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透明细胞肾细胞癌的表观遗传学研究进展
引用本文:高永胜,闫少春,贾小娥,邵国. 透明细胞肾细胞癌的表观遗传学研究进展[J]. 中国病理生理杂志, 2018, 34(1): 178-182. DOI: 10.3969/j.issn.1000-4718.2018.01.031
作者姓名:高永胜  闫少春  贾小娥  邵国
作者单位:1. 包头医学院生物医学研究中心, 基础医学与法医学院, 神经科学研究所, 内蒙古 包头 014060;
2. 包头医学院 第二附属医院, 内蒙古 包头 014030;
3. 内蒙古低氧转化医学重点实验室, 内蒙古 包头 014060;
4. 低氧适应转化医学北京市重点实验室, 首都医科大学宣武医院, 北京 100053
基金项目:国家自然科学基金资助项目(No.81360316;No.81460283;No.81660204);包头医学院科学基金资助项目(No.BYJJ-DF201602;No.BSJJ201617;No.BSJJ201632;No.BYJJ-YF201610)
摘    要:正肾脏肿瘤的发病率在人类泌尿系统肿瘤中排名第3,约占恶性肿瘤的3%,发病年龄主要在50~70岁,每年导致90 000多例患者死亡,且呈递增趋势~([1])。肾癌的具体发病机制不详,除遗传因素外,吸烟、肥胖、污染和辐射等也是重要因素。大多数透明细胞肾细胞癌(clear cell renal cell carcinoma,ccRCC)患者在早期无任何症状,20%~30%患者在

关 键 词:透明细胞肾细胞癌  DNA甲基化  组蛋白修饰  微小RNA  DNA甲基转移酶  
收稿时间:2017-06-12

Progress in epigenetic study of clear cell renal cell carcinoma
GAO Yong-sheng,YAN Shao-chun,JIA Xiao-e,SHAO Guo. Progress in epigenetic study of clear cell renal cell carcinoma[J]. Chinese Journal of Pathophysiology, 2018, 34(1): 178-182. DOI: 10.3969/j.issn.1000-4718.2018.01.031
Authors:GAO Yong-sheng  YAN Shao-chun  JIA Xiao-e  SHAO Guo
Abstract:The epigenetic changes of clear cell renal cell carcinoma (ccRCC) are considered to be the main molecular mechanisms of its pathogenesis, including DNA methylation, histone modification, microRNA change, and so on. DNA methyltransferases (DNMTs) catalyze the occurrence of DNA methylation. DNA methylation changes are manifested in the overall low methylation of the genome and the high methylation of specific sites, which were involved in the development of ccRCC by affecting the expression of tumor suppressor genes. Due to histone-modified enzyme involvement, histone modification is shown as possible genetic reversal. MicroRNA plays an important role in the abnormal expression of ccRCC genes. With the studies of epigenetic mechanism and molecular pathology, it is important to explore the mechanisms and to seek effective early diagnosis, treatment and prognosis intervention of ccRCC.
Keywords:Clear cell renal cell carcinoma  DNA methylation  Histone modification  MicroRNAs  DNA methyltransferases
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