Bhattacharya Resham, Nicoloso Milena, Arvizo Rochelle, Wang Enfeng, Cortez Angelica, Rossi Simona, Calin George A, Mukherjee Priyabrata
Department of Biochemistry, College of Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
Cancer Res. 2009 Dec 1;69(23):9090-5. doi: 10.1158/0008-5472.CAN-09-2552. Epub 2009 Nov 10.
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 miR-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.
在包括卵巢癌在内的多种上皮性恶性肿瘤中均发现了Bmi-1的致癌激活,但Bmi-1过表达的具体机制尚未确定。因此,鉴于Bmi-1在癌症中具有巨大的病理意义,我们想研究微小RNA(miRNA)异常是否在卵巢癌中Bmi-1的调控中发挥作用。在本报告中,我们鉴定出两种miRNA,即miR-15a和miR-16,它们在卵巢细胞系和原发性卵巢组织中表达下调。我们发现这些miRNA直接靶向Bmi-1的3'非翻译区,并且与卵巢癌患者及细胞系中的Bmi-1蛋白水平显著相关。此外,响应miR-15a或miR-16的表达,Bmi-1蛋白水平下调,并导致卵巢癌细胞增殖和克隆生长显著减少。这些发现提示可通过恢复卵巢癌及其他涉及Bmi-1上调的癌症中miR-15a和miR-16的表达来制定治疗策略。