Oncoprotein BMI-1 Induces the Malignant Transformation of HaCaT Cells

被引:13
作者
Wang, Qian [1 ]
Li, Wen-Lin [1 ]
You, Pu [1 ]
Su, Juan [1 ]
Zhu, Ming-Hua [2 ]
Xie, Dong-Fu [1 ]
Zhu, Hai-Yin [1 ]
He, Zhi-Ying [1 ]
Li, Jian-Xiu [1 ]
Ding, Xiao-Yan [3 ]
Wang, Xin [3 ,4 ]
Hu, Yi-Ping [1 ]
机构
[1] Second Mil Med Univ, Dept Cell Biol, Shanghai 200433, Peoples R China
[2] ChangHai Hosp, Dept Pathol, Shanghai 200433, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Mol & Cell Biol, Shanghai 200031, Peoples R China
[4] Univ Minnesota, Stem Cell Inst, Minneapolis, MN 55455 USA
基金
中国国家自然科学基金;
关键词
BMI-1; HaCaT CELL LINE; SKIN CANCER; MALIGNANT TRANSFORMATION; GROUP PROTEIN EZH2; POLYCOMB-GROUP; STEM-CELLS; HUMAN KERATINOCYTES; TUMOR SUPPRESSION; SELF-RENEWAL; CANCER; EXPRESSION; MDM2; IDENTIFICATION;
D O I
10.1002/jcb.21969
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BMI-1 (B-cell-specific Moloney murine leukemia virus integration site 1), a novel oncogene, has attracted much attention in recent years for its involvement in the initiation of a variety of tumors. Recent evidence showed that BMI-1 was highly expressed in neoplastic skin lesions. However, whether dysregulated BMI-1 expression is causal for the transformation of skin cells remains unknown. In this study, we stably expressed BMI-1 in a human keratinocyte cell line, HaCaT. The expression of wild-type BMI-1 induced the malignant transformation of HaCaT cells in vitro. More importantly, we found that expression of BMI-1 promoted formation of squamous cell carcinomas in vivo. Furthermore, we showed that BMI-1 expression led to the downregulation of tumore suppressors, such as p161NK4a and p14ARF, cell adhesion molecules, such as E-Cadherin, and differentiation related factor, such as KRT6. Therefore, our findings demonstrated that dysregulated BMI-1 could indeed lead to keratinocytes transformation and tumorigenesis, potentially through promoting cell cycle progression and increasing cell mobility. J. Cell. Biochem. 106: 16-24, 2009. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:16 / 24
页数:9
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