This article is mentioned in:

Introduction

Breast cancer is the most common malignancy among women and estrogen is an essential stimulant of estrogen receptor (ER)-positive breast cancer (1,2). Tamoxifen (TAM), a non-steroidal anti-estrogen, is the most commonly used therapeutic or preventative agent for ER-positive breast cancer patients (3). However, acquired resistance to TAM is a critical problem with long-term TAM use, and the mechanism underlying this resistance remains unclear (4). We previously established an MCF-7-derived TAM-resistant cell line (TAMR-MCF-7 cells) by long-term incubation with 4-hydroxytamoxifen (5), and determined that TAMR-MCF-7 cells lost polarity and acquired migratory and invasive properties with higher expression of epithelial mesenchymal transition (EMT) marker proteins (6–8). This process is considered a prerequisite for tumor infiltration and metastasis (9). TAMR-MCF-7 cells have also been shown to exhibit enhanced vascular endothelial growth factor (VEGF) expression levels, leading to the promotion of angiogenesis (10).

Several receptors and transcription factors are actively involved in the regulation of cell proliferation and acquisition of migratory and invasive properties in diverse cancer cell types. Among these, the Janus kinase 2 (JAK2)-signal transducer and activator of transcription (STAT) 3 pathway transfers extracellular signals from cytokines and growth factor receptors, including the interleukin-6 receptor (IL-6R) and platelet-derived growth factor receptor (PDGFR), to its downstream target genes (11–13). Activation of the JAK-STAT pathway in cancer cells activates the transcription of several oncogenic genes, including c-myc, ccnd1, and VEGF (14–16). Several studies have indicated that the JAK2-STAT3 signaling pathway is a crucial activator of cell migration and cancer metastasis (17–19).

Ruxolitinib (Jakafi), a potent JAK1/2 inhibitor, was approved by the United States Food and Drug Administration (FDA) in 2011 for the treatment of patients with myeloproliferative neoplasia (MPN). Ruxolitinib directly inhibits JAK1 and JAK2 kinases, with IC50 values of 3.3 and 2.8 nM, respectively (20). Ruxolitinib reduced protein levels of phosphorylated JAK2 and subsequently inhibited protein expression of its downstream target genes, c-Myc, cyclin D1 and Bcl-2 (21). In preclinical studies, ruxolitinib was shown to inhibit the proliferation of JAK2V617F-positive Ba/F3 cells showing a constitutively active mutant form of JAK2, and to alleviate MPN symptoms in JAK2V617F-transgenic mice (20). Moreover, involvement of JAK2 in cell proliferation was experimentally verified in various cancer cell lines, lung cancer cells (H661, H1975, H1563, ADOR, NSCLC1), breast cancer cells (MCF-7, MCF-7-HER18, SUM149, BT474, BT549, SKBR3) and glioblastoma cells (GBM6, GBM12) (21–23). However, the therapeutic effects of ruxolitinib on chemo-resistant breast cancer cells, and especially TAM-resistant cells, remain obscure. In the present study, we demonstrated for the first time that TAM-resistant MCF-7 cells showed higher sensitivity to ruxolitinib compared to parental MCF-7 cells, and the JAK inhibitor blocked the EMT process and VEGF production, consequently suppressing TAMR-MCF-7 cell migration and angiogenesis.

Materials and methods

Cell culture and reagents

MCF-7 (ER-positive human breast cancer cell line) cells were obtained from Korea Cell Line Bank (#30022, 2005), and cultured at 37°C in Dulbecco's modified Eagle's medium (DMEM) containing 10% fetal bovine serum (FBS), 100 U/ml penicillin, and 100 µg/ml streptomycin. TAMR-MCF-7 cells were established as previously described (5,24).

