Warning: mysqli::mysqli() [function.mysqli-mysqli]: (08004/1040): Too many connections in /home/cpr/www/inc/db_con.inc on line 9

Warning: mysqli::query() [function.mysqli-query]: Couldn't fetch mysqli in /home/cpr/www/inc/db_con.inc on line 10

Warning: main() [function.main]: Couldn't fetch mysqli in /home/cpr/www/inc/db_con.inc on line 13
Proteases are Modulated by Fascin in Oral Cancer Invasion
search for




 

Proteases are Modulated by Fascin in Oral Cancer Invasion
Journal of Cancer Prevention 2018;23:141-6
Published online September 30, 2018
© 2018 Korean Society of Cancer Prevention.

Min Kyeong Lee, Ji Hyeon Park, Seol Hwa Gi, and Young Sun Hwang

Department of Dental Hygiene, College of Health Science, Eulji University, Seongnam, Korea
Correspondence to: Young Sun Hwang, Department of Dental Hygiene, College of Health Science, Eulji University, 553 Sanseong-daero, Sujeong-gu, Seongnam 13135, Korea, Tel: +82-31-740-7493, Fax: +82-31-740-7352, E-mail: kiteys@eulji.ac.kr, ORCID: Young Sun Hwang, https://orcid.org/0000-0001-7012-3434
Received August 31, 2018; Revised September 13, 2018; Accepted September 19, 2018.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Background

Cancer invasion is a critical factor for survival and prognosis of patients with cancer. Identifying and targeting factors that influence cancer invasion are an important strategy to overcome cancer. In this study, we investigated the role of fascin known to be associated with cancer invasion.

Methods

Fascin depletion was performed with lentiviral short hairpin RNA against fascin mRNA and stable cell line (Fascindep) was established. Matrigel-Transwell invasion and three-dimensional (3D) culture system were used to observe fascin depletion effects. In order to observe the changes of protease secretion by fascin depleted cancer cells, protease antibody array was performed.

Results

Fascin was highly expressed in invasive cancer cells. Fascin-depleted cells showed decreased cancer invasion in Matrigel-Transwell invasion and 3D culture system. In addition, inhibition of proteases secreation and decrease of intracellular proteases mRNA expression were observed in fascin deplete cells.

Conclusions

These results indicates that fascin is closely involved in proteases activity and cancer invasion. Therefore, fascin is a strategically important factor for controlling cancer invasion.

Keywords : Metalloproteases, Fascin, Head and neck neoplasms, Gene silencing, Tumor microenvironment
INTRODUCTION

Cancer growth and invasiveness are closely related to cancer progression and prognosis.1 Malignant tumors are highly related to poor survival rate of cancer patients. The incidence of oral cancer varies among races and living environments. Oral cancer is one of the 10 most common cancer in the world, accounting for 3% to 5% of total carcinoma in the human body. Oral squamous cell carcinoma (OSCC) is the most common malignant cancer. Like other types of cancer, oral cancer can be restored 80% to 90% in early detection. However, more than half of the patients are diagnosed after the cancer has progressed considerably, leading to poor prognosis.2 Despite extensive studies and improvements in the treatment of OSCC, the 5-year survival rate is only 53%, which is unchanged over the past 40 years.3

Because local recurrence and metastasis to distance organs of oral cancer occur frequently, treatment strategies to reduce or inhibit local recurrence are appropriate to improve the survival rate of patients with oral cancer. Therefore, finding diagnostic factors with high predictive accuracy for cancer invasion and metastasis is important for cancer prognosis. However, oral tissue is composed of heterogenous cells such as teeth, bone, and soft tissues. The location of cancer development also varies, making it difficult to find a suitable diagnostic marker for oral cancer invasion and metastasis.

Invasive cancer cells are known to form a protrusive cellular structure called invadopodia to infiltrate the surrounding matrix and the basement membrane.4 When invasion is needed, cancer cells induce actin polymerization based on Arp2/3 complex and neuronal Wiskott-Aldrich syndrome protein (N-WASP) to stabilize the protruding structure by joining many molecules, such as Tsk5, cortactin, synaptjanin-2, Abl-family kinase Arg4, and integrin. Upon completion of the assembly of invadopodia, proteases are secreted and invasion proceeds. Since inhibition of functional invadopodia formation can effectively inhibit cancer invasion, invadopodia-targeted cancer suppression strategies have been suggested to be very effective. In the present study, we observed changes in cancer invasion induced by fascin, a component of functional invadopodia, and derived related proteases.

