Programmed cell removal: a new obstacle in the road to developing cancer

被引:194
作者
Chao, Mark P. [1 ,2 ]
Majeti, Ravindra [1 ,2 ,3 ]
Weissman, Irving L. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Inst Canc, Div Haematol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Div Haematol, Dept Internal Med, Stanford, CA 94305 USA
关键词
UNFOLDED PROTEIN RESPONSE; RECEPTOR-RELATED PROTEIN; ANTIGEN DOWN-REGULATION; MANNOSE-BINDING LECTIN; ACUTE MYELOID-LEUKEMIA; FIND-ME SIGNAL; APOPTOTIC CELLS; TUMOR-CELLS; PROGNOSTIC-FACTOR; STEM-CELLS;
D O I
10.1038/nrc3171
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of cancer involves mechanisms by which aberrant cells overcome normal regulatory pathways that limit their numbers and their migration. The evasion of programmed cell death is one of several key early events that need to be overcome in the progression from normal cellular homeostasis to malignant transformation. Recently, we provided evidence in mouse and human cancers that successful cancer clones must also overcome programmed cell removal. In this Opinion article, we explore the role of programmed cell removal in both normal and neoplastic cells, and we place this pathway in the context of the initiation of programmed cell death.
引用
收藏
页码:58 / 67
页数:11
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