相关实验视频
Updated: May 13, 2026

Derivation of Thymic Lymphoma T-cell Lines from Atm-/- and p53-/- Mice
Published on: April 3, 2011
随机瘤抑制剂p18通过与ATM/ATR的相互作用对p53进行上调
Bum-Joon Park1, Jin Wook Kang, Sang Won Lee
1National Creative Research Initiatives Center for ARS Network, College of Pharmacy, Seoul National University, Seoul 151-742, South Korea.
研究表明,p18对DNA损伤反应至关重要,并作为瘤抑制剂. 它的缺失导致胚胎致死性和瘤易感性增加,突出其在激活ATM/ATR和p53.3中的作用.
科学领域:
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
- 癌症研究 癌症研究
背景情况:
- p18最初被确定为宏分子tRNA合成酶复合物的组成部分.
- 精确的生物功能p18,特别是在细胞应激反应,仍然在很大程度上不具特征.
研究的目的:
- 为了阐明p18.的体内功能.
- 为了研究p18在DNA损伤反应途径中的作用.
- 确定p18在人类癌症中的临床相关性.
主要方法:
- 产生和分析p18淘汰赛和异构合的小鼠模型.
- 评估DNA损伤反应途径,包括p53激活和ATM/ATR信号.
- 在人类癌症细胞系和组织中分析p18表达.
主要成果:
- 完全失去p18导致胚胎死亡.
- 异卵性p18小鼠对自发瘤形成的敏感性增加.
- p18表达是由DNA损伤引起的,并转移到核中.
- 对于DNA损伤引起的p53升高,p18是必不可少的,并且与ATM/ATR激酶直接相互作用.
- 减少p18表达在人类癌症中很常见.
结论:
- 18作为一个平不充分的瘤抑制剂.
- 作为对DNA损伤的反应,p18是ATM/ATR依赖的p53激活的关键媒介.
- 对p18的调节失调与人类瘤发生有关.
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