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No evidence for germline mutations of the LKB1/STK11 gene in familial pancreatic carcinoma
- Source :
- Cancer letters. 214(1)
- Publication Year :
- 2004
-
Abstract
- Familial pancreatic cancer (FPC) (approximately 3% of all cases) has not been linked to defects in any specific gene. Germline inactivation of the gene LKB1/STK11 have been shown to cause Peutz-Jeghers syndrome (PJS) associated with a approximately 100-fold higher risk for the development of pancreatic cancer. We have analysed 39 index patients from European FPC families for mutations of LKB1/STK11 by sequencing of their DNA. No germline mutation was found within the complete coding region. Therefore, our results indicate that LKB1/STK11 is not altered in the germline of patients with hereditary pancreatic cancer.
- Subjects :
- Adult
Male
congenital, hereditary, and neonatal diseases and abnormalities
Cancer Research
DNA Mutational Analysis
STK11
Biology
Protein Serine-Threonine Kinases
Germline
Germline mutation
AMP-Activated Protein Kinase Kinases
Pancreatic cancer
medicine
Coding region
Humans
Genetic Predisposition to Disease
skin and connective tissue diseases
Gene
Germ-Line Mutation
Aged
Genetics
Carcinoma
Cancer
Middle Aged
medicine.disease
Pedigree
Pancreatic Neoplasms
medicine.anatomical_structure
Oncology
Cancer research
Female
Pancreas
Subjects
Details
- ISSN :
- 03043835
- Volume :
- 214
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Cancer letters
- Accession number :
- edsair.doi.dedup.....a4f94c200645bf7b9c0ba7bf228ead88