Pathological modulation of genome maintenance by cancer/testes antigens (CTAs)

IF 2.7 3区 生物学 Q2 GENETICS & HEREDITY
Cyrus Vaziri , Karly Forker , Xingyuan Zhang , Di Wu , Pei Zhou , Jessica L. Bowser
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引用次数: 0

Abstract

The Cancer Testis Antigens (CTAs) are a group of germ cell proteins that are absent from normal somatic cells yet aberrantly expressed in many cancer cells. When mis-expressed in cancer cells, many CTAs promote tumorigenic characteristics including genome instability, DNA damage tolerance and therapy resistance. Here we highlight some of the CTAs for which their roles in genome maintenance in cancer cells are well established. We consider three broad CTA categories: (1) Melanoma Antigens (MAGEs) (2) Mitotic CTAs and (3) CTAs with roles in meiotic homologous recombination. Many cancer cells rely on CTAs to tolerate intrinsic and therapy-induced genotoxic stress. Therefore, CTAs represent molecular vulnerabilities of cancer cells and may provide opportunities for therapy. Owing to their high-level expression in tumors and absence from normal somatic cells, CTA-directed therapies could have a high level of specificity and would likely be devoid of side-effect toxicity.
癌/睾丸抗原(cta)对基因组维持的病理调节
癌睾丸抗原(cta)是一组生殖细胞蛋白,在正常体细胞中不存在,但在许多癌细胞中异常表达。当在癌细胞中错误表达时,许多cta会促进致瘤性特征,包括基因组不稳定性、DNA损伤耐受性和治疗耐药性。在这里,我们重点介绍了一些cta,它们在癌细胞基因组维持中的作用已经得到了很好的证实。我们考虑了三大类CTA:(1)黑色素瘤抗原(mage);(2)有丝分裂CTA;(3)在减数分裂同源重组中起作用的CTA。许多癌细胞依靠cta来耐受内在的和治疗诱导的基因毒性应激。因此,cta代表了癌细胞的分子脆弱性,可能为治疗提供机会。由于cta在肿瘤中的高水平表达和正常体细胞的缺失,cta定向治疗可能具有高水平的特异性,并且可能没有副作用毒性。
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来源期刊
DNA Repair
DNA Repair 生物-毒理学
CiteScore
7.60
自引率
5.30%
发文量
91
审稿时长
59 days
期刊介绍: DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease. DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.
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