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首页> 外文期刊>Indian journal of clinical biochemistry: IJCB >Therapeutic Targets in Telomerase and Telomere Biology of Cancers
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Therapeutic Targets in Telomerase and Telomere Biology of Cancers

机译:端粒酶的治疗靶点和癌症的端粒生物学

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Telomeres play an important role to conserve genomic integrity by protecting the ends of chromosomes in normal cells. Since, their progressive shortening during successive cell division which lead to chromosomal instability. Notably, telomere length is perpetuated by telomerase in large majority of cancers, thereby ensure indefinite cell proliferation-a hallmark of cancer-and this unique feature has provided telomerase as the preferred target for drug development in cancer therapeutics. Cancer cells have acquired the potential to have telomere length maintenance by telomerase activation- up-regulation of hTERT gene expression in tumor cells is synchronized by multiple genetic and epigenetic modification mechanisms viz hTERT structural variants, hTERT promoter mutation and epigenetic modifications through hTERT promoter methylation which have been implicated in various cancers initiation and progression. In view of these facts, strategies have been made to target the underlining molecular mechanisms involved in telomerase reactivation as well as of telomere structure with special reference to distortion of sheltrin proteins. This review is focussed on extensive understanding of telomere and telomerase biology. which will provide indispensable informations for enhancing the efficiency of rational anticancer drug design. However, there is also an urgent need for better understanding of cell signalling pathways for alternative lengthening of telomere which is present in telomerase negative cancer for therapeutic targets.
机译:端粒通过保护正常细胞中染色体的末端来保护基因组完整性的重要作用。由于它们在连续的细胞划分期间逐渐缩短,导致染色体不稳定性。值得注意的是,端粒长度通过聚端粒酶在大多数癌症中延长,从而确保无限细胞增殖 - 癌症的标志 - 这种独特的特征为端粒酶作为癌症治疗药中药物发育的优选靶标提供。癌细胞已经获得了通过端粒酶激活的肿瘤酶活化肿瘤细胞的激活调节,通过多种遗传和表观遗传改性机制同步,通过HTERT启动子甲基化同步,通过HTERT HTERT结构变体,HTERT启动子突变和表观遗传修饰。已经涉及各种癌症启动和进展。鉴于这些事实,已经进行了策略,以靶向端粒酶再活化的下划线分子机制以及特殊参考涡旋蛋白的变形。本综述主要对端粒和端粒酶生物学的广泛理解。这将为提高Rational抗癌药物设计效率提供不可或缺的信息。然而,还迫切需要更好地理解细胞信号传导途径,以替代地延长端粒酶阴性癌以用于治疗靶标。

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