Snail maintains metastatic potential, cancer stem-like properties, and chemoresistance in mesenchymal mouse breast cancer TUBO‑P2J cells

  • Authors:
    • Sun Young Ma
    • Jin-Hee Park
    • Hana Jung
    • Sung-Min Ha
    • Yeonye Kim
    • Dong Hyen Park
    • Deuk Hee Lee
    • Sooyong Lee
    • In-Ho Chu
    • So Young Jung
    • Il-Hwan Kim
    • Il-Whan Choi
    • Chang Soo Choi
    • Saegwang Park
  • View Affiliations

  • Published online on: July 18, 2017
  • Pages: 1867-1876
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Snail, a zinc-finger transcriptional repressor of E-cadherin expression, is one of the key inducers of epithelial-mesenchymal transition (EMT) in epithelial cancer. In breast cancer, EMT has been associated with malignancies, including metastasis, cancer stem-like properties, and resistance to chemotherapy and radiotherapy. In this study, we analysed the role of Snail in the highly metastatic mesenchymal TUBO‑P2J mouse breast cancer cells, by loss of function using short hairpin RNA. Though silencing Snail did not restore the E-cadherin expression or induce morphological changes, Snail silencing significantly ablated in vitro and in vivo metastatic potentials. In addition, Snail silencing also reduced resistance to chemotherapy drugs and cancer stem-like properties, such as CD44 expression, aldehyde dehydrogenase (ALDH) activity, colony formation, and in vivo tumour formation and growth. However, radioresistance was not decreased by silencing Snail. Collectively, this study suggested that Snail is a main regulator of the maintenance of malignancy potentials and is a good target to prevent cancer metastasis and to increase chemotherapy susceptibility.


Epithelial-mesenchymal transition (EMT) is a process where cells lose epithelial phenotypes, decrease cell-cell recognition and adhesion, and gain mesenchymal phenotypes and an increased potential for metastasis (1). The EMT process is essential in embryonic and breast development. In tumour progression and metastasis, EMT processes are also important. Cells with a mesenchymal phenotype show an increased potential of migration and invasion, anoikis resistance, chemoresistance, radioresistance, and stemness (13). E-cadherin loss is considered a hallmark of EMT. In the EMT process, the expression of E-cadherin is controlled by transcriptional and post-transcriptional regulation. E-cadherin gene (CDH1) expression is modulated by several transcription repressors, which are typically expressed in mesenchymal cells, including Snail genes, Twist, Zeb genes and E47 (1,4). The zinc-finger transcriptional repressor Snail is one of the genes frequently associated with EMT (4,5). Previous studies indicated that Snail may participate in the progression of breast cancer and other types of cancer via the downregulation of CDH1 and the upregulation of mesenchymal genes (4). It was also reported that Snail participates in metastasis, cancer stemness, recurrence, and resistance to chemotherapy and radiotherapy (69).

In a previous study, we reported on the TUBO-P2J spontaneous metastatic mouse breast cancer cell line, which is derived from TUBO, a non-metastatic epithelial breast cancer cell line (10). The TUBO-P2J cell line showed a mesenchymal phenotype compared to TUBO, including a loss of E-cadherin, downregulation of claudin 1 and occludin 1, and a gain of vimentin, α-sm-actin and fibronectin. Various EMT transcription factors (EMT-TF), including Snail, Twist, FoxC2 and ZEB2, are also upregulated in TUBO-P2J cells. In addition, TUBO-P2J cells showed increased resistance to chemotherapy and radiotherapy (10,11). However, it is not clear which factors are critical in the resistance to chemotherapy and radiotherapy.

