Gentian violet (GV), a cationic triphenylmethane dye, is used as an antifungal and antibacterial agent. Recently, attention has been focused on GV as a potential chemotherapeutic and antiangiogenic agent. The present study was undertaken to determine the suppressive effects of GV on human breast cancer MDA-MB-231 cells in vitro. The proliferation of MDA-MB-231 cells was suppressed by culture with GV (1–200 nM). The suppressive effects of GV on cell proliferation were not potentiated in the presence of various inhibitors that induce cell cycle arrest in vitro. This finding suggested that GV inhibits G1 and G2/M phase cell cycle arrest in MDA-MB-231 cells. The suppressive effects of GV on proliferation are mediated through the inhibition of various signaling pathways or nuclear transcription in vitro. Moreover, the suppressive effects of GV on cell proliferation were compared with that of gemcitabine, a strong antitumor agent that induces nuclear DNA damage. Notably, the culture with gemcitabine >50 nM suppressed cell proliferation, while the effects of GV were observed at >1 nM. The suppressive effects of gemcitabine on cell proliferation were not potentiated by GV. Overall, the present study demonstrated that GV exhibits a potential suppressive effect on the proliferation of human breast cancer MDA-MB-231 cells in vitro.
gentian violethuman breast cancerMDA-MB-231 cellscell proliferationcell cyclecell deathIntroduction
Various types of cancer induce bone metastasis, which leads to serious bone loss and fractures. Bone metastasis occurs in 70–80% of patients with advanced stage breast cancer (1–4), and induces severe pathological bone fractures, pain, hypercalcemia, and spinal cord and nerve-compression syndromes (3,5). This bone disorder is frequently causes morbidity and mortality. Tumor invasion of the bone tissues is associated with the recruitment of osteoclasts and osteoblasts, resulting in growth factor liberation from the bone matrix. Furthermore, these growth factors can enhance tumor growth, resulting in a cycle of bone metastasis (4,5).
Breast cancer cells promote osteoclast formation via the secretion of osteoporotic cytokines, including parathyroid hormone-related peptide, tumor necrosis factor-α (TNF-α), prostaglandin E2, leukemia inhibitory factor, and interleukin-1, −6, −8, −11, −15 and −17 (4,6). Constitutively-activated nuclear factor-κB (NF-κB) in breast cancer cells has been shown to play a crucial role in osteolysis, which stimulates osteoclastogenesis. Moreover, breast cancer cells stimulate the production of granulocyte macrophage colony-stimulating factor, which enhances development from monocytes to osteoclasts (7). In addition, progesterone receptor-positive mammary epithelial cancer cells express receptor activator of NF-κB ligand (RANKL), which mediates the proliferation of epithelial cells and carcinogenesis (8). In addition, breast cancer cells suppress the function of osteoblasts. This is demonstrated by an increase in apoptosis and a decrease in proteins required for new bone formation (6). Bone loss induced by breast cancer bone metastasis is based on activated osteoclastic bone resorption and suppressed osteoblastic bone formation.
Bisphosphonate or anti-RANKL antibody (denosumab) is used as the current standard care for patients with bone metastasis (9). Bisphosphonate inhibits osteoclastic bone resorption, but does not possess osteogenic effects. Denosumab suppresses osteoclast maturation by inhibiting the binding of RANKL to RANK, which is the receptor of RANKL in preosteoclasts and mature osteoclasts. These drugs target bone resorption mediated through osteoclasts. However, agents that stimulate osteogenic bone formation to repair bone destruction have been poorly developed.
Gentian violet (GV), a triaminophenylmethane dye, has been used extensively in medicine for a century, and it has a potent anti-microbial action (10). Furthermore, recent studies have suggested the angiogenic and anticancer properties of GV, and this chemical is currently experiencing renewed interest in medical applications (11,12). Our recent study demonstrated that GV inhibits nuclear factor-κB (NF-κB) activity, and that this agent can potently enhance osteoblast differentiation and mineralization, but suppress the differentiation to osteoclasts (13). Thus, GV may regulate the differentiation of bone cells in vitro. Further development of GV as an anti-osteoporotic and/or anti-inflammatory agent may be expected.
Moreover, GV may possess preventive effects on bone loss induced by cancer cell bone metastasis. However, the anticancer effects of GV on human breast cancer bone metastatic cells have been poorly investigated. The present study was undertaken to determine whether GV exhibits a suppressive effect on the proliferation of human breast cancer MDA-MB-231 cells in vitro. The results showed that GV potently suppresses the proliferation of human breast cancer MDA-MB-231 cells.
