In Vitro Growth Inhibition, Caspase-Dependent Apoptosis, and S and G2/M Phase Arrest in Breast Cancer Cells Induced by Fluorine-Incorporated Gold I Compound, Ph3PAu[SC(OMe)=NC6H4F-3]

Gold-based anticancer compounds have been attracting increasing research interest due to their ability to kill cancer cells resistant to platinum-based compounds. Gold I- and gold III-based complexes have shown satisfactory anticancer activities. In this study, two new fluorine-incorporated gold (I) compounds such as Ph3PAu[SC(OMe)=NC6H4F-3] and DPPFeAu2[(SC(OMe)=NC6H4F-3)]2 were evaluated for their in vitro activities against human breast cancer cell lines, primary breast cancer cells, and breast cancer stem cells (parental breast cancer stem cells, BCSC-P, and breast cancer stem cells, BCSC). Assays for growth inhibition and cytotoxicity, including real-time cell analysis, were carried out to screen effective antibreast cancer compounds. In addition, further in vitro assays such as apoptosis, caspase 3/7 activity, and cell cycle analysis were performed to observe the action and mechanism of killing breast cancer cells by the selected gold I compound, Ph3PAu[SC(OMe)=NC6H4F-3]. The gold (I) compound, Ph3PAu[SC(OMe)=NC6H4F-3], showed low toxicity to H9c2 normal cells and significant growth inhibition in MDA-MB-231 and MCF-7 cells, primary breast cancer cells, and breast cancer stem cells (BCSC-P and BCSC). The IC50 doses of the gold (I) compound Ph3PAu[SC(OMe)=NC6H4F-3] against the breast cancer cell lines MDA-MB-231 and MCF-7 were approximately 6-fold lower than that of cisplatin (cis-diamineplatinum (II) dichloride, CDDP). Moreover, the compound Ph3PAu[SC(OMe)=NC6H4F-3] induced caspase 3/7-dependent apoptosis and cell cycle arrest at S and G2/M phases. Ph3PAu[SC(OMe)=NC6H4F-3], a gold (I) compound incorporated with fluorine, is a potential candidate for the treatment of breast cancer.


Introduction
Breast cancer is one of the deadliest diseases among women globally, with a very high incidence, 2.26 million (11.7%) of the total 19.29 million new cancer cases in year 2020 [1]. Moreover, approximately 10-15% of all breast cancer cases are triple-negative as they do not express receptors for estrogen, progesterone, and HER2 [2,3] and are aggressive as well as difficult to treat as they do not respond to hormonal therapy. Despite increased survival rates in recent years due to advancements in technologies for early detection, significant efforts are being devoted to developing new and  2 International Journal of Breast Cancer effective chemotherapeutic compounds against breast cancer. Recent findings have highlighted cancer stem cells as the root cause of cancers; these contribute to cancer recurrence within the first 5 years on average, after remission following treatment [4]. This reemergence of cancer stem cell theory has encouraged researchers to explore novel and effective metal-based compounds against cancer stem cells and advanced breast cancers.
Platinum derivatives have limitations in cancer treatment, considering their toxicity to the neurons and kidneys [5]. Furthermore, they show low effectiveness in cancers that are naturally resistant to cisplatin. The development of acquired resistance in patients previously treated with cisplatin also remains challenging. Overall, the existing metalbased anticancer compounds, including platinum-based compounds, are not very effective against triple-negative   [6][7][8]. The anticancer activity of gold compounds was 8.7-to 20.8-fold higher than that of cisplatin [9]. Therefore, the need to explore more goldbased anticancer compounds to discover new drugs against breast cancer is evident.
Fluorine has unique physical and chemical properties such as being the lightest and the most reactive element among halogens. It can also be found as a trace element in our body parts especially in the teeth, bones, hair, blood, milk, and urine. Fluorine was successfully isolated in 1886 by Henri Moissan who won the Nobel Prize in 1906. Fludrocortisone was the first pharmaceutical item which incorporated fluorine atom to cortisol in 1954. The inclusion of fluorine into the drug design is known to amplify the pharmacological impact on bioactive molecules by increasing the biological activity, enhancing hydrogen bonding interactions and binding affinity to target proteins, and promoting chemical and metabolic stability [10,11].
