Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers

Cited 14 time in Web of Science Cited 14 time in Scopus

Sa, Jason K.; Hwang, Jae Ryoung; Cho, Young-Jae; Ryu, Ji-Yoon; Choi, Jung-Joo; Jeong, Soo Young; Kim, Jihye; Kim, Myeong Seon; Paik, E. Sun; Lee, Yoo-Young; Choi, Chel Hun; Kim, Tae-Joong; Kim, Byoung-Gie; Bae, Duk-Soo; Lee, Yeri; Her, Nam-Gu; Shin, Yong Jae; Cho, Hee Jin; Kim, Ja Yeon; Seo, Yun Jee; Koo, Harim; Oh, Jeong-Woo; Lee, Taebum; Kim, Hyun-Soo; Song, Sang Yong; Seol, Joon; Park, Woong-Yang; Han, Hee Dong; Ahn, Hyung Jun; Sood, Anil K.; Rabadan, Raul; Lee, Jin-Ku; Nam, Do-Hyun; Lee, Jeong-Won

Issue Date
BioMed Central
Genome Biology, Vol.20 No.1, p. 253
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.
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College of Medicine/School of Medicine (의과대학/대학원)Dept. of Biomedical Sciences (대학원 의과학과)Journal Papers (저널논문_의과학과)
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