cells without influencing the expression levels of pFAK and pSTAT3 [25]. Mechanistically, Akt2 induces the expression of miR-200 microRNAs thereby decreasing the expression of E-Cadherin [25], which in turn increases cell invasion. Therefore, it might be interesting to study whether different isoforms of Akt have different functions in regulating melanoma tumor development and metastasis, and if so, how this preferential regulation is occurring. These studies will help addressing some of the key aspects of Akt signaling in melanomas and provide new insights for understanding the mechanistic basis of melanoma tumor development.

2.2. Mechanism Promoting Akt3 Deregulation in Melanomas

A key mechanism for increased Akt activity in cancer cells involves gene copy number increases or mutations leading to constitutive activation. Recently a low-frequency activating mutation (E17K) in the PH domain of Akt3 has been identified in melanoma cell lines and ~4% of patient tumors [111]. This mutation enables Akt3 to get recruited to cell membranes independent of PI3K, which leads to cellular transformation. Genetic amplifications increasing Akt1 or Akt2 expression occur in carcinomas of the stomach, ovary, pancreas, and breast [130–137]. Specifically, Akt2 amplification occurs as part of the 19q13.1–q13.2 amplicon in high-grade aggressive ovarian tumors [138]. Even though no amplifications of Akt genes have been reported in melanomas [139, 140], Akt3 protein is frequently overexpressed [23], as a result of copy number increases of the long arm of chromosome 1 containing the gene [43–45]. No increases in the long arms of chromosome 14 or 19 containing the Akt1 and Akt2 genes, respectively, have been reported [43–45]. Thus, increase in Akt3 copy number is one mechanism contributing to increased expression and activity in melanoma. Since expression of Akt3 protein might not represent the activation status of the protein, it is thought that other processes must also contribute, leading to preferential activation of Akt3 versus the other isoforms in melanomas.

Phosphatases that directly dephosphorylate Akt may also play a role in the preferential activation of Akt3 in melanomas. While the identity of these phosphatases remains uncertain, PP2A phosphatase may be involved in this process [141]. Proteins binding to Akt also have the potential to modulate cellular activity as is observed with the protooncogene TCL1, which enhances oligomerization of Akt1 with Akt3, thereby facilitating activation of Akt3 in leukemia [124–126]. Another example is the heat-shock-protein 90 (Hsp90) that can complex with Akt. Inhibition of Akt-Hsp90 complex formation can inactivate Akt by PP2A-mediated dephosphorylation [142, 143].

Deregulated Akt3 expression and activity could also be controlled by noncoding microRNAs. For example, miR-149 has been shown to inhibit Akt1 activity thereby inducing apoptosis in neuroblastoma and cervival cancers [144]. Ectopic expression of miR-149 induced apoptosis by inhibiting Akt1 expression and activity [144]. However, miRNAs specifically regulating Akt3 expression have not been identified. Only recently, miRNAs 15a and 16 have been shown to inhibit the expression of Akt3 in multiple myelomas [145]. However, these miRNAs also inhibited ribosomal protein-S6, MAP-kinases, and NF-κB activator MAP3KIP3 [145]. Discovering miRNAs specifically regulating Akt3 is important to assess the clinical progression of the disease and for developing novel tools for preventing or treating melanomas.

