Oxidative Medicine and Cellular Longevity
Volume 2018 (2018), Article ID 2492063, 21 pages
https://doi.org/10.1155/2018/2492063

Review Article

Epigenetic versus Genetic Deregulation of the KEAP1/NRF2 Axis in Solid Tumors: Focus on Methylation and Noncoding RNAs

F. P. Fabrizio, A. Sparaneo, D. Trombetta, and L. A. Muscarella

Laboratory of Oncology, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy

Correspondence should be addressed to F. P. Fabrizio; federico_fabrizio@hotmail.it

Received 25 August 2017; Revised 20 November 2017; Accepted 4 December 2017; Published 13 March 2018

Academic Editor: Bhairab N. Singh

Copyright © 2018 F. P. Fabrizio et al. 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.

Oxidative and electrophilic changes in cells are mainly coordinated by the KEAP1/NRF2 (Kelch-like erythroid-derived cap-n-collar homology- (ECH-) associated protein-1/nuclear factor (erythroid-derived 2)-like 2) axis. The physical interaction between these two proteins promotes the expression of several antioxidant defense genes in response to exogenous and endogenous insults. Recent studies demonstrated that KEAP1/NRF2 axis dysfunction is also strongly related to tumor progression and chemo- and radiotherapy resistance of cancer cells. In solid tumors, the KEAP1/NRF2 system is constitutively activated by the loss of KEAP1 or gain of NFE2L2 functions that leads to its nuclear accumulation and enhances the transcription of many cytoprotective genes. In addition to point mutations, epigenetic abnormalities, as aberrant promoter methylation, and microRNA (miRNA) and long noncoding RNA (lncRNA) deregulation were reported as emerging mechanisms of KEAP1/NRF2 axis modulation. This review will summarize the current knowledge about the epigenetic mechanisms that deregulate the KEAP1/NRF2 cascade in solid tumors and their potential usefulness as prognostic and predictive molecular markers.

1. Introduction

Oncogenes and tumor suppressor genes are deregulated in cancer and modify their expression through heterogeneous genetic and epigenetic modifications. All these alterations exert their effects on several cellular processes in which transient modifications of redox balance might occur, such as cell cycle and apoptosis. These transient cellular changes are mainly coordinated by the KEAP1/NRF2 (Kelch-like erythroid-derived cap-n-collar homology- (ECH-) associated protein-1/nuclear factor (erythroid-derived 2)-like 2) signaling pathway [1]. NRF2 is a transcription factor that acts as a master modulator of cellular defense against toxic and oxidative damage, mitochondrial physiology, differentiation, and stem cell maintenance [2–4]. In normal cell conditions, the NRF2 negative regulator KEAP1 forms an ubiquitin ligase complex with cullin 3 (CUL3) and ring-box 1 (RBX1) and targets NRF2 for proteolysis. Upon stress exposure, a specific pattern of KEAP1 cysteine modification arises. By consequence, the KEAP1 releases NRF2 which translocates into the nucleus, where it forms a heterodimeric complex with the small MAF proteins. This complex recognizes the enhancer sequences known as antioxidant response elements (AREs) located in the cytoprotective genes and activates their transcription [5]. Additionally, NRF2 can be subjected to a KEAP1-independent transcriptional and posttranslational regulation, with a consequent alteration of its cellular localization, protein degradation, and DNA-binding capability [6].

Deregulation of the KEAP1/NRF2 axis is actually considered a hallmark in cancer cells, since KEAP1 and NRF2 can modulate oncogenesis, cell proliferation, apoptosis, and tumor cell growth [7].

A decreased levels of KEAP1 protein were firstly reported to be linked to poor outcome in NSCLC patients treated with platinum-based neoadjuvant regimen and in the NSCLC group of patients with lymph node metastases [8, 9].

Actually, the main molecular events that lead to NRF2 abnormal nuclear accumulation in solid tumors can be generally divided into genetic and epigenetic alterations. The final effect is in any case the disruption of protein-protein interaction of the KEAP1/NRF2 crosstalk and its imbalance in expression levels, with a consequent upregulation of cellular detoxifying proteins.

Genetic alterations were the first reported mechanisms of KEAP1/NRF2 axis deregulation. Biallelic changes of the tumor suppressor KEAP1 gene (by point mutations and loss of heterozygosity) were described for the first time in NSCLC [10] and, immediately after, in other several malignancies together with NFE2L2 mutations, the gene that codifies for the NRF2 protein [11]. More recently, the discovery of hypermethylation of the KEAP1 promoter and noncoding RNAs linked to cell-detoxifying network added a new important dimension in the complex regulation of the KEAP1/NRF2 system (Figure 1) [12].

Figure 1: Overview of the main genetic and epigenetic modifications that lead to KEAP1-NFE2L2 impairment and constitutive NRF2 nuclear accumulation in cancer cells. NFE2L2 gene copy number variations (CNV), oncogene activity (KRAS, BRAF, MYC, and PTEN), DNA promoter methylation, and miRNAs contribute in a synergic manner to increase cancerous NRF2 activity as a result of reduction of KEAP1 mRNA or increase of NRF2 mRNA levels and/or protein expression. By contrast, somatic point gain-of-function mutations in NFE2L2 or in loss-of-function in KEAP1 promote the disruption of the interaction between KEAP1 and NRF2 and lead the increase of NRF2 protein quantity which translocates into the nucleus.

This minireview describes the recent updates about the deregulation mechanisms of the KEAP1/NRF2 pathway, with a particular focus on the epigenetic modulation of KEAP1 and NFE2L2 and their cellular significance and potential impact on cancer patient management.

2. The Genetic Deregulation of Keap1/Nrf2 Signaling and Its Translational Impact in Solid Tumors

Among the genetic lesions that affect the KEAP1/NRF2 activity, point mutations are the most frequently investigated ones in solid tumors. They commonly occur in the exonic regions that codify for the KEAP1 and NRF2 interaction sites (the Kelch/DGR domain of KEAP1 and the Neh2 domain of NRF2) and induce a general failure of the ubiquitination process led by the KEAP1 (Figure 2).

(a)

(b)

Figure 2: Domain architecture of the NRF2 (a) and KEAP1 (b) proteins. (a) NRF2 protein is divided into seven highly conserved domains, Neh1 to Neh7 (NRF2-ECH homology: Neh). The coordinates of NRF2 protein domains are shown as follows: Neh2 (16-89aa); Neh2 DLG motif (17-32aa), Neh2 ETGE motif (77-82aa), Neh4 (111-134aa), Neh5 (182-209aa), Neh7 (209-316aa), Neh6 (337-394aa), Neh1 (435-568aa), and Neh3 (569-605aa). (b) KEAP1 protein contains a number of functional domains including the N-terminal region (NTR; 1-60aa), broad complex, tramtrack and bric-a-brac (BTB; 61-179aa), the intervening linker domain (IVR; 180-314aa), the double glycine/Kelch domain harboring six Kelch-repeat domains (315-359aa; 361-410aa; 412-457aa; 459-504aa; 506-551aa; 553-598aa), and the C-terminal region (CTR; 599-624aa).

By consequence, the NRF2 escapes from proteasomal degradation and increases the ARE-target gene expression with an enhancement of the antioxidant defense system and chemo- and radioresistance of cancer cells [13, 14]. Moreover, since the KEAP1 is able to negatively modulate the BCL-2 and p62 degradation, the KEAP1 point mutations also lead to an accumulation of these proteins with a general deregulation of apoptosis, autophagy, and inflammation [15, 16].

