Tumor cells utilize multiple pathways to down-modulate apoptosis - Lessons from a mouse model of islet cell carcinogenesis

被引:32
作者
Hager, JH
Hanahan, D
机构
[1] Univ Calif San Francisco, Hormone Res Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
来源
MECHANISMS OF CELL DEATH: THE SECOND ANNUAL CONFERENCE OF THE CELL DEATH SOCIETY | 1999年 / 887卷
关键词
D O I
10.1111/j.1749-6632.1999.tb07929.x
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
Apoptosis, the process of programmed cell death, plays a critical role in many normal and pathological (disease) processes.(1) In normal tissues, apoptosis functions in the homeostatic maintenance of proper tissue and organ size by eliminating aged cells to offset the birth of new cells that arise by mitosis. In disease, apoptosis can affect the pathological process is two disparate ways. There are diseases that have too much apoptosis such as autoimmune diabetes and Alzheimer's, or those that have too little apoptosis, such as cancer. This review will focus on the latter and, more specifically, detail and summarize some important lessons learned about apoptosis and cancer from studying a transgenic mouse model of islet cell carcinoma, RIP-Tag, as outlined below.
引用
收藏
页码:150 / 163
页数:14
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