3. Cellular Processes Regulated by Akt3 Signaling in Melanomas

3.1. Akt3 Signaling Regulates Cell Survival, Migration, Metastasis, and Chemoresistance

Akt3 has been shown to be a prosurvival kinase in melanomas [23]. SiRNA or pharmacological agents targeting Akt3 protein levels or expression of PTEN selectively lowers Akt3 activity, thereby reducing the tumorigenic potential of melanoma cells by altering apoptotic sensitivity of the cells (Figure 7) [21, 23]. Furthermore, increased activity correlates with tumor progression, providing cells with a selective advantage in the tumor environment [21, 23]. Inhibiting Akt signaling in tumor cells by adenoviral transfer of an Akt kinase-dead mutant, in which the two regulatory phosphorylation sites have been mutated to alanines thereby converting it to a dominant negative, led to selective induction of apoptosis in tumor cells expressing activated Akt [146]. In contrast, a minimal effect was observed in normal or tumor cells expressing low levels of active Akt [146]. In addition, a recent study showed that Akt could act as a molecular switch by increasing angiogenesis and producing superoxides [147]. Experimentally, overexpression of Akt in radial growth phase WM35 cells transformed them into malignant phenotypes by stabilizing cells with extensive mitochondrial DNA mutations, which can generate ROS, and by inducing expression of NOX4, a ROS generating enzyme [147].

(a)

(b)

Figure 7: Targeting Akt3 inhibits melanoma tumor development. SiRNA targeting Akt3 and downstream PRAS40 is introduced into UACC 903 melanoma cells by Amaxa transfection and effect on xenografted subcutaneous tumors measured. The data shows ~50%–60% decreased tumor volume when the expression of Akt3 and PRAS40 is inhibited compared to control cells transfected with a scrambled siRNA, siRNA to C-Raf, or buffer [21]. Inhibiting Akt activity using pharmacological agent ISC-4 that contains selenium also reduced melanoma tumor growth as effectively as siRNA mediated downregulation of Akt3 expression, indicating the potential utility of developing pharmacological agents targeting this key protein in melanomas [122].

The vital role of Akt in melanoma tumor progression and development is further confirmed by showing that hyperactivated Akt signaling upregulated Notch1 via NFκB activity thereby inducing the transformation of melanocytes under prevailing hypoxic conditions in tumors [148]. Upregulated Akt activity in melanoma tumors appears to protect cells from low oxygen pressures and apoptotic cell death induced by various chemotherapeutic agents [48]. For example, a recent study demonstrated that Akt3 mediates the resistance to apoptosis in B-Raf-targeted melanomas [48]. Targeting V600EB-Raf using PLX-4072 rendered invasive melanoma cells susceptible to anoikis, a form of apoptosis generally induced by loss of adhesion and is mediated by BH3-only proteins, Bim-EL and Bcl2-modifying factor (Bmf) [48, 149]. However when expression of Akt3 is induced by adhesion to fibronectin in these cells, the cells exhibited resistance to apoptosis caused by B-Raf inhibition [48]. Therefore, Akt3 is a key regulator of melanoma cell survival and helps protect cells from apoptosis induced by chemotherapeutic agents [48]. Another recent study also demonstrated the induction of chemotherapeutic resistance by Akt activation. Human melanoma cells under endoplasmic reticulum stress showed more resistance to apoptosis induced by microtubule-targeting chemotherapeutic agents such as docetaxel and vincristine, which is mediated by Akt activation [150].

Processes such as metastasis, cell-cell adhesion, cell migration, and development of chemoresistant tumors under hypoxic conditions are also regulated by PI3 kinase and Akt signaling pathways [6, 147, 152]. Activated Akt in metastatic melanoma cells have been shown to regulate Notch1 expression via NFκB thereby promoting tumor development under hypoxic tumor conditions [148]. A different study has shown that Akt inhibits RhoB, a GTPase, in melanomas and thereby induces tumor cell survival, transformation, invasion, and metastasis [153].

3.2. Substrates of Akt3 Kinase Involved in Melanoma Development

Akt substrates can be cytoplasmic or nuclear proteins, and numbers of proteins regulated by Akt continue to increase as studies such as those using the minimal consensus peptide sequence Arg-X-Arg-X-X-[Ser/Thr]-Hyd (where X is any amino acid and Hyd is a bulky hydrophobic amino acid) search for putative substrates [154, 155]. The functions of many of these substrates in cellular processes have been identified, demonstrating that Akt regulates multiple processes in cells including apoptosis and proliferation (Figure 5).

