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J Korean Neurol Assoc. 2005;23(6):784-791.
- Identification of a Novel p53 Intronic Mutation in Cowden's Disease
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Hee-Jung Song
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Department of Neurology, Anseong St. Mary's Hospital, Ansan;
Department of Biochemistry and Molecular Biology, Eulji University School of Medicinea, Daejeon;
Department of Neurology, Chungnam National University Hospitalb, Daejeon, Korea
- p53 유전자의 돌연변이가 발견된 Cowden병
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송희정, 백행운a 정성해b 김지선b 김재문b
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안성성모병원 신경과, 을지의과대학교 생화학-분자생물학교실a, 충남대학교 의과대학 신경과학교실b
- Abstract
- Background
Cowden's disease is a rare disorder, characterized by a multiple harmatoma-neoplasia syndrome. Germline mutations in the Phosphatase and Tensin homolog (PTEN) gene have been identified in some individuals with Cowden's disease. The present study aimed to evaluate abnormalities of PTEN and p53 genes in a patient with Cowden's disease.
Methods
Eleven family members including the patient with Cowden's disease were examined in this study. Sequencing analyses were performed on these people and on the normal control group to identify mutation in PTEN and p53 genes.
Results
DNA sequencing of PTEN gene showed no mutation in the patient and the family members. The G to C germline mutation was identified only in the patient of Cowden disease at 38th base of intron 2 of p53 gene.
Conclusions
Although the exact role of mutation in p53 gene was not identified in the Cowden's disease, the conformational change of the gene would result in the dysfunction of the tumor suppressor effect of p53 gene. Otherwise, an epigenetic silencing can be a mechanism of disease development in a patient without genetic abnormality.KeyWords:Cowden's disease, PTEN, p53, Mutation
Keywords :
- 초록
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