FOXK1 facilitates cell proliferation through regulating the expression of p21, and promotes metastasis in ovarian cancer

被引:27
作者
Li, Li [1 ]
Gong, Miao [1 ]
Zhao, Yu [1 ]
Zhao, Xiujun [1 ]
Li, Quanhai [2 ]
机构
[1] Hebei Med Univ, Dept Histol & Embryol, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Dept Immunol, Shijiazhuang, Hebei, Peoples R China
关键词
FOXK1; proliferation; p21; metastasis; ovarian cancer; TRANSCRIPTION FACTORS; MICE LACKING; FORKHEAD; IDENTIFICATION; PROTEINS; COMPLEX; GROWTH; FOXM1; MMP-9; FHL2;
D O I
10.18632/oncotarget.19713
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer is one of the most common cancer in the world. FOX family plays essential function in multiple cancers. In our work, FOXK1 was found to up-regulate in ovarian cancer tissue samples and cell lines; moreover, the expression of FOXK1 was correlated with tumor size, metastasis and poorly prognosis. To evaluate the function of FOXK1 in ovarian cancer, we performed colony formation analysis, CCK-8 assay and cell cycle analysis to determine the effect of FOXK1 on cell proliferation and cell cycle. We found that FOXK1 obviously improved the ability of cell proliferation through promoting cell cycle. Furthermore, ChIP assay and luciferase reporter assay indicated that FOXK1 facilitated cell cycle through regulating the expression of p21, but FOXK1 had no effect on cell apoptosis. In addition, wound healing assay and transwell invasion analysis demonstrated that FOXK1 promoted migration and invasion in ovarian cancer. In conclusion, our work indicate FOXK1 plays a key function in the ovarian cancer, it promotes cell proliferation and metastasis. FOXK1 serves as a novel molecular therapy target in ovarian cancer.
引用
收藏
页码:70441 / 70451
页数:11
相关论文
共 37 条
[1]   FOXA1 expression in breast cancer - Correlation with luminal subtype A and survival [J].
Badve, Sunil ;
Turbin, Dmitry ;
Thorat, Mangesh A. ;
Morimiya, Akira ;
Nielsen, Torsten O. ;
Perou, Charles M. ;
Dunn, Sandi ;
Huntsman, David G. ;
Nakshatri, Harikrishna .
CLINICAL CANCER RESEARCH, 2007, 13 (15) :4415-4421
[2]  
Banks E, 2000, METH MOLEC MED, V39, P3
[3]   RADIATION-INDUCED CELL-CYCLE ARREST COMPROMISED BY P21 DEFICIENCY [J].
BRUGAROLAS, J ;
CHANDRASEKARAN, C ;
GORDON, JI ;
BEACH, D ;
JACKS, T ;
HANNON, GJ .
NATURE, 1995, 377 (6549) :552-557
[4]   IDENTIFICATION OF 9 TISSUE-SPECIFIC TRANSCRIPTION FACTORS OF THE HEPATOCYTE NUCLEAR FACTOR-III FORKHEAD DNA-BINDING-DOMAIN FAMILY [J].
CLEVIDENCE, DE ;
OVERDIER, DG ;
TAO, WF ;
QIAN, XB ;
PANI, L ;
LAI, EE ;
COSTA, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :3948-3952
[5]   Forkhead-box transcription factors and their role in the immune system [J].
Coffer, PJ ;
Burgering, BMT .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (11) :889-899
[6]   MICE LACKING P21(C/P1/WAF1) UNDERGO NORMAL DEVELOPMENT, BUT ARE DEFECTIVE IN G1 CHECKPOINT CONTROL [J].
DENG, CX ;
ZHANG, PM ;
HARPER, JW ;
ELLEDGE, SJ ;
LEDER, P .
CELL, 1995, 82 (04) :675-684
[7]   Prognostic significance of TIMP-2, MMP-2, and MMP-9 on high-grade serous ovarian carcinoma using digital image analysis [J].
Desmeules, Patrice ;
Trudel, Dominique ;
Turcotte, Stephane ;
Sirois, Jennifer ;
Plante, Marie ;
Gregoire, Jean ;
Renaud, Marie-Claude ;
Orain, Michele ;
Tetu, Bernard ;
Bairati, Isabelle .
HUMAN PATHOLOGY, 2015, 46 (05) :739-745
[8]   Forkhead factor FOXQ1 promotes TGF-β1 expression and induces epithelial-mesenchymal transition [J].
Fan, Dong-Mei ;
Feng, Xiao-Shan ;
Qi, Peng-Wei ;
Chen, Ya-Wei .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2014, 397 (1-2) :179-186
[9]  
Foucher I, 2002, DEVELOPMENT, V129, P4065
[10]   Forkhead box A1 regulates prostate ductal morphogenesis and promotes epithelial cell maturation [J].
Gao, N ;
Ishii, K ;
Mirosevich, J ;
Kuwajima, S ;
Oppenheimer, SR ;
Roberts, RL ;
Jiang, M ;
Yu, XP ;
Shappell, SB ;
Caprioli, RM ;
Stoffel, M ;
Hayward, SW ;
Matusik, RJ .
DEVELOPMENT, 2005, 132 (15) :3431-3443