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Article: Recent Advances of Small Extracellular Vesicles for the Regulation and Function of Cancer-Associated Fibroblasts

TitleRecent Advances of Small Extracellular Vesicles for the Regulation and Function of Cancer-Associated Fibroblasts
Authors
Keywordscancer-associated fibroblasts
crosstalk
small extracellular vesicles
Issue Date1-Dec-2024
PublisherMDPI
Citation
International Journal of Molecular Sciences, 2024, v. 25, n. 23 How to Cite?
AbstractCancer-associated fibroblasts (CAFs) are a heterogeneous cell population in the tumor microenvironment (TME) that critically affect cancer progression. Small extracellular vesicles (sEVs) act as information messengers by transmitting a wide spectrum of biological molecules, including proteins, nucleic acids, and metabolites, from donor cells to recipient cells. Previous studies have demonstrated that CAFs play important roles in tumor progression by regulating tumor cell proliferation, metastasis, therapeutic resistance, and metabolism via sEVs. In turn, tumor-derived sEVs can also regulate the activation and phenotype switch of CAFs. The dynamic crosstalk between CAFs and cancer cells via sEVs could ultimately determine cancer progression. In this review, we summarized the recent advance of the biological roles and underlying mechanisms of sEVs in mediating CAF-tumor cell interaction and its impact on cancer progression. We also reviewed the clinical applications of tumor- and CAF-derived sEVs, which could identify novel potential targets and biomarkers for cancer diagnosis, therapy, and prognosis.
Persistent Identifierhttp://hdl.handle.net/10722/356706
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.179
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiang, Chengdong-
dc.contributor.authorWang, Maoye-
dc.contributor.authorHuang, Yongli-
dc.contributor.authorYam, Judy Wai Ping-
dc.contributor.authorZhang, Xu-
dc.contributor.authorZhang, Xiaoxin-
dc.date.accessioned2025-06-14T00:35:10Z-
dc.date.available2025-06-14T00:35:10Z-
dc.date.issued2024-12-01-
dc.identifier.citationInternational Journal of Molecular Sciences, 2024, v. 25, n. 23-
dc.identifier.issn1661-6596-
dc.identifier.urihttp://hdl.handle.net/10722/356706-
dc.description.abstractCancer-associated fibroblasts (CAFs) are a heterogeneous cell population in the tumor microenvironment (TME) that critically affect cancer progression. Small extracellular vesicles (sEVs) act as information messengers by transmitting a wide spectrum of biological molecules, including proteins, nucleic acids, and metabolites, from donor cells to recipient cells. Previous studies have demonstrated that CAFs play important roles in tumor progression by regulating tumor cell proliferation, metastasis, therapeutic resistance, and metabolism via sEVs. In turn, tumor-derived sEVs can also regulate the activation and phenotype switch of CAFs. The dynamic crosstalk between CAFs and cancer cells via sEVs could ultimately determine cancer progression. In this review, we summarized the recent advance of the biological roles and underlying mechanisms of sEVs in mediating CAF-tumor cell interaction and its impact on cancer progression. We also reviewed the clinical applications of tumor- and CAF-derived sEVs, which could identify novel potential targets and biomarkers for cancer diagnosis, therapy, and prognosis.-
dc.languageeng-
dc.publisherMDPI-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcancer-associated fibroblasts-
dc.subjectcrosstalk-
dc.subjectsmall extracellular vesicles-
dc.titleRecent Advances of Small Extracellular Vesicles for the Regulation and Function of Cancer-Associated Fibroblasts-
dc.typeArticle-
dc.identifier.doi10.3390/ijms252312548-
dc.identifier.pmid39684264-
dc.identifier.scopuseid_2-s2.0-85211961876-
dc.identifier.volume25-
dc.identifier.issue23-
dc.identifier.eissn1422-0067-
dc.identifier.isiWOS:001376455100001-
dc.identifier.issnl1422-0067-

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