MATERIALS AND METHODS

1. Cell culture

YD-10B, HSC-2, HSC-3, Ca9.22 OSCC cells were obtained from the Yonsei University College of Dentistry, Republic of Korea, and all were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM)/F12 (3 : 1 ratio) medium supplemented with 10% FBS, 1 × 10−10 M cholera toxin, 0.4 mg/mL hydrocortisone, 5 μg/mL insulin, 5 μg/mL apotransferrin, and 2 × 10−11 M triiodothronine (T3) in a humidified atmosphere of 5% CO2 at 37°C. PC-3 prostate cancer cells were cultured in RPMI1640 medium with 10% FBS. To establish fascin-depleted YD-10B cell line, fascin 1-specific short hairpin RNA (shRNA) (h) lentiviral particles were transduced in cultured cell with 5 μg/mL polybrene according to the manufacturer protocol (Santa Cruz, Santa Cruz, CA, USA). Continual selection was followed with 1 mg/mL puromycin to establish fascin-depleted stable cell line (Fascindep). Control shRNA (h) lentiviral particles-A (Santa Cruz) was also used as a cell control (Mock). The extent of fascin depletion was evaluated by Western blot.

2. Reagents

All reagents used for cell culture were purchased from Gibco BRL Co. (Rockville, MD, USA). Cholera toxin, hydrocortisone, insulin, apotransferrin, T3, dimethyl sulfoxide (DMSO), and parthenolide were obtained from Sigma-Aldrich (Sigma-Aldrich Chemical Co., St. Louis, MO, USA). The following antibodies were purchased from their respective sources: Fascin (clone 55K-2, monoclonal mouse anti-human) and E-cadherin (clone NCH-38, monoclonal mouse anti-human) (Dako, Carpentaria, CA, USA); β-actin (clone AC-74) (Sigma-Aldrich Chemical Co.).

3. Western blotting

Protein (50 μg) were separated on SDS-PAGE gel and were transferred to a polyvinylidene difluoride membrane (Millipore, Billerica, MA, USA). The membrane was blocked with 10% skim milk in PBS containing 0.1% Tween-20 (PBS-T) and subsequently incubated overnight with a 1 : 1,000 dilution of primary antibody against its specific protein at 4°C. The blots were then incubated with a 1:3,000 dilution of their respective horseradish peroxidase-conjugated secondary antibodies for 2 hours at room temperature and were washed with PBS-T. The targeted proteins were visualized using an enhanced chemiluminescence detection kit (Amersham Life Science, Arlington Heights, IL, USA) according to the manufacturer’s instructions.

4. Invasion assay

Eight μm pore sized polycarbonate nucleopore filter inserts in a 24-well Transwell chamber (Costar; Corning, Cambridge, MA, USA), were coated with Matrigel (30 μg/well; Becton Dickinson, Lincoln Park, NJ, USA). Cells (5 × 104 cells) were added into the upper chamber, and complete medium was added to the bottom chamber and keep for 48 hours at 37°C incubator. Invaded cells on the lower surface of the membrane was fixed with ethanol and noninvasive cells were removed with a cotton swab. Then cells were stained with hematoxylin. Invaded cells from five fields were counted under a microscope.

5. Three-dimensional invasion

Dermal equivalent gel was generated with a Type I-A collagen mixture with eight volumes of ice-cold collagen solution (Nitta Gelatin Inc., Osaka, Japan), one volume of 10× reconstitution solution (0.022 g/mL NaHCO3, 0.0477 g/ml HEPES, 0.05 N NaOH), and one volume 10× DMEM. Immortalized gingiva fibroblast (1 × 105 cells) was added to collagen mixture.5 This mixture was poured into polycarbonate filter inserts (3 μm pore size, 12 mm diameter; Millipore) and placed in 6-well plates (Costar; Corning). After 24 hours incubation at 37°C, YD-10B cells (1 × 105 cells) were loaded on collagen gel and complete medium was added to the 6-well plates. The culture medium was then changed every 2 to 3 days for 2 weeks. Gels were then formalinfixed, paraffin-embedded and histologically examined. To measure invasive areas and depth, the culture tissue was stained with H&E.