Therefore, in this study, the anticancer properties of the novel fluorine-incorporated gold (I) compounds such as tri- 2 (compound 3F3), and their ligand LH (compound 3FL) synthesized by Yeo and colleagues [12,13] were evaluated in breast cancer cells. The compounds were tested for growth inhibition, apoptosis induction, and cell cycle arrest in human breast cancer cell lines such as MDA-MB-231 (triple-negative breast cancer cells) and MCF-7 (estrogen receptor-positive breast cancer cells), primary breast cancer cells (in-house cultured), BCSC, and parental BCSC (BCSC-P). Based on the results, the new gold (I) compound, Ph 3 PAu[SC(OMe)=NC 6 H 4 F-3], showed promising anticancer properties against different types of breast cancers in vitro, in terms of growth inhibition, apoptosis induction, and cell cycle arrest. MDA-MB-231, MCF-7, and H9c2 cells were cultured and maintained in high-glucose Dulbecco's modified Eagle's medium (DMEM) with 10% FBS (heat-inactivated) and 1% pen-strep. Cells were incubated at 37°C in a humidified incubator (CCL-170B-8, ESCO, Singapore) containing 5% CO 2 and 95% air.

Materials and Methods
BCSC-P (Celprogen 36102-29P, USA) and BCSC (Celprogen 36102-29, USA) were cultured in complete medium (Celprogen M36102-29U, USA) and were incubated overnight at 37°C in a humidified incubator (Innova CO14, New Brunswick Scientific, USA) with premixed gas at a ratio of 5% CO 2 , 5% O 2 , and 90% N 2 . The medium was changed once every 2 to 3 days until the cells were 80-90% confluent. Cells were subcultured until the third passage for further experiments.
Primary breast cancer cells were cultured from a patient tissue sample transported in iced cold L15 medium supplemented with 10% FBS and 1% pen-strep. Blood, blood clots, and fat were removed from the tissue sample and washed five times with sterile 1X PBS followed by dissociation it in 2 mL of 0.25% trypsin-EDTA (Gibco 15400-054, USA) and placed it in a conventional cell culture incubator (CCL-050B-8, ESCO, Singapore) for 4 hr. Mechanical dissociation was also done for every 1 hr. Dissociated tissue samples were then cultured in DMEM high glucose supplemented with 10% FBS (heat-inactivated) and 1% pen-strep and were incubated overnight at 37°C in a humidified cell culture incubator with 5% CO 2 and 95% air. After six passages, the cells were subcultured with serum-free DMEM/F12 (Nacalai 0846095, Japan) to inhibit fibroblast growth and promote epithelial cell growth. Primary breast cancer epithelial cells were subcultured until passage 16. were synthesized by Yeo et al. and collected them for this study after confirmation of their purity was tested by using nuclear magnetic resonance [11,12].      [10] followed by a real-time cell analyzer, iCelligence [14,15]. MCF-7, MDA-MB-231, and primary breast cancer (BCA) cells were seeded at 2:5 × 10 4 cells, and H9c2 cells were seeded at 3 × 10 4 cells/well of a flat-bottom 96-well plate each (SPL Life Sciences, Korea), in 100 μL of complete DMEM high glucose and incubated at 37°C in a humidifier incubator supplied with 5% CO 2 and 95% air for 24 h. BCSC-P and BCSC were seeded at 2 × 10 4 cells/well of flat-bottom 96-well plates (Celprogen E36102-29P-96 and Celprogen U36102-29-96), respectively, in 100 μL of complete culture medium (Celprogen, M36102-29US). All cells were in the exponential growth phase. Plates seeded with stem cells were incubated at 37°C in a minihumidified incubator (Innova CO14, New Brunswick Scientific, USA) supplied with premixed gas (5% CO 2 , 5% O 2 , and 90% N 2 ) for 24 h.     International Journal of Breast Cancer The cells were then treated with various concentrations of gold compounds (80 μM, 40 μM, 20 μM, 10 μM, 5 μM, and 2.5 μM). As negative controls, cells were treated with 0.1% DMSO. Cells in positive control wells were treated with freshly prepared IC 50 of cisplatin (Sigma P4394, USA). Twenty microliters each of MTT (5 mg/mL) was added to each well and incubated for 3 h. To dissolve the formazan crystals, medium containing MTT was aspirated gently followed by adding 100 μL DMSO into each well of 96-well plate.
