首都医科大学学报 ›› 2011, Vol. 32 ›› Issue (1): 100-105.

• 神经退行性病的基础研究 • 上一篇    下一篇

p16INK4a/p14ARF基因在细胞衰老和肿瘤抑制中的作用研究进展

王芳1,2关云谦1,2*   

  1. 1. 首都医科大学宣武医院老年病研究所细胞治疗室; 2. 教育部神经变性病重点实验室
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2011-02-21 发布日期:2011-02-21

Role of the p16INK4a/p14ARF Gene in Cell Senescence and Tumor Suppression

WANG Fang1,2, GUAN Yunqian1,2*   

  1. 1. Department of Cell Therapy, Beijing Institute of Geriatrics, Xuanwu Hospital, Capital Medical University;2. Key Laboratory of Neurodegenerative Diseases, Ministry of Education
  • Received:1900-01-01 Revised:1900-01-01 Online:2011-02-21 Published:2011-02-21

摘要:

细胞衰老发生后细胞在形态和生化成分都发生改变,进而发生生理性功能障碍,最终进入凋亡和死亡程序。细胞衰老是生命体在细胞水平防止永生化和恶变、预防肿瘤发生的一种机制。细胞衰老由多种原因引起,近年来的研究发现,p16INK4apRb(视网膜母细胞瘤抗癌蛋白)和p14ARFp53这2条途径的活化与细胞衰老的启动和调节过程密切相关,对细胞衰老的信号传导通路及其调节因子等方面的深入研究,可以进一步认识细胞增生、衰老进程,以及防治肿瘤的规律,并为衰老相关疾病的治疗提示研究方向。

关键词: 细胞衰老, 信号转导通路, p16INK4a, p14ARF

Abstract:

The cell morphology and biochemical composition may be changed after cell senescence, it causes the physiological disorder, and then cells enter the apoptosis and death programs. Cell senescence is a mechanism to prevent immortalization and canceration and to prevent tumorigenesis at the cell level. It is caused by many reasons, during the recent years some researches find that the activation of p16INK4apRb pathway and p14ARFp53 pathway are closely correlated with the priming and adjusting process of cell senescence. The studies about the cell senescence signal transduction pathways and regulation factors can supply the research direction of the further knowledge of cell proliferation and senescence, the regulation of prevention and cure of tumor and the senescence correlated disease.

Key words: cell senescence, signal transduction pathway, p16INK4a, p14ARF

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