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一项关于新型单核苷酸多态性与男性乳腺癌的机制图谱研究。

A study of mechanistic mapping of novel SNPs to male breast cancer.

机构信息

Department of Human Genetics and Molecular Medicine, Central University of Punjab, Bathinda, 151001, India.

Department of Computational Sciences, Central University of Punjab, Bathinda, 151001, India.

出版信息

Med Oncol. 2019 Jun 15;36(8):70. doi: 10.1007/s12032-019-1290-0.

Abstract

Alterations in BRCA2, PALB2, CHEK2, and p53 genes have been identified for their association with male breast cancer in various studies. The incidence of male breast cancer in India is consistent with its global rate. The present study was carried out with an aim to evaluate the genetic alterations in male breast cancer patients from Malwa region of Punjab, India. Four male breast cancer patients belonging to different families were recruited from Guru Gobind Singh Medical College and Hospital, Faridkot, India. A total of 51 genes reported with implications in the pathogenesis of breast cancer were screened using next generation sequencing. Germline variations were found in BRCA1, BRCA2, PMS2, p53, and PALB2 genes, previously reported to be associated with MBC as well as FBC. In addition to these, 13 novel missense alterations were detected in eight genes including STK11, FZR1, PALB2, BRCA2, NF2, BAP1, BARD1, and CHEK2. Impact of these missense alterations on structure and function of protein was also analyzed through molecular dynamics simulation. Structural analysis of these single nucleotide polymorphisms (SNPs) revealed significant impact on the encoded protein functioning.

摘要

BRCA2、PALB2、CHEK2 和 p53 基因的改变已被确定与各种研究中的男性乳腺癌有关。印度男性乳腺癌的发病率与其全球发病率一致。本研究旨在评估来自印度旁遮普省马尔瓦地区男性乳腺癌患者的遗传改变。从印度法里达巴德的古鲁戈宾德辛格医学院和医院招募了属于不同家庭的 4 名男性乳腺癌患者。使用下一代测序筛选了与乳腺癌发病机制相关的 51 个报告基因。在 BRCA1、BRCA2、PMS2、p53 和 PALB2 基因中发现了种系变异,这些基因先前与 MBC 和 FBC 有关。除了这些,在 8 个基因中检测到 13 个新的错义改变,包括 STK11、FZR1、PALB2、BRCA2、NF2、BAP1、BARD1 和 CHEK2。还通过分子动力学模拟分析了这些错义改变对蛋白质结构和功能的影响。这些单核苷酸多态性(SNP)的结构分析显示对编码蛋白功能有重大影响。

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