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Cited 15 time in webofscience Cited 16 time in scopus
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NOTUM Is Involved in the Progression of Colorectal Cancer

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dc.contributor.authorYoon, Jong Hyuk-
dc.contributor.authorKim, Dayea-
dc.contributor.authorKim, Jaeyoon-
dc.contributor.authorLee, Hyeongjoo-
dc.contributor.authorGhim, Jaewang-
dc.contributor.authorKang, Byung Jun-
dc.contributor.authorSong, Parkyong-
dc.contributor.authorSuh, Pann-Ghill-
dc.contributor.authorRyu, Sung Ho-
dc.contributor.authorLee, Taehoon G.-
dc.date.accessioned2023-08-16T09:49:37Z-
dc.date.available2023-08-16T09:49:37Z-
dc.date.created2022-01-13-
dc.date.issued2018-11-
dc.identifier.issn1109-6535-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/718-
dc.description.abstractBackground: There are limitations to current colorectal cancer (CRC)-specific diagnostic methods and therapies. Tumorigenesis proceeds because of interaction between cancer cells and various surrounding cells; discovering new molecular mediators through studies of the CRC secretome is a promising approach for the development of CRC diagnostics and therapies. Materials and Methods: A comparative secretomic analysis was performed using primary and metastatic human isogenic CRC cells. Proliferation was determined by MTT and thymidine incorporation assay, migration was determined by wound-healing assay (ELISA). The level of palmitoleoyl-protein carboxylesterase (NOTUM) in plasma from patients with CRC was determined by enzyme-linked immunosorbent assay. Results: NOTUM expression was increased in metastatic cells. Proliferation was suppressed by inhibiting expression of NOTUM. Knockdown of NOTUM genes inhibited proliferation as well as migration, with possible involvement of p38 and c-JUN N-terminal kinase in this process. The result was verified in patients with CRC. Conclusion: NOTUM may be a new candidate for diagnostics and therapy of CRC.-
dc.language영어-
dc.language.isoen-
dc.publisherINT INST ANTICANCER RESEARCH-
dc.titleNOTUM Is Involved in the Progression of Colorectal Cancer-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoon, Jong Hyuk-
dc.identifier.doi10.21873/cgp.20107-
dc.identifier.scopusid2-s2.0-85055072760-
dc.identifier.wosid000447810900006-
dc.identifier.bibliographicCitationCANCER GENOMICS & PROTEOMICS, v.15, no.6, pp.485 - 497-
dc.relation.isPartOfCANCER GENOMICS & PROTEOMICS-
dc.citation.titleCANCER GENOMICS & PROTEOMICS-
dc.citation.volume15-
dc.citation.number6-
dc.citation.startPage485-
dc.citation.endPage497-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusHEPARAN-SULFATE PROTEOGLYCANS-
dc.subject.keywordPlusMYOTUBE SECRETOME REVEALS-
dc.subject.keywordPlusPROTEOMIC ANALYSIS-
dc.subject.keywordPlusTGF-BETA-
dc.subject.keywordPlusCELL-PROLIFERATION-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusP38-ALPHA-
dc.subject.keywordAuthorNOTUM-
dc.subject.keywordAuthorsecretomics-
dc.subject.keywordAuthorcolorectal cancer-
dc.subject.keywordAuthormigration-
dc.subject.keywordAuthordiagnosis-
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