In this study, we attempted to define the role of Snail in TUBO-P2J cells in the maintenance of mesenchymal cell phenotypes, including the loss of E-cadherin, metastasis, stemness, and resistance to chemotherapy and radiotherapy through a knock-down of Snail with short hairpin RNA (shRNA). Our results showed that Snail is not essential in the maintenance of mesenchymal cell phenotypes, such as cell morphology, the loss of E-cadherin, and resistance to radiation, but is essential for metastasis, stemness and resistance to chemotherapy. In addition, E-cadherin transcription was recovered by DNA methyltransferase (DNMT) inhibitor (5-aza-2′-deoxycytidine, 5-aza-dC) alone, but protein expression was detected only in Snail knock-down cells treated with both 5-aza-dC and an HDAC inhibitor (SAHA).

Materials and methods

Cell culture, shRNA construct and chemicals

The TUBO and TUBO-P2J cell lines were cultured in vitro in high glucose DMEM (HyClone™; Thermo Fisher Scientific, MA, USA) supplemented with heat-inactivated 10% foetal bovine serum (FBS; Thermo Fisher Scientific) and 1% penicillin-streptomycin (HyClone; Thermo Fisher Scientific); the cells were maintained under 5% CO2. Snail shRNA constructs targeting the Mus musculus sequences of Snai1 (NM_011427) were purchased from Sigma (Sh1-sequence: GTACCGGATGTGTC TCCCAGAACTATTTCTCGAGAAATAGTTCTGGGAGAC ACATTTTTTTG, Sh3-sequence: CCGG GATCTTCAACTG CAAATATTGCTCGAGCAATATTTGCAGTTGAAGATCT TTTTG). 5-Aza-dC (DNA methyltransferase inhibitor), SAHA (HDAC inhibitor), epirubicin and doxorubicin was purchased from Sigma.

Generation of Snail knockdown stable cell lines

The lentiviral transduction particles are produced from a library of sequence-verified lentiviral plasmid vectors for mouse snail gene (Sigma). Transduction of lentiviral particles were performed according to the manufacturer's instructions. Transduced cells were selected with 500 µg/ml of puromycin for 3–14 days. Purimycin-resistant colonies and separated single cells were picked. Each single cell was expanded to evaluate the knockdown status of the Snail gene via PCR and western blotting.

Inhibition of DNA methyltransferase and/or histone deacetylase

Cells (1×106/dish) were seeded on 10 cm culture plate and incubated for 5 h for the cells to attach to the dishes. 5-Aza-dc (2.5 µM) and/or SAHA (0.5 or 2 µM) were treated and incubated at 37°C in a humid atmosphere of 5% CO2 for 3 or 7 days, then cells were subcultured with trypsinization to prevent overgrowth.

Reverse transcription-PCR

Total RNA extracted from cultured cells was used as a template for reverse transcriptase reactions. Aliquots of cDNA were amplified using the mouse and human primer pairs (Table I). After an initial denaturation at 94°C for 5 min, the following was performed: 30 cycles of denaturation at 94°C for 30 sec, annealing at 55–60°C for 30 sec, and extension at 72°C for 30 sec. PCR was performed with a 2720 thermo cycler (Applied Biosystems, CA, USA). The reaction products were analysed in 1.5% agarose gels.

Table I.

PCR primer pairs of mouse and human genes.

Table I.

PCR primer pairs of mouse and human genes.

GenesSpeciesNCBI no.Forward (5′-3′)Reverse (5′-3′)Size (bp)
Western blot assay

Cell lysates (40 µg/lane) were electrophoresed on polyacrylamide-SDS gels and then transferred to polyvinylidene fluoride membranes. Immunoblotting was performed by primary antibodies. E-cadherin, Snail-1 and GAPDH antibodies were obtained from Cell Signaling Technology (MA, USA) and estrogen receptor α (ESR1) antibody was purchased from Santa Cruz (TX, USA). HRP-conjugated secondary antibodies were purchased from Jackson Laboratories (Jackson ImmunoResearch, PA, USA).

Flow cytometry

To detect CD24 and CD44 expression, 2×105 cells were stained with 0.5 µg/ml of PE-Cy5-conjugated CD24 and FITC-conjugated CD44 antibody (BioLegend) for 30 min at room temperature in the dark. For aldehyde dehydrogenase (ALDH) activity, cells were stained using the Aldefluor kit (Stem Cell Technologies Inc., Vancouver, Canada) according to the manufacturer's protocol. Stained cells were acquired with the BD FACSCanto II cytometry system and analysed with FlowJo software (version 10).