For BCSC-P and BCSC, 10 μL of MA dye (Biolog 74351, USA) was added to each well. The absorbance of the plates with MA dye was read directly after 3 h incubation without removing the medium-plus dye mixture and adding the solvent DMSO because the MA dye forms soluble formazan crystals and develops color directly.
The plates were analyzed using a microplate reader (MicroStation ELX808BLG, Biolog, USA) at 590 nm with a reference wavelength of 650 nm to measure the absorbance value for each well [13,16]. The percentage of cell viability was calculated using the formula below [17], and IC 50 of the gold compounds against breast cancer cells was determined using GraphPad Prism 7.
Where; Treated:medium, cells and compound Control:medium, cells, and 0.1% DMSO Blank:medium only Further analysis of cell viability was done by real-time cell analysis (RTCA) experiments for MCF-7, MDA-MB-231, and H9c2 cells treated with the compound 3F1. Briefly, 8-well E-plate (L8, ACEA biosciences, USA) was primed with 150 μL of complete DMEM high glucose for 20 min, and the background electrical impedance was measured for 1 min. In total, 2:0 × 10 4 cells/well in 350 μL of complete DMEM high glucose were then seeded into the E-plate, which contained 150 μL/well of complete DMEM high glucose. The E-plate was placed on the RTCA instrument and incubated for 24 h at 37°C in a humidified incubator supplied with 5% CO 2 and 95% air. Cells in the E-plate were then treated with the selected gold compound, 3F1, in duplicate. Cells in the negative control well and positive control well were treated with DMSO (0.1%) and cisplatin at its IC 50 (Sigma P4394, USA), respectively. The E-plate was again placed on the RTCA instrument for 24 h at 37°C in a humidified incubator supplied with 5% CO 2 and 95% air for monitoring the cells in a real-time manner. Data analysis was performed using the RTCA analysis software version 1.0 for determining the normalized cell index at the start of the treatment time-point for time-dependent IC 50 .

Acridine Orange and Propidium Iodide Dual
Fluorescence Cell Viability Assay. MDA-MB-231 and MCF-7 cells were seeded at a density of 4 × 10 5 cells/mL of complete DMEM high glucose to T25 flasks and incubated for 24 h at 37°C in a humidified incubator (CCL-170B-8, ESCO, Singapore) supplied with 5% CO 2 and 95% air for the acridine orange and propidium iodide (AO/PI) cell viability assay using Luna-FL [18,19]. Cells were treated with the respective IC 50 dose of 3F1 (8.5 μM for MDA-MB-231 and 6.5 μM for MCF-7) or 0.1% DMSO (control) and incubated. Total 10 μL of the cell suspension stained with AO/PI dye (Logos Biosystems, F23001, Korea) was loaded onto a PhotonSlide cell counting chamber (Logos Biosystems, L12005, Korea). In Luna-FL AO/PO assay, fluorescence green or yellowish-green captured images are recognized as viable cells, and red fluorescence images are recorded as nonviable cells.  [20][21][22]. The MUSE cell analyzer was used to detect the stained cells, which were segregated into four quadrants of a scattered plot to distinguish between live cells, early apoptotic cells, late apoptotic cells, and necrotic cells. Three independent experiments were carried out.