Loss-of-function mutations of the human KEAP1 gene have been firstly reported in NSCLC with a prevalence of about 20–25%. These mutations were frequently observed in the lung papillary subtype and in TTF-1 negative lung adenocarcinoma [10, 17, 18]. Moreover, KEAP1 point mutations were identified in several human cancers such as gastric (11.1%), liver (2–8%), colorectal (7.8%), prostate (1.3%), gallbladder (30.7%), ovarian (37%), glioma (1.7%), head and neck (42%), and clear renal cell carcinoma (4.7%) [19–29]. More recently, Fernandez-Cuesta et al. and Derks reported KEAP1 genetic alterations as a new uncovered molecular hallmark of LCNEC (lung cancer neuroendocrine) with adenocarcinoma-like features [30, 31]. This last finding was also confirmed by a different group which reported a prevalence of KEAP1-NFE2L2 (31%) alterations in tumors with high neuroendocrine gene expression, mainly cooccurrent with gene mutations [4, 32, 33].

Gain-of-function NFE2L2 mutations are generally mutually exclusive with respect to KEAP1 mutations and are frequently located into the DLG or ETGE motifs. NFE2L2 point mutations were identified in several tumors with squamous histological features, such as esophageal, skin, lung, and laryngeal carcinomas. An increased NFE2L2 gene copy number was also described in lung squamous cell carcinoma. An increased NFE2L2 gene copy number was also described in lung squamous cell carcinoma. All of these mutations are generally missense changes that interfere with the KEAP1 ability to bind to NRF2, thus inducing an escape of NRF2 degradation without changing its gene functionality [34–37]. Somatic lesions linked to KEAP1/NRF2 axis deregulation were also reported in the CUL3 gene, the component of the E3 ligase complex KEAP1/CUL3/RBX1 that marks NRF2 for proteasomal degradation [7, 38]. Mutations in CUL3, together with those in NFE2L2, are frequent in hereditary type 2 papillary renal cell carcinoma (PRCC2). In squamous carcinoma of the head and neck, somatic lesions of CUL3/NFE2L2/KEAP1 have a prevalence of 64% and were associated with a lower patient overall survival (Tables 1 and 2) [25, 39–41].

Table 1: Functionally investigated KEAP1 gene mutations in tumor tissues and cell lines.

Cancer tissue or cell line types
Nucleotide change
Amino acid change
Mutation type/clinical prediction
Protein domain
Functional effects of KEAP1 mutant

Breast cell line and ductal carcinoma
c.68G>A
p.C23Y
Missense/pathogenic
NTR
Repression of NRF2-dependent transcription activity and ubiquitination defects

Lung AC, lung SCC
c.212G>T
p.R71L
Missense/pathogenic
BTB
Wild-type behavior

Stomach AC
c.246G>T
p.Q82H
Missense/pathogenic
BTB
Impaired effect on NRF2 pathway activation

EOC
c.319T>C
p.F107L
Missense/pathogenic
BTB
Enhance the NRF2 nuclear localization and its transcription activity

BUC, EOC
c.347G>C
p.R116P
Missense/pathogenic
BTB
Enhance the NRF2 nuclear localization and its transcription activity

Lung AC, lung SCC
c.463G>T
p.V155F
Missense/pathogenic
BTB
Enhance the binding of KEAP1 to NRF2 and facilitate NRF2 ubiquitination

EOC
c.475G>A
p.A159T
Missense/pathogenic
BTB
Enhance the NRF2 nuclear localization and its transcription activity

Lung AC, lung SCC
c.499G>T
p.V167F
Missense/pathogenic
BTB
Weakly affect the bind of KEAP1 to NRF2 without suppressing the NRF2 activity

BTC
c.543_544insC
p.S181fs∗11
Frameshift/NS
IVR
Induce the loss of KEAP1 repression activity on NRF2

HCC
c.548A>G
p.N183S
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Lung AC
c.556G>C
p.G186R
Missense/pathogenic
IVR
Induce an enhanced binding of KEAP1 to NRF2 and facilitate its ubiquitination without suppressing NRF2-mediated transcription

EOC
c.563C>T
p.A188V
Missense/pathogenic
IVR
Enhance activation of NRF2 pathway and an increase of its transcriptional activity and nuclear localization

Lung AC
c.599A>C
p.H200P
Missense/pathogenic
IVR
Wild-type behavior

Lung SCC
c.671C>A
p.S224Y
Missense/pathogenic
IVR
Wild-type behavior

Lung SCC
c.691C>G
p.L231V
Missense/pathogenic
IVR
Wild-type behavior

Stomach AC
c.698G>A
p.S233N
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

CESC, colorectal AC
c.700C>T
p.R234W
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Lung AC
c.706G>C
p.D236H
Missense/pathogenic
IVR
Reduce KEAP1-mediated repression of NRF2

Lung SCC, liver
c.706G>T
p.D236Y
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Lung AC
c.711delG
p.L237fs∗1
Frameshift (stop codon)/NS
IVR
Reduce KEAP1-mediated repression of NRF2

Lung AC
c.724G>A
p.E242K
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Lung SCC
c.728C>G
p.S243C
Missense/pathogenic
IVR
Induce an enhanced binding of KEAP1 to NRF2 and facilitate its ubiquitination without suppressing NRF2-mediated transcription

BUC, lung AC
c.730G>A
p.E244K
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

BTC, stomach
c.746G>A
p.C249Y
Missense/pathogenic
IVR
Mutant KEAP1 fails to repress NRF2-dependent transactivation

Breast AC
c.767A>G
p.D256G
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

PF
c.790G>A
p.V264I
Missense/pathogenic
IVR
Reduce KEAP1-mediated repression of NRF2

Lung AC
c.814C>T
p.R272C
Missense/pathogenic
IVR
Reduce KEAP1-mediated repression of NRF2 (impaired Nrf2 degradation)

Stomach AC
c.838T>C
p.F280L
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Stomach AC
c.842T>C
p.L281P
Missense/pathogenic
IVR
Induce an impaired binding of KEAP1 to the CUL3 ubiquitin ligase

Lung AC, lung LCC
c.851A>T
p.Q284L
Missense/pathogenic
IVR
Reduce KEAP1-mediated repression of NRF2

Stomach AC
c.863G>A
p.C288Y
Missense/pathogenic
IVR
Induce and impair binding of KEAP1 to NRF2 and facilitate NRF2 ubiquitination and its degradation

Lung AC, liver
c.880G>T
p.D294Y
Missense/pathogenic
IVR
Lead to deleterious effect on protein stability

Lung SCC
c.953C>T
p.P318L
Missense/pathogenic
KELCH1
Wild-type behavior

Lung SCC
c.?
p.P318_fs
Frameshift/NS
KELCH1
Impact on the KEAP1-NRF2 association and NRF2 degradation

EOC
c.1234C>T
p.P319S
Missense/NS
KELCH1
Enhance activation of NRF2 pathway and an increase of its transcriptional activity and nuclear localization

Lung SCC
c.959G>A
p.R320Q
Missense/pathogenic
KELCH1
Induce an enhanced binding of KEAP1 to NRF2 and facilitate its ubiquitination without suppressing NRF2-mediated transcription

Lung AC, lung SCC
c.965C>T
p.P322L
Missense/pathogenic
KELCH1
Lead to deleterious effects on KEAP1 protein stability

Colorectal AC
c.989C>T
p.T330I
Missense/pathogenic
KELCH1
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Lung AC
c.994G>T
p.G332C
Missense/pathogenic
KELCH1
Induce an enhancement of the NRF2 activity