Migration and invasion assays

The migration and invasion assays were performed using 8.0-µm pore size 24-well insert systems (BD Falcon) with 2 mg/ml of Matrigel coating (invasion) or not (migration). Then, 5×104 cells (migration) or 5×105 cells (invasion) were added to the upper chamber and incubated for 4–6 h (migration) or 72 h (invasion). After incubation, the upper surface of the membrane was wiped with a cotton-tipped applicator to remove residual cells. Cells in the bottom compartment were fixed and stained with H&E. Cells in ten randomly selected fields at ×40 magnification were counted.

Soft agar colony-forming assay

Six-well plates were covered with a layer of 0.5% agar in medium supplemented with 10% foetal bovine serum. Cells were prepared in 0.3% agar and seeded in triplicate at 3 different dilutions ranging from 1×103 to 5×105. The plates were incubated at 37°C in a humid atmosphere of 5% CO2 for 2 weeks. Each experiment was repeated at least 3 times. Colonies were photographed between 10 and 12 days at an original magnification of ×40 under phase contrast.

Chemo-susceptibility test

The chemo-susceptibility was measured with an In Vitro Toxicology assay kit (TOX6, Sigma). Briefly, 0.5–1×104 cells/well were seeded and attached in 96-well culture plates. Indicated doses of chemo-drugs were administered for 72 h. Cells were fixed in 10% trichloroacetic acid for 1 h at 4°C, stained with SRB for 15 min, and washed 3 times with 1% acetic acid. The incorporated dye was solubilized with 10 mM Tris base, pH 8.8. Absorbance was spectrophotometrically measured at 565 nm using an EL800 microplate reader (Bio-Tek Instruments, Winooski, VT, USA).

Radiation susceptibility test

Cells were harvested with trypsin and suspended in 15 ml conical tubes at 1×104 cells/ml. After irradiation with the indicated doses with X-ray generator (RapidArc®; Varian Medical Systems Inc., Palo Alto, CA, USA), cells were diluted 10-fold and seeded in 6-well plates. After 72 h, the cells were stained with 0.5% crystal violet for 10 min and fixed with 4% paraformaldehyde. Colonies were counted under a microscope. For in vivo radiation treatment, TUBO-P2J/NC (1.5×105) and TUBO-P2J/shSnail (2×105) cells were implanted subcutaneously and tumour tissues were locally irradiated at 15-Gy with an X-ray generator under anaesthesia (ketamine 90 mg/kg and xylazine 10 mg/kg).

In vivo animal study

All of the procedures involving animals were approved by the INJE University College of Medicine Institutional Animal Care and Use Committee. All of the mice (BALB/C, 6–8 weeks of age) used in this study were purchased from Orient Bio (Taejun, Korea). To evaluate the tumour formation ability and growth, 1×105 or 1×104 cells were subcutaneously implanted on the backside of the mice. Tumour development was followed every day, and tumour sizes were measured two times per week. Tumour volumes were measured along three orthogonal axes (x, y, and z) and calculated as tumour volume = (xyz)/2. To analyse experimental metastasis, 2×104 cells were intravenously injected through the tail vein and lung tissues were collected at day 19.


Differences between groups were analysed using an unpaired t-test. Error bars represent ± SD. All statistical analyses were conducted using Graph-Pad Prism Version 4.0 (GraphPad Software). Unless specified, statistically significant differences of p<0.05, 0.01, and 0.001 are noted.