Materials and methodsMaterials
Dulbecco's modified Eagle's medium (DMEM) with 4.5 g/l glucose, L-glutamine and sodium pyruvate, and antibiotics [penicillin and streptomycin (P/S); 5,000 U/ml and 5,000 µg/ml, respectively] were purchased from Gibco Laboratories (Grand Island, NY, USA). Fetal bovine serum (FBS) was obtained from HyClone (Logan, UT, USA). Gentian violet, sodium butyrate, roscovitine, sulforaphane, PD98059, staurosporine, wortmannin, 5,6-dichloro-1-β-D-ribofuranosylbenzimidazole (DRB) and all other reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA) unless otherwise specified. Gemcitabine was obtained from Hospira, Inc. (Lake Forest, IL, USA). Gemcitabine was diluted in phosphate-buffered saline (PBS) and other reagents were dissolved in 100% ethanol to use in the experiments.
Cancer cells
MDA-MB-231 human breast cancer cells lack the receptors for progesterone, estrogen and human epithelial growth factor receptor 2, and are therefore considered as triple negative (14). However, MDA-MB-231 cells do express epithelial growth factor receptor (EGFR) at high levels, and activation of this receptor and its downstream signaling events enhance the migration, proliferation, invasion and progression of the malignant phenotype of breast cancer cells (14). The present study used estrogen-independent bone-seeking triple negative human breast cancer MDA-MB-231 cells (1×106 cells/ml of DMEM containing 10% FBS and 0.1% P/S), which were stored at −80°C. The cells were obtained from the American Type Culture Collection (Rockville, MD, USA).
Proliferation in cancer cells
The breast cancer MDA-MB-231 cells (1×105/ml per well) were cultured in a 24-well plate using DMEM containing 10% FBS and 1% P/S in the presence or absence of GV (1, 10, 50, 100 or 200 nM) for 1, 3, 7 or 14 days in a water-saturated atmosphere containing 5% CO2 and 95% air at 37°C (15–17). In separate experiments, the MDA-MB-231 cells (1×105/ml per well) were cultured in DMEM containing 10% FBS and 1% P/S in the presence of either ethanol (0.1% final concentration; control), sodium butyrate (10 and 100 µM), roscovitine (10 and 100 nM), sulforaphane (1 and 10 nM), PD98059 (1 µM), staurosporin (0.1 µM), wortmannin (1 µM), DRB (1 µM) or gemcitabine (100 nM) for 3–7 days. Subsequent to the culture process, the cells were detached from each culture dish and counted (16,17). In addition, to determine the effects of GV on MDA-MB-231 cells that reached confluence, the cells (1×105 cells/ml per well) were cultured using a 24-well plate in DMEM containing 10% FBS and 1% P/S in the absence of GV for 7 days until they reached confluence, and then the cells were cultured in the presence of GV (1, 10, 50, 100 or 200 nM) for 3 days (18). Following this, the cells were detached from each culture dish and counted.
Cell counting
Following trypsinization of each culture dish using 0.2% trypsin plus 0.02% EDTA in Ca2+/Mg2+-free PBS for 2 min at 37°C, detached cells from the dishes were collected after centrifugation at 150 × g for 5 min (16–18). The cells were resuspended in PBS solution and stained with eosin. Cell numbers were counted under a microscope (Olympus MTV-3; Olympus, Tokyo, Japan) using a hemocytometer plate. For each dish, the average of two counts was used. Cell number is shown as the number per well of each plate.
Statistical analysis
Statistical significance was determined using GraphPad InStat version 3 for Windows XP (GraphPad Software Inc., La Jolla, CA, USA). Multiple comparisons were performed by one-way analysis of variance with Tukey-Kramer multiple comparisons post-hoc test for parametric data as indicated. P<0.05 was considered to indicate a statistically significant difference.
Results
To determine the effects of GV on the proliferation of human breast cancer MDA-MB-231 cells in vitro, the cancer cells were cultured in the presence of GV for 3 or 7 days. Cell numbers were increased with increasing culture periods. This increase was suppressed after culture with GV (1–200 nM) for 3 (Fig. 1A) and 7 (Fig. 1B) days. Thus, GV was found to exhibit suppressive effects on the proliferation of the MDA-MB-231 cells in vitro. In addition, the MDA-MB-231 cells that reached confluence after culture for 7 days were cultured for an additional 3 days in the presence of GV (1–200 nM). Cell number was significantly (P=0.001) decreased after culture with GV (10–200 nM) (data not shown), suggesting that GV partly stimulates cell death.