Substrates for Akt3 do not appear to be specific but rather seem to be identical to those acted on by all three Akt isoforms. Substrates of Akt3 involved in melanoma development include (a) Bad-whose inactivation promotes cell survival [156]; (b) NFκB-inhibition of Akt activity led to increased apoptosis and decreased NFκB promoter activity in melanoma cells [115]; (c) hTERT-inhibition of Akt reduced hTERT peptide phosphorylation and telomerase activity [157]; and (d) Rac1-targeting Akt decreased phosphorylated serine 71 of Rac1 thereby modulating the Rac1 signal transduction pathway in SK-MEL-28 melanoma cells [158] (Figure 5).

Recently, Akt3 has been reported to phosphorylate V600EB-Raf on S364 and/or S428 to reduce its activity to levels that promote rather than inhibit melanoma development from melanocytes [46]. Ectopic expression of V600EB-Raf in primary cell lines such as melanocytes has been shown to induce cellular senescence not only by elevating the levels of MAPK activity for unusually longer periods but also by upregulating the expression of cyclin-dependent kinase (cdk) inhibitors [159, 160]. Therefore, genetic changes such as loss of tumor suppressor genes (PTEN, p53 or p16INK4A) or upregulation of cooperating oncogenes is necessary to progress into advanced metastatic stages [161]. For example, activation of Akt3 has been demonstrated to facilitate the progression of quiescent melanocytic nevi into aggressive vertical and metastatic stages by inhibiting V600EB-Raf activity thereby releasing cells from a senescence block [46, 162]. This demonstrates that in melanomas, Akt3 kinase not only increases cell survival but also aids early melanoma development [46]. Likewise, a recent study demonstrated the induction of melanomas only when PTEN is silenced [47]. Using a conditional mouse model it has been demonstrated that V600EB-Raf induction resulted in the development of melanocytic hyperplasias, which failed to progress into melanomas [47]. However, when the PTEN gene was silenced while maintaining the expression of V600EB-Raf, melanocytic hyperplasias progressed into melanomas with 100% penetrance, short latency, and metastatic ability [47].

PRAS40 is another substrate regulated by Akt3. PRAS40 is a cytosolic protein found ubiquitously in all eukaryotes [118] and is phosphorylated by Akt at T246 [118]. Phosphorylated PRAS40T246 protects neuronal cells from ischemic injury by inhibiting caspase-3-mediated apoptotic cell death [163]. Expression of pPRAS40 levels are also associated with tumor malignancy [164]. Compared to paired control normal cells, cancer cell lines (MCF10A/MCF7, BEAS/H1170) exhibited high pPRAS40 expression [164]. However, the detailed functional characterization, in vitro and in vivo, was not reported. Compared to normal melanocyte controls, 43 to 60% of flash frozen tumors collected from melanoma patients express high pPRAS40 and pAkt [21]. Furthermore, targeted inhibition of PRAS40 using siRNA reduced melanoma tumor growth in xenografted melanoma studies (Figure 8) [21]. Mechanistically, PRAS40 inhibition induced caspase-3/7-mediated apoptosis in melanoma cells and increased sensitivity to apoptosis inducers such as staurosporine [21]. However, the molecular basis for caspase-3/7 activity inhibition by pPRAS40 in melanomas remains unknown.

(a)

(b)

Figure 8: Akt3 and downstream PRAS40 are the key regulators of melanoma cell survival. SiRNA-mediated downregulation of Akt3 and PRAS40 induced apoptosis in subcutaneous melanoma tumors. Shown are the representative pictures of TUNEL assay performed on size- and time-matched tumors. The bar graph shows the percentage TUNEL positive cells in the tumors [21].

Recent reports have demonstrated that PRAS40 is a physiological target of mTORC1 kinase and regulates its activity by functioning as a direct inhibitor of substrate binding [119, 165, 166]. PRAS40 has two additional phosphorylation sites S183 and S221 other than the one phosphorylated by Akt [167]. A recent study demonstrated that phosphorylation of T246 by Akt facilitates the phosphorylation of S183 and S221 by mTORC1 [167]. 14-3-3 proteins via physical interactions sequester phosphorylated PRAS40 thereby release mTOR. Therefore, increased pPRAS40T246 may releasing its inhibitory effects on mTORC1 kinase and downregulate caspase-3/7 activity. Although phosphorylation of PRAS40 at threonine 246 by Akt is primarily involved in inhibiting cellular apoptosis and increasing survival, the role of unphosphorylated PRAS40 in the cancer cells needs further investigation.