TUBO-P2J displays a cancer stem cell phenotype and resistance to chemotherapy and radiotherapy

Previously we reported on the the highly metastatic mouse breast cancer cell line TUBO-P2J, derived from the non-metastatic TUBO cell line (10). TUBO cells were morphologically epithelial in nature. In contrast, TUBO-P2J cells were spindle-shaped mesenchymal-type cells. TUBO-P2J cells showed a gain of Snail and loss of E-cadherin. In flow cytometry analysis and soft agar colony assays, the TUBO-P2J cell line was characterized as stem cell-like with a prominent CD44high population (Fig. 1A) and 5 times higher colony number (Fig. 1B) than TUBO cells. Chemo and radiation susceptibility tests revealed that TUBO-P2J cells were more resistant to chemotherapy and radiation therapy (Fig. 1C and D). Snail expression levels were associated with poor prognosis phenotypes, including metastatic potential, soft agar colony formation capacity and resistance to chemotherapy and radiotherapy.

Before Snail silencing, we compared the migration potentials of TUBO-P2J cell line with other breast cancer cell lines, such as MCF7, MDA-MD-231, HCC70, 4T1, and original TUBO cell lines (Fig. 2A). The migration activity of TUBO-P2J was higher than that of human breast cancer MDA-MB-231, which is a well-known cell line with a highly metastatic potential. TUBO-P2J cell line also showed the highest level of snail expression among the tested breast cancer cell lines (Fig. 2B). In addition, TUBO-P2J cell line did not express estrogen receptor α1 (ESR1) similarly to MDA-MB-231, triple-negative breast cancer cell line (Fig. 2C). Even though TUBO-P2J is a mouse tumour cell line, it is derived spontaneously in vivo and could be exactly compared with parent TUBO cells which showed less malignant phenotypes, including metastatic potential, stemness, chemoresistance and radioresistance (10). Based on these data, we chose the TUBO-P2J cell line for Snail silencing experiments with efficient lentiviral transfection system.

Downregulation of Snail does not induce mesenchymal-epithelial transition in TUBO-P2J cells

To examine the role of Snail in maintaining the mesenchymal phenotype and the suppression of E-cadherin, we produced a stable Snail knockdown TUBO-P2J cell line (TUBO-P2J/shSnail) by lentiviral transfection. Two independent stable shSnail-expressing clones (Sh1 and Sh3, one clone from each construct) and a stable negative control shRNA clone (NC) were analysed for Snail mRNA expression. Sh1 and Sh3 showed 50–90% downregulation of Snail mRNA, whereas the control clone did not exhibit any significant reduction in Snail mRNA (Fig. 3A). Knockdown of Snail in TUBO-P2J cells was confirmed with western blot analysis (Fig. 3B). Snail protein levels were correlated with mRNA levels. The morphology of Snail knockdown cells (Sh1 and Sh3) and control cells (NC) was not different, as all of the cells showed a spindle-shaped mesenchymal phenotype (Fig. 3C). Next, we evaluated the expression of E-cadherin with RT-PCR and western blot analysis (Fig. 3D and E). In TUBO-P2J cells, Snail knockdown did not induce transcription of E-cadherin. Based on Snail expression levels, we chose the Sh1 clone as TUBO-P2J/shSnail for further experiments.

E-cadherin expression was controlled by DNA methylation, histone deacetylation, and Snail in TUBO-P2J cells

Lim et al (12) reported that Snail represses the transcription of E-cadherin through binding to E-boxes of this gene and inducing DNA methylation of its promoter by recruiting HDAC1 and DNMT. To evaluate the reason that E-cadherin was not expressed in TUBO-P2J/shSnail cells, cells were treated with 5-aza-dC and/or SAHA. By the third day of 5-azaC treatment, E-cadherin mRNA was detected in all TUBO-P2J cells regardless of Snail knockdown (Fig. 4A). However, E-cadherin protein was detected only in shSnail cells by treatment of 5-azaC and SAHA for 7 days (Fig. 4B). These data suggest that Snail might suppress the expression of E-cadherin through a translation step co-operating with HDAC in TUBO-P2J cells.

