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The good oncogene: When bad genes identify good outcome in cancer
被引:6
|作者:
Lee, Jonathan M.
[1
]
机构:
[1] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
关键词:
ELONGATION-FACTOR EEF1A2;
STEM-CELL FACTOR;
RECEPTOR TYROSINE KINASE;
C-KIT;
BREAST-CANCER;
PIK3CA MUTATIONS;
SELF-RENEWAL;
EXPRESSION;
OVARIAN;
LIGAND;
D O I:
10.1016/j.mehy.2010.10.015
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Some cancer patients live many decades after diagnosis while others are not so fortunate. Understanding why this occurs is a fundamental issue in cancer research. We hypothesize that among the factors controlling favorable outcome are a class of genes that we describe as "good oncogenes". These genes have a paradoxical function in cancer in that they are prognostic markers for favorable survival but have strong transforming and tumour-promoting properties. As such, good oncogenes both promote neoplasia and constrain it. We propose that good oncogenes enhance outcome probability by allowing early tumor detection, sensitizing cancer cells to senescence or by attenuating metastatic progression and tumour self-renewal. We believe that understanding the signaling pathways regulated by good oncogenes provides mechanistic insight into the biochemical basis for long-term survival in cancer. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:259 / 263
页数:5
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