Gallbladder
c.996_996delC
p.G332fs∗67
Frameshift/NS
KELCH1
Lead a loss of NRF2 repression by KEAP1

Lung AC
c.997G>T
p.G333C
Missense/pathogenic
KELCH1
Induce misfolding effects and decrease the KEAP1 stability and capability to bind NRF2

Lung
c.1001>T
p.Y334F
Missense/NS
KELCH1
Disrupt the integrity of the Kelch domain of KEAP1

HCC
c.1007G>A
p.R336Q
Missense/pathogenic
KELCH1
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Gallbladder AC, breast AC
c.1013C>T
p.S338L
Missense/pathogenic
KELCH1
Mutant KEAP1 fails to repress NRF2-dependent transactivation

HCC
c.1024C>A
p.L342M
Missense/pathogenic
KELCH1
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Lung AC
c.1036InsT
p.S346_fs
Frameshift (stop codon)/pathogenic
KELCH1
Lead to a premature termination and truncated KEAP1 protein

PF
c.1043insG
p.348_fs
Frameshift (stop codon)/NS
KELCH1
Result in a frameshift and produce a truncated KEAP1 protein, with a lower KEAP1-mediated repression of NRF2

Lung AC, stomach cell lines
c.1048G>A
p.G350S
Missense/NS
KELCH1
Reduce KEAP1-mediated repression of NRF2

Prostate
c.1069G>A
p.D357N
Missense/pathogenic
KELCH1
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Colorectal AC
c.1075C>T
p.Q359X
Nonsense/pathogenic
KELCH1
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Lung AC samples and cell lines
c.1090G>T
p.G364C
Missense/pathogenic
KELCH2
Abolish the KEAP1-NRF2 interaction

Lung AC
c.GCC1098TTA
p.L367_fs
Frameshift/pathogenic
KELCH2
Produce a truncated KEAP1 protein

Lung AC
c.1106T>C
p.V369A
Missense/pathogenic
KELCH2
Lead to deleterious effects on KEAP1 protein stability

Gallbladder AC, HCC
c.1136G>A
p.G379D
Missense/pathogenic
KELCH2
Mutant KEAP1 fails to repress NRF2-dependent transactivation. Induce a misfolding effects on the KEAP1 protein and decrease its ability to bind NRF2

Lung AC
c.1238G>T
p.L413R
Missense/pathogenic
KELCH3
Mutant KEAP1 fails to repress NRF2-dependent transactivation. Induce misfolding effects on the KEAP1 protein and decrease its ability to bind NRF2

Lung AC
c.DelGG?
p.L413_fs
Frameshift (stop codon)/NS
KELCH3
Reduce KEAP1-mediated repression of NRF2

Lung AC
c.1243C>G
p.R415G
Missense/pathogenic
KELCH3
Affect the ability of KEAP1 to repress NRF2 and lost the ability to bind and sequester NRF2 in the cytoplasm

Lung SCC, ESCC
c.1264G>A
p.D422N
Missense/pathogenic
KELCH3
Enhance the binding of KEAP1 to NRF2 and facilitate NRF2 ubiquitination

Lung AC, lung SCC
c.1268G>T
p.G423V
Missense/pathogenic
KELCH3
Enhance the binding of KEAP1 to NRF2 and facilitate NRF2 ubiquitination

Lung AC
c.1280C>T
p.A427V
Missense/pathogenic
KELCH3
Reduce KEAP1-mediated NRF2 repression ability but Kelch domain should still be able to interact effectively with the ETGE and the DLG sites of NRF2

Lung AC
c.1288G>T
p.G430C
Missense/pathogenic
KELCH3
Induce a misfolding effect on the KEAP1 protein and decrease its ability to bind NRF2 and sequester NRF2 in the cytoplasm.

Lung AC cell line
c.1329T>G
p.Y443_fs
Frameshift (stop codon)/NS
KELCH3
Reduce KEAP1-mediated repression of NRF2

Lung AC
c.1370delG
p.L457fs∗1
Frameshift (stop codon)/NS
KELCH3
Result in a frameshift and produce a truncated KEAP1 protein, with a lower KEAP1-mediated repression of NRF2

Lung AC
c.1396G>C
p.A466P
Missense/pathogenic
KELCH4
Lead to deleterious effects on KEAP1 protein stability

Lung SCC
c.?
p.N469fs
Frameshift/NS
KELCH4
Impact on the KEAP1-NRF2 association and the KEAP1 ability to suppress NRF2

Lung AC, lung SCC, ESCC, UADT
c.1408C>T
p.R470C
Missense/pathogenic
KELCH4
Exhibit enhanced binding to NRF2 and facilitate NRF2 ubiquitination

Lung LCC
c.1426G>A
p.G476R
Missense/NS
KELCH4
Induce a misfolding effect on the KEAP1 protein and decrease its ability to bind NRF2 and sequester NRF2 in the cytoplasm.

Lung SCC
c.1438G>T
p.G480W
Missense/pathogenic
KELCH4
Reduce the KEAP1-NRF2 binding

Lung AC
c.1448G>A
p.R483H
Missense/pathogenic
KELCH4
Reduce the KEAP1-NRF2 binding

Lung AC
c.1477G>C
p.E493Q
Missense/pathogenic
KELCH4
Induce an upregulation of the NRF2 activity

Lung SCC
c.1632G>T
p.W544C
Missense/pathogenic
KELCH5
Reduce the KEAP1-NRF2 binding

Liver, lung AC
c.1661G>A
p.R554Q
Missense/pathogenic
KELCH6
Reduce the KEAP1-NRF2 binding

Liver
c.1662G>A
p.W554X
Missense/pathogenic
KELCH6
Decrease the NRF2 repression activity

PF
c.1663_1680del18
p.S555_T560del
In frame/NS
KELCH6
Reduce KEAP1-mediated repression of NRF2

Lung AC
c.1709G>T
p.G570V
Missense/pathogenic
KELCH6
Reduce the KEAP1-NRF2 binding

Lung AC
c.1772G>T
p.W591L
Missense/pathogenic
KELCH6
Impair the KEAP1 binding to NRF2 through the KEAP1 DC pocket (lower affinity)

Colorectal AC
c.1816G>A
p.V606M
Missense/pathogenic
CTR
Induce an upregulation of the NRF2 activity

EOC
c.1831G>A
p.E611K
Missense/pathogenic
CTR
Enhance activation of NRF2 pathway and an increase of its transcriptional activity and nuclear localization

Cosmic (Catalogue of Somatic Mutations in Cancer) database IP (http://cancer.sanger.ac.uk/cosmic/gene/analysis?ln=KEAP1#variants). AC: adenocarcinoma; BUC: bladder urothelial carcinoma; CESC: cervical squamous cell carcinoma; DC: C-terminal β-propeller domain; EOC: epithelial ovarian cancer; ESCC: esophageal squamous cell carcinoma; HCC: hepatocellular carcinoma; LCC: large cell carcinoma; PF: pleural fluid; SCC: squamous cell carcinoma; UADT: upper aerodigestive tract; NS: not specified.

Table 2: Functional investigated NFE2L2 gene mutations in tumor tissues and cell lines.