The antibodies used in the present study were as follow: phospho-STAT3 (p-STAT3) (Y705, cat. no. 9131S), STAT3 (cat. no. 4904S), Bcl-2 (cat. no. 2876S) and hypoxia inducible factor (HIF)-1α (cat. no. 3716S) were purchased from Cell Signaling Technology (Beverly, MA, USA), c-Myc (cat. no. sc-40), c-Jun (cat. no. sc-1694), Cyclin B1 (cat. no. sc-245), Cyclin D1 (cat. no. sc-753), vimentin (cat. no. sc-32322), twist (cat. no. sc-81417) were obtained from Santa Cruz Biotechnology (Dallas, TX, USA), and glyceraldehyde 3-phosphate dehydrogenase (GAPDH, Calbiochem, Gibbstown, NJ, USA; cat. no. CB-1001), β-actin (Sigma-Aldrich, St. Louis, MO, USA; cat. no. a2228), E-cadherin (BD Biosciences, San Jose, CA, USA; cat. no. 610181), N-cadherin (BD Biosciences; cat. no. 610920), snail (Abcam, Cambridge, UK; cat. no. ab53519) were used. VEGF-luc plasmids were kindly donated from Dr. Lee (Chonnam National University, Gwangju, Korea).

Western blot analysis

Cells were lysed with lysis buffer containing 20 mM Tris-Cl (pH 7.5), 1% Triton X-100, 137 mM sodium chloride, 10% glycerol, 2 mM EDTA, 1 mM sodium orthovanadate, 25 mM β-glycerophosphate, 2 mM sodium pyrophosphate, 1 mM phenylmethylsulfonylfluoride and 1 µg/ml leupeptin. The cell lysates were centrifuged at 13,000 × g for 15 min to remove insoluble material, the supernatants were quantified using the Bradford method (25) and fractionated using polyacrylamide gel, and electrophoretically transferred to nitrocellulose membranes. Horseradish peroxidase (HRP)-conjugated anti-IgG antibodies were used as the secondary antibodies (cat. no. 7076S, 7074S, 1:5,000 dilution; Cell Signaling Technology). The nitrocellulose papers were developed using an ECL chemiluminescence system (Milipore, Billerica, MA, USA). For ECL chemiluminescence detection, LAS-3000 mini system (Fujifilm, Tokyo, Japan) was used.

Immunocytochemistry

MCF-7 and TAMR-MCF-7 cells were cultured overnight on coverslips. After treatment with 10 µM ruxolitinib or vehicle, the cells were fixed with 4% paraformaldehyde and blocked with 1% bovine serum albumin at room temperature for 1 h. The cells were incubated with Alexa Fluor 488-conjugated Phalloidin antibody (1:200 dilution, Thermo Fisher Scientific, Waltham, MA, USA) in 0.1% Tween-20-containing phosphate-buffered saline at 4°C overnight. Mouse monoclonal E-cadherin or N-cadherin antibody (1:200 dilution, BD Biosciences) were also incubated in the same buffer at 4°C overnight. After twice washing with PBS, the coverslips were incubated with goat anti-mouse Alexa Fluor 568 IgG (1:2,000 dilution; Thermo Fisher Scientific, Inc., Waltham, MA, USA) at room temperature for 1 h. Finally, the coverslips were washed thoroughly with PBS and then mounted with ProLong Gold Antifade reagent with 4′,6-diamidino-2-phenylindole (DAPI; Invitrogen, Carlsbad, CA, USA). Images were obtained using CELENAS Digital Imaging System (Logos Biosystems, Anyang, South Korea).

Cell proliferation assay

MCF-7 and TAMR-MCF-7 cells were seeded in 96-well plate (3×103 cells/well) and cultured for 96 h in the presence or absence of ruxolitinib (0.1–10 µM). The kinetics of viable cell numbers were counted using IncuCyte ZOOM live-cell analysis system (Essen BioScience, Ann Arbor, MI, USA) and monitored using the IncuCyte label-free cell monolayer confluence algorithm. IncuCyte provides the ability to acquire phase-contrast images and an integrated confluence metric as a surrogate for cell number.

Transwell migration assay

TAMR-MCF-7 cells were seeded in the upper chamber of the transwell plate (Essen BioScience) and the lower side of the upper chamber was covered with type I collagen (Sigma-Aldrich). The lower chamber was filled with 200 µl FBS-containing culture media. The cells were incubated at 5% CO2 for 18 h. The migrated cell numbers were counted using IncuCyte ZOOM live-cell analysis system.

