Loss of anti-mitotic effects of Bcl-2 with retention of anti-apoptotic activity during tumor progression in a mouse model

被引:43
作者
Furth, PA
Bar-Peled, U
Li, ML
Lewis, A
Laucirica, R
Jäger, R
Weiher, H
Russell, RG
机构
[1] Univ Maryland, Ctr Med Biotechnol, Inst Human Virol, Sch Med,Dept Med,Div Infect Dis, Baltimore, MD 21201 USA
[2] Baltimore Vet Affairs Med Ctr, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Methodist Hosp, Houston, TX 77030 USA
[6] Forschungszentrum Karlsruhe, Inst Genet, D-76021 Karlsruhe, Germany
[7] Inst Diabet Forsch, D-80804 Munich, Germany
关键词
Bcl-2; cancer progression; mitosis; apoptosis; mouse model;
D O I
10.1038/sj.onc.1203073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bcl-2 is an anti-apoptotic and anti-proliferative protein over-expressed in several different human cancers including breast, Gain of Bcl-2 function in mammary epithelial cells was superimposed on the WAP-TAg transgenic mouse model of breast cancer progression to determine its effect on epithelial cell survival and proliferation at three key stages in oncogenesis: the initial proliferative process, hyperplasia, and cancer. During the initial proliferative process, Bcl-2 strongly inhibited both apoptosis and mitotic activity. However as tumorigenesis progressed to hyperplasia and adenocarcinoma, the inhibitory effects on mitotic activity were lost. In contrast, anti-apoptotic activity persisted in both hyperplasias and adenocarcinomas. These results demonstrate that the inhibitory effect of Bcl-2 on epithelial cell proliferation and apoptosis can separate during cancer progression. In this model, retention of anti-apoptotic activity with loss of anti-proliferative action resulted in earlier tumor presentation.
引用
收藏
页码:6589 / 6596
页数:8
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