Hereditary pancreatitis and familial pancreatic cancer

被引:33
作者
Finch, MD
Howes, N
Ellis, I
Mountford, R
Sutton, R
Raraty, M
Neoptolemos, JP
机构
[1] Univ Liverpool, Dept Surg, Liverpool L69 3GA, Merseyside, England
[2] Univ Liverpool, Dept Clin Genet, Liverpool L69 3GA, Merseyside, England
[3] Univ Liverpool, Dept Mol Genet, Liverpool L69 3GA, Merseyside, England
关键词
cationic trypsinogen; chronic pancreatitis; secondary screening; genetics;
D O I
10.1159/000201502
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Important advances in the understanding of pancreatic diseases have taken place through the application of molecular methods in the study of the inherited form of pancreatitis and pancreas cancer. Mutations of the cationic trypsinogen gene have been found to be causative for hereditary pancreatitis with important implications for the molecular pathogenesis of acute and chronic pancreatitis. A variety of cancer syndromes involving the PI6 and BRCA2 genes, for example, also lead to pancreatic cancer, but the gene responsible for familial pancreatic cancer has not been identified so far. The establishment of a European Registry of Hereditary Pancreatitis and Pancreatic Cancer (EUROPAC) will facilitate future developments.
引用
收藏
页码:564 / 569
页数:6
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