Another well-known substrate of Akt is GSK3 [6, 117], which is present in cells as two structurally similar GSK3α and GSK3β isoforms [168]. Akt has been shown to phosphorylate S9 of GSK3β and S21 of GSK3α to inhibit their activity thereby promoting cell proliferation by stabilizing cyclin-D1 protein [29, 117]. Therefore, unphosphorylated active GSK3 is considered as an apoptosis inducing tumor suppressor. However, recent studies have shown that GSK3 expression is elevated in advanced cancers and deregulation of GSK3 activity increases malignant transformation of cells [168–171]. Recently it has been observed that inhibition of GSK3β enhances sorafenib-induced apoptosis in melanoma cells [172]. Furthermore, targeting GSK3β using organometallic inhibitors (DW1/2) decreased Mdm2 activity thereby elevating p53-mediated apoptosis in melanoma cell lines expressing wild-type p53 protein [173]. Finally, GSK3α and not GSK3β has been shown to regulate pancreatic cell survival [174]. However, similar studies have not been reported in melanomas. Therefore, identifying the actual isoform regulating melanoma development by selectively inhibiting these isoforms using siRNA is warranted. Furthermore, studies are also warranted to demonstrate which isoform is expressed in melanoma patient tumors in order to establish its clinical relevance.

4. Clinical Implications of Targeting the PI3k-Akt3 Signaling Cascade in Melanomas

Targeting PI3K-Akt3 signaling has significant clinical potential for inhibiting melanoma tumor development [23]. For example, introduction of PTEN into melanoma cells or inhibiting Akt3 using siRNA or small molecule inhibitors such as ISC-4 inhibited melanoma tumors growth in vitro and in animals [175, 176]. Furthermore, expression of PTEN or reduction of Akt3 activity has been found to increase melanoma cell sensitivity to apoptotic stimuli that occurs with most chemotherapeutic agents [9, 21, 176].

4.1. PTEN Reexpression Prevents Melanoma Development

Tumor suppressor PTEN has been demonstrated to inhibit melanoma development in cultured cells and in spontaneous melanoma models [9, 21, 47]. For example, introduction of PTEN into advanced-stage melanoma cells via a chromosomal transfer or ectopic expression using a plasmid-based vector inhibited tumor development in xenografted melanoma models [8, 15, 177]. Thus, targeted delivery of PTEN into melanoma cells has potential to be an effective therapeutic agent. Restoration of functional PTEN in these cells would increase the therapeutic efficacy of antimelanoma agents [8, 9, 21]. For example, isogenic cell lines expressing PTEN containing low pAkt are sensitive to staurosporine-induced apoptotic cell death, whereas cell lines that lost PTEN are resistant to therapeutic agents [8, 9, 21] (Figures 1 and 2). Furthermore, if PTEN expression was regulated by endogenous microRNAs, inhibiting using antimers could significantly upregulate PTEN activity thereby restoring the chemosensitivity of the melanoma cells. However, PTEN regulation by microRNAs has not yet been reported in melanomas.