Cancer tissue or cell line types
Nucleotide change
Amino acid change
Mutation type/clinical prediction
Protein domain
Functional effects of NFE2L2 mutant

HCC
c.68T>G
p.L23R
Missense/pathogenic
Neh2 DLG
Disrupt the intramolecular interactions for KEAP1-DLGex binding and are associated with the strongest increase of NRF2 activity

PRCC, ESCC
c.70T>C
p.W24R
Missense/pathogenic
Neh2 DLG
NFE2L2 mutant with gain-of-function activity, which is partly resistant to KEAP1-mediated inhibition

Lung SCC, SCLC, ESCC
c.72G>C
p.W24C
Missense/pathogenic
Neh2 DLG
Affect the binding to the KEAP1 dimer and inhibit the KEAP1-mediated degradation of NRF2 and a stronger increase of the NRF2 activity

ESCC
c.76C>G
p.Q26E
Missense/pathogenic
Neh2 DLG
NFE2L2 mutant with gain-of-function activity, which is partly resistant to KEAP1-mediated inhibition

Lung SCC
c.77A>T
p.Q26L
Missense/pathogenic
Neh2 DLG
Only present in TCGA report

Lung SCC
c.77A>C
p.Q26P
Missense/pathogenic
Neh2 DLG
Only present in TCGA report

HCC
c.78A>C
p.Q26H
Missense/pathogenic
Neh2 DLG
Lead to an activation of NRF2 signaling

Lung SCC
c.79G>C
p.D27H
Missense/pathogenic
Neh2 DLG
Only present in TCGA report

ESCC
c.79G>T
p.D27Y
Missense/pathogenic
Neh2 DLG
Block proper KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

Lung SCC, ESCC
c.83T>C
p.I28T
Missense/pathogenic
Neh2 DLG
Lead to weaker KEAP1-binding DLG region and inhibit the KEAP1-mediated degradation of NRF2

HCC, lung AC, SCC-UADT
c.85G>C
p.D29H
Missense/pathogenic
Neh2 DLG
Lead and increase NRF2 levels

Lung SCC
c.85G>A
p.D29N
Missense/pathogenic
Neh2 DLG
Inhibit the KEAP1-mediated degradation of NRF2, resulting in a stabilization and a nuclear accumulation of NRF2

Cervix SCC, PRCC, lung AC, lung SCC
c.85G>T
p.D29Y
Missense/pathogenic
Neh2 DLG
Lead to a constitutive activation of NRF2 at E3 ligase recognition sites

HCC, lung SCC, ESCC, SCC-UADT
c.86A>G
p.D29G
Missense/pathogenic
Neh2 DLG
Lead to weaker KEAP1-binding DLG region and inhibit the KEAP1-mediated degradation of NRF2

ccRCC
c.86A>T
p.D29V
Missense/pathogenic
Neh2 DLG
Lead to a constitutive activation of NRF2 at E3 ligase recognition sites

Liver, lung SCC, ESCC, skin, SCC-UADT
c.88C>T
p.L30F
Missense/pathogenic
Neh2 DLG
Affect the binding ability of NRF2 to the KEAP1 dimer with a lower NRF2 ubiquitination and an enhancement of its transcriptional activity into the nucleus

EEA
c.89T>G
p.L30R
Missense/pathogenic
Neh2 DLG
Disrupt the KEAP1/NRF2 interaction due to lack of binding of NRF2 to Kelch domain of KEAP1

Central nervous system
c.91G>A
p.G31R
Missense/pathogenic
Neh2 DLG
Gain-of-function mutation with an increased NRF2 stabilization

ccRCC, lung SCC, ESCC, skin SCC
c.92G>C
p.G31A
Missense/pathogenic
Neh2 DLG
NFE2L2 mutant with a gain-of-function activity, which is partly resistant to KEAP1-mediated inhibition

ESCC
c.92G>A
p.G31E
Missense/pathogenic
Neh2 DLG
Affect the binding ability of NRF2 to interact with the Kelch domain of KEAP1

SCC-UADT, skin SCC
c.93_95delAGT
p.V32del
In frame/NS
Neh2 DLG
Lead to weaker KEAP1-binding DLG region and inhibit the KEAP1-mediated degradation of NRF2

HCC
c.95T>A
p.V32E
Missense/pathogenic
Neh2 DLG
Mutational target that leads to its aberrant activation

Lung SCC
c.95T>G
p.V32G
Missense/pathogenic
Neh2 DLG
Lead to weaker KEAP1-binding DLG region and inhibit the KEAP1-mediated degradation of NRF2

EEA, lung SCC
c.100C>G
p.R34G
Missense/pathogenic
Neh2
Inhibit the KEAP1-mediated degradation of NRF2, resulting in an increase of its stabilization and nuclear accumulation

Lung SCC, ESCC
c.101G>C
p.R34P
Missense/pathogenic
Neh2
Lead to a constitutive activation of NRF2 at E3 ligase recognition sites

Cervix SCC, lung SCC, ESCC, SCC-UADT
c.101G>A
p.R34Q
Missense/pathogenic
Neh2
Lead to weaker KEAP1-binding DLG region and inhibit the KEAP1-mediated degradation of NRF2

PRCC
c.105_107delAGT
p.V36del
In frame/NS
Neh2
NFE2L2 mutant is insensitive to KEAP1-mediated degradation (NFE2L2 mutant is stable even with ectopic expression of KEAP1 occurs)

ESCC, UADT
c.225A>C
p.Q75H
Missense/pathogenic
Neh2
Impair two-site substrate of KEAP1 recognition and inhibit the KEAP1-mediated degradation of NRF2

SCC-UADT
c.229G>A
p.D77N
Missense/pathogenic
Neh2 ETGE
Block the KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

Liver
c.229G>T
p.D77Y
Missense/pathogenic
Neh2 ETGE
Affect the NRF2 binding to Kelch domain surface of the KEAP1

Lung SCC
c.230A>C
p.D77A
Missense/pathogenic
Neh2 ETGE
Block the KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

HCC, lung SCC, ESCC
c.230A>G
p.D77G
Missense/pathogenic
Neh2 ETGE
NFE2L2 mutant with a gain-of-function activity, partly resistant to the KEAP1-mediated inhibition

Lung SCC,ESCC
c.230A>T
p.D77V
Missense/pathogenic
Neh2 ETGE
Compromise the association of NRF2 with KEAP1-DC and inhibit the KEAP1-mediated degradation of NRF2

ESCC
c.232G>A
p.E78K
Missense/pathogenic
Neh2 ETGE
NFE2L2 mutant with gain-of-function activity, which is partly resistant to the KEAP1-mediated inhibition

Lung SCC, ESCC
c.235G>A
p.E79K
Missense/pathogenic
Neh2 ETGE
Reduce the ability of NRF2 to interact with KEAP1 and inhibit the KEAP1-mediated degradation of NRF2, thus promoting the nuclear localization and transcriptional activity of NRF2

Cervix SCC, lung AC, lung SCC, SCC-UADT
c.235G>C
p.E79Q
Missense/pathogenic
Neh2 ETGE
Compromise the association of NRF2 with KEAP1-DC and inhibit the KEAP1-mediated degradation of NRF2

HCC, SCC-UADT
c.236A>G
p.E79G
Missense/pathogenic
Neh2 ETGE
Block the KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

HCC, ESCC
c.238A>C
p.T80P
Missense/pathogenic
Neh2 ETGE
NFE2L2 mutant with a gain-of-function activity, partly resistant to the KEAP1-mediated inhibition

HCC, UADT
c.239C>T
p.T80I
Missense/pathogenic
Neh2 ETGE
Impair the two-site substrate recognition of KEAP1 and inhibit KEAP1-mediated degradation of NRF2

Lung SCC
c.239C>G
p.T80R
Missense/pathogenic
Neh2 ETGE
Reduce the ability of NRF2 to interact with KEAP1

