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The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer.
Zogopoulos, George; Rothenmund, Heidi; Eppel, Ayelet; Ash, Colleen; Akbari, Mohammad Reza; Hedley, David; Narod, Steven A; Gallinger, Steven.
Affiliation
  • Zogopoulos G; Sam Minuk Cancer Genetics and Biomarker Laboratories, Samuel Lunenfeld Research Institute, Toronto, Ontario, Canada.
Hum Genet ; 121(5): 635-7, 2007 Jun.
Article in En | MEDLINE | ID: mdl-17415588
The P239S palladin variant has recently been suggested to play a role in hereditary pancreatic cancer. We estimated the contribution of the P239S variant, and surrounding sequence, to familial and early-onset pancreatic cancer. The P239S germline variant was identified in one of 84 high-risk cases and one of 555 controls. The case reported an elderly relative with pancreas cancer. We conclude that this variant does not appear to account for a significant fraction of hereditary or early-onset pancreas cancer.
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Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Phosphoproteins / Genetic Predisposition to Disease / Cytoskeletal Proteins Limits: Aged / Humans / Male Language: En Journal: Hum Genet Year: 2007 Type: Article Affiliation country: Canada
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Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Phosphoproteins / Genetic Predisposition to Disease / Cytoskeletal Proteins Limits: Aged / Humans / Male Language: En Journal: Hum Genet Year: 2007 Type: Article Affiliation country: Canada