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p16INK4a-mediated suppression of telomerase in normal and malignant human breast cells

机译:p16INK4a介导的正常和恶性人类乳腺细胞端粒酶的抑制

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摘要

SummaryThe cyclin-dependent kinase inhibitor p16INK4a (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.
机译:概述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通过触发被称为细胞衰老的细胞增殖的不可逆止的抑制作用来抑制癌症的发展。在这里,我们描述了p16的另一种抗癌功能,不仅可以阻止细胞周期进程。我们显示p16的瞬时表达稳定地抑制正常和恶性乳腺癌上皮细胞中的hTERT基因,编码端粒酶的催化亚基。短期p16表达增加与hTERT启动子结合的赖氨酸27(H3K27)上三甲基化的组蛋白H3的量,导致转录沉默,可能是由多梳复合物介导的。我们的结果表明,短暂的p16暴露可能通过不可逆转的基因(如hTERT)阻止了分裂细胞的恶性进展,而hTERT等基因的活性对于广泛的自我更新是必不可少的。

著录项

  • 来源
    《Aging Cell》 |2010年第5期|p.736-746|共11页
  • 作者单位

    Department of Laboratory Medicine, University of California, San Francisco, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

    Department of Laboratory Medicine, University of California, San Francisco, CA, USA;

    Ludwig Institute For Cancer Research, University of California, San Diego, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA|Buck Institute for Age Research, Novato, CA, USA;

    Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA;

    Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA;

    Institute of Pathology, University of Lausanne, 1011 Lausanne, Switzerland;

    Ludwig Institute For Cancer Research, University of California, San Diego, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA|Buck Institute for Age Research, Novato, CA, USA;

    Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    heterochromatin; histone methylation; hTERT; INK4a; senescence;

    机译:异染色质;组蛋白甲基化;hTERT;INK4a;衰老;

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