Reduced miR-100 expression in cervical cancer and precursors and its carcinogenic effect through targeting PLK1 protein

被引:101
|
作者
Li, Bao Hua
Zhou, Jian Song
Ye, Feng
Cheng, Xiao Dong
Zhou, Cai Yun [2 ]
Lu, Wei Guo
Xie, Xing [1 ]
机构
[1] Zhejiang Univ, Dept Gynecol Oncol, Womens Reprod Hlth Key Lab Zhejiang Prov, Womens Hosp,Sch Med, Hangzhou 310006, Zhejiang, Peoples R China
[2] Zhejiang Univ, Dept Pathol, Womens Hosp, Sch Med, Hangzhou 310006, Zhejiang, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
miR-100; PLK1; Human papillomavirus; Viral oncoproteins; Cervical carcinogenesis; OVARIAN-CANCER; CELLS; INFECTION; E6; DIFFERENTIATION; REPLICATION; ONCOPROTEIN; MICRORNAS; SURVIVAL; MIR-34A;
D O I
10.1016/j.ejca.2011.04.037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: Although aberrant miRNAs expression has been documented, altered miR-100 expression in cervical cancer and precursor tissues and its carcinogenic effect and mechanism remain unexplored. The aim of our study was to investigate the role of miR-100 alteration in cervical carcinogenesis. Methods: The expression of miR-100 was examined by quantitative real-time reverse transcriptase PCR (qRT-PCR) in 125 cervical tissues including normal cervical epithelium, cervical intraepithelial neoplasia (CIN), and cervical cancer, as well as in five cervical cell lines. Through modulating miR-100 expression using miR-100 inhibitor or mimic in vitro, cell growth, cycle and apoptosis were tested separately by MTT or flow cytometry and meanwhile Polo-like kinase1 (PLK1) mRNA and protein expressions were detected by qRT-PCR and immunoblotting. The expression of PLK1 in 125 cervical tissues was also examined by immunohistochemical staining and the correlation between miR-100 and PLK1 expression in the same tissues was analysed. Finally, HPV-16 E6/E7 expression was modulated by gene transfection and subsequently the level of miR-100 was examined by qRT-PCR. Results: The miR-100 expression showed a significantly and gradually reduced tendency from low-grade CIN, high-grade CIN to cervical cancer tissues and a significant decrease in HPV positive cervical cancer cell lines. The modulation of miR-100 expression remarkably influenced cell proliferation, cycle and apoptosis, as well as the level of PLK1 protein, but not mRNA, in vitro experiments. PLK1 expression was negatively correlated with miR-100 expression in CIN3 and cervical cancer tissues. The modulation of HR-HPV E6/E7 expression did not change miR-100 level. Conclusions: The reduced miR-100 expression participates in the development of cervical cancer at least partly through loss of inhibition to target gene PLK1, which probably occurs in a relative late phase of carcinogenesis. HR-HPV E6/E7 may not directly regulate miR-100 expression in cervical cells. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2166 / 2174
页数:9
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