4.2. Therapeutic Agents Targeting PI3K and Akt3 Signaling Cascades in Melanoma

Targeting Akt3 alone or in combination inhibits growth by inducing apoptosis, decreasing survival, and inhibiting proliferation of melanoma cells [5, 9, 21]. Several synthetic and naturally occurring small molecule inhibitors specifically inhibiting Akt activity have been developed and efficacy tested for inhibiting melanoma development in cultured cells and xenografted animal models [6, 9, 21, 46, 122, 151, 176, 178]. For example, isoselenocyanate ISC-4 has been demonstrated to inhibit early melanocytic lesions and advanced xenografted melanoma tumors in animals [122]. Compared to known inhibitors of Akt signaling such as API-2, the selenium containing ISC-4 appears to be more effective for melanoma treatment [122]. BI-69A11 is another Akt inhibitor, demonstrated to effectively inhibit melanoma tumors [179]. However, clinical utility of these inhibitors for decreasing melanoma development has not been evaluated yet. Similarly, safety and efficacy of other inhibitors of PI3K-Akt signaling such as GSK690693 (developed by GlaxoSmithKline), a novel ATP-competitive inhibitor of Akt kinases [180] and SR13668 (developed by SRI international), an NCI approved Akt inhibitor [181, 182], also need to be tested in clinic.

Since the efficacy of a particular inhibitor in vitro or in preclinical animal models may not exactly reflect the potency of the compound in clinical trials, testing these new inhibitors in clinic is highly recommended. For example, perifosine, the alkylsphophocholine analogue, is found to be very effective (inhibiting growth of cancer cells at 0.2 to 0.3 μM concentration) in vitro and in animal models. However, a Phase-II study using perifosine in 18 previously untreated patients with metastatic melanoma demonstrated no objective response [183].

4.3. Targeting Multiple Pathways to Synergistically Treat Melanoma

Several lines of evidence now suggest that it might be required to target multiple signaling pathways to inhibit melanoma development. For example, a recent study shows that inhibiting V600EB-Raf using PLX-4720 induced resistance to apoptosis by activating Akt signaling [48, 149]. Furthermore, it is also now well established that targeting V600EB-Raf not only induces resistance to various therapeutic agents but also stimulates the activity of C-Raf and wt B-Raf signaling thereby triggering the formation of keratoacanthomas and basal cell carcinomas [7, 184]. Therefore, it is important to target multiple signaling cascades to inhibit melanoma development. However, it is not completely known which targets should be inhibited. Studies have provided some directions in this regard by showing synergistically acting melanoma tumor inhibition by simultaneously targeting PI3K/Akt3 and MAP kinase signaling pathways [32, 46, 151, 185–187]. For example (a) delivering siRNAs inhibiting Akt3 and V600EB-Raf synergistically inhibited melanoma tumor cells growth in culture or in xenografted melanoma tumors [46, 151] (Figures 9 and 10); (b) combining nanoliposomal ceramide with sorafenib synergistically reduced melanoma cell growth [188]; (c) pharmacological agents inhibiting MAPK (U0126, PD98059 and PD325901) and mTORC1 (using rapamycin) more effectively reduced melanoma cells growth compared to either of the agents tested singly [24, 189, 190]; (d) topical application of LY-294002 and U0126 in combination effectively decreased melanoma tumor incidence in the transgenic TPRas mouse model when compared to either of these agents alone [191]; (e) targeting PI3K and mTOR using dual inhibitors NVP-BBD130 and NVP-BEZ235 effectively reduced the size of primary melanoma tumors and inhibited cervical lymph node metastasis in a syngenic mouse melanoma model. Although these studies demonstrate the potential therapeutic efficacy of combined target inhibition, no complete tumor reduction occurred in any of these studies, warranting the identification of other candidates and target combinations for treating this disease.

Figure 9: Cotargeting Akt3 and V600EB-Raf inhibits melanoma cell proliferation in vitro. Two hundred picomoles of siRNA targeting Akt3 and increasing (3, 6, and 12 picomoles) amounts of siRNA inhibiting V600EB-Raf were introduced alone or in combination into UACC 903 melanoma cell line by Amaxa transfection and effect on anchorage independent growth ability measured using MTS assay. The data shows a dose-dependent inhibition of cell viability when Akt3 and V600EB-Raf were inhibited. However, maximal effect was observed only when Akt3 and V600EB-Raf targeted together, indicating the necessity of inhibiting multiple signaling cascades [46, 151].

