黑色素瘤生长和转移中的基因突变和泛素化

IF 1.4 Q4 ONCOLOGY
Anushka Dikshit, Jennifer Y. Zhang
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引用次数: 0

摘要

在肿瘤转化后,黑色素瘤本质上容易发生转移,这标志着该疾病最危险的方面,并将其称为最具挑战性的癌症之一。BRAF/MEK肿瘤激酶抑制剂和免疫疗法在一些患者中显示出相当大的前景,但由于耐药性的快速发展,临床益处往往是短暂的。近年来,泛素化酶已成为潜在的治疗靶点。这些酶可以靶向增加肿瘤抑制因子的表达,阻碍介导细胞增殖和组织侵袭的致癌信号通路的激活。本章描述了黑色素瘤的一些常见基因突变、泛素化和去泛素化酶,它们与黑色素瘤的进展、转移和治疗耐药性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Mutations and Ubiquitination in Melanoma Growth and Metastasis
Upon neoplastic transformation, melanoma is intrinsically prone to metastasis, which marks the most dangerous aspect of the disease and dubs it one of the most challenging cancers to treat. BRAF/MEK oncokinase inhibitors and immunotherapies have shown considerable promise in some patients, but the clinical benefits are often short-lived due to rapid development of resistance. Recently, ubiquitination enzymes have emerged as potential therapeutic targets. These enzymes can be targeted to increase expression of tumor suppressors and impede activation of oncogenic signaling pathways mediating cell proliferation and tissue invasion. This chapter describes some of the common genetic mutations in melanoma, ubiquitinating and deubiquitinating enzymes that are linked to melanoma progression, metastasis, and therapeutic resistance.
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来源期刊
CiteScore
3.20
自引率
5.30%
发文量
460
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