Snail increases metastatic potential in TUBO-P2J cells

Because processes of EMT have been linked with metastasis, we next evaluated the metastatic potential of PLKO and Sh1 cells. By silencing Snail, migration was significantly decreased from 195.3±7.5 (mean ± SE) cells/fields to 86.7±4.7 cells/fields (56% decrease) (Fig. 5A) and invasion was decreased even more from 127.1±47.6 cells/fields to 10.7±2.7 cells/fields (93% decrease) (Fig. 5B). An in vivo metastasis assay using tail vein injection also showed that lung colony numbers of shSnail cells were reduced to one-third of that of control cells (Fig. 5C). These data suggest that inactivation of Snail could reduce the metastatic potentials of breast cancer cells without driving MET.

Snail maintains cancer stem cell-like properties and in vivo tumourigenicity of TUBO-P2J cells

As Snail is expressed in CD44high compared to CD44low cells, we examined whether Snail could affect the expression of CD44, a breast cancer stem cell marker. Snail silenced TUBO-P2J cells showed a slight decrease in the CD44high population (37.5%) compared to their control counterparts (52.9%) (Fig. 6A). Aldehyde dehydrogenase (ALDH) activity was also reduced significantly by Snail silencing (Fig. 6B). Next, we used a soft agar colonization assay to evaluate the role of Snail in anchorage-independent growth. Data showed that the sizes of the colonies were not different with Snail silencing, but the numbers were significantly reduced by 40% compared to that of control cells (Fig. 6C). In vivo tumourigenicity was tested with subcutaneous implantation of TUBO-P2J, TUBO-P2J/NC, and TUBO-P2J/shSnail (1×104 or 1×105 cells/mouse). In all of the mice implanted with parent TUBO-P2J and TUBO-P2J/NC cells, tumours developed at day 14, but tumours developed in two mice out of seven at 30 days when 1×104 of TUBO-P2J/shSnail cells were implanted (Table II). Moreover, a decrease in tumour size was observed in tumours established with Snail silenced cells compared with those from parent and control cells (Fig. 6D). These in vitro and in vivo data demonstrate that Snail has an important role in the maintenance of breast cancer stem cell properties.

Figure 6.

Silencing Snail induces downregulation of tumourigenicity and chemoresistance but not conneted radioresistance. (A) CD44 and CD24 expression levels of TUBO-P2J/NC and TUBO-P2J/shSnail cells were quantified by flow cytometry. (B) ALDH1 activity of TUBO-P2J/NC and TUBO-P2J/shSnail cells. Cells were treated with an Aldefluor substrate in the presence or absence of ALDH inhibitors DEAB. After treatment, the samples were analysed by flow cytometry for the presence of ALDHhigh cells. (C) A soft agar colony-formation assay for TUBO-P2J/NC and TUBO-P2J/shSnail cells. (D) Tumour growth curves: 1×105 tumour cells were implanted subcutaneously on the backs of mice. Tumour growth was monitored twice per week, and the data are presented as the mean tumour size ± SD of 4 tumours per group. The data shown are representative of two independent experiments. (E and F) TUBO-P2J/NC and TUBO-P2J/shSnail cells were treated with epirubicin (E) and doxorubicin (F) for 72 h. Cell viability was measured with a Tox-6 assay, and the data are presented as mean ± SD. (G) TUBO-P2J/NC and TUBO-P2J/shSnail cells were irradiated with the indicated dose and seeded in 6-well plates at a 10-fold-dilution. After 72 h, the cells were stained with crystal violet and counted under a microscope. (H) Tumour-bearing mice were irradiated locally with 15 Gy, and tumour sizes were measured twice per week. The data are presented as the relative tumour size compared to the tumour size when treatment was started (mean ± SD). *p<0.01; ***p<0.001.

Table II.

Incidence of tumour growth.

Table II.

Incidence of tumour growth.

