Literature DB >> 20367983

Mutation analysis in a Chinese family with multiple endocrine neoplasia type 1.

Bing-bing Zha1, Wang Liang, Jun Liu, Juan Cheng, Xiao-wu Hong, Jing Liu, Yi-ming Li, Duan Ma.   

Abstract

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome which is caused by germline mutations of the tumor suppressor gene MEN1. This study aimed to identify mutations in a Chinese pedigree with MEN1.
METHODS: A large Chinese family with MEN1 was collected. All of the coded regions and their adjacent sequences of the MEN1 gene were amplified and sequenced.
RESULTS: In this family, a heterozygous cytosine insertion in exon 10 (c.1546_1547insC) inducing a frame shift mutation of MEN1 was found in the proband and the other two suffering members of his family. This mutation was linked to a novel single nucleotide polymorphism (SNP) in intron 3 (IVS3 + 18C > T).
CONCLUSIONS: The mutation in exon 10 of MEN1 gene might induce development of parathyroid hyperplasia and pituitary adenoma and cosegregate with MEN1 syndrome. The significance of the new found IVS3 + 18C > T of MEN1 needs a further investigation.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20367983

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  2 in total

1.  A novel intronic mutation and a missense mutation of MEN1 identified in two Chinese families with multiple endocrine neoplasia type 1.

Authors:  B Han; Z Y Song; J J Wu; W Liu; B L Liu; X P Ye; X Chen; C M Pan; H Y Xu; L Li; H Zhu; Y L Lu; W L Wu; M D Chen; H D Song; J Qiao
Journal:  J Endocrinol Invest       Date:  2012-04-05       Impact factor: 4.256

2.  Multiple endocrine neoplasia type 1: a new germline "homozygous" variant (c.201delC) caused by detection errors.

Authors:  Fan Zhang; Xiaohui Yu; Xiaoli Wang; Hua Shao
Journal:  Hered Cancer Clin Pract       Date:  2022-03-07       Impact factor: 2.857

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.