DLGAP5通过MYC稳定调节糖酵解增强膀胱癌化疗耐药。

IF 12.4 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Theranostics Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI:10.7150/thno.102730
Zhao Deng, Fenfang Zhou, Mingxing Li, Wan Jin, Jingtian Yu, Gang Wang, Kaiyu Qian, Lingao Ju, Yi Zhang, Yu Xiao, Xinghuan Wang
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引用次数: 0

摘要

理由:膀胱癌(BLCA)是最致命的泌尿系统肿瘤之一,具有很高的复发率和化疗耐药性,特别是对吉西他滨(GEM)。了解GEM耐药机制对于改善治疗效果至关重要。我们的研究探讨了DLGAP5通过调节BLCA细胞的糖酵解和MYC蛋白稳定性来促进GEM耐药的作用。方法:利用多种BLCA细胞系和临床组织样本,分析dgap5对GEM耐药的影响。通过生化分析、蛋白质相互作用研究和基因表达分析,我们研究了DLGAP5如何与USP11和MYC相互作用,评估了对MYC去泛素化和稳定性的影响。通过小鼠皮下异种移植模型和自发BLCA模型评估这些相互作用对糖酵解活性和GEM耐药性的影响。结果:我们的研究结果表明,DLGAP5通过USP11介导的去泛素化过程稳定MYC蛋白,从而增强GEM耐药性。DLGAP5被发现促进USP11和MYC之间的相互作用,促进DLGAP5自身MYC驱动的转录,从而形成一个正反馈循环。这个循环导致MYC持续积累和糖酵解活性增加,导致BLCA细胞对GEM产生耐药性。结论:该研究强调了DLGAP5在调节MYC蛋白稳定性中的关键作用,并提示破坏DLGAP5- usp11 -MYC轴可能为克服BLCA GEM耐药提供一种新的治疗方法。DLGAP5是缓解膀胱癌BLCA化疗耐药的治疗干预的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DLGAP5 enhances bladder cancer chemoresistance by regulating glycolysis through MYC stabilization.

Rationale: Bladder cancer (BLCA), one of the most lethal urological tumors, exhibits high rates of recurrence and chemoresistance, particularly to gemcitabine (GEM). Understanding the mechanisms of GEM resistance is crucial for improving therapeutic outcomes. Our study investigates the role of DLGAP5 in promoting GEM resistance through modulation of glycolysis and MYC protein stability in BLCA cells. Methods: We utilized various BLCA cell lines and clinical tissue samples to analyze the impact of DLGAP5 on GEM resistance. Through biochemical assays, protein interaction studies, and gene expression analyses, we examined how DLGAP5 interacts with USP11 and MYC, assessed the effects on MYC deubiquitination and stability. The influence of these interactions on glycolytic activity and GEM resistance was also evaluated via mouse subcutaneous xenograft model and spontaneous BLCA model. Results: Our findings indicate that DLGAP5 enhances GEM resistance by stabilizing MYC protein via deubiquitination, a process mediated by USP11. DLGAP5 was found to facilitate the interaction between USP11 and MYC, promoting MYC-driven transcription of DLGAP5 itself, thereby creating a positive feedback loop. This loop leads to sustained MYC accumulation and increased glycolytic activity, contributing to GEM resistance in BLCA cells. Conclusion: The study highlights the critical role of DLGAP5 in regulating MYC protein stability and suggests that disrupting the DLGAP5-USP11-MYC axis may provide a novel therapeutic approach to overcome GEM resistance in BLCA. DLGAP5 represents a potential target for therapeutic intervention aimed at mitigating chemoresistance in bladder cancer BLCA.

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来源期刊
Theranostics
Theranostics MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
25.40
自引率
1.60%
发文量
433
审稿时长
1 months
期刊介绍: Theranostics serves as a pivotal platform for the exchange of clinical and scientific insights within the diagnostic and therapeutic molecular and nanomedicine community, along with allied professions engaged in integrating molecular imaging and therapy. As a multidisciplinary journal, Theranostics showcases innovative research articles spanning fields such as in vitro diagnostics and prognostics, in vivo molecular imaging, molecular therapeutics, image-guided therapy, biosensor technology, nanobiosensors, bioelectronics, system biology, translational medicine, point-of-care applications, and personalized medicine. Encouraging a broad spectrum of biomedical research with potential theranostic applications, the journal rigorously peer-reviews primary research, alongside publishing reviews, news, and commentary that aim to bridge the gap between the laboratory, clinic, and biotechnology industries.
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