Evidence map›Paper›PMID 38707742›Full record

ArticleCancer diagnosis & prognosis

High Frequency of BRCA2 c.5576_5579del Carriers in Kakogawa, Japan.

Haruna Nakamura, Sachiko Mizumoto, Hirokazu Tanino, Yui Niwa, Mitsutoshi Ogino, Yoko Sakoda, Kazuhiko Tsuchiya, Seishi Kono, Muneharu Konishi, Sayaka Ueno and 1 more

Abstract read
In one paragraph

Article in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Haruna NakamuraDepartment of Breast Surgery, Kakogawa Central City Hospital, Kakogawa, Japan.
Sachiko MizumotoDivision of Breast and Endocrine Surgery, Graduate School of Medicine, Kobe University, Kobe, Japan.
Hirokazu TaninoDepartment of Thoracic and Cardiovascular Surgery, Wakayama Medical University, Wakayama, Japan.
Yui NiwaDepartment of Clinical Genetics, Kobe University Hospital, Kobe, Japan.
Mitsutoshi OginoDepartment of Breast Surgery, Kakogawa Central City Hospital, Kakogawa, Japan.
Yoko SakodaDepartment of Breast Surgery, Kakogawa Central City Hospital, Kakogawa, Japan.
Kazuhiko TsuchiyaDepartment of Breast Surgery, Kakogawa Central City Hospital, Kakogawa, Japan.
Seishi KonoDepartment of Breast Surgery, Hyogo Prefectural Harima-Himeji General Medical Center, Himeji, Japan.
Muneharu KonishiDepartment of Surgery, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.
Sayaka UenoDepartment of Genomic Medicine, School of Medicine, Fujita Health University, Toyoake, Japan.
Tomonari KunihisaDivision of Breast and Endocrine Surgery, Graduate School of Medicine, Kobe University, Kobe, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: Certain germline pathogenic variants (PVs), known as founder mutations, have been frequently observed in specific regions and ethnic groups. In Japan, several pathogenic variants of BRCA1/2 have been identified as founder mutations, with their distribution varying across different regions. This retrospective study aimed to further investigate the detailed distribution and correlation between genotype and clinical features among breast cancer patients. Patients and Methods: This study was conducted at Kobe University Hospital and three collaborating institutions. It included breast cancer patients who underwent BRCA1/2 genetic testing between July 1, 2018, and March 31, 2021, and were found to have germline PVs. Clinical characteristics and breast cancer subtypes were compared between carriers of BRCA2 c.5576_5579del and those with other PVs. Additionally, the detection rate of BRCA2 c.5576_5579del was compared with that observed in a previous report. Results: A total of 38 breast cancer patients were included; PVs in BRCA1 and BRCA2 were detected in 12 and 26 patients, respectively, 12 of whom were BRCA2 c.5576_5579del carriers. BRCA2 c.5576_5579del carriers were more likely to develop triple negative breast cancers among all BRCA2 PV carriers. BRCA2 c.5576_5579del accounted for 30.8% of the PVs detected, with a particularly high frequency of 72.7% at Kakogawa Central City Hospital. Conclusion: BRCA2 c.5576_5579del was detected with a particularly high frequency in Hyogo Prefecture, especially in Kakogawa city. In the future, a survey of the distribution of the BRCA2 c.5576_5579del carriers may provide more clarity regarding their localization.

Indexed as

BRCA2 c5576_5579delBreast cancerfounder mutationhereditary breast and ovarian cancerJapan

Identifiers

PMID38707742
PMCPMC11062150

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