RNA 结合蛋白 IGF2BP1 在癌症多药耐药性中的作用

IF 5.3 2区医学 Q1 PHARMACOLOGY & PHARMACY

Biochemical pharmacology Pub Date : 2024-09-25 DOI:10.1016/j.bcp.2024.116555

Aldana Magalí Gola , María Bucci-Muñoz , Juan Pablo Rigalli , María Paula Ceballos , María Laura Ruiz

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引用次数: 0

摘要

胰岛素样生长因子-2 mRNA 结合蛋白 1（IGF2BP1）是单链 RNA 结合蛋白（IGF2BP1-3）保守家族的成员，在胎儿组织、胎盘和超过 16 种癌症类型中广泛表达，但只在数量有限的正常成人组织中表达。IGF2BP1 需要通过影响某些 mRNA 的稳定性、翻译或定位，将其从细胞核转运到细胞质，这些 mRNA 在胚胎发生、癌变和多药耐药性（MDR）中发挥着重要作用。本综述旨在收集和介绍癌症中 MDR 机制的相关信息，以及 IGF2BP1 在其中的重要作用。在这篇综述中，我们将概述 IGF2BP1，包括其组织分布、表达、肿瘤发生过程中的分子靶点及其抑制剂。我们的主要重点是阐明 IGF2BP1 与 MDR 之间的相互作用，尤其是 ABC 转运体介导的化疗耐药性。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Role of the RNA binding protein IGF2BP1 in cancer multidrug resistance

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Role of the RNA binding protein IGF2BP1 in cancer multidrug resistance

The insulin-like growth factor-2 mRNA-binding protein 1 (IGF2BP1), a member of a conserved family of single-stranded RNA-binding proteins (IGF2BP1-3), is expressed in a broad range of fetal tissues, placenta and more than sixteen cancer types but only in a limited number of normal adult tissues. IGF2BP1is required for the transport from nucleus to cytoplasm of certain mRNAs that play essential roles in embryogenesis, carcinogenesis, and multidrug resistance (MDR), by affecting their stability, translation, or localization. The purpose of this review is to gather and present information on MDR mechanisms in cancer and the significance of IGF2BP1 in this context. Within this review, we will provide an overview of IGF2BP1, including its tissue distribution, expression, molecular targets in the context of tumorigenesis and its inhibitors. Our main focus will be on elucidating the interplay between IGF2BP1 and MDR, particularly with regard to chemoresistance mediated by ABC transporters.

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来源期刊

Biochemical pharmacology 医学-药学

CiteScore

10.30

自引率

1.70%

发文量

420

审稿时长

17 days

期刊介绍： Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.