1. A novel Lynch syndrome pedigree bearing germ-line MSH2 missense mutation c.1808A>T (Asp603Val)
- Author
-
Katsunori Iijima, Tatsuro Yamaguchi, Risako Sekine, Koji Fukuda, Kazuhiro Shimazu, Daiki Taguchi, Yusato Suzuki, Daisuke Nakano, Hiroshi Nanjyo, Hiroyuki Shibata, and Taichi Yoshida
- Subjects
Male ,Proband ,congenital, hereditary, and neonatal diseases and abnormalities ,Cancer Research ,Mutation, Missense ,Mutant protein ,Humans ,Medicine ,Missense mutation ,Radiology, Nuclear Medicine and imaging ,Germ-Line Mutation ,business.industry ,Endometrial cancer ,nutritional and metabolic diseases ,Cancer ,General Medicine ,Middle Aged ,medicine.disease ,Colorectal Neoplasms, Hereditary Nonpolyposis ,digestive system diseases ,Lynch syndrome ,Pedigree ,Germ Cells ,MutS Homolog 2 Protein ,Oncology ,MSH2 ,Mutation (genetic algorithm) ,Cancer research ,Female ,MutL Protein Homolog 1 ,business - Abstract
We report the first pedigree of Lynch syndrome bearing a germ-line MSH2 missense mutation c.1808A>T (Asp603Val). Until now, this missense mutation, in exon 12 of MSH2, was identified as a variant of unknown significance in the International Society for Gastrointestinal Hereditary Tumours database. In vitro induction mutagenesis experiments indicated that the MSH2 mutant protein (Asp603Val) is easily degraded in embryonic stem cells, albeit there is no clinical information concerning this mutant. Our pedigree includes four patients with Lynch syndrome-associated malignancies and clinically matches the Amsterdam II criteria. The proband, a female, first had an endometrial cancer at the age of 49 and then mantle cell lymphoma, colonic and gastric adenocarcinomas and neuroendocrine carcinoma, successively. Her mother also had Lynch syndrome-associated malignancies, including colonic, uterine and gastric cancers, and her elder son had rectal cancer. In the germline of the proband and her son, an MSH2 missense mutation c.1808A>T was discovered. Immunohistochemical analyses indicated that the expression of the MSH2 protein was decreased in the tumors, such as gastric cancer and neuroendocrine carcinoma, due to the missense mutation c.1808A>T. This study showed that the MSH2 missense mutation c.1808A>T (Asp603Val) is a likely pathogenic mutation and is responsible for typical Lynch syndrome-associated malignancies, including neuroendocrine carcinoma.
- Published
- 2021
- Full Text
- View/download PDF