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JMJD4 promotes tumor progression via inhibition of the PDCD5-TP53 pathway

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dc.contributor.author박수연-
dc.contributor.author윤호근-
dc.contributor.author이수연-
dc.contributor.author유정윤-
dc.date.accessioned2025-05-02T00:09:07Z-
dc.date.available2025-05-02T00:09:07Z-
dc.date.issued2025-02-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/205294-
dc.description.abstractProgrammed cell death 5 (PDCD5) regulates cell death and suppresses tumor progression. Since the stability and nuclear translocation of PDCD5 are regulated by TP53-dependent cell death stimuli, knowledge of the regulatory mechanism of PDCD5 function is required to better understand the TP53-signaling pathway. We identified Jumonji domain-containing protein 4 (JMJD4) to be a PDCD5-interacting protein using liquid chromatography- mass spectrometry (LC-MS). Interestingly, JMJD4 upregulates cell proliferation and chemo-resistance under genotoxic stress conditions by colony-formation assay and decreases TP53-related apoptotic genes (BAX, PUMA) by suppressing protein levels of PDCD5. Additionally, using the Cancer Genome Atlas and the Gene Expression Omnibus database to confirm the clinical correlation between JMJD4 and cancer patients, we verified that JMJD4 is associated with a poor prognosis in colon cancer and lung cancer patients. Therefore, this study demonstrates that JMJD4 directly interacts with PDCD5, regulates cancer cell death negatively, and could be a potential therapeutic target for cancer development.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherKorean Society for Biochemistry and Molecular Biology-
dc.relation.isPartOfBMB REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHApoptosis / genetics-
dc.subject.MESHApoptosis Regulatory Proteins* / genetics-
dc.subject.MESHApoptosis Regulatory Proteins* / metabolism-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Proliferation / genetics-
dc.subject.MESHColonic Neoplasms / genetics-
dc.subject.MESHColonic Neoplasms / metabolism-
dc.subject.MESHColonic Neoplasms / pathology-
dc.subject.MESHDisease Progression-
dc.subject.MESHGene Expression Regulation, Neoplastic-
dc.subject.MESHHumans-
dc.subject.MESHJumonji Domain-Containing Histone Demethylases* / genetics-
dc.subject.MESHJumonji Domain-Containing Histone Demethylases* / metabolism-
dc.subject.MESHLung Neoplasms / genetics-
dc.subject.MESHLung Neoplasms / metabolism-
dc.subject.MESHLung Neoplasms / pathology-
dc.subject.MESHNeoplasm Proteins* / genetics-
dc.subject.MESHNeoplasm Proteins* / metabolism-
dc.subject.MESHNeoplasms / genetics-
dc.subject.MESHNeoplasms / metabolism-
dc.subject.MESHNeoplasms / pathology-
dc.subject.MESHSignal Transduction-
dc.subject.MESHTumor Suppressor Protein p53* / genetics-
dc.subject.MESHTumor Suppressor Protein p53* / metabolism-
dc.titleJMJD4 promotes tumor progression via inhibition of the PDCD5-TP53 pathway-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Biochemistry and Molecular Biology (생화학-분자생물학교실)-
dc.contributor.googleauthorHyunsik Kim-
dc.contributor.googleauthorSubhin Jang-
dc.contributor.googleauthorSoo Yeon Lee-
dc.contributor.googleauthorJae-Hwan Kwon-
dc.contributor.googleauthorSeunghee Byun-
dc.contributor.googleauthorJung-Yoon Yoo-
dc.contributor.googleauthorSungryul Yu-
dc.contributor.googleauthorSoo-Yeon Park-
dc.contributor.googleauthorHo-Geun Yoon-
dc.identifier.doi10.5843/BMBRep.2024-0027-
dc.contributor.localIdA01534-
dc.contributor.localIdA02625-
dc.relation.journalcodeJ00348-
dc.identifier.eissn1976-670X-
dc.identifier.pmid39567206-
dc.contributor.alternativeNamePark, Soo Yeon-
dc.contributor.affiliatedAuthor박수연-
dc.contributor.affiliatedAuthor윤호근-
dc.citation.volume58-
dc.citation.number2-
dc.citation.startPage64-
dc.citation.endPage69-
dc.identifier.bibliographicCitationBMB REPORTS, Vol.58(2) : 64-69, 2025-02-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers

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