PRCC, lung SCC, ESCC
c.239C>A
p.T80K
Missense/pathogenic
Neh2 ETGE
Compromise the association of NRF2 with KEAP1-DC. Also inhibit KEAP1-mediated degradation of NRF2 and promote nuclear localization and transcriptional activity of NRF2

HCC, lung SCC
c.241G>A
p.G81S
Missense/pathogenic
Neh2 ETGE
NFE2L2 mutant with gain-of-function activity, with an increased NRF2 stabilization due to alteration of the binding ability to KEAP1

Breast, lung AC, lung SCC, ESCC
c.242G>A
p.G81D
Missense/pathogenic
Neh2 ETGE
NFE2L2 mutant with a gain-of-function activity, partly resistant to the KEAP1-mediated inhibition

HCC, lung SCC, ESCC
c.242G>T
p.G81V
Missense/pathogenic
Neh2 ETGE
Block the KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

HCC, lung AC, lung SCC, ESCC
c.244G>C
p.E82Q
Missense/pathogenic
Neh2 ETGE
Block the KEAP1-NRF2 binding and inhibit the KEAP1-mediated degradation of NRF2

PRCC, HCC, lung SCC, UADT
c.245A>G
p.E82G
Missense/pathogenic
Neh2 ETGE
Stabilize NRF2 by disrupting its ability to bind KEAP1 although the NRF2 transcriptional activity remains unchanged

ESCC
c.245A>T
p.E82V
Missense/pathogenic
Neh2 ETGE
Affect the repressive activity of KEAP1 on NRF2 signaling

HCC, lung AC, ESCC
c.246A>C
p.E82D
Missense/pathogenic
Neh2 ETGE
Impair the two-site substrate recognition of KEAP1 and inhibit KEAP1-mediated degradation of NRF2

Cosmic (Catalogue of Somatic Mutations in Cancer) database IP (http://cancer.sanger.ac.uk/cosmic/gene/analysis?ln=NFE2L2#variants). AC: adenocarcinoma; ccRCC: clear cell renal cell carcinoma; DC: C-terminal β-propeller domain; DLGex: extended DLG motif; EEA: endometrioid endometrial adenocarcinoma; ESCC: esophageal squamous cell carcinoma; HCC: hepatocellular carcinoma; PRCC: papillary renal cell carcinoma; SCC: squamous cell carcinoma; SCLC: small cell lung cancer; UADT: upper aerodigestive tract; NS: not specified.

Dysfunction of the KEAP1/NRF2 axis by genetic mutations is gradually becoming a milestone to understand cancer development, progression, and resistance to conventional and biological treatments [42]. It is now well known that loss-of-function mutations of the KEAP1 gene or gain-of-function mutations in NFE2L2 enhance the resistance of cancer cells to anticancer drugs, such as etoposide and carboplatin, and it is associated with poor outcome of platinum-based advanced NSCLC patients [43]. Nuclear accumulation of NRF2 was also correlated with a poor survival of lung SqCC and pancreatic adenocarcinomas and a worse progression free survival (PFS) in patients treated with surgery only [44–47]. Aberrant NRF2 activation due to KEAP1 alterations is also reported as one of the molecular mechanisms of chemoresistance of gallbladder cancer under 5-FU-based regimen and of colorectal cancer under demethylase and methyltransferase treatments [20, 48, 49].

Jeong and coworkers suggested a new role for KEAP1 and NFE2L2 mutations in radiotherapy resistance of NSCLC patients and in identifying patients who might benefit from radiation dose escalation [50]. Knockdown experiments reported that radiochemosensitization was led by CDK20 that competes with NRF2 for KEAP1 binding and induces nuclear translocation of NRF2 and the enhancement of its transcriptional activity. This ultimately results in proliferation defects and provides new insights into the cellular response to NRF2-mediated DNA damage [51].

An interesting link between the KEAP1/NRF2 axis and target therapies was recently reported. Cell proliferation in cancer was demonstrated to be cross-regulated by KEAP1/NRF2 and EGFR signaling. Moreover, cells expressing oncogenic allele of KRAS are able to activate NRF2 via the MAPK pathway in mouse embryonic fibroblasts [52, 53]. In the same way, the loss of KEAP1 by the CRISPR-Cas9 system cooperates with the tumor mutational landscape in modulating the response to BRAF, MEK, EGFR, and ALK inhibition and in allowing cancer cells to increase their ability to resist to treatments and proliferate [54]. KRAS activity confers in NSCLC chemoresistance also by upregulating NRF2 through the link with TPA response element (TRE) located in exon 1 of the NFE2L2. In the same context of resistance to target therapy, it is possible that NFE2L2 mutations can contribute to survival under crizotinib treatment and can allow the cells to acquire additional resistance mutations over time. In line with these hypotheses, Krall et al. recently identified a hotspot mutation in NFE2L2 in a patient with acquired resistance to ALK inhibitors that could exert a synergic effect with a secondary ALK mutation in the resistance to second-generation ALK inhibitors [55].

Recent additional studies in this field gave the first hint of the prognostic role of single-nucleotide polymorphisms (SNPs) of the KEAP1 gene in breast cancer without inducing any evident and detectable variations of the protein structure or conformation. More specifically, five tagging SNPs (rs34197572, rs9676881, rs1048290, rs11085735, and rs8113472) located in the KEAP1 were genotyped and appeared to be in allelic linkage disequilibrium (LD) with each other. This finding suggests the existence of a haplotype block at the KEAP1 gene locus that might correlate with specific clinical features of cancer patients [56]. The two SNPs rs9676881 and rs1048290 resulted to be significantly associated with a shorter PFS survival in invasive breast cancer patients. The main hypothesis is that they reside into cell type-specific regulatory elements that modulate the binding capability of critical transcriptional factors, which in turn change target gene expression. Thus, it might explain the observed correlation with the high KEAP1 protein expression levels and the high cytoplasmic localization of NRF2 in breast tissues [57]. The SNP rs1048290 is located in the DGR domain, so it may affect the maintenance of physiological levels of NRF2.

Tumor susceptibility SNPs might be also associated with specific miRNA/lncRNA binding regions [58, 59]. The SNP rs1048290 was found in LD with the SNP rs9676881, which is located in a putative enhancer region, few bases downstream of the 3-untraslated region (3-UTR) of the KEAP1 gene and 410 bp from the miR-200a binding site. By consequence, it is clear to suppose that a LD may exist with these silent variations and the specific miRNA binding site. However, the role of KEAP1 SNPs in predicting patient survival remains controversial. The two SNPs rs9676881 and rs1048290 appeared to be the most interesting ones and resulted to be significantly associated with a shorter PFS survival in both invasive and ER-positive tamoxifen-treated invasive breast cancer patients [60].

3. The Aberrant Methylation of the Keap1-Nrf2 Axis and Its Translational Impact in Solid Tumors

Gene promoter hypermethylation at the specific CpGs and chromatin remodeling are two of the main epigenetic events that can modulate gene expression by spatial interfering with the ability to work with the transcriptional machinery.

