Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Sa, Jason K. | - |
dc.contributor.author | Hwang, Jae Ryoung | - |
dc.contributor.author | Cho, Young-Jae | - |
dc.contributor.author | Ryu, Ji-Yoon | - |
dc.contributor.author | Choi, Jung-Joo | - |
dc.contributor.author | Jeong, Soo Young | - |
dc.contributor.author | Kim, Jihye | - |
dc.contributor.author | Kim, Myeong Seon | - |
dc.contributor.author | Paik, E. Sun | - |
dc.contributor.author | Lee, Yoo-Young | - |
dc.contributor.author | Choi, Chel Hun | - |
dc.contributor.author | Kim, Tae-Joong | - |
dc.contributor.author | Kim, Byoung-Gie | - |
dc.contributor.author | Bae, Duk-Soo | - |
dc.contributor.author | Lee, Yeri | - |
dc.contributor.author | Her, Nam-Gu | - |
dc.contributor.author | Shin, Yong Jae | - |
dc.contributor.author | Cho, Hee Jin | - |
dc.contributor.author | Kim, Ja Yeon | - |
dc.contributor.author | Seo, Yun Jee | - |
dc.contributor.author | Koo, Harim | - |
dc.contributor.author | Oh, Jeong-Woo | - |
dc.contributor.author | Lee, Taebum | - |
dc.contributor.author | Kim, Hyun-Soo | - |
dc.contributor.author | Song, Sang Yong | - |
dc.contributor.author | Seol, Joon | - |
dc.contributor.author | Park, Woong-Yang | - |
dc.contributor.author | Han, Hee Dong | - |
dc.contributor.author | Ahn, Hyung Jun | - |
dc.contributor.author | Sood, Anil K. | - |
dc.contributor.author | Rabadan, Raul | - |
dc.contributor.author | Lee, Jin-Ku | - |
dc.contributor.author | Nam, Do-Hyun | - |
dc.contributor.author | Lee, Jeong-Won | - |
dc.date.accessioned | 2024-01-19T18:34:23Z | - |
dc.date.available | 2024-01-19T18:34:23Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2019-11-26 | - |
dc.identifier.issn | 1474-760X | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/119309 | - |
dc.description.abstract | Background: Gynecologic malignancy is one of the leading causes of mortality in female adults worldwide. Comprehensive genomic analysis has revealed a list of molecular aberrations that are essential to tumorigenesis, progression, and metastasis of gynecologic tumors. However, targeting such alterations has frequently led to treatment failures due to underlying genomic complexity and simultaneous activation of various tumor cell survival pathway molecules. A compilation of molecular characterization of tumors with pharmacological drug response is the next step toward clinical application of patient-tailored treatment regimens. Results: Toward this goal, we establish a library of 139 gynecologic tumors including epithelial ovarian cancers (EOCs), cervical, endometrial tumors, and uterine sarcomas that are genomically and/or pharmacologically annotated and explore dynamic pharmacogenomic associations against 37 molecularly targeted drugs. We discover lineage-specific drug sensitivities based on subcategorization of gynecologic tumors and identify TP53 mutation as a molecular determinant that elicits therapeutic response to poly (ADP-Ribose) polymerase (PARP) inhibitor. We further identify transcriptome expression of inhibitor of DNA biding 2 (ID2) as a potential predictive biomarker for treatment response to olaparib. Conclusions: Together, our results demonstrate the potential utility of rapid drug screening combined with genomic profiling for precision treatment of gynecologic cancers. | - |
dc.language | English | - |
dc.publisher | BMC | - |
dc.subject | EPITHELIAL OVARIAN-CANCER | - |
dc.subject | PHASE-II | - |
dc.subject | GENOMIC CHARACTERIZATION | - |
dc.subject | DRUG-SENSITIVITY | - |
dc.subject | BREAST-CANCER | - |
dc.subject | ENDOMETRIAL | - |
dc.subject | RECURRENT | - |
dc.subject | MUTATIONS | - |
dc.subject | RIDAFOROLIMUS | - |
dc.subject | EVEROLIMUS | - |
dc.title | Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers | - |
dc.type | Article | - |
dc.identifier.doi | 10.1186/s13059-019-1848-3 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | GENOME BIOLOGY, v.20, no.1 | - |
dc.citation.title | GENOME BIOLOGY | - |
dc.citation.volume | 20 | - |
dc.citation.number | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000511881900001 | - |
dc.identifier.scopusid | 2-s2.0-85075652379 | - |
dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
dc.relation.journalWebOfScienceCategory | Genetics & Heredity | - |
dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
dc.relation.journalResearchArea | Genetics & Heredity | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | EPITHELIAL OVARIAN-CANCER | - |
dc.subject.keywordPlus | PHASE-II | - |
dc.subject.keywordPlus | GENOMIC CHARACTERIZATION | - |
dc.subject.keywordPlus | DRUG-SENSITIVITY | - |
dc.subject.keywordPlus | BREAST-CANCER | - |
dc.subject.keywordPlus | ENDOMETRIAL | - |
dc.subject.keywordPlus | RECURRENT | - |
dc.subject.keywordPlus | MUTATIONS | - |
dc.subject.keywordPlus | RIDAFOROLIMUS | - |
dc.subject.keywordPlus | EVEROLIMUS | - |
dc.subject.keywordAuthor | Gynecologic malignancy | - |
dc.subject.keywordAuthor | Pharmacogenomic analysis | - |
dc.subject.keywordAuthor | PARP inhibitor | - |
dc.subject.keywordAuthor | TP53 mutations | - |
dc.subject.keywordAuthor | ID2 | - |
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