6. Protease array

Wild type control Mock and Fascindep cells were cultured in 1% medium and harvested after 24 hours. Harvested medium was centrifuged in 3,000 × g for 10 minutes and used as conditioned media (CM) for protease array. The protein concentration of the CM was normalized by dilution with serum-free media. Then CM was incubated for 24 hours with the Proteome Profiler Human Protease Array Kit (R&D Systems, St. Louis, MO, USA). The relative expression levels of the proteases were determined according to the manufacturer’s protocol and signal intensities were compared using ImageJ software program.

7. Reverse transcription-PCR

Total RNA was isolated using TRIzol reagent (Life Technologies, Foster City, CA, USA) according to the instructions provided by the manufacturer. Reverse transcription to obtained cDNA and amplification by PCR using specific primer pairs. Primer sequences are given in Table 1. The reaction products were electrophoresed on 2% agarose gel. The obtained bands were visualized with Quantity One software and the Gel Doc 2000 system (Bio-Rad Laboratories, Hercules, CA, USA).

8. Statistical analysis

The statistical analysis was performed using InStat GraphPad Prism ver. 5.01 statistical software (GraphPad Software, Inc., San Diego, CA, USA). Results are expressed as mean ± SD. P-values < 0.05 were considered significant.

RESULTS

1. Effect of fascin on cancer invasion

Expression of fascin was confirmed in various cancer cell lines. As shown in Figure 1A, Western blot analysis revealed that fascin was clearly expressed in cancer cell lines. Relatively high fascin expression was observed in highly invasive cancer cells such as YD-10B, HSC-3, and Ca9.22. PC-3 was analyzed as a fascin positive control. To confirm the role of fascin in cancer invasion, fascin-depleted YD-10B cell (Fascindep) was established using lentiviral short hairpin (Fig. 1B). In Matrigel-coated Transwell invasion, Fascindep showed significantly lower invasion activity compared to control Mock cells (Fig. 1C). The level of E-cadherin expression was lower in the control Mock, but increased in the Fascindep (Fig. 1D). In addition, as a result of invasion activity, invasive areas into organotypic dermal equivalents (COL-matrix) were deeply extended in control Mock whereas Fascindep showed low infiltration (Fig. 1E).

2. Effect of fascin on expression and secretion of proteases

In order to define whether the decrease in invasion activity due to inhibition of fascin expression was caused by changes in protease activity, protease secreation was first observed. Protease array analysis showed that various protease were secreated from control Mock cells (Fig. 2A). However, the amount and type of protease secreated by fascin-depleted cells were reduced. Especially, release of matrix metalloproteinase (MMP)-9, MMP-10, cathepsin B, and cathepsin D were significantly decreased in Fascindep cells. On protease array analysis, only kallilrein 5 secreation was increased in Fascindep cells than that in control Mock. mRNA expression levels of MMP-9, MMP-10, cathepsin B, and cathepsin D in Fascindep cells were also decreased compared to those in control Mock whereas those of Kallikrein 5 (KLK5) were increased (Fig. 2B). These results indicate that fascin is associated with cancer invasion activity and that expression loss of fascin inhibits the expression and secretion of proteases, thereby decreasing cancer invasion.

DISCUSSION

Appropriate protease secretion by cancer cells is crucial for cancer invasion activity. Cancer forms a protruding structure called invadopodia to facilitates invasion.6 When protease is secreted intensively around the invadopodia, the extracellular matrix is deeply degraded, acting as a mechanism to increase cancer cell invasion.4 Inhibition of factors involved in functional invadopodia formation such as LIMK (LIM kinase) can reduce protease activity, thereby inhibiting matrix degradation.7 Fascin is a component of invadopodia. It acts as a cross-link between actin filaments to stabilize the protruding structure of leading edges, thereby facilitating extracellular matrix invasion.8,9 In the present study, high level of fascin was expressed in a various of highly invasive cancer cells whereas fascin down-regulation significantly reduced cancer invasiveness. From this result, we analyzed proteases regulated by fascin. Despite the fact that fascin highly expressed in various cancer tissues, there is little research on the alteration of protease activity by fascin expression.

