MicroRNA-200c overexpression in cancer-associated fibroblasts decreases interleukin-2 secretion
dc.contributor.author | Shariati, L. | |
dc.contributor.author | Vaseghi, G. | |
dc.contributor.author | Vaziri, N. | |
dc.contributor.author | Shenavar, N. | |
dc.contributor.author | Zarrabi, A. | |
dc.contributor.author | Haghjooy, Javanmard, S. | |
dc.date.accessioned | 2024-05-19T14:33:31Z | |
dc.date.available | 2024-05-19T14:33:31Z | |
dc.date.issued | 2022 | |
dc.department | İstinye Üniversitesi | en_US |
dc.description.abstract | miR-200c-3p is demonstrated to play the role of tumour suppressor in different tumours. However, the miR-200c-3p biological function in normal fibroblast (NF) and cancer-associated fibroblast (CAF) remains unclear. This investigation aims to study the regulatory role of miR-200c-3p in the secretion of Interleukin-2 (IL-2) in CAF and NF. CAFs and NFs were isolated from tumour and normal tissue specimens respectively. Immunocytochemistry was used to confirm the presence of a fibroblast specific marker, alpha-actin smooth muscle, in NFs and CAFs. NF and CAF were transfected with scramble and miR-200c-3p utilizing the lipofectamine 2000 reagent. The protein levels of IL-2 were measured in CAFs, NFs, and transfected groups with miR-200c-3p and scrambled using an IL-2 enzyme-linked immunoassay kit. miR-200c decreased secretion of IL-2 in transfected CAF and NF compared to controls. Results elucidated that transfection of MiR-200c-3p can decrease the IL-2 secretion and consequently reduce IL-induced tumourigenic manner in the CAF. © 2022 The Authors. Clinical and Translational Discovery published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics. | en_US |
dc.description.sponsorship | Isfahan University of Medical Sciences, IUMS: 297184 | en_US |
dc.description.sponsorship | This work was supported by Isfahan University of Medical Sciences [grant number 297184]. | en_US |
dc.identifier.doi | 10.1002/ctd2.90 | |
dc.identifier.issn | 2768-0622 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopus | 2-s2.0-85165482850 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.uri | https://doi.org/10.1002/ctd2.90 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/4260 | |
dc.identifier.volume | 2 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Blackwell Publishing | en_US |
dc.relation.ispartof | Clinical and Translational Discovery | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.snmz | 20240519_ka | en_US |
dc.subject | Breast Cancer | en_US |
dc.subject | Cancer-Associated Fibroblast | en_US |
dc.subject | Mir-200c-3p | en_US |
dc.subject | Normal Fibroblast | en_US |
dc.title | MicroRNA-200c overexpression in cancer-associated fibroblasts decreases interleukin-2 secretion | en_US |
dc.type | Article | en_US |