Genetic characterization of BRCA1 and BRCA2 variants in cancer and high-risk family screening cohorts in the UAE population.

IF 2.7 3区 医学 Q3 ONCOLOGY
Abeer Arif Abdalla Abutalib Al Ali, Moza Mohamed Alechleh Al Ali, Dalia Mahmoud Abdel-Hamid El-Shourbagy, Syed Hammad Hassan Tirmazy, Imran Mirza, Afsheen Raza, Muhammad Farooq Latif, Hemad Yasaei
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引用次数: 0

Abstract

Introduction: Germline BRCA1/2 (gBRCA1/2) variants are strongly associated with hereditary cancers, and screening for these variants in high-risk populations is recommended for personalized management. This study aims to comprehensively characterize gBRCA1/2 variants in cancer and family screening cohorts from the Dubai Emirate, UAE.

Material and methods: A total of 443 patients with breast, ovarian, prostate and pancreatic cancer were tested for gBRCA1/2 variants from 2017 to 2022 using whole-gene sequencing, and data were analysed using variant interpretation and in-silico prediction tools. All BRCA1/2 variants were classified as P/LP or variants of uncertain significance (VUS) according to ACMG guidelines.

Results: In the cancer cohort, 38 out of 306 patients harboured gBRCA1/2 P/LP or VUS variants. Of these, 23 (7.5%) were classified as BRCA1/2 P/LP, while 15 (4.9%) were categorized as VUS. These variants were predominantly observed in estrogen receptor-positive/progesterone receptor-positive (ER + /PR +) and triple-negative breast cancer patients. Common BRCA1 P/LP variants included deletion frameshift variants (c.4065_4068del, c.68_69delAG, c.3228_3229delAG), an insertion frameshift variant (c.1140dup), and a nonsense variant (c.5251C > T). BRCA2 P/LP variants included a nonsense variant (c.5645C > A), a missense variant (c.7007G > A), and a deletion frameshift variant (c.2254_2257del). In the family screening cohort, 14 out of 137 samples harboured BRCA1/2 P/LP orVUS. Of these, five (3.6%) were classified as P/LP, while nine (6.6%) were VUS. Pathogenic BRCA1 variants included deletions (c.4065_4068del, c.3756_3759del) and a nonsense variant (c.5095C > T), while BRCA2 PVs included a deletion frameshift (c.771_775del) and a novel missense variant (c.8377G > A). In both cohorts, novel distinct variants were observed.

Conclusion: gBRCA1/2 variant prevalence in cancer and family screening cohorts can serve as beneficial personalized tool for management and treatment of cancer patients. Larger studies from other emirates of UAE will serve as a foundation for robust risk assessment and implementation of treatment and prevention strategies.

阿联酋人群中癌症和高危家庭筛查队列中BRCA1和BRCA2变异的遗传特征
生殖系BRCA1/2 (gBRCA1/2)变异与遗传性癌症密切相关,建议在高危人群中筛查这些变异以进行个性化管理。本研究旨在全面表征来自阿联酋迪拜酋长国的癌症和家庭筛查队列中的gBRCA1/2变异。材料和方法:使用全基因测序技术对2017年至2022年443例乳腺癌、卵巢癌、前列腺癌和胰腺癌患者进行gBRCA1/2变异检测,并使用变异解释和计算机预测工具对数据进行分析。根据ACMG指南,所有BRCA1/2变异被分类为P/LP或不确定意义变异(VUS)。结果:在癌症队列中,306例患者中有38例携带gBRCA1/2 P/LP或VUS变体。其中,23例(7.5%)被归类为BRCA1/2 P/LP, 15例(4.9%)被归类为VUS。这些变异主要见于雌激素受体阳性/孕激素受体阳性(ER + /PR +)和三阴性乳腺癌患者。常见的BRCA1 P/LP变体包括删除移码变体(c.4065_4068del, c.68_69delAG, c.3228_3229delAG),插入移码变体(c.1140dup)和无义变体(c.5251C > T)。BRCA2 P/LP变体包括一个无义变体(c.5645C > a),一个错义变体(c.7007G > a)和一个删除移码变体(c.2254_2257del)。在家庭筛查队列中,137个样本中有14个携带BRCA1/2 P/LP或vus。其中5例(3.6%)为P/LP, 9例(6.6%)为VUS。致病性BRCA1变异包括缺失(c.4065_4068del, c.3756_3759del)和无义变异(c.5095C > T),而BRCA2 PVs包括缺失移码(c.771_775del)和新的错义变异(c.8377G > a)。在这两个队列中,观察到新的明显变异。结论:gBRCA1/2变异在癌症中的患病率和家庭筛查队列可以作为癌症患者管理和治疗的有益的个性化工具。来自阿联酋其他酋长国的更大规模的研究将作为强有力的风险评估和实施治疗和预防战略的基础。
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来源期刊
CiteScore
4.00
自引率
2.80%
发文量
577
审稿时长
2 months
期刊介绍: The "Journal of Cancer Research and Clinical Oncology" publishes significant and up-to-date articles within the fields of experimental and clinical oncology. The journal, which is chiefly devoted to Original papers, also includes Reviews as well as Editorials and Guest editorials on current, controversial topics. The section Letters to the editors provides a forum for a rapid exchange of comments and information concerning previously published papers and topics of current interest. Meeting reports provide current information on the latest results presented at important congresses. The following fields are covered: carcinogenesis - etiology, mechanisms; molecular biology; recent developments in tumor therapy; general diagnosis; laboratory diagnosis; diagnostic and experimental pathology; oncologic surgery; and epidemiology.
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