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논문 기본 정보

자료유형
학술저널
저자정보
Tomoko Akahane (Department of Obstetrics and Gynecology Keio University School of Medicine Tokyo Japan) Kenta Masuda (Department of Obstetrics and Gynecology Keio University School of Medicine Tokyo Japan) Akira Hirasawa (Center for Medical Genetics Keio University School of Medicine Tokyo Japan) Yusuke Kobayashi (Keio University School of Medicine) Arisa Ueki (Genomics Unit Keio Cancer Center Keio University School of Medicine Tokyo Japan) Miho Kawaida (Department of Diagnostic Pathology Keio University School of Medicine Tokyo Japan) Kumiko Misu (Center for Medical Genetics Keio University School of Medicine Tokyo Japan) Kohei Nakamura (Genomics Unit Keio Cancer Center Keio University School of Medicine Tokyo Japan) Shimpei Nagai (Department of Obstetrics and Gynecology Keio University School of Medicine Tokyo Japan) Tatsuyuki Chiyoda (Keio University School of Medicine) Wataru Yamagami (Keio University School of Medicine) Shigenori Hayashi (Department of Obstetrics and Gynecology Keio University School of Medicine Tokyo Japan) Fumio Kataoka (Department of Obstetrics and Gynecology International University of Health and Welfare School of Me) Kouji Banno (Keio University School of Medicine) Kokichi Sugano (Center for Medical Genetics Keio University School of Medicine Tokyo Japan) Hajime Okita (Department of Diagnostic Pathology Keio University School of Medicine Tokyo Japan) Kenjiro Kosaki (Center for Medical Genetics Keio University School of Medicine Tokyo Japan) Hiroshi Nishihara (Genomics Unit Keio Cancer Center Keio University School of Medicine Tokyo Japan) Daisuke Aoki (Keio University)
저널정보
대한부인종양학회 Journal of Gynecologic Oncology Journal of Gynecologic Oncology Vol.33 No.4
발행연도
2022.7
수록면
1 - 13 (13page)
DOI
https://doi.org/10.3802/jgo.2022.33.e50

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초록· 키워드

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Objective: Precursor lesions may be identified in fallopian tube tissue after risk-reducing salpingo-oophorectomy (RRSO) in patients with pathogenic variants of . Serous tubal intraepithelial carcinoma (STIC) is considered a precursor of high-grade serous carcinoma, whereas the significance of the p53 signature remains unclear. In this study, we investigated the relationship between the p53 signature and the risk of ovarian cancer. Methods: We analyzed the clinicopathological findings and conducted DNA sequencing for variants of p53 signatures and STIC lesions isolated using laser capture microdissectionin 13 patients with pathogenic variants of who underwent RRSO and 17 control patients with the benign gynecologic disease. Results: pathogenic variants were detected significantly higher in RRSO group than control (p<0.001). No difference in the frequency of p53 signatures were observed between groups (53.8% vs 29.4%; p=0.17). sequencing and next-generation sequencing analysis in a patient with STIC and occult cancer revealed 2 mutations causing different p53 staining for STICs and another mutation shared between STIC and occult cancer. Conclusion: The sequence analysis for revealed 2 types of p53 signatures, one with a risk of progression to STIC and ovarian cancer with pathological variants in and the other with a low risk of progression without pathological variants in as seen in control.

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