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Biobanking of gynecologic cancer biospecimens: Development, quality control, and translational applications

Authors
 Kim, Jue Young  ;  Lee, Yoo-Kyung  ;  Shin, Ha-Yeon  ;  Kim, Yoon Joo  ;  Jeon, Mi Ae  ;  Yang, Wookyeom  ;  Jun, Anna  ;  Kim, Kyungmin  ;  Cho, Hanbyoul  ;  Kim, Min-A  ;  Kim, Jae-Hoon 
Citation
 PLOS ONE, Vol.21(3), 2026-03 
Article Number
 e0345861 
Journal Title
PLOS ONE
Issue Date
2026-03
MeSH
Animals ; Biological Specimen Banks* / standards ; Cell Line, Tumor ; Female ; Genital Neoplasms, Female* / genetics ; Genital Neoplasms, Female* / pathology ; Humans ; Mice ; Ovarian Neoplasms / genetics ; Ovarian Neoplasms / pathology ; Quality Control ; Republic of Korea ; Specimen Handling ; Translational Research, Biomedical ; Whole Genome Sequencing
Abstract
Introduction This study presents a nationwide infrastructure for the collection and utilization of gynecologic cancer biospecimens, established through the Korea Biobank Project. We comprehensively describe the biobanking strategy, quality control protocols, and development of secondary resources to support future translational and discovery-based research.Methods We established a gynecologic cancer biobank within the Korea Biobank Project (KBP) through a multi-institutional consortium. Biospecimens, including blood, tumor tissue, urine, and ascites, were collected from 294 patients with endometrial, cervical, or ovarian cancers. Pre-analytical variables were documented using the Standard PREanalytical Code (SPREC), and all samples were tracked with 2D barcodes. Secondary resources were developed, including whole-genome sequencing (WGS) datasets, immortalized human ovarian surface epithelial (IHOSE) cell lines, patient-derived xenografts (PDX), tumor organoids, and tissue microarrays (TMAs).Results A total of 6,168 biospecimens were archived. WGS was performed on 386 cancer samples, including 172 paired tumor-normal sets. Four IHOSE cell lines were authenticated and validated for stability, 14 PDX models retained histological fidelity across passages, and patient-derived ovarian cancer organoids demonstrated drug sensitivity consistent with clinical response patterns. TMAs were constructed from 519 tumors, supporting large-scale molecular profiling. Industry collaborations further highlighted the translational utility of these resources.Conclusions This study describes the development and application of a gynecologic cancer biobank that integrates standardized biospecimen collection, rigorous QC, and the generation of diverse secondary resources. By linking these resources with clinical and epidemiological data, the biobank provides a scalable and accessible platform for precision oncology and academic-industry collaboration.
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DOI
10.1371/journal.pone.0345861
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Min A(김민아)
Kim, Jae Hoon(김재훈) ORCID logo https://orcid.org/0000-0001-6599-7065
Kim, Ju Young(김주영)
Shin, Ha Yeon(신하연)
Yang, Wookyeom(양우겸)
Lee, Yoo Kyung(이유경)
Cho, Hanbyoul(조한별) ORCID logo https://orcid.org/0000-0002-6177-1648
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/211867
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