Epigenetic mechanisms are clearly implicated in the complex regulation of the KEAP1/NRF2 axis and are actually considered the most frequent mechanisms of KEAP1 silencing in solid tumors [61]. The first hypothesis of an epigenetic dysregulation of the KEAP1 gene comes from the intriguing observation that the KEAP1 mutations were not frequent enough to justify alone the frequency of aberrant NRF2 nuclear accumulation reported in lung tumor cells [8]. All the scientific findings on the hypermethylation of the KEAP1 promoter and its effects on the KEAP1/NRF2 pathway are summarized in Table 3. The first report in this field was in human NSCLC and prostate DU-145 cancer cell lines. The promoter CpGs affected by this phenomenon are grouped into one island located at the P1 region of KEAP1, near the transcriptional start site [62–64]. The KEAP1 promoter hypermethylation was described in neoplastic tissues of patients affected by glioma, breast cancer (51%), and primary NSCLC (47%). In lung cancer, the presence of epigenetic abnormalities in the KEAP1 gene plus its point mutations/LOH matched with the prevalence of NRF2 nuclear accumulation in NSCLC tissues and was associated with an increased risk of lung cancer progression in surgically resected patients [65–67]. In clear renal cell carcinoma (ccRCC), the epigenetic modulation of KEAP1 was shown to be the leading mechanism of KEAP1 deregulation (48.6%), thus supporting a driver role of the KEAP1/NRF2 axis in renal cancer. TCGA (The Cancer Genome Atlas) concomitant data analysis suggested that KEAP1 hypermethylation is able to strongly predict patient survival [68]. In primary breast cancers and preinvasive lesions, an aberrant KEAP1 promoter methylation was seen to be more recurrent in ER-positive, HER2-negative than in triple-negative breast cancers and was hypothesized to be a prognostic marker since a higher mortality risk in triple-negative patients was predicted. Moreover, KEAP1 promoter silencing by methylation was also predictive of a lower risk of tumor relapse in patients treated with sequential therapy of anthracyclines and cyclophosphamide followed by taxanes [67]. Gliomas are the second tumor described by our group to have a promoter hypermethylation. In these tumors, it was reported that KEAP1 epigenetic modifications were associated with poor prognosis and contribute to the prediction of the disease progression of patients subjected to radiotherapy and temozolomide treatment [65]. The role of KEAP1/NRF2 in radiation has been also elucidated in A549 lung adenocarcinoma cell line under DNMT inhibitor genistein treatment. The pharmacological demethylation of the KEAP1 CpG promoter islands was demonstrated to induce an increase in transcript levels and a consequent overexpression of NRF2, GSS, and HO-1 [69].

Table 3: Effect of KEAP1/NRF2 expression by promoter methylation in human cancers (tissues and cell lines) and correlation with clinical patients’ outcomes.

Molecular target
Cancer model
Methylation status
Functional effects
Clinical outcome
Refs

NRF2
Prostate cancer cell line (LNCaP) and tissues ()
Hypermethylation
↓NRF2 mRNA
↓HO-1 mRNA and protein
↓NQO1 mRNA and protein
Increment of Gleason score from normal to advanced stage prostate cancer
[121]

Human colon cancer cells (SNU-C5)
Hypomethylation
↑NRF2 mRNA
↑HO-1 mRNA and protein
NA
[59, 60]

KEAP1
Lung cancer cell lines (SPC-A1, A549, and NCI-H460) and tissues ()
Hypermethylation
↓KEAP1 mRNA
↑ NRF2 protein
↑HO-1 mRNA and protein
↑GSH mRNA and protein
NA
[48,116, 122]

NSCLC tissues ()
Hypermethylation
↓KEAP1 mRNA
Worst prognosis associated to KEAP1 double alterations
[52]

Malignant gliomas ()
Hypermethylation
↓KEAP1 mRNA
Lowest risk to progress in patients treated with radiotherapy and temozolomide
[51]

Primary breast cancers () and preinvasive breast lesions ()
Hypermethylation
↓KEAP1 mRNA
Worse prognosis in triple-negative phenotype and reduced risk of relapse in patients treated with EC/D chemotherapy
[53]

Human colorectal cancer cell lines () and tissues ()
Hypermethylation
↓KEAP1 mRNA
↑ NRF2 protein
↑NQO1 mRNA
↑AKR1C1 mRNA
NA
[55]

Prostate cancer cell DU-145
Hypermethylation
↓KEAP1 mRNA
↑NRF2 mRNA
↑NQO1 mRNA
↑HO-1 mRNA
↑GCLC mRNA
NA
[49]

ccRCC tissues ()
TCGA dataset ()
Hypermethylation
↓KEAP1 mRNA
Worse overall survival (OS) and association with increased of tumor grading
[54]

AKR1C1: aldo-keto reductase family 1 member C1; ccRCC: clear renal cell carcinoma; GCLC: glutamate-cysteine ligase catalytic subunit; GSH: glutathione; HO-1: heme oxygenase-1; KEAP1: Kelch-like ECH-associated protein 1; NQO1: NAD(P)H-quinone oxidoreductase 1; NRF2: nuclear factor erythroid 2-related factor 2; NSCLC: non-small-cell lung cancer; NA: not applicable.

Aberrant KEAP1 methylation was also reported in 53% of colorectal cancer and head and neck cancer tissues (29.3%) and was also linked to the worse prognosis of these tumors [70, 71]. In pancreatic cancer cell lines, the suppression of KEAP1 protein was demonstrated to be correlated with UHRF1, a scaffold protein for DNA methyltransferase DNMT1 [72].

A possible role of epigenetic variations in the modulation of NRF2 expression is less investigated. Li and colleagues showed that a low methyltransferase EZH2 expression correlates both lung cancer cell lines and tissues with an elevated expression of NRF2, NQO1 (NAD(P)H-quinone oxidoreductase 1), and HO-1 (heme oxygenase 1). Since the EZH2 is involved in the establishment and/or maintenance of chromatin architecture and histone methylation, its downstream effect was attributed to a decrease in the trimethylation of lysine 27 on histone H3 (H3K27Me3) in the NFE2L2 promoter region [73]. Recently, Kang and colleagues focused on the causative relationship between NRF2 expression and its epigenetic alterations, especially in the context of DNA methylation at cytosines and histone methylation status during 5-fluorouracil- (5-FU-) induced oxidative stress in colon cancer cells. They found that elevated reactive oxygen species (ROS) level induced by 5-FU activates TET (ten-eleven translocation) DNA demethylases and produces a hypomethylation of the NFE2L2 promoter with consequent activation of NRF2 translation. This, in turn, upregulates the expression of the antioxidant enzymes and generates the resistance to 5-FU in cancer cells [48, 49].

4. MicroRNAs Directly Targeting the Keap1/Nrf2 Pathway

An intriguing epigenetic way of KEAP1/NRF2 pathway deregulation in tumor cells comes from miRNAs that act in cancer as oncogenes or tumor suppressors [74]. miRNAs are proximately 22 nucleotide single-stranded noncoding RNA molecules which regulate gene expression at posttranscriptional levels by binding to the 3-untranslated regions (UTRs) of specific mRNAs. They generally affect the translation or stability of mRNA molecules through the interaction of specific mRNAs with complementary base pairing.

Two different blocks of miRNAs can be distinguished in the context of posttranscriptional regulation of the KEAP1/NRF2 pathway (Table 4) [75]. The first group includes the miRNAs that directly target NFE2L2 and usually negatively regulate the KEAP1/NRF2 pathway by decreasing the NRF2 protein levels. The second one comprises those miRNAs that directly interact with KEAP1 and indirectly influence the NRF2 signaling. In addition, a lot of miRNAs are reported to indirectly modulate the ARE-mediated redox signaling through their interaction with additional factors located in the crossing points of the NRF2 network (Figure 3). All of these interactions are complex and still remain to be fully elucidated. So we focalized our attention on the main findings concerning NRF2 and KEAP1.

