Literature DB >> 30078507

BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls.

Ang Li1, Rong Xie2, Qihuan Zhi1, Yixiao Deng1, Yangming Wu1, Weiwei Li1, Lu Yang1, Zinan Jiao1, Jiaqi Luo1, Yi Zi1, Gang Sun1, Jiajia Zhang1, Yujian Shi3, Jian Liu4.   

Abstract

OBJECTIVE: To investigate the BRCA status in Chinese patients with ovarian cancer (OC). Though there were two large prevalence studies in Chinese OC patients, this was the first time to observe it in healthy controls.
METHODS: We performed BRCA mutation screening using next-generation sequencing to determine the prevalence of BRCA germline deleterious mutations in an unselected cohort of Chinese OC patients (n = 1331) versus healthy controls (n = 1763) and describe the types and spectrum of BRCA deleterious variants.
RESULTS: Among the 1331 patients with OC, 227 (17.1%) carried deleterious variants in BRCA1 and 70 (5.3%) carried deleterious variants in BRCA2. Of 1763 control subjects, 6 (0.3%) and 2 (0.1%) had deleterious variants in BRCA1 and BRCA2. No patient carried mutations in both BRCA1 and BRCA2 simultaneously. Sixty-three novel mutations were identified, and three Chinese specific hot-spot mutations were notified as BRCA1 c.5470_5477delATTGGGCA, BRCA1 c.981_982delAT, and BRCA1 c.3770_3771delAG. Interestingly, all these high-frequency recurrent mutations were distributed on exon 10, which may also be the Chinese OC BRCA mutations' distinct characteristics. In addition, in our study, the estimated odds ratio (OR) of OC associated with BRCA1 positive variants were approximately 34.6 (95% CI, 12.5-95.7) in age group under 40 and 42.4 (95% CI, 5.9-305.2) in group older than 50 in the Chinese population, respectively.
CONCLUSIONS: We recommend BRCA testing to all Chinese OC patients and those general Chinese who have family members with hereditary breast and ovarian related cancer (HBOC)-related cancers. Variants carriers would not only benefit from early prevention of OC but also for the medical management.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BRCA gene; Case-control studies; Chinese genetic testing; Exon mutation; High-throughput nucleotide sequencing; Ovarian neoplasms

Mesh:

Substances:

Year:  2018        PMID: 30078507     DOI: 10.1016/j.ygyno.2018.07.024

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  14 in total

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Authors:  Pongtawat Lertwilaiwittaya; Ekkapong Roothumnong; Panee Nakthong; Peerawat Dungort; Chutima Meesamarnpong; Warisara Tansa-Nga; Khontawan Pongsuktavorn; Supakit Wiboonthanasarn; Warunya Tititumjariya; Wanna Thongnoppakhun; Sirisak Chanprasert; Chanin Limwongse; Manop Pithukpakorn
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Journal:  Cancer Sci       Date:  2019-12-31       Impact factor: 6.716

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9.  Identification of BRCA1:c.5470_5477del as a Founder Mutation in Chinese Ovarian Cancer Patients.

Authors:  Jun Li; Sile Han; Cuiyun Zhang; Yanlin Luo; Li Wang; Ping Wang; Yi Wang; Qingxin Xia; Xiaoyan Wang; Bing Wei; Jie Ma; Hongle Li; Yongjun Guo
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Review 10.  Differences in Ovarian and Other Cancers Risks by Population and BRCA Mutation Location.

Authors:  Masayuki Sekine; Koji Nishino; Takayuki Enomoto
Journal:  Genes (Basel)       Date:  2021-07-08       Impact factor: 4.096

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