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端粒、癌症与衰老:长生不老?

Telomeres, cancer & aging: live long & prosper?

作者信息

Eissenberg Joel C

机构信息

Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, USA.

出版信息

Mo Med. 2013 Jan-Feb;110(1):11-6.

PMID:23457740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6179622/
Abstract

Like our clothes, our chromosomes fray at the edges with age. Some believe that if we could discover a molecular tailor to patch our age-abraded chromosome ends, we could become modern Methuselahs. Notably, cancer cells achieve immortality by protecting their chromosome ends. Drugs that selectively fray the ends of cancer cell chromosomes would be potent and general anti-cancer therapies. Here, I summarize data on the role of chromosome ends in cellular and organismal aging.

摘要

如同我们的衣物,我们的染色体末端也会随着年龄增长而磨损。一些人认为,如果我们能找到一位分子裁缝来修补因年龄而磨损的染色体末端,我们就能成为现代的玛士撒拉(译注:《圣经》中最长寿的人)。值得注意的是,癌细胞通过保护其染色体末端来实现永生。能够选择性地磨损癌细胞染色体末端的药物将是强大而通用的抗癌疗法。在此,我总结了关于染色体末端在细胞和机体衰老中作用的数据。

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Telomeres, cancer & aging: live long & prosper?端粒、癌症与衰老:长生不老?
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2
Cellular senescence, cancer and aging: the telomere connection.细胞衰老、癌症与衰老:端粒联系
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The implication of telomerase activity and telomere stability for replicative aging and cellular immortality (Review).端粒酶活性和端粒稳定性对复制性衰老及细胞永生化的意义(综述)
Oncol Rep. 1998 Sep-Oct;5(5):1043-52. doi: 10.3892/or.5.5.1043.
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Signaling on telomerase: a master switch in cell aging and immortalization.端粒酶信号传导:细胞衰老与永生化的主控开关
Biogerontology. 2002;3(1-2):107-16. doi: 10.1023/a:1015232102470.
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Telomeres and telomerase: implications for cancer and aging.端粒与端粒酶:对癌症和衰老的影响
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引用本文的文献

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Beating the Odds on Lifespan.战胜寿命的不利因素。
Mo Med. 2018 Jul-Aug;115(4):337-338.
2
Hungering for Immortality.渴望不朽。
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3
MR molecular imaging of tumors based on an optimal hTERT promoter tyrosinase expression system.基于优化的人端粒酶逆转录酶(hTERT)启动子酪氨酸酶表达系统的肿瘤磁共振分子成像
Oncotarget. 2016 Jul 5;7(27):42474-42484. doi: 10.18632/oncotarget.9888.
4
Labeling of Chromosomes in Cell Development and the Appearance of Monozygotic Twins.细胞发育过程中染色体的标记与同卵双胞胎的出现
Biomed Res Int. 2015;2015:628092. doi: 10.1155/2015/628092. Epub 2015 Jun 21.
5
Global Characteristics of CSIG-Associated Gene Expression Changes in Human HEK293 Cells and the Implications for CSIG Regulating Cell Proliferation and Senescence.人HEK293细胞中与CSIG相关的基因表达变化的全球特征及其对CSIG调节细胞增殖和衰老的意义。
Front Endocrinol (Lausanne). 2015 May 15;6:69. doi: 10.3389/fendo.2015.00069. eCollection 2015.
6
Copy neutral loss of heterozygosity is more frequent in older ovarian cancer patients.杂合性丢失在老年卵巢癌患者中更为常见。
Genes Chromosomes Cancer. 2013 Sep;52(9):794-801. doi: 10.1002/gcc.22075. Epub 2013 May 28.

本文引用的文献

1
Telomeres and adversity: Too toxic to ignore.端粒与逆境:毒性太强不容忽视。
Nature. 2012 Oct 11;490(7419):169-71. doi: 10.1038/490169a.
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Comparative biology of mammalian telomeres: hypotheses on ancestral states and the roles of telomeres in longevity determination.哺乳动物端粒的比较生物学:关于祖先状态的假说和端粒在寿命决定中的作用。
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Is telomere length a biomarker of aging? A review.端粒长度是衰老的生物标志物吗?一篇综述。
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Constitutive telomerase expression promotes mammary carcinomas in aging mice.组成型端粒酶表达促进衰老小鼠的乳腺癌发生。
Proc Natl Acad Sci U S A. 2002 Jun 11;99(12):8191-6. doi: 10.1073/pnas.112515399. Epub 2002 May 28.
9
Telomere dysfunction and evolution of intestinal carcinoma in mice and humans.端粒功能障碍与小鼠和人类肠道癌的演变
Nat Genet. 2001 Jun;28(2):155-9. doi: 10.1038/88871.
10
Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesis.端粒短的端粒酶缺陷型小鼠对皮肤肿瘤发生具有抗性。
Nat Genet. 2000 Sep;26(1):114-7. doi: 10.1038/79089.