Exosomal miR‑3681‑3p from M2‑polarized macrophages confers cisplatin resistance to gastric cancer cells by targeting MLH1

Cisplatin (DDP) is a key chemotherapeutic agent in the treatment of gastric cancer; however, its efficacy is often limited by chemoresistance, a notable challenge in clinical oncology. The present study aimed to investigate the influence of exosomes derived from M2-polarized macrophages, which promo...

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Vydáno v:	Molecular medicine reports Ročník 31; číslo 4
Hlavní autoři:	Wei, Wujun, Li, Jiaxing, Huang, Jingjing, Jiang, Qi, Lin, Cheng, Hu, Rentong, Wei, Jiazhu, Li, Qiao, Xu, Guidan, Chang, Zhengyi
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Greece D.A. Spandidos 01.04.2025 Spandidos Publications Spandidos Publications UK Ltd
Témata:	Animals Antibodies Antineoplastic Agents - pharmacology Apoptosis Apoptosis - drug effects Biotechnology Calnexin Cancer cells Cancer therapies Care and treatment CD163 antigen CD9 antigen Cell differentiation Cell growth Cell Line, Tumor Chemoresistance Chemotherapy Cisplatin Cisplatin - pharmacology cisplatin resistance Cytokines Dosage and administration Drug resistance Drug Resistance, Neoplasm - genetics Exosomes Exosomes - genetics Exosomes - metabolism Gastric cancer Gene Expression Regulation, Neoplastic - drug effects Genetic aspects Health aspects Humans Immunofluorescence Immunotherapy Invoices M2 macrophages Macrophages Macrophages - drug effects Macrophages - metabolism Mice microRNA-3681-3p MicroRNAs MicroRNAs - genetics MicroRNAs - metabolism Microscopy miRNA MLH1 MLH1 protein MutL protein MutL Protein Homolog 1 - genetics MutL Protein Homolog 1 - metabolism Physiological aspects RNA-mediated interference siRNA Stomach cancer Stomach Neoplasms - drug therapy Stomach Neoplasms - genetics Stomach Neoplasms - metabolism Stomach Neoplasms - pathology Therapeutic targets Transfection Transmission electron microscopy Tumor necrosis factor-TNF China M2 macrophages gastric cancer MLH1 microRNA‑3681‑3p cisplatin resistance
ISSN:	1791-2997, 1791-3004, 1791-3004
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Popis
Shrnutí:	Cisplatin (DDP) is a key chemotherapeutic agent in the treatment of gastric cancer; however, its efficacy is often limited by chemoresistance, a notable challenge in clinical oncology. The present study aimed to investigate the influence of exosomes derived from M2-polarized macrophages, which promote this resistance, on the response of gastric cancer cells to DDP, examining both the effects and the underlying mechanisms. M2 macrophages, differentiated from mouse bone marrow cells with interleukin (IL)-13 and IL-4, were identified using immunofluorescence staining for CD206 and CD163. Exosomes derived from these macrophages were characterized using transmission electron microscopy and protein markers, including calnexin, tumor susceptibility gene 101 and CD9. The role of exosomal microRNA (miR)-3681-3p in DDP resistance was assessed using Cell Counting Kit-8 and apoptosis assays, while a luciferase reporter assay was used to elucidate the interaction between miR-3681-3p and MutL protein homolog 1 (MLH1). Co-culturing gastric cancer cells with M2 macrophages enhanced DDP resistance, an effect amplified by exosomes from M2 macrophages enriched with miR-3681-3p. This microRNA directly targeted and reduced MLH1 protein expression. Overexpression of miR-3681-3p through mimic transfection, along with MLH1 silencing by small interfering RNA transfection, significantly increased DDP resistance, as evidenced by elevated IC50 values in AGS cells. By contrast, the overexpression of MLH1 effectively reversed the drug resistance of AGS cells to DDP caused by miR-3681-3p mimic transfection, as evidenced by a decrease in the IC50 value. In conclusion, exosomal miR-3681-3p from M2 macrophages may have a key role in conferring DDP resistance to gastric cancer by suppressing MLH1, offering a new therapeutic target for overcoming chemoresistance.
Bibliografie:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Contributed equally
ISSN:	1791-2997 1791-3004 1791-3004
DOI:	10.3892/mmr.2025.13459