Table 4: Main miRNAs interacting with KEAP1 and NRF2 and downstream effects observed in cancer cells.

Target
miRNA ID
Functional validations

Downstream effects
Cancer model
Methods
Refs

NRF2
↑ hsa-miR-28
↓NRF2
Human breast cancer cells
Luciferase assay, qRT-PCR, WB, and coimmunoprecipitation
[76]

↓ hsa-miR-155
↑NRF2, ↑HO-1, ↑GSH, ↑NO, ↑SOD,
↑ colony formation,
↑ arsenite resistance
Human bronchiolar epithelial cells
Mimic and miRNA inhibitor transfection, qRT-PCR, WB, measurements of ROS and enzymatic activity, cell cycle, cell migration, and colony formation assays
[78]

↑ hsa-miR-144
↓NRF2, ↓GSH,
↓ cell viability,
↑ apoptosis,
↓ 5-FU resistance
Leukemia cells,
human hepatocellular cancer cells, neuroblastoma cells
Luciferase reporter assay, cell viability assay, ROS and enzymatic activity measurements, qRT-PCR, WB
[82]

MicroRNA microarray analysis, luciferase reporter assay, qRT-PCR, WB, ELISA
[83]

Luciferase reporter assay, drug sensitivity assay, qRT-PCR, WB
[84]

↓ hsa-miR-93
↑NRF2,
↑ mammosphere formation,
↓ apoptosis,
↑ DNA damage
Rat breast cancer cells
siRNA (small interfering RNA) transfection, qRT-PCR, WB, clonogenic cell survival assay, mammosphere formation assay, cell migration, and cell apoptosis assays
[85]

↑ hsa-miR-153
↓NRF2, ↓GCLC, ↓GSR,
↓ cell migration,
↓ cell invasion
Neuroblastoma cells, breast cancer cells, oral squamous cell carcinoma
miRNA mimic and inhibitor transfection, cell proliferation assay and colony forming assays, cell migration analysis, cell cycle analysis, measurement of ROS and enzymatic activity, qRT-PCR, WB
[87]

MicroRNA microarray analysis, luciferase reporter assay, qRT-PCR, WB, cell migration, and invasion assays
[88]

↑ hsa-miR-27 ↑ hsa-miR 142
↓NRF2, ↓GCLC, ↓GSR
Neuroblastoma cells
Transient transfection, WB, qRT-PCR, measurement of ROS, and enzymatic activity
[86]

↑ hsa-miR-340
↓NRF2,
↓ cisplatin resistance
Esophageal cancer cells
MicroRNA microarray analysis, luciferase reporter assay, drug sensitivity assay, qRT-PCR, WB
[89]

↑ hsa-miR-507
↑ hsa-miR-634
↑ hsa-miR-450
↑ hsa-miR-129
↓NRF2, ↓ME1,
↓ cell growth,
↓ cisplatin resistance
Esophageal cancer cells
Measurement of ROS, qRT-PCR, WB, siRNA, drug sensitivity assays
[90, 91]

KEAP1
↑ hsa-miR-141
↓KEAP1, ↑NRF2,
↑HO-1,
↓ apoptosis,
↑ cisplatin resistance,
↑ 5-FU resistance
Ovarian cancer cells, hepatocellular carcinoma
MicroRNA microarrays analysis, luciferase reporter assay, qRT-PCR, WB, apoptosis assay
[92]

MicroRNA microarray analysis, miRNA mimic and inhibitor transfection, luciferase reporter assay, qRT-PCR, WB, cell viability assay, apoptosis assay, drug sensitivity assay
[93]

↑ hsa-miR-200
↓KEAP1, ↑NRF2
Breast cancer cells, esophageal cancer cells
Luciferase reporter assay, qRT-PCR, mRNA stability assay, WB, ChIP, anchorage-independent cell growth assay, IHC
[60]

Transfection reporter assay, qRT-PCR, ChIP
[95]

↑ hsa-miR-7
↓KEAP1, ↑NRF2, ↑GSH
Neuroblastoma cells
Cell viability assay, LC-MS/MS, qRT-PCR, WB, enzymatic activity measurements
[96]

↑ hsa-miR-432
↓KEAP1, ↑NRF2,
↑ chemoresistance
Esophageal cancer cells
CRISPR/Cas9 system, cell survival assay, siRNAs, luciferase reporter assay, qRT-PCR, WB, mRNA stability assay, ChIP
[98]

GCLC: glutamate-cysteine ligase catalytic subunit; GSH: glutathione; GSR: glutathione reductase; HO-1: heme oxygenase-1; KEAP1: Kelch-like ECH-associated protein 1; ME1: malic enzyme 1; NO: nitric oxide; NRF2: nuclear factor erythroid 2-related factor 2; SOD: superoxide dismutase; 5-FU: 5-fluorouracil; WB: Western blot; FC: flow cytometry; IHC: immunohistochemistry; LC-MS/MS: liquid chromatography tandem mass spectrometry; MTT: (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay; qRT-PCR: quantitative real-time PCR.

Figure 3: Left and right panels show how miRNA modifications may contribute to down and upregulate the KEAP1/NRF2 signaling in cancer. Representative scheme on the left side summarizes a group of miRNAs that directly target KEAP1 mRNA and indirectly impact on the transcriptional activity of the NRF2 into the nucleus. Other miRNAs modulate BACH1, a transcription factor that competes with NRF2 leading to the link at the antioxidant response element (ARE) of detoxifying genes. The schematic model on the right side depicts those miRNAs that directly target NFE2L2 and impact on the general mRNA and protein levels of NRF2 and, by consequence, on the activation of detoxification NRF2 target genes with a great impact on chemo- and radioresistance, survival, growth, and proliferation of tumor cells.

Several miRNAs predicted to target the KEAP1/NRF2 axis were identified by bioinformatic analysis of miRNA databases [76]. Some of these were experimentally proven to directly target and repress the NRF2 activity. The negative effects on the NRF2 expression by miR-28 were firstly documented in MCF-7 breast cancer cells [77]. A similar activity was described for miR-155 in 16-HBE human bronchiolar epithelial cells under arsenite treatment, together with an observed upregulation of glutathione (GSH), nitric oxide (NO), and superoxide dismutase (SOD) [78]. The increased expression of miR-155 correlates with radiation-induced severe fibrosis in a murine skin model [79], similar to miR-140, whose deficiency increased activation of TGF-β1 signaling, inflammation, and myofibroblast differentiation in fibrotic lung tissue after radiation treatment [80, 81]. Among functionally validated miRNAs that regulate NRF2, miR-144 recently emerged as having a central role in the modulation of cellular stress response in blood malignancies and solid tumors. In K562 cell line and primary erythroid progenitor cells, it was seen that increased levels of miR-144 were associated with reduced NRF2 levels in HbSS reticulocytes. By contrast, inhibition of miR-144-3p in human leukemia HL-60 cells reduced cell viability and prompted apoptosis by interfering with NRF2 activity. In hepatocellular carcinoma cell lines, miR-144 overexpression was reversely correlated with an enhancement of 5-fluorouracil- (5-FU-) induced cytotoxicity and apoptosis and with GSH biosynthesis in neuroblastoma SH-SY5Y cells via NRF2 [82–84].

A direct effect of miR-93 on nuclear accumulation of NRF2 was well described by Singh et al. using a rat model of breast carcinogenesis. A significant reduction in carcinogenesis-associated phenotypes such as mammosphere development, antiapoptosis, and DNA damage was observed [85].

