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长链非编码RNA RP11-214F16.8 促进乳腺癌细胞增殖
引用本文:陈向宙,叶嘉慧,黎谢梦丹,贾小婷,贺智敏.长链非编码RNA RP11-214F16.8 促进乳腺癌细胞增殖[J].中国生物化学与分子生物学报,2018,34(8):900-904.
作者姓名:陈向宙  叶嘉慧  黎谢梦丹  贾小婷  贺智敏
作者单位:广州医科大学附属肿瘤医院肿瘤研究所,广州恶性肿瘤治疗转化医学重点实验室,广州510095
基金项目:国家自然科学基金(No.81602016);广东省医学科学技术研究基金(No.A2017362)和广州市医药卫生科技项目(No.20171A011321)
摘    要:长链非编码RNAs (long non-coding RNAs, lncRNAs)在乳腺癌发生发展中的作用备受瞩目。本研究通过大数据分析发现,lncRNA RP11-214F16.8在乳腺癌组织中的表达量显著高于正常组织,且其表达量与乳腺癌患者预后负相关。因此,本文采用qRT-PCR技术,在收集的临床样本中验证RP11-214F16.8的表达,证实其在乳腺癌组织中相对表达量为5.65±0.72,其在癌旁组织中表达量为2.63±0.35,且RP11-214F16.8的表达量与乳腺癌瘤体大小和临床TNM分期相关。此外发现,RP11-214F16.8在乳腺癌细胞中的表达量高于正常乳腺上皮细胞。在乳腺癌MCF-7细胞中,过表达RP11-214F16.8后,MCF-7细胞的增殖能力显著增强。而在MDA-MB-231细胞中,敲低RP11-214F16.8的表达,获得相反的结果。进一步研究发现,RP11-214F16.8可上调细胞周期蛋白 D3、CDK4的表达,而下调p18蛋白表达量,进而加速细胞增殖。总之,RP11-214F16.8在乳腺癌中高表达,且促进乳腺癌细胞增殖,进而推动乳腺癌进程。这一研究发现,将为乳腺癌发生发展的网络机制研究提供新的理论依据。

关 键 词:长链非编码RNA    RP11-214F16.8    增殖  乳腺癌  
收稿时间:2018-03-12

Long Non-coding RNA RP11-214F16.8 Enhances Proliferation of Breast Cancer Cells
CHEN Xiang-Zhou,YE Jia-Hui,LI-XIE Meng-Dan,JIA Xiao-Ting,HE Zhi-Min.Long Non-coding RNA RP11-214F16.8 Enhances Proliferation of Breast Cancer Cells[J].Chinese Journal of Biochemistry and Molecular Biology,2018,34(8):900-904.
Authors:CHEN Xiang-Zhou  YE Jia-Hui  LI-XIE Meng-Dan  JIA Xiao-Ting  HE Zhi-Min
Institution:Cancer Research Institute, Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou Key Laboratory of Translational Medicine on Cancer Treatment, Guangzhou 510095, China
Abstract:Long non-coding RNAs (lncRNAs) were highlighted in the progression of breast cancer. In this study, it was found that RP11-214F16.8 was significantly enhanced in breast cancer tissues in data set analysis by GEPIA software, comparing with that in normal. Moreover, RP11-214F16.8 was negatively correlated with the prognosis of breast cancer patients. Furthermore, qRT PCR assay was performed to determine the expression levels of RP11-214F16.8 in breast cancer and normal tissues collected at our hospital. The results showed that RP11-214F16.8 was highly expressed in breast cancer tissues (5.65±0.72) than that in normal tissues (2.63±0.35). RP11-214F16.8 expression was positively correlated with tumor size and TNM stage of breast cancer. Similarly, it was demonstrated that RP11-214F16.8 was evidently accelerated in breast cancer cells, comparing with that in mammary MCF-10A epithelial cells. Restoring RP11-214F16.8 enhanced proliferation of MCF-7 cells, while silencing RP11-214F16.8 reduced MDA-MB-231 cells proliferation. RP11-214F16.8 could upregulate cyclin D3 and CDK4 protein expression while downregulated p18 protein expression. To sum up, RP11-214F16.8 was highly expressed in breast cancer and enhanced proliferation of breast cancer cells. This investigation can provide new insight into the molecular mechanisms of breast cancer progression.
Keywords:long non-coding RNAs(lncRNAs)  RP11-214F16  8  proliferation  breast cancer cells  
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