Semi-quantitative polymerase chain reaction (sqPCR)

Total RNA was isolated from MCF-7 and TAMR-MCF-7 cells using Trizol® reagent (Invitrogen), and cDNA was synthesized by reverse transcriptase using an oligo (dT) primer. PCR was performed using the selective primers for human VEGF (sense: 5′-GCTACTGCCATCCAATCGAG-3′, antisense: 5′-TGCATTCACATTTGTTGTGC-3′), human GAPDH (sense: 5′-AAGGCTGAGAACGGGAAG-3′, antisense: 5′-GCCCCACTTGATTTTGGA-3′) as the housekeeping gene. sqPCR was performed for 40 cycles (denaturation at 98°C for 30 sec, annealing at 60°C for 30 sec, and then a final extension at 60°C for 5 min). After PCR, 6 µl samples of the products were subjected to 2.0% agarose gel electrophoresis and stained with ethidium bromide. Densitometric analyses were performed using Quantity One 1-D Analysis Software version 4.6.2 (Bio-Rad Laboratories, Inc., Hercules, CA, USA).

Reporter gene assay

MCF-7 and TAMR-MCF-7 cells (1×105 cells/well) were seeded in 48-well plates, then transfected with luciferase reporter plasmids containing VEGF-luc reporter plasmid containing the luciferase structural gene and the human VEGF promoter and pRL-SV plasmids (Renilla luciferase expression for normalization). The transfected cells were exposed to compound for 24 h, and the promoter activity was measured using a dual-luciferase reporter assay system (Promega, Madison, WI, USA). The firefly and Renilla luciferase activities were measured using a luminometer (LB941, Berthold Technologies, Bad Wildbad, Germany).

Chick chorioallantoic membrane (CAM) assay

Fertilized eggs were purchased from Siprigol Poultry Farm (Gyeongsan, South Korea) and the CAM was prepared as described previously (26–28). The surfaces of 10-day-old post-fertilization chick eggs were sterilized and the CAM was exposed by cutting a window (1 cm2) on one side of the egg using the false air sac technique. TAMR-MCF-7 cells were placed on the exposed CAM and the windows were sealed with transparent tape. The eggs were then incubated in a humidified incubator at 37°C. The CAMs were examined at 3 days after inoculation using a SV6 stereomicroscope (Carl Zeiss, Hamburg, Germany) at 50 × magnification. The CAM experiments were terminated at 13th embryonic day. After extraction of chorioallantoic membrane, chick embryos should be dead due to the excess hemorrhage. Then the dead cadaver was disposed in accordance with the biological waste treatment procedures. Digital images of CAM sections were collected using a 3-charge coupled device color video camera system (Toshiba, Tokyo, Japan). The number of vessel branch points contained in a circular region was counted. The experimental studies were approved by the Institutional Animal Care and Use Committee of Yeungnam University (Gyeongsangbuk, Korea).

Statistical analysis

Statistical analysis was performed using Sigma plot 12.0 (Systat Software, Inc., San Jose, CA, USA) with one-way analysis of variance and Tukey's post hoc multiple comparisons test to determine the differences. P<0.05 was considered to indicate a statistically significant difference.

Results

Ruxolitinib inhibits STAT3 activation in TAMR-MCF-7 cells

We compared JAK2 activity between MCF-7 and TAMR-MCF-7 cells by determining the extent of Tyr705 STAT3 phosphorylation. Immunoblot results showed that STAT3 phosphorylation was much higher in TAMR-MCF-7 cells than in control MCF-7 cells (Fig. 1A). We then assessed whether ruxolitinib disturbed the JAK2-STAT3 signaling pathway in both breast cancer cell types, and found that p-STAT3 levels decreased with ruxolitinib treatment (0.1–10 µM) in a concentration-dependent manner in both MCF-7 and TAMR-MCF-7 cells (Fig. 1B). Many studies have reported that STAT3 activation is required for the transactivation of several oncoproteins and survival factors, including c-Myc, c-Jun, Cyclin B1, Cyclin D1, Bcl-2, and HIF-1α (29,30). In comparison to protein levels of MCF-7 cells, those of c-Myc, c-Jun, Cyclin B1, Cyclin D1, Bcl-2, and HIF-1α were upregulated in TAMR-MCF-7 cells, and this enhanced expression was markedly inhibited by ruxolitinib (0.1–10 µM, Fig. 1C). These results demonstrate that ruxolitinib attenuates activation of the JAK2-STAT3 pathway in TAMR-MCF-7 cells.

