A MicroRNA Expression Signature for Cervical Cancer Prognosis

被引:257
|
作者
Hu, Xiaoxia [1 ]
Schwarz, Julie K. [1 ]
Lewis, James S., Jr. [2 ]
Huettner, Phyllis C. [2 ]
Rader, Janet S. [3 ]
Deasy, Joseph O. [1 ]
Grigsby, Perry W. [1 ,3 ]
Wang, Xiaowei [1 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Obstet & Gynecol, St Louis, MO 63110 USA
关键词
MESENCHYMAL TRANSITION; MIR-200; FAMILY; TARGET PREDICTION; REPRESSORS ZEB1; CELLS; IDENTIFICATION; DELIVERY; GROWTH; GENES; SITES;
D O I
10.1158/0008-5472.CAN-09-3289
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Invasive cervical cancer is a leading cause of cancer death in women worldwide, resulting in about 300,000 deaths each year. The clinical outcomes of cervical cancer vary significantly and are difficult to predict. Thus, a method to reliably predict disease outcome would be important for individualized therapy by identifying patients with high risk of treatment failures before therapy. In this study, we have identified a microRNA (miRNA)-based signature for the prediction of cervical cancer survival. miRNAs are a newly identified family of small noncoding RNAs that are extensively involved in human cancers. Using an established PCR-based miRNA assay to analyze 102 cervical cancer samples, we identified miR-200a and miR-9 as two miRNAs that could predict patient survival. A logistic regression model was developed based on these two miRNAs and the prognostic value of the model was subsequently validated with independent cervical cancers. Further-more, functional studies were done to characterize the effect of miRNAs in cervical cancer cells. Our results suggest that both miR-200a and miR-9 could play important regulatory roles in cervical cancer control. In particular, miR-200a is likely to affect the metastatic potential of cervical cancer cells by coordinate suppression of multiple genes controlling cell motility. Cancer Res; 70(4); 1441-8. (C) 2010 AACR.
引用
收藏
页码:1441 / 1448
页数:8
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