2.6. Caspase-3/-7 Activity Assay. MDA-MB-231 and MCF-7 cells were seeded at a density of 5 × 10 5 cells/mL with complete DMEM high glucose (Nacalai, Japan) in T25 flasks and incubated for 24 h at 37°C in a humidified incubator (CCL-170B-8, ESCO, Singapore) with 5% CO 2 and 95% air. Cells were treated with 0.1% DMSO (control) or with the IC 50 dose of the 3F1 compound. Single-cell suspension at the recommended density between 1 × 10 5 and 5 × 10 6 cells/mL in 1X assay buffer BA was prepared. Staining the cells with DNA-binding dye coupled with DEVD peptide substrate was performed according to the manufacturer's instructions [23,24]. The results were analyzed using MUSE analysis software version 1.5. Stained cells were distinguished into four quadrants in a scattered plot.

Cell Cycle Analysis
Assay. MUSE cell analysis assay kit (Millipore, USA) that contains PI and RNase A premixed reagent was used for cell cycle analysis. MDA-MB-231 and MCF-7 cells were seeded at a density of 5 × 10 5 cells/mL in complete DMEM high glucose (Nacalai, Japan) in T25 flasks  50 , lower than IC 50 , higher than the IC 50 to evaluate whether the compound 3F1 consistently affected the cell cycle of these breast cancer cells. Treated and control cells were incubated for 24 h at 37°C in a humidified incubator supplied with 5% CO 2 and 95% air followed by fixation and staining of the cells by manufacturer instructions of the kit. Analysis was done using the MUSE cell analyzer (Merck-Millipore, USA) followed by ModFit LT version 5 to generate the histograms and the percentage of cells in each cell cycle phase.

Statistical
Analysis. Data presented were mean ± SD from three independent experiments with at least duplicate or triplicate. IC 50 and statistical comparisons were calculated using GraphPad Prism software version 7 (GraphPad, San  Figure 2). The compound 3F1 demonstrated significant growth inhibition of BCA, BCSC-P, and BCSC, and IC 50 doses against these breast cancer cells were found to be less than the IC 50 dose for H9c2 normal cardiomyoblasts too (Table 1). In addition to the endpoint IC 50 generated by MTT assay, RTCA assays were also performed to determine IC 50 of the compound 3F1, and it was found that both endpoint IC 50 doses generated from MTT and RTCA were comparable ( Figure 3 and Table 2).
AO/PI cell viability assays were used to check further whether the identified IC 50 Figure 4 and Table 3, respectively. The Luna AO/PI cell viability assay showed 29.29% and 64.54% viable cells in the treated MDA-MB-231 and MCF-7 cells, respectively.

Apoptosis Induction in Breast Cancer Cell Lines by
Compound 3F1. Annexin V, a cellular protein found in eukaryotic cells, has a high affinity to phosphatidylserine (PS), a phospholipid found on the inner surface or the cytoplasmic face of the cell membrane [25]. PS molecules are translocated to the outer membrane surface when cells undergo the apoptotic process [26]. Translocated PS molecules present in early and late apoptotic cells were bound by Annexin V-PE. Dead cells were detected by 7-AAD. Therefore, cells were distinguished into four groups in a scattered plot: viable cells (Annexin V -/7-AAD -) at lower left quadrant, early apoptotic cells (Annexin V + /7-AAD -) in the lower right quadrant, late apoptotic cells together with secondary necrotic cells (Annexin V + /7-AAD + ) in the upper right quadrant, and necrotic cells without going through the apoptotic pathway (Annexin V -/7-AAD + ) at the upper left quadrant. Breast cancer cell death via apoptotic pathway was detected by treating the breast cancer cells with the respective IC 50 dose of 3F1 compound for 24 h and analyzed them using the MUSE Annexin V and dead cell kit (Merck-Millipore, USA) on the MUSE flow cytometer ( Figure 5). Breast cancer cells treated with compound 3F1 showed an increasing average total apoptotic cell population (early apoptotic plus late apoptotic cells) compared with the control or the cells treated with CDDP (MDA-MB-231: control 4:60 ± 2:19%, CDDP 37:62 ± 12:07%, and 3F1 60:44 ± 5:55%; MCF-7: control 4:52 ± 2:53%, CDDP 34:64 ± 5:35%, 3F1 44:49 ± 9:85%).