Figure 1. Inhibition of the STAT3 signaling pathway by ruxolitinib in TAMR-MCF-7 cells. (A) Expression of pSTAT3 and STAT3 in MCF-7 and TAMR-MCF-7 cells. β-actin levels were utilized as the loading controls. (B) Inhibition of STAT3 phosphorylation by ruxolitinib. MCF-7 and TAMR-MCF-7 cells were treated with vehicle or ruxolitinib (0.1–10 µM) for 24 h. (C) Effects of ruxolitinib on the expression of downstream target genes of the JAK-STAT pathway. The protein levels of c-Myc, c-Jun, Cyclin B1, Cyclin D1, Bcl-2 and HIF-1α were determined in MCF-7 and TAMR-MCF-7 cells 24 h following ruxolitinib treatment (0.1–10 µM). All of the experiments were repeated at least three times. JAK, Janus kinase; STAT, signal transducer and activator of transcription; pSTAT, phosphorylated STAT; HIF-1α, hypoxia inducible factor-1α; Bcl-2, B-cell lymphoma 2; TAMR, tamoxifen resistant.

Ruxolitinib inhibits TAMR-MCF-7 cell proliferation

To determine the effect of ruxolitinib on breast cancer cell proliferation, real-time, live-cell monitoring and analysis were performed using IncuCyte ZOOM. Ruxolitinib significantly inhibited the growth of MCF-7 cells at a concentration of 10 µM (Fig. 2A). However, TAMR-MCF-7 cells showed enhanced sensitivity to ruxolitinib (Fig. 2B). When ruxolitinib at the concentration of 1 or 3 µM was exposed to TAMR-MCF7 cells, the inhibiting effect of cell growth was slight but significant. Also, this inhibitory effect was not observed in MCF-7 cells treated with ruxolitinib at the same concentration ranges. These data suggest that TAMR-MCF-7 cell proliferation is partially dependent on the JAK2-STAT3 pathway and that ruxolitinib preferentially suppresses TAM-resistant breast cancer cell proliferation.

Figure 2. Anti-proliferation effects of ruxolitinib in breast cancer cells. (A and B) Effects of ruxolitinib on the cell proliferation of (A) MCF-7 and (B) TAMR-MCF-7 cells. MCF-7 and TAMR-MCF-7 cells were cultured in 96-well plate and cell proliferation was determined by IncuCyte ZOOM live-cell analysis system for 96 h. Data represent means ± standard deviation (n=6). ***P<0.005 vs. vehicle-treated control. Rxb, ruxolitinib; TAMR, tamoxifen resistant.

Ruxolitinib inhibits cell migration and EMT progression in TAMR-MCF-7 cells

Because the JAK2-STAT3 pathway plays an important role in cancer cell migration and invasion, we performed a transwell migration assay to assess TAMR-MCF-7 cell migration. We previously reported that TAMR-MCF-7 cells possess greater in vitro migratory ability than MCF-7 cells (8). TAMR-MCF-7 cell migration was significantly suppressed under treatment with 10 µM ruxolitinib (Fig. 3A). Because TAMR-MCF-7 cells acquire the migratory phenotype via EMT progression (7), we then examined whether JAK2-STAT3 inhibition by ruxolitinib affects the expression of EMT markers in TAMR-MCF-7 cells. Representative biochemical markers of EMT include loss of the epithelial adherence protein E-cadherin and upregulation of the mesenchymal protein N-cadherin (9). Immunocytochemistry for E-cadherin, N-cadherin, and phalloidin in MCF-7 and TAMR-MCF-7 cells showed that E-cadherin downregulation and N-cadherin upregulation in TAMR-MCF-7 cells were partially reversed by treatment with 10 µM ruxolitinib (Fig. 3B). Western blot analyses confirmed that higher expression of mesenchymal marker proteins, such as N-cadherin, vimentin, snail, or twist, was suppressed in TAMR-MCF-7 cells by ruxolitinib in a concentration-dependent manner (Fig. 3C). Although E-Cadherin was slightly detected in TAMR-MCF-7 cells by immunocytochemistry, E-cadherin was not detectable by immunoblottings in TAMR-MCF7 cells (Fig. 3C) (8). It may result from the difference in detection sensitivity between immunoblotting and immunocytochemistry. These results demonstrate that ruxolitinib may inhibit cell migration in TAMR-MCF-7 cells, presumably by blocking EMT.

