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MDMX:结构、功能、调控及其抑制剂的研究进展

刘书琪 王洪波

肿瘤药学2025,Vol.15Issue(2):152-160,9.
肿瘤药学2025,Vol.15Issue(2):152-160,9.DOI:10.3969/j.issn.2095-1264.2025.02.02

MDMX:结构、功能、调控及其抑制剂的研究进展

MDMX:advances in structure,function,regulation and its inhibitors

刘书琪 1王洪波1

作者信息

  • 1. 烟台大学 药学院,山东 烟台,264005
  • 折叠

摘要

Abstract

Murine double minute X(MDMX)is an oncogenic protein which is aberrantly overexpressed in multiple ma-lignant tumors,and its overexpression is closely associated with poor patient prognosis.In-depth elucidation of its function-al mechanisms and regulatory networks holds significant importance for developing novel anticancer drugs targeting MDMX as a druggable vulnerability.However,due to the unique structural characteristics of MDMX,the development of MDMX in-hibitors currently faces many challenges,such as poor specificity and insufficient activity.Overcoming these bottlenecks has become a critical research focus and challenge in this field.In recent years,emerging technologies represented by prote-olysis-targeting chimeras(PROTAC)have demonstrated unique advantages and achieved preliminary progress in this area.This review systematically summarizes the research progress of the structural characteristics,biological functions,regulato-ry networks and targeting inhibitors of MDMX,aiming to provide valuable insights for mechanistic research and therapeutic strategy optimization in related diseases.

关键词

MDMX/结构/生物学功能、调控/转录调控/肿瘤治疗/抑制剂

Key words

MDMX/Structure/Biological function/Regulation/Transcriptional regulation/Cancer treatment/Inhibitor

分类

医药卫生

引用本文复制引用

刘书琪,王洪波..MDMX:结构、功能、调控及其抑制剂的研究进展[J].肿瘤药学,2025,15(2):152-160,9.

基金项目

国家自然科学基金项目(82273969、82473967). (82273969、82473967)

肿瘤药学

2095-1264

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