MiR-15a and MiR-16 Control Bmi-1 Expression in Ovarian Cancer

被引:207
作者
Bhattacharya, Resham [1 ]
Nicoloso, Milena [3 ]
Arvizo, Rochelle [1 ]
Wang, Enfeng [1 ]
Cortez, Angelica [3 ]
Rossi, Simona [3 ]
Calin, George A. [3 ]
Mukherjee, Priyabrata [1 ,2 ]
机构
[1] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Biomed Engn, Rochester, MN 55905 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
MICRORNA EXPRESSION; TELOMERASE ACTIVITY; DOWN-REGULATION; SELF-RENEWAL; LUNG-CANCER; PROFILES; MANAGEMENT; CELLS;
D O I
10.1158/0008-5472.CAN-09-2552
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncogenic activation of Bmi-1 is found in a wide variety of epithelial malignancies including ovarian cancer, yet a specific mechanism for overexpression of Bmi-1 has not been determined. Thus, realizing the immense pathologic significance of Bmi-1 in cancer, we wanted to investigate if microRNA (miRNA) aberrations played a role in the regulation of Bmi-1 in ovarian cancer. In this report, we identify two miRNAs, miR-15a and mill-16, that are underexpressed in ovarian cell lines and in primary ovarian tissues. We show that these miRNAs directly target the Bmi-1 3'untranslated region and significantly correlate With Bmi-1 protein levels in ovarian cancer patients and cell lines. Furthermore, Bmi-1 protein levels are downregulated in response to miR-15a or miR-16 expression and lead to significant reduction in ovarian cancer cell proliferation and clonal growth. These findings suggest the development of therapeutic strategies by restoring miR-15a and miR-16 expression in ovarian cancer and in other cancers that involve upregulation of Bmi-1. [Cancer Res 2009;69(23):9090-5]
引用
收藏
页码:9090 / 9095
页数:6
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