国际肿瘤学杂志 ›› 2012, Vol. 39 ›› Issue (1): 60-63.

• 综述 • 上一篇    下一篇

3号染色体短臂抑癌基因与肾透明细胞癌

向威, 赵军   

  1. 430022 华中科技大学同济医学院附属协和医院泌尿外科
  • 出版日期:2012-01-08 发布日期:2013-11-11
  • 通讯作者: 赵军,E-mail:zhaojun21@yahoo.com E-mail:zhaojun21@yahoo.com

Chromosome 3p tumour suppressor genes and clear cell renal cell carcinoma

XIANG  Wei, ZHAO  Jun   

  1. Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
  • Online:2012-01-08 Published:2013-11-11
  • Contact: Corresponding author: ZHAO Jun, E-mail: zhaojun21@yahoo.com E-mail:zhaojun21@yahoo.com

摘要: 人类3号染色体短臂(3p)上抑癌基因的异常改变(如缺失突变、转录失活或沉默等)被认为是包括肾癌尤其是肾透明细胞癌在内的人类多种肿瘤起始发生的关键步骤,而它们与肿瘤的后续发展演变亦关联紧密。大量研究发现并证实诸如VHL、RASSF1A、SEMA3B、SETD2、PBRM1、NPRL2、GPX1等3p基因的缺失或下调在肾透明细胞癌的形成与发展中扮演了极为重要的角色,这为进一步阐释肾透明细胞癌分子形成机制奠定了基础,是当前研究的重要方向。而关于其具体调控路径及作用机制的研究除部分基因已初步明晰外,余尚在继续进行中。

关键词: 肾肿瘤, 基因, 肿瘤抑制, 3号染色体断臂

Abstract: The abnormal changes of tumor suppressor genes such as deletion mutant, transcription inactivation or silence on human chromosome 3p (pter) were considered as a key step which was closely related to the tumorigenesis of several kinds of cancers, especially clear cell renal cell carcinoma, one kind of renal cancer. And on this basis, it has been confirmed that the deletion and downregulation of multiple 3p genes such as VHL, RASSF1A, SEMA3B, SETD2, PBRM1, NPRL2 and so on, play a vital important role in the tumorigenesis and development of clear cell renal cell carcinoma. And they provide a further way to explain the molecular mechanism of the tumorigenesis of kidney cancer. However, when the regulatory pathway and mechanism research of some genes were known to us, the other genes, especially those newly founded, which were still not clear and need to be further investigated.