To determine a mechanistic characterization, the present study determined whether the suppressive effects of GV on the proliferation of MDA-MB-231 cells are altered using various inhibitors that induce cell cycle arrest in vitro (Fig. 2). Cells were cultured for 3 days with or without butyrate (10 and 100 µM), roscovitine (10 and 100 nM) or sulforaphane (1 and 10 nM) (17,19,20). The proliferation of the MDA-MB-231 cells, which were cultured in the absence of GV, was suppressed in the presence of these inhibitors (Fig. 2A). The suppressive effects of these inhibitors on cell proliferation was not altered in the presence of GV (100 nM) (Fig. 2B). This finding suggested that GV induces G1 and G2/M phase cell cycle arrest in MDA-MB-231 cells.
Next, the study determined whether the suppressive effects of GV on the proliferation in MDA-MB-231 cells are changed by various signaling factors that suppress proliferation. The suppressive effects of GV (100 nM) on the proliferation of the MDA-MB-231 cells were not altered in the presence of PD98059 (1 µM), an extracellular signal-regulated kinase (ERK) inhibitor (21), or staurosporin (0.1 µM), an inhibitor of protein kinase C (22) (Fig. 3A). In addition, the suppressive effects of GV on cell proliferation were not enhanced in the presence of wortmannin (1 µM), an inhibitor of phosphatidylinositol 3-kinase (PI3K) (23), or DRB (1 µM), an inhibitor of transcriptional activity with RNA polymerase II inhibition (24) (Fig. 3B).
Moreover, the suppressive effects of GV on the proliferation of the MDA-MB-231 cells were compared with those of gemcitabine, a strong antitumor agent that induces nuclear DNA damage (25). Culture with gemcitabine (50, 100 and 300 nM) for 7 days suppressed cell proliferation, while such effects were not observed at a concentration of 10 nM gemcitabine (Fig. 4A). The suppressive effects of gemcitabine (10 and 50 nM) on proliferation were not potentiated in the presence of GV (10 nM), which exhibited suppressive effects on the proliferation of the MDA-MB-231 cells (Fig. 4B).
Discussion
The present study demonstrated that GV exhibits a potent suppressive effect on the proliferation of human breast cancer MDA-MB-231 cells in vitro. The suppressive effects of GV on cell proliferation were characterized using various factors that inhibit cell cycle-related signaling processes. The suppressive effects of GV on the proliferation of the MDA-MB-231 cells were not changed by the presence of butyrate, roscovitine or sulforaphan, which induce cell cycle arrest. Roscovitine is a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2m and cdk5 (19), sulforaphane induces G2/M phase cell cycle arrest (20) and butyrate induces the inhibition of G1 progression (17). In the present study, GV was suggested to induce G1 and G2/M phase cell cycle arrest in the MDA-MB-231 cells.
The suppressive effects of GV on the proliferation of the MDA-MB-231 cells were not altered in the presence of various inhibitors that regulate intracellular signaling pathways in vitro. The suppressive effects of GV on cell proliferation were not potentiated in the presence of PD98059, an inhibitor of the ERK/mitogen-activated protein kinase (MAPK) signaling pathway (21), staurosporin, an inhibitor of the calcium-dependent protein kinase C signaling pathway (22), or wortmannin, an inhibitor of the PI3K/Akt signaling pathway (23). GV appeared to suppress cell proliferation, which is mediated through the inhibition of various signaling pathways associated with ERK/MAPK, calcium and PI3/Akt in breast cancer MDA-MB-231 cells.
Moreover, the suppressive effects of GV on cell proliferation were not altered in the presence of DRB, an inhibitor of transcriptional activity with RNA polymerase II inhibition (24). GV may also suppress transcriptional activity in the nuclei of MDA-MB-231 cells. Gemcitabine is an antitumor agent that induces nuclear DNA damage (25). This agent suppresses cell proliferation and stimulates apoptotic cell death in various types of cancer cells. In the present study, the effects of GV on proliferation and cell death were not enhanced in the presence of gemcitabine in the MDA-MB-231 cells, suggesting that GV partly acts in a process involved in the action of gemcitabine. Notably, GV exhibited suppressive effects on cell proliferation at lower concentrations compared with gemcitabine, indicating that GV exhibits a potential effect in breast cancer cells. GV may provide a useful tool as a novel antitumor agent.
GV has been shown to potently prevent TNF-α-induced suppression of osteoblastic mineralization and RANKL-induced stimulation of osteoclastogenesis by antagonizing the activation of NF-κB signaling in preosteoblastic cells and RAW267.4 preosteoclastic cells in vitro (13). Moreover, GV has been demonstrated to potently prevent suppressed osteoblastic mineralization and enhanced osteoclastogenesis induced by MDA-MB-231 cells in bone marrow culture in vitro (26). From these findings, it has been suggested that GV exhibits a potent suppressive effect on the activation of NF-κB signaling in MDA-MB-231 cells.