Involvement of Caspase-3/-7 in Breast Cancer Cell
Apoptosis Induced by Compound 3F1. Induction of the apoptosis pathway by compound 3F1 was tested by the detection of caspase-3/-7 activity. The bright fluorescent signals from caspase-dependent apoptotic cells were detected after

Discussion
In A compound demonstrating in vitro antitumor activity at less than 10 μM is considered an active hit-to-lead compound in drug discovery [27,28]. In our screening, the compound 3F1 was considered a hit-to-lead compound as the respective IC 50 dose against breast cancer cells such as MDA-MB-231 (8:435 μM ± 0:809), MCF-7 (6:174 μM ± 0:660), BCA (5:770 μM ± 0:907), and BCSC-P (4:522 μM ± 0:537) was less than 10 μM, though this was not observed for BCSC, which showed an IC 50 of 10:170 μM ± 0:417. This finding is aligned with the common clinical perspectives wherein cancer stem cells are difficult to kill and have the potential for drug resistance [29]. Antitumor compounds usually target fast-growing tumor masses compared to slow dividing cells such as normal  13 International Journal of Breast Cancer cells and stem cells, including cancer stem cells [30][31][32]. In other words, cells with high metabolic rates are killed faster than those with normal or slow metabolic rates. An accelerated metabolic rate of glucose is observed in cancer cells via aerobic glycolysis, wherein pyruvate is converted to lactate, also known as the Warburg effect [33]. We found that the IC 50 dose of compound 3F1 was approximately sixfold lower than that of cisplatin (cis-diamineplatinum (II) dichloride). Alternatively, the novel gold-based compound 3F1 demonstrated sixfold stronger anticancer properties than cisplatin. In our study, endpoint IC 50 does of compound 3F1 from MTT assay was confirmed by iCelligence RTCA. RTCA is one of the latest technologies useful for in vitro experiments to monitor cell proliferation, viability, morphology, and migration in a realtime manner. RTCA data are recorded based on the electrical impedance changes in gold electrodes due to the attachment of live cells [14]. Several RTCA assays have been previously conducted using the same types of breast cancer cells. For example, the effect of 6-bromo-indirubin on MDA-MB-231, the cytotoxicity of platinum II complexes against MDA-MB-231 and MCF-7, and the long-term effects of aluminum against MDA-MB-231 were determined by RTCA analyses [25][26][27]. The cell viability and dose-dependent cytotoxicity data from RTCA were in agreement with the MTT results [34]. From this study, we confirmed that endpoint IC 50 doses were comparable between MTT assays and RTCA assays.
