The association of piR-651 and piR-823 on metastaticand invasive characteristics of triple negative breastcancer cells
dc.authorid | 0000-0003-3771-3277 | |
dc.contributor.author | Öner, Çağrı | |
dc.contributor.author | Köser, Faruk | |
dc.contributor.author | Çolak, Ertuğrul | |
dc.date.accessioned | 2025-01-07T13:23:46Z | |
dc.date.available | 2025-01-07T13:23:46Z | |
dc.date.issued | 2024 | |
dc.department | Fakülteler, Tıp Fakültesi | |
dc.description.abstract | PIWI-Interacting RNAs are small non-coding RNAs derived fromsingle-stranded RNAs which plays a crucial role in epigeneticregulation through transposon silencing and mRNA degrada-tion via deamination. This study aimed to inhibit piR-651 andpiR-823 in MDA-MB-231 triple-negative breast cancer cells andto explore their potential effects on healthy HUVEC cells. Non-target, anti-piR-651, and anti-piR-823 sequences were trans-fected in bothHUVEC and MDA-MB-231 cells usingLipofectamine. Proliferation and motility were assessed at 24,48, and 72 h post-transfection in both cell lines. Based on themotility findings, MDA-MB-231 cells were underwent an inva-sion assay using crystal violet staining. The expressions of Ki-67,HIF-1α, MMP-2, and MMP-9 genes were measured at 48 h,when both cell lines exhibited the most significant effects ofinhibition. The optimal time for proliferation of anti-piR-651 andanti-piR-823 transfected MDA-MB-231 cells was determined tobe at 48 h, as indicated by decreased motility and invasionassay results (p < 0.001). NeverthelessHowever, there was no sig-nificant difference in the motility and proliferation of HUVECsstransfected with anti-piR-651 and anti-piR-823 compared to thecontrol group (p > 0.05). Asides from MMP-2 in anti-piR-823transfected HUVECs and HIF-1α in anti-piR-823 transfectedMDA-MB-231 cells, gene expressions of Ki-67, HIF-1α, MMP-2,and MMP-9 were reduced in both cell lines (p < 0.001). Inhibitionof piR-651 and piR-823 decreased the survival and metastasisof cancer cells, without causing vital structural changes inhealthy cells. Future research in cancer gene therapy or geneticmodification may benefit from investigating piR-651 and piR-823 as possible inhibitors of breast cancer invasion andmetastasis. | |
dc.identifier.citation | Öner, Ç., Köser, F. ve Çolak, E. (2024). The association of piR-651 and piR-823 on metastaticand invasive characteristics of triple negative breastcancer cells, Nucleosides Nucleotides & Nucleic Acids, Taylor & Francis Group, s.1-17. | |
dc.identifier.doi | 10.1080/15257770.2024.2437037 | |
dc.identifier.endpage | 17 | |
dc.identifier.issn | 1525-7770 | |
dc.identifier.startpage | 1 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12415/13213 | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Group | |
dc.relation.ispartof | Nucleosides Nucleotides & Nucleic Acids | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Invasion | |
dc.subject | Metastasis | |
dc.subject | PIWI interacting RNA | |
dc.subject | piR-651 | |
dc.subject | piR-823 | |
dc.subject | Triple Negativebreast Cancer | |
dc.title | The association of piR-651 and piR-823 on metastaticand invasive characteristics of triple negative breastcancer cells | |
dc.type | Article | |
dspace.entity.type | Publication |
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