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p16(INK4a) 介导的正常和恶性人乳腺细胞中端粒酶的抑制作用。

p16(INK4a) -mediated suppression of telomerase in normal and malignant human breast cells.

机构信息

Department of Laboratory Medicine, University of California, San Francisco, USA.

出版信息

Aging Cell. 2010 Oct;9(5):736-46. doi: 10.1111/j.1474-9726.2010.00599.x. Epub 2010 Jul 14.

Abstract

The cyclin-dependent kinase inhibitor p16(INK4a) (CDKN2A) is an important tumor suppressor gene frequently inactivated in human tumors. p16 suppresses the development of cancer by triggering an irreversible arrest of cell proliferation termed cellular senescence. Here, we describe another anti-oncogenic function of p16 in addition to its ability to halt cell cycle progression. We show that transient expression of p16 stably represses the hTERT gene, encoding the catalytic subunit of telomerase, in both normal and malignant breast epithelial cells. Short-term p16 expression increases the amount of histone H3 trimethylated on lysine 27 (H3K27) bound to the hTERT promoter, resulting in transcriptional silencing, likely mediated by polycomb complexes. Our results indicate that transient p16 exposure may prevent malignant progression in dividing cells by irreversible repression of genes, such as hTERT, whose activity is necessary for extensive self-renewal.

摘要

细胞周期蛋白依赖性激酶抑制剂 p16(INK4a)(CDKN2A) 是一种重要的抑癌基因,在人类肿瘤中经常失活。p16 通过触发称为细胞衰老的细胞增殖不可逆停滞来抑制癌症的发展。在这里,我们除了描述 p16 阻止细胞周期进程的能力之外,还描述了 p16 的另一种抗癌功能。我们发现,p16 的瞬时表达在正常和恶性乳腺上皮细胞中稳定地抑制编码端粒酶催化亚基的 hTERT 基因。短期的 p16 表达增加了与 hTERT 启动子结合的组蛋白 H3 赖氨酸 27 三甲基化 (H3K27) 的量,导致转录沉默,可能由多梳复合物介导。我们的结果表明,瞬时的 p16 暴露可能通过不可逆地抑制 hTERT 等基因来防止分裂细胞的恶性进展,因为 hTERT 的活性对于广泛的自我更新是必需的。

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