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具有连锁不平衡的BRCA基因中的良性多态性与癌症特征相关。

Benign polymorphisms in the BRCA genes with linkage disequilibrium is associated with cancer characteristics.

作者信息

Lee Kuo-Ting, Chen Dao-Peng, Loh Zhu-Jun, Chung Wei-Pang, Wang Chih-Yang, Chen Pai-Sheng, Cheung Chun Hei Antonio, Chang Chih-Peng, Hsu Hui-Ping

机构信息

Department of Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

Kim Forest Enterprise Co., Ltd., New Taipei, Taiwan.

出版信息

Cancer Sci. 2024 Dec;115(12):3973-3985. doi: 10.1111/cas.16364. Epub 2024 Oct 12.

DOI:10.1111/cas.16364
PMID:39394900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11611775/
Abstract

Germline pathogenic mutation of the BRCA gene increases the prevalence of breast cancer. Reports on the benign variants of BRCA genes are limited. However, the definition of these variants might be altered with the accumulation of clinical evidence. Therefore, in the present study, we focused on benign single nucleotide polymorphisms (SNPs) of BRCA genes. Linkage disequilibrium was calculated from whole genome sequencing of the BRCA genes obtained from 500 healthy controls and 49 breast cancer patients. Sanger sequencing was used to confirm the mutation. The linkage disequilibrium was noted for seven and three SNPs in the BRCA1 and BRCA2 genes, respectively. Breast cancer with BRCA1/2 linkage disequilibrium was not correlated with a personal history of benign diseases or family history of cancer. Nevertheless, breast cancer with BRCA1 linkage disequilibrium was correlated with high tumor-infiltrating lymphocytes and positive extensive intraductal components. The patients with BRCA1 linkage disequilibrium tended to have worse disease-specific survival. Cancers with BRCA2 linkage disequilibrium are associated with a lower ratio of grade III cancer. Moreover, patients with BRCA2 linkage disequilibrium tended to have better overall survival. In conclusion, linkage disequilibrium from benign SNPs of the BRCA genes potentially affects cancer characteristics.

摘要

BRCA基因的种系致病突变会增加乳腺癌的患病率。关于BRCA基因良性变异的报道有限。然而,随着临床证据的积累,这些变异的定义可能会发生改变。因此,在本研究中,我们聚焦于BRCA基因的良性单核苷酸多态性(SNP)。通过对500名健康对照者和49名乳腺癌患者的BRCA基因进行全基因组测序来计算连锁不平衡。采用桑格测序法来确认突变。在BRCA1和BRCA2基因中,分别发现7个和3个SNP存在连锁不平衡。具有BRCA1/2连锁不平衡的乳腺癌与良性疾病个人史或癌症家族史无关。然而,具有BRCA1连锁不平衡的乳腺癌与高肿瘤浸润淋巴细胞和广泛的导管内成分阳性相关。具有BRCA1连锁不平衡的患者疾病特异性生存率往往较差。具有BRCA2连锁不平衡的癌症与III级癌症的比例较低有关。此外,具有BRCA2连锁不平衡的患者总生存率往往较好。总之,BRCA基因良性SNP的连锁不平衡可能会影响癌症特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/3b32bc19682b/CAS-115-3973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/556637e3b77f/CAS-115-3973-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/8460dafb4da3/CAS-115-3973-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/08c6e32b8fcd/CAS-115-3973-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/9eb9a63ae28b/CAS-115-3973-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/786f4bdf0e3f/CAS-115-3973-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/3b32bc19682b/CAS-115-3973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/556637e3b77f/CAS-115-3973-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/8460dafb4da3/CAS-115-3973-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/08c6e32b8fcd/CAS-115-3973-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/9eb9a63ae28b/CAS-115-3973-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/786f4bdf0e3f/CAS-115-3973-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1034/11611775/3b32bc19682b/CAS-115-3973-g001.jpg

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