首页|hucMSC-Exs缓解IBD恶性转化机制的研究进展(综述)

hucMSC-Exs缓解IBD恶性转化机制的研究进展(综述)

Research progress on the mechanism of hucMSC-Exs in alleviating malignant transformation of IBD

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炎症性肠病(IBD)长期迁延不愈,易恶性转化导致结直肠癌(CRC)发生,目前临床上仍缺乏有效治疗IBD的方法.人脐带间充质干细胞(hucMSCs)及其来源的外泌体(Exs)能修复DSS诱导的小鼠IBD.人脐带间充质干细胞来源外泌体(hucMSC-Exs)抑制了由AOM/DSS诱导的小鼠IBD恶性转化,可能是通过下调小分子泛素样修饰体-1(SUMO1)的表达进而影响相关信号通路的调控,但确切的机制亟待阐明.该文试图通过相关文献综述,阐明hucMSC-Exs作用的结直肠黏膜组织靶细胞及靶细胞对hucMSC-Exs的应答,揭示hucMSC-Exs下调靶细胞中SUMO1表达的关键分子及相关信号通路,深入探讨hucMSC-Exs抑制IBD恶性转化的作用机制,为hucMSC-Exs治疗IBD及其恶性转化提供新的思路.
Objective:Prolonged inflammatory bowel disease(IBD)is prone to malignant transformation,which can lead to colorectal cancer(CRC),and there is still a lack of effective treatment for IBD in the clinic.Recent studies have shown that human umbilical cord mesenchymal stem cells(hucMSCs)and their derived exosomes(Exs)can repair DSS induced mouse IBD,and human umbilical cord mesenchymal stem cell derived exosomes(hucMSC-Exs)inhibit AOM/DSS induced malignant transformation of mouse IBD,possibly by downregulating the expression of small ubiquitin-like modifier-1(SUMO 1)and affecting the regulation of related signaling pathways.However,the exact mechanism needs to be elucidated.This article attempts to elucidate the target cells of colorectal mucosal tissue affected by hucMSC-Exs and their response to hucMSC-Exs,reveal the key molecules and related signaling pathways that downregulate SUMO1 expression in target cells by hucMSC-Exs,and deeply explore the mechanism of hucMSC-Exs inhibiting IBD malignant transformation,providing new ideas and experimental basis for hucMSC-Exs treatment of IBD and its malignant transformation.

IBDhucMSC-Exsmalignant transformation mechanismresearch progress

方安宁、严家来

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安徽医学高等专科学校 安徽合肥 230601

炎症性肠病 人脐带间充质干细胞来源外泌体 恶性转化机制 研究进展

安徽省高校自然基金重点项目安徽省质量工程项目

KJ2020A08572021jxtd141

2024

安徽医专学报
安徽医学高等专科学校

安徽医专学报

影响因子:0.441
ISSN:2097-0196
年,卷(期):2024.23(3)