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人乳头瘤病毒在宫颈癌中对miR-9的激活作用。

Activation of miR-9 by human papillomavirus in cervical cancer.

作者信息

Liu Weijun, Gao Ge, Hu Xiaoxia, Wang Yuhui, Schwarz Julie K, Chen Jason J, Grigsby Perry W, Wang Xiaowei

机构信息

Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.

People's Hospital of Guangxi Province, Nanning, China. Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.

出版信息

Oncotarget. 2014 Nov 30;5(22):11620-30. doi: 10.18632/oncotarget.2599.

Abstract

Cervical cancer is the third most common cancer in women worldwide, leading to about 300,000 deaths each year. Most cervical cancers are caused by human papillomavirus (HPV) infection. However, persistent transcriptional activity of HPV oncogenes, which indicates active roles of HPV in cervical cancer maintenance and progression, has not been well characterized. Using our recently developed assays for comprehensive profiling of HPV E6/E7 transcripts, we have detected transcriptional activities of 10 high-risk HPV strains from 87 of the 101 cervical tumors included in the analysis. These HPV-positive patients had significantly better survival outcome compared with HPV-negative patients, indicating HPV transcriptional activity as a favorable prognostic marker for cervical cancer. Furthermore, we have determined microRNA (miRNA) expression changes that were correlated with tumor HPV status. Our profiling and functional analyses identified miR-9 as the most activated miRNA by HPV E6 in a p53-independent manner. Further target validation and functional studies showed that HPV-induced miR-9 activation led to significantly increased cell motility by downregulating multiple gene targets involved in cell migration. Thus, our work helps to understand the molecular mechanisms as well as identify potential therapeutic targets for cervical cancer and other HPV-induced cancers.

摘要

宫颈癌是全球女性中第三大常见癌症,每年导致约30万例死亡。大多数宫颈癌是由人乳头瘤病毒(HPV)感染引起的。然而,HPV癌基因的持续转录活性,这表明HPV在宫颈癌维持和进展中起积极作用,但尚未得到充分表征。使用我们最近开发的用于全面分析HPV E6/E7转录本的检测方法,我们在分析的101例宫颈肿瘤中的87例中检测到了10种高危HPV毒株的转录活性。与HPV阴性患者相比,这些HPV阳性患者的生存结果明显更好,表明HPV转录活性是宫颈癌的一个有利预后标志物。此外,我们确定了与肿瘤HPV状态相关的微小RNA(miRNA)表达变化。我们的分析和功能研究确定miR-9是HPV E6以不依赖p53的方式激活的最活跃的miRNA。进一步的靶点验证和功能研究表明,HPV诱导的miR-9激活通过下调多个参与细胞迁移的基因靶点导致细胞运动性显著增加。因此,我们的工作有助于了解宫颈癌和其他HPV诱导的癌症的分子机制,并识别潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0138/4294330/73b36a523338/oncotarget-05-11620-g001.jpg

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