In conclusion, the present study demonstrated that GV potently suppresses the proliferation of human breast cancer MDA-MB-231 cells in vitro, and that this effect of GV has potential compared with that of gemcitabine, which is clinically used as an anticancer drug (25). GV may be a novel useful tool in the prevention and therapy of breast cancer in vivo.
ReferencesBoyceBFYonedaTGuiseTAFactors regulating the growth of metastasis cancer in boneEndocr Relat Cancer6333347199910.1677/erc.0.006033310516850MundyGRMetastasis to bone: Causes, consequences and therapeutic opportunitiesNat Rev Cancer2584593200210.1038/nrc86712154351RoodmanCDMechanism of bone metastasisN Engl J Med35016551664200410.1056/NEJMra03083115084698AkhtariMMansuriJNewmanKAGuiseTMSethPBiology of brest cancer bone metastasisCancer Biol Ther739200810.4161/cbt.7.1.516318059174ColemanREMetastatic bone disease: Clinical features, pathophysiology and treatment strategiesCancer Treat Rev27165176200110.1053/ctrv.2000.021011417967ChenYCSosnoskiDMMastroAMBreast cancer metastasis to the bone: Mechanisms of bone lossBreast Cancer Res12215201010.1186/bcr278121176175ParkBKZhangHZengQDaiJKellerETGiordanoTGuKShahVPeiLZarboRJNF-kappaB in breast cancer cells promotes osteolytic bone metastasis by inducing osteoclastogenesis via GM-CSFNat Med136269200710.1038/nm151917159986Gonzalez-SuarezEJacobAPJonesJMillerRRoudier-MeyerMPEnwertRPinkasJBranstetterDDougallWCRANK ligand mediates progestin-induced mammary epithelial proliferation and carcinogenesisNature468103107201010.1038/nature0949520881963WeilbaecherKNGuiseTAMcCauleyLKCancer to bone: A fatal attractionNat Rev Cancer11411425201110.1038/nrc305521593787BerriosRLArbiserJLEffectiveness of gentian violet and similar products commonly used to treat pyodermasDermatol Clin296973201110.1016/j.det.2010.08.00921095530PerryBNGovindarajanBBhandarkarSSKnausUGValoMSturkCCarrilloCOSohnACerimeleFDumontDPharmacologic blockade of angiopoietin-2 is efficacious against model hemangiomas in miceJ Invest Dermatol12623162322200610.1038/sj.jid.570041316741507ZhangXZhengYFriedLEDuYMontanoSJSohnALefkoveBHolmgrenLArbiserJLHolmgrenALuJDisruption of the mitochondrial thioredoxin system as a cell death mechanism of cationic triphenylmethanesFree Radic Biol Med50811820201110.1016/j.freeradbiomed.2010.12.03621215310YamaguchiMVikulina1TArbiserJLWeitzmannMNSuppression of NF-κB activation by gentian violet promotes osteoblastogenesis and suppresses osteoclastogenesisCurr Mol Med14783792201410.2174/156652401466614072410484225056540YonedaTWilliamsPJHiragaTNiewolnaMNishimuraRA bone-seeking clone exhibits different biological properties from the MDA-MB-231 parental human breast cancer cells and a brain-seeking clone in vivo and in vitroJ Bone Miner Res1614861495200110.1359/jbmr.2001.16.8.148611499871YamaguchiMZhuSWeitzmannMNSnyderJPShojiMCurcumin analog UBS109 prevents bone marrow osteoblastogenesis and osteoclastogenesis disordered by coculture with breast cancer MDA-MB-231 bone metastatic cells in vitroMol Cell Biochem401110201510.1007/s11010-014-2286-x25416449MisawaHInagakiSYamaguchiMSuppression of cell proliferation and deoxyribonucleic acid synthesis in cloned rat hepatoma H4-II-E cells overexpressing regucalcinJ Cell Biochem84143149200110.1002/jcb.127411746523YamaguchiMDaimonYOverexpression of regucalcin suppresses cell proliferation in cloned rat hepatoma H4-II-E cells: Involvement of intracellular signaling factors and cell cycle-related genesJ Cell Biochem9511691177200510.1002/jcb.2049015962315IzumiTYamaguchiMOverexpression of regucalcin suppresses cell death in cloned rat hepatoma H4-II-E cells induced by tumor necrosis factor-alpha or thapsigarginJ Cell Biochem92296306200410.1002/jcb.2005615108356MeijerLBorgneAMulnerOChongJPBlowJJInagakiNInagakiMDelerosJGMoulinouxJPBiochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5Eur J Biochem243527536199710.1111/j.1432-1033.1997.t01-2-00527.x9030781SinghSVHerman-AntosiewiceASinghAVLewKLStrivastavaSKKamathRBrownKDZhangLBaskaranRSulforaphan-induced