CHMP4C promotes pancreatic cancer progression by inhibiting necroptosis via the RIPK1/RIPK3/MLKL pathway

IF 13 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Journal of Advanced Research Pub Date : 2025-11-01 Epub Date: 2025-01-25 DOI:10.1016/j.jare.2025.01.040
Longchen Yu , Qining Guo , Yaping Li , Mai Mao , Zhenping Liu , Tingting Li , Lei Wang , Xin Zhang
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Abstract

Introduction

Pancreatic cancer (PC) cannot currently be completely cured and has a poor prognosis. Necroptosis is a distinct form of regulated cell death that differs from both necrosis and apoptosis. Understanding the role of necroptosis during PC progression would open new avenues for targeted therapy.

Objectives

The purpose of this study is to examine the impact of necroptosis on the progression of PC and related mechanisms.

Methods

RNA sequencing was performed to identify necroptosis-related genes that are differentially expressed in PC tissues. The biological functions of CHMP4C and its necroptosis effects were determined in vitro and in vivo. RNA immunoprecipitation, MeRIP-qPCR, Co-immunoprecipitation assays were conducted to evaluate the interaction among CHMP4C, YBX1 and caspase-8 mRNA. Extracellular vesicles were isolated using the differential ultracentrifugation method. The expression of CHMP4C, p-MLKL and CD117 were detected on a PC tissue microarray using multiplex immunofluorescence staining.

Results

CHMP4C was significantly overexpressed in PC cells and tissues. It promoted cell growth and suppressed necroptosis of PC cells in both in vivo and in vitro settings. Mechanistically, CHMP4C interacted with YBX1 to mediate m5C modification of caspase-8 mRNA, resulting in increased caspase-8 expression and inhibition of RIPK1/RIPK3/MLKL pathway phosphorylation. Furthermore, CHMP4C promoted extracellular exocytosis of p-MLKL to further suppress necroptosis. Additionally, PC cells used CHMP4C within extracellular vesicles to recruit and stimulate mast cells (MCs), which in turn promoted PC cell proliferation. In PC tissues, the expression of CHMP4C showed a negative correlation with p-MLKL and a positive association with CD117. High expression levels of CHMP4C in patients were associated with poorer overall survival outcomes.

Conclusions

CHMP4C promotes PC progression by inhibiting necroptosis, which has potential as a biomarker and therapeutic target in PC.

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CHMP4C通过RIPK1/RIPK3/MLKL通路抑制坏死下垂促进胰腺癌进展
胰腺癌(PC)目前不能完全治愈,预后较差。坏死性上睑下垂是一种不同于坏死和细胞凋亡的细胞死亡形式。了解坏死性上睑下垂在PC进展中的作用将为靶向治疗开辟新的途径。目的探讨坏死性上睑下垂对PC进展的影响及相关机制。方法采用srna测序方法鉴定PC组织中差异表达的坏死相关基因。在体外和体内研究了CHMP4C的生物学功能及其对坏死性坏死的影响。采用RNA免疫沉淀法、MeRIP-qPCR、共免疫沉淀法评价CHMP4C、YBX1和caspase-8 mRNA的相互作用。用差示超离心法分离细胞外囊泡。应用多重免疫荧光染色技术在PC组织芯片上检测CHMP4C、p-MLKL和CD117的表达。结果schmp4c在PC细胞和组织中显著过表达。在体内和体外,它促进细胞生长,抑制PC细胞坏死。机制上,CHMP4C与YBX1相互作用介导m5C修饰caspase-8 mRNA,导致caspase-8表达增加,抑制RIPK1/RIPK3/MLKL通路磷酸化。此外,CHMP4C促进p-MLKL的细胞外胞吐,进一步抑制坏死。此外,PC细胞利用胞外囊泡内的CHMP4C募集和刺激肥大细胞(MCs),从而促进PC细胞增殖。在PC组织中,CHMP4C的表达与p-MLKL呈负相关,与CD117呈正相关。患者中CHMP4C的高表达水平与较差的总生存结果相关。结论schmp4c通过抑制坏死下垂促进PC的进展,具有作为PC生物标志物和治疗靶点的潜力。
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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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