Figure 3. Effects of ruxolitinib on cell migration and EMT phenotype changes in TAMR-MCF-7 cells. (A) Effect of ruxolitinib on TAMR-MCF-7 cell migration. Transwell migration assays were performed in TAMR-MCF-7 cells 18 h post-treatment with ruxolitinib (0.1–10 µM). Representative pictures of migrated cells (red circles) were shown (left panel). The relative cell numbers of migrated cells were counted (right panel). Data are presented as the mean ± standard deviation (n=4). *P<0.05 vs. vehicle-treated control. (B) Immunofluorescence staining of EMT markers in MCF-7 and TAMR-MCF-7 cells. TAMR-MCF-7 cells cultured on coverslips were incubated with or without 10 µM ruxolitinib for 24 h, and then the fixed cells were stained with specific antibodies against phalloidin, E-cadherin or N-cadherin. Representative images were captured using a CELENAS Digital Imaging System. Magnification, ×40. (C) Expression of EMT markers in TAMR-MCF-7 cells. EMT phenotype markers were determined following the exposure of TAMR-MCF-7 cells to 0.1–10 µM ruxolitinib for 24 h. EMT, epithelial mesenchymal transition; TAMR, tamoxifen resistant.

Ruxolitinib inhibits angiogenesis and tumor growth

A clinical feature of TAM resistance in human breast cancer is an increase in microvessel counts (31). We previously reported that angiogenic potential was enhanced in TAMR-MCF-7 cells by VEGF upregulation (10). In the current study, high basal VEGF mRNA expression was observed in TAMR-MCF-7 cells, but not in MCF-7 cells (Fig. 4A). Consistent with the inhibitory effects of ruxolitinib on cell migration and EMT progression of TAMR-MCF-7 cells, ruxolitinib (0.1–10 µM) reduced VEGF mRNA levels in TAMR-MCF-7 cells (Fig. 4A). Moreover, a VEGF-luc reporter gene assay further revealed that VEGF promoter binding activity was significantly diminished by treatment with 0.3–1 µM ruxolitinib (Fig. 4B). As ruxolitinib above 3 µM causes a significant cell death in the reporter gene analysis condition because of the lipid carrier-based membrane damage (32), MCF-7 and TAMR-MCF-7 cells were exposed to 0.3–1 µM ruxolitinib. These results suggest that the overexpression of VEGF gene transcription in TAMR-MCF-7 cells was partly a result of JAK2-STAT3 pathway activation. We then performed chorioallantoic membrane (CAM) assays by placing TAMR-MCF-7 cells on CAMs to verify the effect of ruxolitinib on angiogenesis. Numbers of vessel branch points in TAMR-MCF-7 cells were significantly decreased by ruxolitinib in a concentration-dependent manner (Fig. 4C).

Figure 4. Effect of ruxolitinib on VEGF-induced angiogenesis in breast cancer cells. (A) mRNA levels of VEGF. sqPCR was performed in MCF-7 and TAMR-MCF-7 cells. The mRNA expression levels were normalized to GAPDH mRNA. (B) Concentration-dependent effects of ruxolitinib on VEGF gene transcription in MCF-7 and TAMR-MCF-7 cells. MCF-7 and TAMR-MCF-7 cells were transfected with VEGF-luc and pRL-SV plasmids and the cells were incubated with or without 0.1–1 µM ruxolitinib for 24 h. (C and D) Inhibitory effects of ruxolitinib on TAMR-MCF-7-induced (C) angiogenesis and (D) tumor growth (scale bars, 5 mm). Representative images of angiogenesis originated from TAMR-MCF-7. The control CAM of a 10-day-old chick embryo was exposed to PBS. The additional embryos were implanted with TAMR-MCF-7 cells (2×106 cells/CAM) and exposed to 0.1–3 µM ruxolitinib. The quantitation of new branches formed from existing blood vessels was performed 3 days following cancer cell implantation. Data are presented as the mean ± standard deviation from 6 different samples. *P<0.05 and **P<0.01 vs. vehicle-treated control. CAM, chorioallantoic membrane; VEGF, vascular endothelial growth factor; sqPCR, semi-quantitative polymerase chain reaction; TAMR, tamoxifen resistant.