Apoptosis of breast cancer cells treated by compound 3F1 was detected by Annexin V assay. Following 24 h treatment with the compound, an increased percentage of the total apoptotic cell population was observed in MDA-MB-231 (60:44 ± 5:55%) and MCF-7 (44:49 ± 9:85%). Anticancer agents that induce apoptosis are highly desirable because malignant cells bypass apoptosis for their survival [35]. Induction of apoptosis is preferable over necrosis in therapeutics, including cancer treatments, as apoptosis requires a shorter period in the process of cell death [36]. Therefore, the novel gold compound 3F1, which induces apoptosis in breast cancer cells, is a potentially efficient chemotherapeutic agent against breast cancer. Apoptosis of breast cancer cells induced by compound 3F1 was further analyzed to check if it was involved in caspase activity. Caspases in human are divided into three subfamilies such as ICE-like protease (caspase-1, -4, -5, and -13), CED-3 protease (caspase-3, -6, -7, -8, -9, and -10) and the orphan caspase, caspase-2. Apoptosis can be executed through either caspase-dependent or caspase-independent pathways. Caspase-independent pathways have not been examined until recently [37]. To date, only two major caspase-dependent apoptosis pathways, i.e., the intrinsic pathway (via mitochondria) and extrinsic pathway (via cell surface death receptors), have been reported. The endoproteases, caspase-3/-7/-6, also named effectors or executioner caspases, are activated intracellularly by the initiators as a downstream cascade in response to apoptotic signals and lead cellular breakdown eventually. Both the extrinsic and intrinsic pathways of apoptosis must finally undergo activation of the executioner caspase-3/-7 and -6 [38,39]. The intrinsic apoptotic pathway signals originate within the cells from DNA damage, cellular stress due to growth factor insufficiency, and cytoskeletal disruption. Once DNA damage occurs in cells, signaling molecules such as ATM-Chk2 and ATR-Chk1 activate p53 (tumor suppressor protein) and other oncogenes. Activated p53 blocks the cells from progressing to further stages in the cell cycle. Simultaneously, P53 starts to recruit the apoptosis regulator 14 International Journal of Breast Cancer protein, BAX, which eventually induced pores in the mitochondria. These pores help to release cytochrome c to the cytosol, which later binds Apaf-1 protein [40]. The cytochrome c bound with Apaf-1 triggers a set of downstream protein cascade reactions that finally activate procaspase-9 to caspase-9. Caspase-9 further activates procaspase-3/-7 and -6 to caspase-3/-7/-6, which eventually cleaves the inhibitors of nucleases [41]. Activated nucleases such as poly (ADP-ribose) polymerase (PARP) enter the nucleus and cause DNA degradation leading to cell death. On the contrary, extrinsic pathway signals originate from outside the cells. Upon binding of the extrinsic signal molecule ligands to any of the death receptors such as Fas, TNFαR, DR3, DR4, and DR5, the death domain receptor inside the cell is activated and induces the death-induced signaling cascade (DISC) due to interactions between multiple death receptors that are closely located to one another. Caspase-8, which plays a vital role in the extrinsic apoptotic pathway, is first activated. Caspase-8 activates procaspase-3/-7/-6 to caspase-3/-7/-6, which finally activates nucleases to degrade DNA. Although caspase-8 is a major protease of the extrinsic apoptotic pathway, it is also involved in the intrinsic apoptotic pathway by activating BID protein to tBID, which activates the Bcl-2 family members. BAX and BAK proteins are responsible for making holes in the mitochondrial membrane, triggering the intrinsic apoptotic pathway, as mentioned previously. Caspase-3 is regarded as the main executioner of caspase, and caspase-7 is responsible for cell detachment as a supportive role in apoptosis [42]. MCF-7 cells that we used here do not exist caspase-3 gene as the cells were originated from a breast cancer tissue without the caspase-3 protein-coding gene [43]. Therefore, caspase activity detected in the treated MCF-7 cells may be involved mainly with caspase-7 and other associated proteases of subfamily member CED-3. Further investigations are required to carry out in the future to identify other caspases involved in inducing apoptosis of such MCF-7 cells deficient