DU145型
生物
前列腺癌
癌症研究
前列腺
基因
LNCaP公司
癌症
分子生物学
遗传学
作者
B Ren,Guoying Yu,George C. Tseng,Kathleen Cieply,Tim Gavel,James B. Nelson,George K. Michalopoulos,Yang Yu,J-H Luo
出处
期刊:Oncogene
[Springer Nature]
日期:2005-10-17
卷期号:25 (7): 1090-1098
被引量:187
标识
DOI:10.1038/sj.onc.1209134
摘要
The genomic DNA profiles of prostate cancers with aggressive features were compared to the profiles of matched normal DNA to identify genes that are selectively amplified in the cancer cells. One of the identified genes, MCM7, which is a component of the DNA replication licensing complex, has been studied extensively both at the DNA and protein levels in human prostate tissues. Approximately half of the prostate cancer specimens studied showed MCM7 gene amplification, and 60% of the aggressive prostate cancer specimens had increased MCM7 protein expression. Amplification or overexpression of MCM7 was significantly associated with relapse, local invasion and a worse tumor grade. Constitutive expression of MCM7 in a human prostate cancer cell line, DU145, resulted in markedly increased DNA synthesis and cell proliferation compared to vector-only controls, and an increased cell invasion in vitro. Indeed, MCM7 overexpression produced primary tumors 12 times larger than vector-only controls and resulted in a rapid demise of mice bearing those tumors. These studies implicate MCM7, and the DNA replication licensing gene family, in prostate cancer progression, growth and invasion.
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