Many types of secreted proteases were detected in CM of oral cancer. However, several proteases were found to be limitedly secreted in fascin-depleted cell line. Secretion of MMP-9, MMP-10, cathepsin B, and cathepsin D were significantly reduced. These results were varified as mRNA expression levels of these proteases in fascin-depleted cells were also decresed. MMPs, also known as matrixins, are proteases that not only degrade all kinds of extracellular matrix proteins, but also process many bioactive molecules. They are involved in the cleavage of cell surface receptor, the release of apoptotic ligands, and chemokine activation.10 Cathepsins are also proteases found in all animals. Especially, cathepsin B is implicated in the progression of various human tumors including ovarian cancer.11 Elevated levels of cathepsin D in tumor cells have been reported to be associated with greater invasiveness.12 The reduction of cancer invasion by fascin depletion is a result of suppression of proteases transcription and secretion. However, KLK5 was increased in fascin-depleted cells in this study. KLK5 is a secreted serin protease. It cleaves various extracellular matrix components. It also activates several other KLK proteases, triggering proteolytic cascades of tissue micro-environment. Elevated level of KLK5 was detected in serum of patients with ovarian and breast cancer.13 Therefore, over-expression of KLK5 is an indicator of poor prognosis in ovarian cancer. Interestingly, KLK5 expression levels was reported to be down-regulated in malignant specimens of mammary gland compared to benign ones.14 KLK5 expression in breast tissue biopsies has been suggested as an independent biomarker for differential diagnosis between malignant tumors and benign tumors of the breast. Therefore, further clinical study is needed to compare KLK5 expression between malignant and benign oral tumors.

Epithelial-mesenchymal transition (EMT) is the process by which epithelial cells lose their cell polarity and cell-cell adhesion to gain migratory and invasive properties and become mesenchymal stem cells.15 Since EMT occurs not only in wound healing and organ fibrosis, but also in the cancer progression, cancer invasion mechanisms are understood through EMT. Epithelial cells express high levels of E-cadherin whereas mesenchymal cells express high levels of N-cadherin, fibronectin, and vimentin. Thus, EMT entails profound morphological and phenotypic changes to cell. Loss of E-cadherin is considered to be a fundamental event in EMT. E-cadherin expression is decreased in epithelial malignancies including oral cancer. It is associated with decreased cell adhesiveness and increased malignancy. Therefore, E-cadherin is a significant prognostic factor associated with relapse and survival rate.16 In this study, decreased invasion activity and increased expression of E-cadherin were observed in fascin-depleted cells. These results suggest that inhibition of fascin expression may result from suppression of EMT progression. Recent studies have indicated that invadopodia is regulated by tumor environment signals including growth factors,4,17 hypoxia,18 pH,19 metabolism,20 and stromal cell interactions.21 The formation of invadopodia induced by growth factors such as epidermal growth factor, TGF-β or platelet-derived growth factor has been reported.22 The expression of fascin induced by growth factors has also been reported. TGF-β increases fascin expression in gastric cancer as a Smad3 phosphorylation-dependent response.23 Induction of fascin expression by interleukin-6 and TNF-α in metastatic breast cancer cells has also been reported.24 These reports indicate that fascin expression and invadopodia formation are regulated by paracrine signaling pathways in the cancer microenvironment. Thus cancer invasion studies should be considered together with the tumor surrounding microenvironment.

In conclusion, fascin expression affects proteases activity for matrix degradation and regulates cancer invasion and progression. Thus, a molecular mechanism study on the regulation of the activity of proteases by fascin is important in understanding cancer invasion. Fascin may be an important target for controlling cancer invasion.

ACKNOWLEDGMENTS

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2015R1D1A1A01056946 and 2018R1D1A1B07042035).

CONFLICTS OF INTEREST

No potential conflicts of interest were disclosed.

