Seashols-Williams S J, Budd W, Clark G C, Wu Q, Daniel R, Dragoescu E, Zehner Z E
Department of Biochemistry & Molecular Biology, Virginia Commonwealth University, Richmond, Virginia, United States of America.
Department of Bioinformatics, Virginia Commonwealth University, Richmond, Virginia, United States of America.
PLoS One. 2016 Jul 22;11(7):e0159601. doi: 10.1371/journal.pone.0159601. eCollection 2016.
Identification of dysregulated microRNAs (miRNAs) in prostate cancer is critical not only for diagnosis, but also differentiation between the aggressive and indolent forms of the disease. miR-9 was identified as an oncomiR through both miRNA panel RT-qPCR as well as high-throughput sequencing analysis of the human P69 prostate cell line as compared to its highly tumorigenic and metastatic subline M12, and found to be consistently upregulated in other prostate cell lines including DU-145 and PC3. While miR-9 has been characterized as dysregulated either as an oncomiR or tumour suppressor in a variety of other cancers including breast, ovarian, and nasopharyngeal carcinomas, it has not been previously evaluated and proven as an oncomiR in prostate cancer. miR-9 was confirmed an oncomiR when found to be overexpressed in tumour tissue as compared to adjacent benign glandular epithelium through laser-capture microdissection of radical prostatectomy biopsies. Inhibition of miR-9 resulted in reduced migratory and invasive potential of the M12 cell line, and reduced tumour growth and metastases in male athymic nude mice. Analysis showed that miR-9 targets e-cadherin and suppressor of cytokine signalling 5 (SOCS5), but not NF-ĸB mRNA. Expression of these proteins was shown to be affected by modulation in expression of miR-9.
鉴定前列腺癌中失调的微小RNA(miRNA)不仅对诊断至关重要,而且对于区分该疾病的侵袭性和惰性形式也很关键。通过miRNA芯片RT-qPCR以及对人P69前列腺细胞系与其高致瘤性和转移性亚系M12进行高通量测序分析,miR-9被鉴定为一种癌基因miRNA,并且发现在包括DU-145和PC3在内的其他前列腺细胞系中持续上调。虽然miR-9在包括乳腺癌、卵巢癌和鼻咽癌在内的多种其他癌症中已被表征为作为癌基因miRNA或肿瘤抑制因子失调,但它此前尚未在前列腺癌中被评估并证实为癌基因miRNA。通过对前列腺癌根治术活检组织进行激光捕获显微切割发现,与相邻良性腺上皮相比,miR-9在肿瘤组织中过表达,从而证实其为癌基因miRNA。抑制miR-9导致M12细胞系的迁移和侵袭潜能降低,并减少雄性无胸腺裸鼠的肿瘤生长和转移。分析表明,miR-9靶向E-钙黏蛋白和细胞因子信号传导抑制因子5(SOCS5),但不靶向NF-κB mRNA。这些蛋白质的表达显示受miR-9表达调节的影响。