Cell numbers injected

Tumour cells105104
Snail increases chemoresistance but not radioresistance

As Snail is expressed in chemo- and radioresistant cells, TUBO-P2J, we examined whether Snail could induce chemo- and radioresistance. Our data revealed that silencing Snail increased the susceptibility to epirubicin and doxorubicin (Fig. 6E and F); however, susceptibility to radiation therapy was not affected by Snail silencing (Fig. 6G and H). These results suggested that Snail silencing might be a good strategy to overcome chemoresistance.

The expression of SLUG and Vimentin and the β-catenin signaling are not changed by Snail silencing

To test whether the phenotype changes in Snail silent cells were mediated by other EMT related genes, we evaluated mRNA levels of EMT related genes such as SLUG (Snail2), vimentin, fibrinectin, Twist, DDR2, and FoxC2 (Fig. 7A). Data revealed that silencing of Snail reduced the expressions of fibronectin and DDR2 but did not influence on the expressions of other EMT related genes including vimentin, SLUG, and Twist. In addition, silencing of Snail did not change the activation status of β-catenin (Fig. 7B). These data suggested that the malignant phenotypes of TUBO-P2J cell lines which are increased stemness, metastasis, and chemoresistance are mediated by the increased expression of Snail and the role of Snail in this model was not linked with the expression of vimentin and SLUG and Wnt/β-catenin signaling pathway.


This study demonstrates that Snail, one of the master EMT genes in breast cancer cells, maintains metastatic potential, clonogenicity, and drug resistance without restoration of E-cadherin expression or morphological changes. In addition, our results also revealed that Snail is required for tumour initiation and growth in vivo. Our data suggested that inhibition of Snail activity could be a good strategy to inhibit tumour metastasis and to enhance the biological effects of anticancer agents.

Loss of E-cadherin is a hallmark of the EMT process. E-cadherin expression is controlled by various transcription factors, Snail genes, Twist, Zeb genes and E47 (1,4). Snail was discovered first and is the most important transcriptional repressor of E-cadherin (6). Snail binds to the E-box of the E-cadherin promoter through C2H2-type zinc fingers and represses transcription (13). Many reports have demonstrated that silencing Snail can restore E-cadherin expression in various cancer cells including breast cancer (1420). In TUBO-P2J cells, however, silencing Snail did not restore the expression of E-cadherin. This finding might be because: i) Snail sufficiently represses E-cadherin during the initial stages of EMT while subsequent maintenance may require cooperation of other transcription factors (21), or ii) Snail can play a role as a mediator of epigenetic changes through recruiting histone deacetylases (HDAC) and DNA methyltransferase (DNMT) to the E-cadherin promoter (12,14). Though we cannot rule out the possibility that other transcription factors repress the expression of E-cadherin, epigenetic changes are a main regulator for E-cadherin expression in TUBO-P2J cells. Interestingly, the transcription of E-cadherin was restored by 5-aza-dC treatment within 3 days regardless of the presence of Snail, but the E-cadherin protein was detected only in TUBO-P2J/shSnail cells treated with both 5-aza-dC and SAHA at day 7. These data suggested that Snail may regulate E-cadherin expression at post-transcriptional steps with HDAC. Further studies to define the exact mechanisms of Snail in the post-transcriptional regulation of E-cadherin and which types of HDAC participate would be required.