Figures
Fig. 1. Effect of fascin depletion on cancer invasion. (A) Fascin expression in various cancer cells. PC-3 was loaded as fascin positive control. 棺-actin was used as loading control. aP < 0.01 versus PC-3. (B) Fascin-depleted cell (Fascindep) was prepared using fascin short hairpin RNA (shRNA) lentiviral particles and puromycine resistance clone was analyzed by Western blot for reduction of fascin level. Control shRNA lentiviral particles-A was used to prepare control stable cell line (Mock). aP < 0.01 versus Mock. (C) Matrigel-coated transwell invasion activity of Mock and Fascindep cells. Invasion assay was proceeded for 48 hours. Invading cells were detected by hematoxylin staining and counted. aP < 0.01 versus Mock. (D) E-cad-herin expression in Mock and Fascindep cells. aP < 0.05, bP < 0.01 versus Mock. (E) Three-dimensional (3D) invasion of Mock and Fascindep cells. Cells on Type I-A collagen mixture (COL-matrix) was culture for 10 days. Invasion of cells within dermal equivalent was analyzed by H&E staining. Scale bars; 50 關m.
Fig. 2. Effect of fascin depletion on proteases activity. (A) Released protease in Mock and Fascindep cells. Conditioned media from Mock and Fascindep cells was incubated with Protease Array Kit and relative signal intensities were determined using ImageJ software program. Results were plotted. aP< 0.01 versus Mock. Proteases with large signal changes are indicated by circled numbers. (B) Expression of proteases mRNA in Mock and Fascindep cells. Reverse transcription-PCR products were loaded into agarose gel and glyceraldehyde-3-phosphate dehydrogen-ase (GAPDH) was used as RNA loading control. Results were plotted. bP < 0.05, aP < 0.01 versus Mock. MMP, matrix metalloproteinase.
Tables

Primer sequences, product sizes, and annealing temperatures for reverse transcription-PCR

Target genePrimer sequenceAnnealing temperature (°C)
MMP-9Sense; 5′-GATGCGTGGAGAGTCGAAAT-3′
Antisense; 5′-CACCAAACTGGATGACGATG-3′
65
MMP-10Sense; 5′-GACCCCAGACAAATGTGATCCT-3′
Antisense; 5′-TTCAGGCTCGGGATTCCA-3′
60
Cathepsin BSense; 5′-GAAGAAGCTGTGTGGCACTG-3′
Antisense; 5′-GTTCGGTCAGAAATGGCTTC-3′
58
Cathepsin DSense; 5′-AGGTGAAGGAGCTGCAGAAG-3′
Antisense; 5′-ATTCCCATGAAGCCACTCAG-3′
58
Kallikrein 5Sense; 5′-CCCCAAGTGCACTTCCCTAA-3′
Antisense; 5′-TCGTGTAGACACCCGGTCTG-3′
60
GAPDHSense; 5′-ATCCCTCCAAAATCAAGTGGG-3′
Antisense; 5′-TGAAGACGCCAGTGGACTCC-3′
60

MMP, matrix metalloproteinase; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.