In silico analysis and in vitro studies on different sets of tumor cell lines recently provided more additional insights into the role of KEAP1/NRF2 axis modulation by miRNAs. In SH-SY5Y neuroblastoma cells, the 3-UTR of NFE2L2 is targeted by miR-153, miR27a, and miR-142-5p, with a consequent decrease in Gclc glutamate-cysteine ligase (GCLC) and glutathione-disulfide reductase (GSR) expression levels [86]. The functional impact of miR-153-3p/NRF2 interaction was firstly reported in breast cancer cell lines and recently highlighted by microarray studies in oral squamous cell carcinoma cell lines and tissues. Low expression levels of miR-153-3p significantly correlate with tumor cell migration and invasion [87, 88]. In the same histological pattern of esophageal cell carcinoma, miR-340 was shown to directly modulate the NRF2 expression levels, thus interfering with the chemoresistance phenotype under cisplatin treatment [89]. Finally, miR-507, miR-634, miR-450a, and miR-129-5p appeared to negatively modulate the NRF2 activity by targeting both the NFE2L2 and ME1 transcripts, a well-known target of NRF2 [90]. In NSCLC A549 cells, this group of miRNAs exerts a synergic effect in increasing sensitivity of cell growth suppression under cisplatin treatment [91].

By looking at the KEAP1 regulation side, miR-141 was the first reported miRNA to target KEAP1 by binding to its 3-UTR sequence site in ovarian carcinoma cell lines [92]. The upregulation of miR-141 expression decreases the 5-FU-mediated effects and apoptosis in hepatocellular carcinoma cell lines by inducing nuclear translocation of NRF2 and activation of HO-1 gene transcription [93]. A direct inhibition effect of miR-200a on KEAP1 was elucidated in human MDA-MB-231 and Hs578T breast and esophageal squamous cell carcinoma cells under methylseleninic acid (MSA) treatment. MSA acts as a chemopreventive agent that is able to induce miR-200a expression and inhibits KEAP1 through the Krüpple-like factor 4 (KLF4) [60, 94, 95]. Interesting results came from the investigation by Hartikainen et al. In their work, SNP rs1048290 has been found in LD with SNP rs9676881, which is located in a putative enhancer region, few bases downstream of the 3-untranslated region (3-UTR) of the KEAP1 gene, the specific target region of miR-200a [56]. More recently, a direct action of miR-7 on KEAP1 expression was described in the human neuroblastoma cells. By targeting the 3-UTR of KEAP1 mRNA, miR-7 enhances the nuclear localization of NRF2 and induces an increased expression of HO-1 and glutamate-cysteine ligase modifier subunit (GCLM). The control of cell survival under stress by miR-7 was amplified by the observed variation of intracellular hydroperoxide levels and increases in the reduced form of glutathione levels [83, 96]. A similar effect was described for miR-196 in human hepatoma cells against hepatitis C virus infection [97]. The CRISPR/Cas9 system was used to prove the direct binding to the coding region of KEAP1 by miR-432-3p in the esophageal squamous cell carcinoma (ESCC). In this tumor, miR-432-3p overexpression correlates with a downregulation of the KEAP1 expression, thus inducing a decrease in the sensitivity of tumor cells to cisplatin and other chemotherapy drugs [98].

A lot of miRNAs were also reported to regulate the KEAP1/NRF2 pathway independently from the KEAP1 or NRF2 activity. The let-7 family modulates the DICER expression and represents the first example of cancer regulation by miRNA in humans [99]. Not less importantly, let-7 showed to inhibit the expression of several oncogenes involved in cellular proliferation, such as RAS (rat sarcoma), MYC (avian myelocytomatosis viral oncogene homolog), and HMGA2 (high-mobility group AT-hook 2) [100, 101]. The miRNAs let-7b and let-7c were firstly demonstrated to negatively modulate the expression of BACH1 in the liver, a transcription factor that works in association with the small MAF proteins in a dominant condition in respect of NRF2 [102, 103]. By consequence, the repression of BACH1 induces an upregulation of HO-1 expression via NRF2 transcription [104].

5. Long Noncoding RNAs Linked to the Keap1/Nrf2 Pathway

Long noncoding RNAs (lncRNAs) are non-protein-coding transcripts longer than 200 nucleotides which are expressed in a sense, antisense, or bidirectional manner. Different to protein-coding genes, they show a high density of DNA methylation around their transcription start sites, independent of their expression status [105]. A growing number of evidences elucidated the role of lncRNAs in the initiation, progression, and stem cell pluripotency of cancer cells [106]. Little is known about the role of lncRNAs in the modulation of the detoxification processes of cells.

The most recent findings are those related to smoke and cancer-associated lncRNA 1 (SCAL1) and lncRNA regulator of reprogramming (ROR). The SCAL1 is the first characterized long noncoding RNA activated by NRF2 and is considered one of the downstream mediators of NRF2-induced oxidative stress protection in airway epithelial cells. Under stress induced by cigarette smoke, the SCAL1 expression increases in lung cancer cell lines and appears to be directly correlated with NFE2L2 mutations [107]. In human bronchial epithelial cells, a knockdown gene approach revealed that NRF2 can regulate the expression level of SCAL1 by binding to the nuclear factor erythroid-derived 2 (NF-E2) motif located in the promoter region of its gene [108]. Conversely to SCAL1, Zhang and colleagues proved that in breast cells, NRF2 controls the ROR lncRNA expression by binding two different NRF2 response elements flanking the ROR promoter region. NFE2L2 knockdown leads to the overexpression of lncRNA ROR in mammary embryonic stem cells [109].

6. Concluding Remarks

Significant advances have been made in these last years to understand the regulation mechanisms of the KEAP1/NRF2 system. However, although KEAP1/NRF2 dysfunction is now well known to confer resistance to chemo- and radiotherapy, the KEAP1-NFE2L2 mutational status assessment is not used to make treatment decisions in lung cancer yet. Moreover, molecular profiling of these two proteins in pretreated and resistant tumor samples will help to elucidate if the loss of KEAP1 or the gain of NFE2L2 may be clinically relevant mechanisms of acquired and intrinsic resistance to therapies in lung cancer and other solid tumors or not. A general limitation to clarify these issues remains and consists of a lack of available rebiopsy tissue specimens.

From an epigenetic point of view, the effects produced by KEAP1 hypermethylation on the KEAP1/NRF2 signaling in cancer remain partially understood. Firstly, it is natural to wonder what the real role of P1 CpG island methylation is and if the methylation status of KEAP1 exclusively affects its expression or could additionally interfere with the ability to bind to NRF2 in promoting tumor progression and resistance to therapies. According to these observations, it would be of great interest to determine if in tumors with different origins there are similar or different methylation CpG density patterns at the P1 region and if demethylation of the KEAP1 promoter in neoplastic tissues could really suppress tumor progression and enhance resistance to therapies.

Given that posttranscriptional modifications play important roles in regulating the stability and translation of mRNAs, more studies on the regulation of the KEAP1/NRF2 pathway by miRNAs will corroborate their key roles in clinical practice. However, this approach will require a greater knowledge of how drug treatment influences miRNA expression and how miRNA expression could influence the multifaced KEAP1/NRF2 network.

Conflicts of Interest

The authors declare that they have no competing financial interests.

Acknowledgments

This work was supported by the Italian Ministry of Health (Ricerca Corrente, RC1703LO41 to L.A. Muscarella) by “5 × 1000” voluntary contributions to Casa Sollievo della Sofferenza and AIRC/MFAG Grant 12983 (to L.A. Muscarella).

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