In breast cancer, Snail expression has been detected at the invasive area, coincidently with E-cadherin downregulation, and has been associated with lymph node metastasis and recurrence (17,22). Previous studies demonstrated that Snail participates in the EMT-MET process, tumour metastasis, cancer stemness, recurrence, and resistance to chemotherapy and radiotherapy (69,23). In these studies, however, the expression of Snail was linked with E-cadherin expression and morphological changes, such as EMT or MET. Therefore, it is not clear whether these poor prognostic potentials are induced by Snail-induced EMT or by Snail expression itself. In the metastatic potential, silencing Snail significantly reduced in vitro migration and invasion and in vivo lung colonization. These data revealed that Snail plays a role as a central regulator of metastasis. For the breast cancer stem cell markers, CD44 expression levels and ALDH activity were also decreased by Snail silencing. In human breast cancer, various markers, such as CD24, CD44, CD133, CD166 and ALDH1, were identified as cancer stem cell markers, as cells with the phenotype CD44+/CD24low/− and/or ALDH1+ are most consistently associated with stem-like characteristics (2428). In our study, CD24 expression levels were not different between epithelial non-metastatic TUBO cells and mesenchymal metastatic TUBO-P2J cells and were not linked with colony formation ability. In these mouse breast cancer cell lines, CD44 expression levels were linked with colony formation ability and in vivo tumour formation and growth and were regulated by Snail expression. ALDH1 activities in TUBO and TUBO-P2J cells were similar (data not shown); however, silencing Snail reduced ALDH1 activity in TUBO-P2J cells. Though the reasons that CD24 expression was not linked with cancer stemness remain unknown, it is clear that CD44 expression levels are closely related with cancer stemness and are regulated by Snail expression. Regarding resistance to chemo-drugs, while we tested only two anthracyline drugs, our results are consistent with prior studies that suggested that EMT is associated with an increased chemoresistance of cancer cells (8). However, there are some controversies regarding the link between EMT or Snail and chemoresistance. Mezencev et al (23) reported that Snail-induced EMT in MCF7 cells induced resistance to gemcitabine and mitomycin C, but increased sensitivity to doxorubicin, methotrexate, cisplatin, and 5-fluorouracil. In our previous study, we showed that mesenchymal TUBO-P2J cells were less sensitive to 12 breast cancer chemo-drugs than parental epithelial TUBO cells (10). It is still difficult to generalize whether Snail or EMT increase the resistance of breast cancer cells to most chemo-drugs, but our results suggest the possibility that Snail inhibition can reduce the resistance to some chemo-drugs. A number of studies have reported that EMT and cancer stem cell-like properties are also associated with radioresistance in breast cancer cells (9,2931). However, it is not clear whether Snail regulates radioresistance in breast cancer. Mezencev et al (23) showed that mesenchymal MCF7-Snail cells are more sensitive to radiation that their parental cells. Zhang et al (32) demonstrated that radioresistance can be induced and maintained by ZEB1, not by Twist and Snail, using gene expression and silencing techniques. Our results also showed that silencing Snail without E-cadherin restoration or morphological changes did not increase the sensitivity to radiation. Considering cancer stem-like properties were decreased by Snail silencing and there was no detection of ZEB1 in TUBO-P2J cells (10), radioresistance might be regulated by unknown factors in TUBO-P2J cells.

Based on this study, Snail is thought to be a critical element in the machinery that maintains the metastatic potential, stem-like properties and chemoresistance in mesenchymal breast cancer. In addition, Snail inhibition would be a good target for breast cancer treatment.


This study was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (NRF-2015R1A2A2A01008394).



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September 2017
Volume 38 Issue 3

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Ma, S.Y., Park, J., Jung, H., Ha, S., Kim, Y., Park, D.H. ... Park, S. (2017). Snail maintains metastatic potential, cancer stem-like properties, and chemoresistance in mesenchymal mouse breast cancer TUBO‑P2J cells. Oncology Reports, 38, 1867-1876.
Ma, S. Y., Park, J., Jung, H., Ha, S., Kim, Y., Park, D. H., Lee, D. H., Lee, S., Chu, I., Jung, S. Y., Kim, I., Choi, I., Choi, C. S., Park, S."Snail maintains metastatic potential, cancer stem-like properties, and chemoresistance in mesenchymal mouse breast cancer TUBO‑P2J cells". Oncology Reports 38.3 (2017): 1867-1876.
Ma, S. Y., Park, J., Jung, H., Ha, S., Kim, Y., Park, D. H., Lee, D. H., Lee, S., Chu, I., Jung, S. Y., Kim, I., Choi, I., Choi, C. S., Park, S."Snail maintains metastatic potential, cancer stem-like properties, and chemoresistance in mesenchymal mouse breast cancer TUBO‑P2J cells". Oncology Reports 38, no. 3 (2017): 1867-1876.