理解和靶向EGFR-TKIs在人类癌症中耐药的表观遗传调控。

IF 2.5 4区 医学 Q3 ONCOLOGY
Lan Sun, Lingyue Gao, Yingxi Zhao, Yuqing Wang, Qianhui Xu, Yiru Zheng, Jiali Chen, He Wang, Lihui Wang
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引用次数: 4

摘要

背景:肿瘤的发生和发展是遗传和表观遗传学失调的结果。表观遗传调控可以在不改变DNA结构的情况下可逆地影响基因转录活性。组蛋白的共价修饰在基因表达的表观遗传调控中是至关重要的。此外,表皮生长因子受体(epidermal growth factor receptor, EGFR)对细胞的发生、增殖、抗肿瘤耐药等有显著影响。过度表达EGFR促进癌症的发展。因此,egfr靶向药物已成为肿瘤治疗的重点。随着表皮生长因子受体酪氨酸激酶抑制剂(epidermal growth factor receptor tyrosine kinase inhibitors, EGFR-TKIs)的出现,EGFR-TKIs的耐药性大约半年到一年发生一次,已经成为癌症治疗的一个障碍。目的:本研究的目的是探讨在多种肿瘤中克服EGFR-TKIs耐药的方法。方法:采用表观遗传药物与其他药物联合治疗。结果:两药联合用药可克服EGFR-TKIs耐药,延长患者生存期。结论:本文阐述了EGFR-TKIs耐药的表观遗传学概念和机制,阐述了EGFR-TKIs耐药与表观遗传学机制的关系。最后讨论了利用表观遗传药物逆转人类肿瘤EGFR-TKIs耐药的临床研究和最新专利。在未来,可能会发现更多新的靶点来克服对EGFR-TKIs的耐药性,而不仅仅是在组蛋白去乙酰化酶(hdac)上。表观遗传药物联合治疗的给药过程和给药方式有待进一步研究。这一综述为利用表观遗传药物克服EGFR-TKIs耐药性提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding and Targeting the Epigenetic Regulation to Overcome EGFR-TKIs Resistance in Human Cancer.

Background: The occurrence and progression of cancer are the results of the dysregulation of genetics and epigenetics. Epigenetic regulation can reversibly affect gene transcription activity without changing DNA structure. Covalent modification of histones is crucial in the epigenetic regulation of gene expression. Furthermore, epidermal growth factor receptor (EGFR) significantly affects cell tumorigenesis, proliferation, antitumor drug resistance, etc. Overexpression of EGFR promotes cancer development. Therefore, EGFR-targeted drugs have become the focus of tumor therapy. With the advent of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), EGFR-TKIs resistance, which occurs about half a year to a year, has become an obstacle in cancer treatment.

Objective: The objective of this study is to discuss the ways to overcome EGFR-TKIs resistance in a variety of tumors.

Methods: The combination therapy of epigenetic drugs and other drugs is used.

Results: The combination of the two drugs can overcome the resistance of EGFR-TKIs and prolong the survival of patients.

Conclusion: This article depicts the concepts of epigenetics and the mechanism of EGFR-TKIs resistance and then illustrates the relationship between epigenetic mechanisms and EGFR-TKIs resistance. Finally, it discusses the clinical research and the latest patents for using epigenetic drugs to reverse EGFR-TKIs resistance in human cancer. In the future, more novel targets may be discovered for overcoming resistance to EGFR-TKIs, not just on histone deacetylases (HDACs). The dosing course and mode of administration of the combination therapy containing epigenetic drugs need further study. This review provides new ideas for using epigenetic agents to overcome EGFR-TKIs resistance.

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来源期刊
CiteScore
4.50
自引率
7.10%
发文量
55
审稿时长
3 months
期刊介绍: Aims & Scope Recent Patents on Anti-Cancer Drug Discovery publishes review and research articles that reflect or deal with studies in relation to a patent, application of reported patents in a study, discussion of comparison of results regarding application of a given patent, etc., and also guest edited thematic issues on recent patents in the field of anti-cancer drug discovery e.g. on novel bioactive compounds, analogs, targets & predictive biomarkers & drug efficacy biomarkers. The journal also publishes book reviews of eBooks and books on anti-cancer drug discovery. A selection of important and recent patents on anti-cancer drug discovery is also included in the journal. The journal is essential reading for all researchers involved in anti-cancer drug design and discovery. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to anti-cancer drug discovery.
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