PTPN2 及其小分子抑制剂/降解剂对蛋白质磷酸化的调控作为一种潜在的疾病治疗策略

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-08-12 DOI:10.1016/j.ejmech.2024.116774
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引用次数: 0

摘要

蛋白酪氨酸磷酸酶非受体 2 型(PTPN2)是一种能使具有酪氨酸残基的蛋白质去磷酸化的酶,从而调节体内的相关信号通路。根据具体情况,PTPN2 可作为肿瘤抑制因子或肿瘤促进因子。在某些癌症(如结直肠癌和肺癌)中,PTPN2 的缺陷可能会损害蛋白酪氨酸激酶通路(癌细胞中的蛋白酪氨酸激酶通路往往被过度激活),从而抑制肿瘤的发展和恶化。然而,PTPN2 还能通过调节免疫细胞和细胞因子抑制肿瘤免疫。本文综述了 PTPN2 在各种肿瘤细胞中的结构、功能和底物。并总结了小分子 PTPN2 抑制剂和降解剂的研究现状。本文还强调了开发 PTPN2 抑制剂作为抗癌药物的潜在机遇和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Regulation of protein phosphorylation by PTPN2 and its small-molecule inhibitors/degraders as a potential disease treatment strategy

Protein tyrosine phosphatase nonreceptor type 2 (PTPN2) is an enzyme that dephosphorylates proteins with tyrosine residues, thereby modulating relevant signaling pathways in vivo. PTPN2 acts as tumor suppressor or tumor promoter depending on the context. In some cancers, such as colorectal, and lung cancer, PTPN2 defects could impair the protein tyrosine kinase pathway, which is often over-activated in cancer cells, and inhibit tumor development and progression. However, PTPN2 can also suppress tumor immunity by regulating immune cells and cytokines. The structure, functions, and substrates of PTPN2 in various tumor cells were reviewed in this paper. And we summarized the research status of small molecule inhibitors and degraders of PTPN2. It also highlights the potential opportunities and challenges for developing PTPN2 inhibitors as anticancer drugs.

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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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