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miR-4742–5p promotes invasiveness of gastric cancer via targeting Rab43: An in vitro study

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dc.contributor.authorBae, WJ-
dc.contributor.authorWoo, KJ-
dc.contributor.authorAhn, JM-
dc.contributor.authorYang, CM-
dc.contributor.authorKim, YS-
dc.contributor.authorKim, S-
dc.contributor.authorLee, D-
dc.date.accessioned2023-03-24T06:26:52Z-
dc.date.available2023-03-24T06:26:52Z-
dc.date.issued2022-
dc.identifier.issn0006-291X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/25081-
dc.description.abstractmiRNA (miR)-4742-5p is a recently identified microRNA regarding progression and metastasis in gastric cancer (GC). However, the biological function of this novel miRNA is largely unknown. We identified that the miR-4742-5p expression level was variably increased in GC cell lines. Suppression of miR-4742-5p using miR-inhibitor reduced the proliferation, migration, and invasion of GC cells with high miR-4742-5p expression, whereas overexpression of miR-4742-5p-mimic enhanced the aforementioned properties in GC cells with low miR-4742-5p expression. miR-4742-5p expression induced the decreases of Zo-1 and E-cadherin expression as well as the increases of vimentin and N-cadherin expression, leading to epithelial-mesenchymal transition (EMT) of cancer cells. RNA sequencing results indicated Ras-related GTP-binding protein 43 (Rab43) as a potential target gene. We identified that the expression of Rab43 is associated with activation of AKT and nuclear factor-kappa B (NF-kappaB) which are key oncogenic pathways in cancer cells. Our results demonstrate a new component in GC progression, promising a potential therapeutic strategy.-
dc.language.isoen-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Movement-
dc.subject.MESHCell Proliferation-
dc.subject.MESHEpithelial-Mesenchymal Transition-
dc.subject.MESHGene Expression Regulation, Neoplastic-
dc.subject.MESHHumans-
dc.subject.MESHMicroRNAs-
dc.subject.MESHNeoplasm Invasiveness-
dc.subject.MESHStomach Neoplasms-
dc.titlemiR-4742–5p promotes invasiveness of gastric cancer via targeting Rab43: An in vitro study-
dc.typeArticle-
dc.identifier.pmid35597125-
dc.subject.keywordGastric cancer-
dc.subject.keywordInvasion-
dc.subject.keywordmiR-4742–5p-
dc.subject.keywordRab43-
dc.contributor.affiliatedAuthorKim, YS-
dc.contributor.affiliatedAuthorKim, S-
dc.contributor.affiliatedAuthorLee, D-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.bbrc.2022.05.044-
dc.citation.titleBiochemical and biophysical research communications-
dc.citation.volume613-
dc.citation.date2022-
dc.citation.startPage180-
dc.citation.endPage186-
dc.identifier.bibliographicCitationBiochemical and biophysical research communications, 613. : 180-186, 2022-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn1090-2104-
dc.relation.journalidJ00006291X-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
Journal Papers > School of Medicine / Graduate School of Medicine > Pathology
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