To estimate the inhibitory effect of ruxolitinib on tumor growth, we analyzed the tumor weight of TAMR-MCF-7 cells on CAMs. Implanted tumor growth was strongly suppressed by ruxolitinib (0.3–3 µM) (Fig. 4D), which implies that JAK2-STAT3 signaling is also critical to in vivo tumor growth in TAM-resistant breast cancer.

Discussion

As a selective ER modulator, TAM is the most widely used treatment for ER-positive breast cancer in both premenopausal and postmenopausal patients (3). Approximately 70% of breast cancer patients express ER; therefore, ER is the major target for luminal breast cancer therapy (33). Nonetheless, intrinsic or acquired resistance to hormonal therapy is the main challenge to clinicians, with 50% of advanced metastatic breast cancer patients developing resistance to TAM (34). Several studies have suggested potential mechanisms underlying the acquisition of TAM resistance, and therapeutic targets that may cause drug sensitivity in TAM-resistant breast cancer. Overexpression or formation of ER variants, coregulator switching, abnormal microRNA expression, and genetic polymorphism have been suggested as possible mechanisms for TAM resistance (34,35). In addition, the dysregulation of intracellular signaling has been seen during the acquisition of TAM resistance in several contexts, including growth factor receptors [epidermal growth factor receptor (EGFR/HER2), fibroblast growth factor receptor, type-I insulin-like growth factor receptor (IGFIR)), phosphoinositide 3-kinase (PI3K)-phosphatase and tensin homolog (PTEN)/AKT/mammalian target of rapamycin (mTOR), and nuclear factor-κB (NF-κB) (36). In particular, the activation of EGFR/HER2 or IGFR is a key molecular pathway implicated in TAM resistance (4). However, clinical trials combining anti-estrogens with EGFR inhibitors have provided minimal, or no, clinical benefit to patients over anti-estrogens alone (37,38). Because hormone resistance to breast cancer typically appears to be caused by diverse factors, identifying a new therapeutic target for the prevention of cancer relapse under continued hormone therapy remains problematic.

Activation of the JAK-STAT pathway has been considered an essential downstream signaling response to interferon (IFN)-α, IFN-γ, and IL-6 (39). Because the JAK-STAT pathway is also involved in the proliferation, differentiation, migration, and apoptosis of cancer cells (40–42), diverse inhibitors have been developed to target the JAK family (43–46). Among these, tofacitinib (Xeljanz) and ruxolitinib have been approved for the treatment of rheumatoid arthritis, myelofibrosis, and polycythemia vera (PCV), and are now in clinical trials for novel therapeutic applications, such as colitis and various solid tumors (pancreatic cancer, breast cancer, and non-small-cell lung cancer (NSCLC) (45). It has been reported that ruxolitinib suppresses Hodgkin's lymphoma (HL) and primary mediastinal B-cell lymphoma (PMBL) growth in vitro, and increases programmed cell death against lymphoma cells (47). Ruxolitinib has also been shown to significantly inhibit tumor growth and improve survival in HL and PMBL xenograft mice (47). In the current study, we showed for the first time that STAT3 activity was highly increased in TAMR-MCF-7 cells, and that ruxolitinib inhibited cell proliferation and tumor growth in TAM-resistant breast cancer cells, though the inhibition intensity is marginal. We believe that the functional role of JAK2, which can be inhibited by ruxolitinib, is not mainly involved in the growth of TAMR-MCF7 cells. Lim et al (21) recently demonstrated that ruxolitinib and calcitriol possessed synergistic anticancer effect in MCF-7 cells. Although ruxolitinib showed marginal inhibition rate in cell growth of MCF-7 cells, synergistic inhibition of cell proliferation was observed by ruxolitinib/calcitriol combination. Based on the finding, we believe that ruxolitinib could be used as a regimen for combination therapy in TAM-resistant breast cancer patients. In fact, JAK-STAT has been reported to be constitutively active in a triple-negative breast cancer (TNBC) cell line, MDA-MB-cells, and TNBC tumor tissues (12,48–50), and an oral JAK inhibitor suppresses tumor growth and metastasis of TNBC cells in vitro and in vivo (51). In a terminated clinical study, single administration of ruxolitinib showed no objective responses in a treatment-refractory TNBC patient population (52). The authors indicated that the discrepancy between clinical outcomes and on-target activity may be due to intratumoral heterogeneity within individual TNBC biopsies (50). Considering our cell-based results, tamoxifen-resistant breast cancer patients may be able to enroll in new clinical studies using ruxolitinib.