References
  1. Guan, X (2015). Cancer metastases: challenges and opportunities. Acta Pharm Sin B. 5, 402-18.
    Pubmed KoreaMed CrossRef
  2. Noguti, J, De Moura, CF, De Jesus, GP, Da Silva, VH, Hossaka, TA, and Oshima, CT (2012). Metastasis from oral cancer: an overview. Cancer Genomics Proteomics. 9, 329-35.
    Pubmed
  3. Mehrotra, R, and Gupta, DK (2011). Exciting new advances in oral cancer diagnosis: avenues to early detection. Head Neck Oncol. 3, 33.
    Pubmed KoreaMed CrossRef
  4. Eddy, RJ, Weidmann, MD, Sharma, VP, and Condeelis, JS (2017). Tumor cell invadopodia: invasive protrusions that orchestrate metastasis. Trends Cell Biol. 27, 595-607.
    Pubmed KoreaMed CrossRef
  5. Hwang, YS, Park, KK, and Chung, WY (2013). Epigallocatechin-3 gallate inhibits cancer invasion by repressing functional invadopodia formation in oral squamous cell carcinoma. Eur J Pharmacol. 715, 286-95.
    Pubmed CrossRef
  6. Paz, H, Pathak, N, and Yang, J (2014). Invading one step at a time: the role of invadopodia in tumor metastasis. Oncogene. 33, 4193-202.
    KoreaMed CrossRef
  7. Lagoutte, E, Villeneuve, C, Lafanech챔re, L, Wells, CM, Jones, GE, and Chavrier, P (2016). LIMK regulates tumor-cell invasion and matrix degradation through tyrosine phosphorylation of MT1-MMP. Sci Rep. 6, 24925.
    Pubmed KoreaMed CrossRef
  8. Bryan, J, and Kane, RE (1978). Separation and interaction of the major components of sea urchin actin gel. J Mol Biol. 125, 207-24.
    Pubmed CrossRef
  9. Li, A, Dawson, JC, Forero-Vargas, M, Spence, HJ, Yu, X, and K철nig, I (2010). The actin-bundling protein fascin stabilizes actin in invadopodia and potentiates protrusive invasion. Curr Biol. 20, 339-45.
    Pubmed KoreaMed CrossRef
  10. Newby, AC (2006). Matrix metalloproteinases regulate migration, proliferation, and death of vascular smooth muscle cells by degrading matrix and non-matrix substrates. Cardiovasc Res. 69, 614-24.
    CrossRef
  11. Nishikawa, H, Ozaki, Y, Nakanishi, T, Blomgren, K, Tada, T, and Arakawa, A (2004). The role of cathepsin B and cystatin C in the mechanisms of invasion by ovarian cancer. Gynecol Oncol. 92, 881-6.
    Pubmed CrossRef
  12. Johnson, MD, Torri, JA, Lippman, ME, and Dickson, RB (1993). The role of cathepsin D in the invasiveness of human breast cancer cells. Cancer Res. 53, 873-7.
    Pubmed
  13. Yousef, GM, Polymeris, ME, Grass, L, Soosaipillai, A, Chan, PC, and Scorilas, A (2003). Human kallikrein 5: a potential novel serum bio-marker for breast and ovarian cancer. Cancer Res. 63, 3958-65.
    Pubmed
  14. Avgeris, M, Papachristopoulou, G, Polychronis, A, and Scorilas, A (2011). Down-regulation of kallikrein-related peptidase 5 (KLK5) expression in breast cancer patients: a biomarker for the differential diagnosis of breast lesions. Clin Proteomics. 8, 5.
    Pubmed KoreaMed CrossRef
  15. De Craene, B, and Berx, G (2013). Regulatory networks defining EMT during cancer initiation and progression. Nat Rev Cancer. 13, 97-110.
    Pubmed CrossRef
  16. Shiozaki, H, Tahara, H, Oka, H, Miyata, M, Kobayashi, K, and Tamura, S (1991). Expression of immunoreactive E-Cadherin adhesion molecules in human cancers. Am J Pathol. 139, 17-23.
    Pubmed KoreaMed
  17. Gould, CM, and Courtneidge, SA (2014). Regulation of invadopodia by the tumor microenvironment. Cell Adh Migr. 8, 226-35.
    Pubmed KoreaMed CrossRef
  18. Lucien, F, Brochu-Gaudreau, K, Arsenault, D, Harper, K, and Dubois, CM (2011). Hypoxia-induced invadopodia formation involves activation of NHE-1 by the p90 ribosomal S6 kinase (p90RSK). PLoS One. 6, e28851.
    CrossRef
  19. Rosenthal, CK (2012). pH-dependent invadopodia control. Nature Cell Biology. 14, 50.
    CrossRef
  20. van Horssen, R, Buccione, R, Willemse, M, Cingir, S, Wieringa, B, and Attanasio, F (2013). Cancer cell metabolism regulates extracellular matrix degradation by invadopodia. Eur J Cell Biol. 92, 113-21.
    Pubmed CrossRef
  21. Cao, H, Eppinga, RD, Razidlo, GL, Krueger, EW, Chen, J, and Qiang, L (2016). Stromal fibroblasts facilitate cancer cell invasion by a novel invadopodia-independent matrix degradation process. Oncogene. 35, 1099-110.
    CrossRef
  22. Murphy, DA, and Courtneidge, SA (2011). The 쁦ns and 쁮uts of podosomes and invadopodia: characteristics, formation and function. Nat Rev Mol Cell Biol. 12, 413-26.
    Pubmed KoreaMed CrossRef
  23. Li, L, Cao, F, Liu, B, Luo, X, Ma, X, and Hu, Z (2015). TGF-棺 induces fascin expression in gastric cancer via phosphorylation of smad3 linker area. Am J Cancer Res. 5, 1890-6.
    KoreaMed
  24. Snyder, M, Huang, J, Huang, XY, and Zhang, JJ (2014). A signal transducer and activator of transcription 3쨌nuclear factor 觀B(Stat3쨌NF觀B) complex is necessary for the expression of fascin in metastatic breast cancer cells in response to interleukin (IL)6 and tumor necrosis factor (TNF)-慣. J Biol Chem. 289, 30082-9.
    Pubmed KoreaMed CrossRef


September 2018, 23 (3)
Full Text(PDF) Free

Social Network Service

Cited By Articles
  • CrossRef (0)

Services

Warning: mysqli::close() [function.mysqli-close]: Couldn't fetch mysqli in /home/cpr/www/inc/bottom.inc on line 64