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Suh, Pann-Ghill
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dc.citation.startPage 93 -
dc.citation.title EXPERIMENTAL AND MOLECULAR MEDICINE -
dc.citation.volume 50 -
dc.contributor.author Park, Soyeon -
dc.contributor.author Park, Ji-Hwan -
dc.contributor.author Jung, Hee-Jung -
dc.contributor.author Jang, Jin-Hyeok -
dc.contributor.author Ahn, Sanghyun -
dc.contributor.author Kim, Younah -
dc.contributor.author Suh, Pann-Ghill -
dc.contributor.author Chae, Sehyun -
dc.contributor.author Yoon, Jong Hyuk -
dc.contributor.author Ryu, Sung Ho -
dc.contributor.author Hwang, Daehee -
dc.date.accessioned 2023-12-21T20:19:33Z -
dc.date.available 2023-12-21T20:19:33Z -
dc.date.created 2018-08-30 -
dc.date.issued 2018-08 -
dc.description.abstract Increased fatty acid (FA) is often observed in highly proliferative tumors. FAs have been shown to modulate the secretion of proteins from tumor cells, contributing to tumor survival. However, the secreted factors affected by FA have not been systematically explored. Here, we found that treatment of oleate, a monounsaturated omega-9 FA, promoted the proliferation of HepG2 cells. To examine the secreted factors associated with oleate-induced cell proliferation, we performed a comprehensive secretome profiling of oleate-treated and untreated HepG2 cells. A comparison of the secretomes identified 349 differentially secreted proteins (DSPs; 145 upregulated and 192 downregulated) in oleate-treated samples, compared to untreated samples. The functional enrichment and network analyses of the DSPs revealed that the 145 upregulated secreted proteins by oleate treatment were mainly associated with cell proliferation-related processes, such as lipid metabolism, inflammatory response, and ER stress. Based on the network models of the DSPs, we selected six DSPs (MIF, THBS1, PDIA3, APOA1, FASN, and EEF2) that can represent such processes related to cell proliferation. Thus, our results provided a secretome profile indicative of an oleate-induced proliferation of HepG2 cells -
dc.identifier.bibliographicCitation EXPERIMENTAL AND MOLECULAR MEDICINE, v.50, pp.93 -
dc.identifier.doi 10.1038/s12276-018-0120-3 -
dc.identifier.issn 1226-3613 -
dc.identifier.scopusid 2-s2.0-85051072611 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/25580 -
dc.identifier.url https://www.nature.com/articles/s12276-018-0120-3 -
dc.identifier.wosid 000440852400002 -
dc.language 영어 -
dc.publisher NATURE PUBLISHING GROUP -
dc.title A secretome profile indicative of oleate-induced proliferation of HepG2 hepatocellular carcinoma cells -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Medicine, Research & Experimental -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Research & Experimental Medicine -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.subject.keywordPlus ENDOPLASMIC-RETICULUM-STRESS -
dc.subject.keywordPlus MIGRATION INHIBITORY FACTOR -
dc.subject.keywordPlus UNSATURATED FATTY-ACIDS -
dc.subject.keywordPlus BREAST-CANCER CELLS -
dc.subject.keywordPlus CANDIDATE SEROLOGICAL BIOMARKERS -
dc.subject.keywordPlus THIOL OXIDOREDUCTASE ERP57 -
dc.subject.keywordPlus UNFOLDED PROTEIN RESPONSE -
dc.subject.keywordPlus PANCREATIC-CANCER -
dc.subject.keywordPlus MASS-SPECTROMETRY -
dc.subject.keywordPlus INDUCED APOPTOSIS -

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