miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer

Abstract Background Cancer-associated fibroblasts (CAFs) aggravate gastric cancer (GC) development. Methods Combined with bioinformatics analysis and literature review, miR-223-3p had high expression in microvesicles (MVs) derived from GC CAFs, and it could modulate SORBS1. miR-223-3p and SORBS1 mRN...

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Main Authors: Xiaoli Jin, Xi Qiu, Yi Huang, Hang Zhang, Kaibo Chen
Format: Article
Language:English
Published: BMC 2022-02-01
Series:Cancer Cell International
Subjects:
Online Access:https://doi.org/10.1186/s12935-022-02513-1
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author Xiaoli Jin
Xi Qiu
Yi Huang
Hang Zhang
Kaibo Chen
author_facet Xiaoli Jin
Xi Qiu
Yi Huang
Hang Zhang
Kaibo Chen
author_sort Xiaoli Jin
collection DOAJ
description Abstract Background Cancer-associated fibroblasts (CAFs) aggravate gastric cancer (GC) development. Methods Combined with bioinformatics analysis and literature review, miR-223-3p had high expression in microvesicles (MVs) derived from GC CAFs, and it could modulate SORBS1. miR-223-3p and SORBS1 mRNA levels were assessed by qRT-PCR. The levels of CAFs markers, MVs markers, epithelial-mesenchymal transition (EMT)-associated proteins, and SORBS1 protein were assessed by western blot. MVs isolated from fibroblasts were observed by transmission electron microscopy. Combined with immunofluorescence and co-culture experiments, GC cells were determined to absorb MVs carrying miR-223-3p. Cell functions were measured using CCK-8, transwell, flow cytometry and colony formation assays. The binding of miR-223-3p and SORBS1 was determined by dual-luciferase assay and RNA immunoprecipitation. The cancer-promoting effect of MVs carrying miR-223-3p on experimental animals was verified in vivo by tumor-bearing experiment in nude mice. Results miR-223-3p was upregulated in the MVs secreted by GC CAFs and could be transmitted to GC cells through MVs, to boost the malignant progression of tumor cells. Additionally, it was also revealed that miR-223-3p targeted SORBS1 and accelerated progression along with EMT in GC. Conclusions CAFs-derived MVs could carry miR-223-3p to GC cells to target SORBS1, thereby promoting the malignant progression of GC.
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spelling doaj.art-fe69b477425449e088266f8812fb57f22022-12-22T01:33:59ZengBMCCancer Cell International1475-28672022-02-0122111510.1186/s12935-022-02513-1miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancerXiaoli Jin0Xi Qiu1Yi Huang2Hang Zhang3Kaibo Chen4Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Zhejiang University School of MedicineDepartment of Hematology, The Second Affiliated Hospital of Zhejiang University School of MedicineDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Zhejiang University School of MedicineDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Zhejiang University School of MedicineDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Zhejiang University School of MedicineAbstract Background Cancer-associated fibroblasts (CAFs) aggravate gastric cancer (GC) development. Methods Combined with bioinformatics analysis and literature review, miR-223-3p had high expression in microvesicles (MVs) derived from GC CAFs, and it could modulate SORBS1. miR-223-3p and SORBS1 mRNA levels were assessed by qRT-PCR. The levels of CAFs markers, MVs markers, epithelial-mesenchymal transition (EMT)-associated proteins, and SORBS1 protein were assessed by western blot. MVs isolated from fibroblasts were observed by transmission electron microscopy. Combined with immunofluorescence and co-culture experiments, GC cells were determined to absorb MVs carrying miR-223-3p. Cell functions were measured using CCK-8, transwell, flow cytometry and colony formation assays. The binding of miR-223-3p and SORBS1 was determined by dual-luciferase assay and RNA immunoprecipitation. The cancer-promoting effect of MVs carrying miR-223-3p on experimental animals was verified in vivo by tumor-bearing experiment in nude mice. Results miR-223-3p was upregulated in the MVs secreted by GC CAFs and could be transmitted to GC cells through MVs, to boost the malignant progression of tumor cells. Additionally, it was also revealed that miR-223-3p targeted SORBS1 and accelerated progression along with EMT in GC. Conclusions CAFs-derived MVs could carry miR-223-3p to GC cells to target SORBS1, thereby promoting the malignant progression of GC.https://doi.org/10.1186/s12935-022-02513-1Cancer-associated fibroblastsMicrovesiclesmiR-223-3pSORBS1Gastric cancer
spellingShingle Xiaoli Jin
Xi Qiu
Yi Huang
Hang Zhang
Kaibo Chen
miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
Cancer Cell International
Cancer-associated fibroblasts
Microvesicles
miR-223-3p
SORBS1
Gastric cancer
title miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
title_full miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
title_fullStr miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
title_full_unstemmed miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
title_short miR-223-3p carried by cancer-associated fibroblast microvesicles targets SORBS1 to modulate the progression of gastric cancer
title_sort mir 223 3p carried by cancer associated fibroblast microvesicles targets sorbs1 to modulate the progression of gastric cancer
topic Cancer-associated fibroblasts
Microvesicles
miR-223-3p
SORBS1
Gastric cancer
url https://doi.org/10.1186/s12935-022-02513-1
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