Telomerase, telomerase inhibition, and cancer.

Ali Ahmed, Trygve O Tollefsbol
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引用次数: 36

Abstract

Telomeres, located at the ends of eukaryotic chromosomes, are synthesized by the enzyme telomerase and are responsible for maintaining chromosome length. The absence of telomerase in most somatic cells has been associated with telomere shortening and aging of these cells. In contrast, high levels of telomerase activity are observed in over 90% of human cancer cells. The absence of telomerase in normal and aging cells is considered a natural defense against development of cancer. However, we do not know what triggers the reappearance of telomerase in cancer cells. Telomerase activity is directly correlated with the expression of its active catalytic component, the human telomerase reverse transcriptase (hTERT), which is believed to be controlled primarily at the level of transcription. Elucidation of the control of telomerase in aging and in cancer as an age-related disease has considerable potential in leading to novel approaches in anti-aging medicine.

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端粒酶,端粒酶抑制,和癌症。
端粒位于真核生物染色体的末端,由端粒酶合成,负责维持染色体的长度。在大多数体细胞中,端粒酶的缺失与这些细胞的端粒缩短和衰老有关。相比之下,在超过90%的人类癌细胞中观察到高水平的端粒酶活性。正常细胞和衰老细胞中端粒酶的缺失被认为是抵御癌症发展的天然屏障。然而,我们不知道是什么触发了端粒酶在癌细胞中的重现。端粒酶活性与其活性催化成分——人类端粒酶逆转录酶(hTERT)的表达直接相关,而hTERT被认为主要在转录水平上受到控制。阐明端粒酶在衰老和癌症中作为一种年龄相关疾病的控制具有相当大的潜力,可以引导抗衰老药物的新方法。
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