in caspase-3. Time-dependent treatments are also recommended so that treatment duration required to attain the maximum number of early apoptotic cell population can be identified before treated cells enter the late apoptosis or secondary necrosis phase after 24 h of treatment. Targeting cell cycle arrest is an attractive therapeutic property for anticancer compounds. In fact, interferonalpha, an effective anticancer agent clinically used to treat liver cancer, also induces cell cycle arrest at the S and G2/ M phases [44]. Other anticancer agents that induce cell cycle arrest at both the S and G2/M phases are selenomethionine (SeMet), gatifloxacin, and 7-hydroxystauro-sporine [45][46][47]. MDA-MB-231 cells treated with 4.5 μM (lower than IC 50 ), 8.5 μM (IC 50 ), or 12.5 μM (higher than IC 50 ) of compound 3F1 showed higher percentages in the S phase (18:08 ± 1:66%, 17:88 ± 0:33%, and 21:33 ± 1:49%) and G2/ M phase (30:29 ± 6:17%, 35:58 ± 4:35%, and 36:59 ± 2:82% ), respectively, compared with control cells in the S phase (11:66 ± 3:94%) and G2/M phase (24:15 ± 6:04%). MCF-7 cells treated with 3.5 μM (lower than IC 50 ), 6.5 μM (IC 50 ), or 9.5 μM (higher than IC 50 ) of compound 3F1 also showed higher percentages in the S phase (18:10 ± 1:80%, 20:74 ± 3:24%, and 22:19 ± 2:38%) and G2/M phase (30:17 ± 1:90%, 32:91 ± 3:32%, and 35:86 ± 2:76%), respectively, compared with MCF-7 control cells in the S phase (16:94 ± 0:36) and G2/M phase (26:86 ± 1:13%). Along with accumulation at the S and G2/M phases, a concomitant decrease in the percentage of G0/G1 phase cells was observed in the treated MDA-MB-231 (from the control at 64:20 ± 7:38% to 51:63 ± 7:58%, 46:53 ± 4:24%, and 42:07 ± 3:74%) and MCF-7 (from the control at 56:19 ± 0:98% to 51:84 ± 0:69%, 46:35 ± 0:19%, and 41:95 ± 0:85%) cells, respectively. Therefore, based on these consistent findings, we suggest that the novel gold compound 3F1 induced cell cycle arrest at both the S and G2/M phases.
Malignant cells grow uncontrollably due to disruption of cell cycle regulations by overexpression of cyclins and failure of cyclin-dependent kinase (CDK) inhibitor expression. Furthermore, incompetent checkpoint control also causes the division of genetically damaged cells resulting in the emergence of cancer cells. Both CDK4-cyclin D and CDK6cyclin D are responsible for the G1 phase, whereas CDK2cyclin A is responsible for the S phase. The G2/M phase is controlled by CDK1-cyclin A and CDK1-cyclin B, respectively [48]. For more detailed information regarding the cell cycle arrest induced by compound 3F1, it is necessary to determine the duration of each phase in the cell cycle to identify and quantify the respective CDKs with their associated cyclin proteins and CDK inhibitors specific to each phase of the cell cycle in tumor cells [49][50][51]. Our study suffers from some limitations. Normal breast cancer cells, e.g., MCF-10/-10A, should have also been tested with the compound 3F1 in addition to H9c2 cells. However, in other similar studies, the same H9c2 cell type was the only cells that had been tested without using normal breast too [52][53][54][55]. Normal breast cells may have more tolerance to the compound 3F1 than H9c2 cardiomyoblasts. Moreover, other caspases activities and the length of each cell cycle phase could have been carried out to present comprehensive findings.

Conclusions
Among newly synthesized gold (I) compounds, 3F1, 3F3, and the ligand 3FL, the compound 3F1 (triphenylphosphanegold(I) O-methyl-N-3-fluorophenyl thiocarbamate) demonstrated significant inhibition of the in vitro growth of triple-negative breast cancer cells (MDA-MB-231), estrogen receptor-positive breast cancer cells (MCF-7), BCA, BCSC-P and BCSC. The compound 3F1 induced apoptosis in both MDA-MB-231 and MCF-7 cells. Execution of MDA-MB-231 cell death was via activation of the caspase 3/7 pathway that is responsible for both extrinsic (death receptors and ligands) and intrinsic (mitochondrial-initiated) caspasedependent apoptosis. IC 50 doses of the 3F1 compound were approximately at least 6-fold lower than those of the commonly used anticancer compound, cisplatin (CDDP). Furthermore, 3F1 induced cell cycle arrest of treated MDA-MB-231 and MCF-7 cells at the S and G2/M phases. In summary, the compound 3F1, Ph 3 PAu[SC(OMe)=NC 6 H 4 F-3], is a potential anticancer compound, and findings from this