Increased metastasis and angiogenesis are the representative clinical characteristics of TAM-resistant breast cancer (31). We and other groups have shown that EMT contributes to the enhanced migration ability of TAM-resistant breast cancer cells, which may be required for higher rates of metastasis (7–9). During EMT progression, morphological changes to highly motile mesenchymal cancer cells are associated with several molecular characteristics, including increased levels of N-cadherin and vimentin, reduced levels of E-cadherin and claudins, and the release of matrix remodeling enzymes such as matrix metalloproteinases (52). Changes in the expression patterns of these proteins have been shown to result from induction of EMT-activating transcription factors, such as the snail family of zinc finger transcription factors, basic helix-loop-helix factors, and twist (53). In the current study, protein expression of mesenchymal phenotype markers and transcription factors upregulated in TAMR-MCF-7 cells was diminished by ruxolitinib treatment. Consistent with our results, JAK1/2 inhibition by ruxolitinib suppressed STAT3-mediated expression of ZEB1 and snail as well as the emergence of a mesenchymal phenotype in hepatocellular carcinoma (54). It has been also reported that the JAK-STAT pathway is involved in VEGF gene transcription (55,56). VEGF mRNA expression and gene transcription were highly upregulated in TAMR-MCF-7 cells, but were suppressed by ruxolitinib. Consistent with sqPCR results, a reporter gene assay using the VEGF-luc promoter showed that ruxolitinib inhibited the activation of VEGF gene transcription. It has been reported that protein expression and secretion of VEGF mainly depend on the transcriptional activation of the VEGF gene (10). Considering our findings that ruxolitinib inhibits both the VEGF-luc reporter activity and VEGF mRNA expression, VEGF protein levels may be down-regulated by ruxolitinib in TAMR-MCF-7 cells. The fact that we did not quantify the amount of secreted VEGF would be a limitation of our study. CAM assay results clearly demonstrated that ruxolitinib can suppress TAMR-MCF7-induced angiogenesis, where this effect was mediated by VEGF. In conclusion, ruxolitinib, a potent JAK-STAT pathway inhibitor, blocked the EMT process and VEGF production, consequently suppressing TAMR-MCF-7 cell migration and angiogenesis. These results hold great promise in improving the clinical outcomes of TAM-resistant breast cancer patients.

Acknowledgements

Not applicable.

Funding

The present study was supported by the National Research Foundation of Korea (NRF) grant (grant nos. NRF-2018R1A2B2003590 and 2017R1A4A1015860).

Availability of data and materials

The dataset generated and/or analysed during this study are available from the corresponding author on reasonable request.

Author's contributions

KWK and JAK designed the research. JWK, JG and JEK performed the research. JWK and JEK contributed to the western blot analysis, cell culture, sqPCR, luciferase assay and immunocytochemistry assay. JG contributed to the CAM assay and data analysis.

Ethics approval and consent to participate

The experimental studies were approved by the Institutional Animal Care and Use Committee of Yeungnam University (Gyeongsangbuk, Korea).

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Glossary

Abbreviations

Abbreviations:

References