Figure 10: Akt3 synergizes with V600EB-Raf in melanomas. UACC 903 cells transfected with siRNA targeting Akt3 and V600EB-Raf alone and in combination were subcutaneously injected into mice and effect on tumor development measured. Cotargeting these two key kinases inhibited melanoma development more effectively than inhibiting each of these kinases alone [46, 151].

Other key targets regulating melanoma development have been recently identified. For example, Yang et al. showed the effect conditional ablation of Ikkb on melanoma tumor development using an established HRasV12 mouse model of spontaneous melanoma [192]. Ink4a/Arf−/− mice with melanocyte-specific deletion of Ikkb were protected from HRasV12-initiated melanoma only when p53 was expressed. Ikkb ablation was found to decrease Aurora-A kinase and IL-6 in melanomas [192]. Therefore Ikkb and Aurora-A could be potential targets in melanomas [192]. However, it is not known whether targeting these pathways would synergize with Akt inhibition. In support of this direction of investigation, a recent study reported that Aurora-A regulates cancer cell survival by inducing Akt activity and inhibiting Aurora kinase with VX-680 synergizes with pharmacological inhibition of Akt (wortmannin) activity [193]. However, experimental evidence pertaining to which Aurora kinase isoform needs to be targeted for the greater synergistic effect is currently unknown.

It is fairly certain that both MAP and PI3 kinase pathways will need to be targeted for inhibiting melanoma. For example, hybrid compounds that inhibit these pathways such as HMBA (hexamethylene bisacetamide—HMBA), which simultaneously inhibits Akt and MAPK pathways and represses NFκB activity in breast cancer cell lines, needs to be tested in melanomas [194]. Similarly, recent studies have demonstrated the utility of a novel selenium containing iNOS inhibitor, called PBISe, for inhibiting melanoma cell growth in vitro and in vivo [195]. Intraperitoneally administered or topically applied PBISe inhibited iNOS and PI3K/Akt3 signaling thereby inducing significant apoptosis in melanoma cells. Furthermore, PBISe-mediated inhibition of Akt3 signaling induced cell senescence by upregulating pErk1/2 to inhibitory levels which triggered the induction of cell cycle inhibitors p21, p16, and p27 [196, 197]. Inhibitors targeting PI3K also have potential to inhibit melanoma growth [67]. For example, SF1126, a conjugate of LY294002 and a pan-PI3K inhibitor, developed by Semafore Pharmaceuticals, is currently in Phase-I clinical trial for solid tumors [198]. Other PI3K inhibitors that are under clinical investigation include GDC-0941, an inhibitor of p110α subunit developed by Genentech, Inc; and XL-147 and XL-765, developed by Exelixis [198]. However, it is not known whether these inhibitors could synergistically inhibit melanoma development when combined with agents inhibiting other key signaling cascades.

5. Conclusions

Activation of Akt3 is a key event regulating the development of melanomas. Enzymes involved in this signaling pathway regulate cell survival, proliferation, metastasis and are implicated in development of resistance to a variety of chemotherapeutic agents. Mechanisms regulating Akt3 phosphorylation such as loss of PTEN, and activation of PI3K signaling need to be further unraveled to aid in the design of novel therapeutic strategies for treating melanoma. Therefore, PI3K-Akt3 signaling remains an attractive target in melanomas. Although this review provides an overview of the PI3K-Akt signaling in melanomas, several aspects need further investigation. Several unanswered questions also remain pertaining to this key signaling cascade. For example, it is not known (a) which microRNAs are regulating Akt signaling in melanomas, (b) whether endogenous Akt3 is also regulating metastasis development in human melanomas, and (c) how Akt2 is regulating melanoma metastasis and whether targeting Akt2 alone could inhibit metastasis development? Addressing these questions might provide a better understanding of the role of Akt signaling in melanoma and help design more potent selective agents for targeting this disease.

Acknowledgment

Grant support from NIH CA-127892-01A, the Foreman Foundation for Melanoma Research (GPR), Melanoma Research Foundation (SVM) and the American Cancer Society are gratefully Acknowledged.

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