载脂蛋白E通过诱导trim25介导的AR泛素化促进对AR靶向治疗的原发性耐药,并使前列腺癌免疫治疗增敏。

IF 12.4 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Theranostics Pub Date : 2025-04-21 eCollection Date: 2025-01-01 DOI:10.7150/thno.109994
Chaofan Liu, Xi Wang, Qinyu Li, Xintao Gao, Kai Zeng, Beining Li, Jianping Miao, Bolong Zheng, Jihong Liu, Zhihua Wang, Xianglin Yuan, Bo Liu
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引用次数: 0

摘要

理由:前列腺癌(PCa)的生长是由雄激素受体(AR)及其下游信号通路促进的,因此AR靶向治疗对于晚期治疗至关重要。尽管如此,对ar靶向治疗的反应是不一致的,很大一部分患者甚至从一开始就表现出对治疗的无反应,称为原发性耐药。因此,一个完善的分类框架是必要的及时检测耐药表型和探索新的治疗途径。方法:采用组织微阵列和临床队列来描述APOE对PCa患者预后和治疗抵抗的影响。利用流式细胞术、免疫沉淀和质谱分析,我们剖析了APOE在赋予ar靶向干预的抗性中的作用的分子基础。单细胞RNA测序揭示了APOE表达升高的PCa复杂的转录组谱。此外,严格评估了抗pd - l1药物治疗APOE诱导PCa的治疗潜力。结果:在本研究中,我们阐明了APOE通过抑制AR信号通路介导PCa对AR靶向治疗的原发性耐药的关键作用。从机制上讲,APOE通过介导e3连接酶TRIM25与AR之间的相互作用,增强AR的泛素化和随后的降解,同时抑制AR的转录活性。此外,APOE表达升高与抗pd - l1治疗的增强反应相关,这暗示了在APOE高的PCa背景下免疫治疗的治疗优势。结论:APOE表达可以作为一种预后生物标志物,对预测ar靶向治疗和免疫治疗的反应至关重要,从而为PCa治疗方式的个性化选择提供了一种创新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apolipoprotein E promotes primary resistance to AR-targeted therapy via inducing TRIM25-mediated AR ubiquitination and sensitizes immunotherapy in prostate cancer.

Rationale: Prostate cancer (PCa) growth is facilitated by the androgen receptor (AR) and its downstream signaling pathways, making AR-targeted therapy crucial for treating advanced stages. Despite this, the response to AR-targeted therapies is inconsistent, with a significant proportion of patients even exhibiting unresponsiveness to therapy from the outset, known as primary resistance. Therefore, a refined categorization framework is imperative for the timely detection of resistant phenotypes and the exploration of novel therapeutic avenues. Methods: Tissue microarrays and clinical cohorts were employed to delineate the impact of APOE on the prognostic outcomes and therapeutic resistance in PCa patients. Employing flow cytometry, immunoprecipitation, and mass spectrometry, we dissected the molecular underpinnings of APOE's role in conferring resistance to AR-targeted interventions. Single-cell RNA sequencing elucidated the intricate transcriptomic profiles of PCa with elevated APOE expression. Additionally, the therapeutic potential of anti-PD-L1 agents in treating PCa with APOE induction was rigorously assessed. Results: In this study, we elucidated the pivotal role of APOE in mediating primary resistance to AR-targeted therapy in PCa through the suppression of AR signaling pathways. Mechanistically, APOE was found to enhance the ubiquitination and subsequent degradation of AR by mediating the interaction between the E3-ligase TRIM25 and AR, concurrently dampening the transcriptional activity of AR. Additionally, elevated APOE expression was correlated with an augmented response to anti-PD-L1 treatment, hinting at the therapeutic advantage of immunotherapy in APOE-high PCa contexts. Conclusions: APOE expression could serve as a prognostic biomarker, pivotal for forecasting responses to both AR-targeted therapy and immunotherapy, thereby offering an innovative strategy for the personalized selection of treatment modalities in PCa.

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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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