Nakamura T, Monden Y, Kawashima K, Naruke T, Nishimura S
Laboratory of Cancer Research, Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories, Tsukuba, Ibaraki.
Jpn J Cancer Res. 1996 Dec;87(12):1204-9. doi: 10.1111/j.1349-7006.1996.tb03134.x.
The functions of the transcription factor E2F-1 are regulated by the RB protein through the RB-binding domain of E2F-1 and this factor is considered to be an important molecule that functions downstream of the RB protein. In order to determine whether E2F-1 that cannot bind to RB might be associated with various human cancers, we searched for mutations in the RB-binding domain of E2F-1 using samples of DNA from various clinical specimens obtained from 406 cancer patients (with lung, pancreatic, stomach, colon, esophageal, and hepatic cancers) by analysis of polymerase chain reaction-mediated single-strand conformational polymorphism. No mutations or deletions were detected in genes for E2F-1 from any of the tumor tissues examined. These results suggest that a mutation or deletion in E2F-1 that might affect binding of the RB protein is not involved in human cancers.
转录因子E2F-1的功能通过E2F-1的RB结合结构域受RB蛋白调控,并且该因子被认为是在RB蛋白下游发挥作用的重要分子。为了确定不能与RB结合的E2F-1是否可能与多种人类癌症相关,我们通过聚合酶链反应介导的单链构象多态性分析,使用从406例癌症患者(患有肺癌、胰腺癌、胃癌、结肠癌、食管癌和肝癌)获得的各种临床标本的DNA样本,搜索E2F-1的RB结合结构域中的突变。在所检查的任何肿瘤组织的E2F-1基因中均未检测到突变或缺失。这些结果表明,可能影响RB蛋白结合的E2F-1中的突变或缺失不参与人类癌症。