Cited 8 times in
TMED9 Expression Level as a Biomarker of Epithelial Ovarian Cancer Progression and Prognosis
DC Field | Value | Language |
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dc.contributor.author | 김재훈 | - |
dc.contributor.author | 윤희 | - |
dc.contributor.author | 조한별 | - |
dc.date.accessioned | 2023-03-03T02:10:29Z | - |
dc.date.available | 2023-03-03T02:10:29Z | - |
dc.date.issued | 2022-11 | - |
dc.identifier.issn | 1109-6535 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/192749 | - |
dc.description.abstract | Background: Transmembrane emp24 domain-containing protein 9 (TMED9) belongs to the TMED/p24 family that transports, modifies, and packs proteins and lipids into vesicles for delivery to specific locations and is important in innate immune signaling via the endoplasmic reticulum-Golgi cargo pathway. TMED9 has been implicated in various cancer types; however, its role in epithelial ovarian cancer (EOC) is unclear. In this study, we aimed to elucidate the role and clinical significance of TMED9 in EOC. Materials and methods: mRNA and protein levels of TMED9 and their associations with clinicopathological features in EOCs were evaluated using RNA-sequencing and immunohistochemistry data. Functional studies assessing the tumorigenic role of TMED9 in EOC cell lines were also performed. Results: The mRNA expression of TMED9 was up-regulated in EOC compared to that in normal ovarian epithelium. TMED9 protein expression increased in progression from normal ovarian epithelium to EOC (p<0.001). Moreover, high expression of TMED9 was associated with advanced stage, serous cell type and poor histological grade in EOC and demonstrated independent prognostic significance for both disease-free and overall survival. Further functional studies showed that TMED9 knockdown reduced migration, invasion, cell proliferation, and colony formation of EOC cells. Conclusion: Overall, our results support the use of TMED9 as a valuable prognostic biomarker and provide evidence for targeting of TMED9 as a novel strategy for EOC treatment. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | International Institute of Anticancer | - |
dc.relation.isPartOf | CANCER GENOMICS & PROTEOMICS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Biomarkers, Tumor / metabolism | - |
dc.subject.MESH | Carcinoma, Ovarian Epithelial / metabolism | - |
dc.subject.MESH | Cell Line, Tumor | - |
dc.subject.MESH | Cell Proliferation / genetics | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Gene Expression Regulation, Neoplastic | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Neoplasms, Glandular and Epithelial* / genetics | - |
dc.subject.MESH | Ovarian Neoplasms* / pathology | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | RNA, Messenger / genetics | - |
dc.title | TMED9 Expression Level as a Biomarker of Epithelial Ovarian Cancer Progression and Prognosis | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Obstetrics and Gynecology (산부인과학교실) | - |
dc.contributor.googleauthor | Gwan Hee Han | - |
dc.contributor.googleauthor | Hee Yun | - |
dc.contributor.googleauthor | Joon-Yong Chung | - |
dc.contributor.googleauthor | Jae-Hoon Kim | - |
dc.contributor.googleauthor | Hanbyoul Cho | - |
dc.identifier.doi | 10.21873/cgp.20352 | - |
dc.contributor.localId | A00876 | - |
dc.contributor.localId | A06203 | - |
dc.contributor.localId | A03921 | - |
dc.relation.journalcode | J03713 | - |
dc.identifier.eissn | 1790-6245 | - |
dc.identifier.pmid | 36316042 | - |
dc.subject.keyword | TMED9 | - |
dc.subject.keyword | biomarker | - |
dc.subject.keyword | diagnosis | - |
dc.subject.keyword | ovarian cancer | - |
dc.subject.keyword | prognosis | - |
dc.contributor.alternativeName | Kim, Jae Hoon | - |
dc.contributor.affiliatedAuthor | 김재훈 | - |
dc.contributor.affiliatedAuthor | 윤희 | - |
dc.contributor.affiliatedAuthor | 조한별 | - |
dc.citation.volume | 19 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 692 | - |
dc.citation.endPage | 702 | - |
dc.identifier.bibliographicCitation | CANCER GENOMICS & PROTEOMICS, Vol.19(6) : 692-702, 2022-11 | - |
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