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衰老与癌症:端粒与端粒酶的联系

Ageing and cancer: the telomere and telomerase connection.

作者信息

Shay J W, Wright W E

机构信息

University of Texas Southwestern Medical Center at Dallas, Department of Cell Biology, 5323 Harry Hines Boulevard, Dallas, TX 75390-9039, USA.

出版信息

Novartis Found Symp. 2001;235:116-25; discussion 125-9, 146-9.

Abstract

Telomeres are repetitive DNA sequences at the ends of linear chromosomes. Telomerase, a cellular reverse transcriptase, helps stabilize telomere length in human stem, reproductive and cancer cells by adding TTAGGG repeats onto the telomeres. Each time a telomerase-negative cell divides some telomeric sequences are lost. When telomeres are short, cells enter an irreversible growth arrest state called replicative senescence. In most instances cells become senescent before they can become cancerous, thus the growth arrest induced by short telomeres may be a potent anti-cancer mechanism. Since most cancers express telomerase, maintenance of telomere stability is likely to be required for the long-term viability of tumours. Inhibition of telomerase results in gradual erosion of telomeres followed by cessation of proliferation or apoptosis, and thus may be a promising target for cancer therapy. Introduction of the telomerase catalytic protein component into telomerase-silent cells is sufficient to restore telomerase activity and extend cellular life span. However, cells with introduced telomerase are not cancer cells since they have not accumulated the other changes needed to become cancerous. This indicates that telomerase-induced telomere length manipulations may have utility for tissue engineering and for dissecting the molecular mechanisms underlying genetic diseases including cancer.

摘要

端粒是线性染色体末端的重复DNA序列。端粒酶是一种细胞逆转录酶,通过在端粒上添加TTAGGG重复序列,帮助稳定人类干细胞、生殖细胞和癌细胞中的端粒长度。每当端粒酶阴性细胞分裂时,一些端粒序列就会丢失。当端粒缩短时,细胞进入一种不可逆的生长停滞状态,称为复制性衰老。在大多数情况下,细胞在癌变之前就会衰老,因此短端粒诱导的生长停滞可能是一种有效的抗癌机制。由于大多数癌症都表达端粒酶,维持端粒稳定性可能是肿瘤长期存活所必需的。抑制端粒酶会导致端粒逐渐缩短,随后细胞增殖停止或凋亡,因此可能是癌症治疗的一个有前景的靶点。将端粒酶催化蛋白成分导入端粒酶沉默细胞足以恢复端粒酶活性并延长细胞寿命。然而,导入端粒酶的细胞不是癌细胞,因为它们没有积累癌变所需的其他变化。这表明端粒酶诱导的端粒长度操纵可能在组织工程以及剖析包括癌症在内的遗传疾病的分子机制方面具有应用价值。

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