G2/M phase cell cycle arrest involves checkpoint kinase 2-mediated phosphorylation of cell division cycle 25CJ Biol Chem2792581325822200410.1074/jbc.M31353820015073169ChenSWangYRuanWWangXPanCReversing multidrug resistance in hepatocellular carcinoma cells by inhibiting extracellular signal-regulated kinase/mitogen-activated protein kinase signaling pathway activityOncol Lett823332339201425295120ChenQWEdvinssonLXuCBRole of ERK/MAPK in endothelin receptor signaling in human aortic smoth muscle cellsBMC Cell Biol1052200910.1186/1471-2121-10-5219575782Serrano-NascimentoCda SilvaTeixeira SNicolaJPNachbarRTMasini-RepisoAMNunesMTThe acute inhibitory effect of iodide excess on sodium/iodide symporter expression and activity involves the PI3K/Akt signaling pathwayEndocrinology15511451156201410.1210/en.2013-166524424051PalangatMGrassJALangelierMFCoulombeBLandickRThe RPB2 flap loop of human RNA polymerase II is dispensable for transcription initiation and elongationMol Cell Biol3133123325201110.1128/MCB.05318-1121670157TangSCChenYCNovel therapeutic targets for pancreatic cancerWorld J Gastroenterol201082510844201410.3748/wjg.v20.i31.1082525152585YamaguchiMVikulinaTWeitzmannMNGentian violet inhibits MDA-MB-231 human breast cancer cells proliferation, and reverses the stimulation of osteoclastogenesis and suppression of osteoblast activity induced by cancer cellsOncol Rep3421562162201526260090
Gentian violet (GV) potently suppresses MDA-MB-231 human breast cancer cell proliferation in vitro. Cells were cultured in Dulbecco's modified Eagle's medium in the presence or absence of GV (1–200 nM) for (A) 3 or (B) 7 days. After culture, the number of attached cells on each dish was counted. Data are presented as the mean ± standard deviation of 2 replicate wells per dataset using different dishes and cell preparations. *P<0.001 vs. control (one-way analysis of variance, Tukey-Kramer post-hoc test).
Gentian violet (GV) induces cell cycle arrest in human breast cancer MDA-MB-231 cells in vitro. Cells were cultured for 3 days in the (A) absence or (B) presence of GV (100 nM) with or without butyrate (10 and 100 µM), roscovitine (10 and 100 nM) or sulforaphane (1 and 10 nM). After culture, the number of attached cells on each dish was counted. Data are presented as the mean ± standard deviation of 2 replicate wells per dataset using different dishes and cell preparations. *P<0.001 vs. control (white bar) (one-way analysis of variance, Tukey-Kramer post-hoc test).
Suppressive effects of gentian violet (GV) on cell proliferation are not altered in the presence of inhibitors associated with intracellular signaling and transcriptional activity in MDA-MB-231 human breast cancer cells in vitro. (A) Cells were culture for 3 days in the presence of GV (100 nM) with or without PD98059 (1 µM) or staurosporin (0.1 µM). (B) Cells were cultured for 3 days in the presence of GV (100 nM) with or without wortmannin (1 µM) or DRB (1 µM). After culture, the number of attached cells on each dish was counted. Data are presented as the mean ± standrad deviation of 2 replicate wells per dataset using different dishes and cell preparations. *P<0.001 vs. control (grey bar). DRB, 5,6-dichloro-1-β-D-ribofuranosylbenzimidazole.
Suppressive effects of gentian violet (GV) on human breast cancer MDA-MB-231 cells show potential as compared with gemcitabine (GC) in vitro. (A) Cells were cultured for 7 days in the presence of gemcitabine (10, 50, 100 or 200 nM). (B) Cells were cultured for 7 days in the presence of GV (10 nM) with or without gemcitabine (10 or 50 nM). After culture, the number of attached cells on each dish was counted. Data are presented as the mean ± standard deviation of 2 replicate wells per dataset using different dishes and cell preparations. *P<0.001 vs. control (grey bar) (one-way analysis of variance, Tukey-Kramer post-hoc test).