Chek2 gene alterations in the forkhead-associated domain, 1100delC and del5395 do not modify the risk of sporadic pancreatic cancer

Beatrice Mohelnikova-Duchonova, Ondrej Havranek, Ivona Hlavata, Lenka Foretova, Zdenek Kleibl, Petr Pohlreich, Pavel Soucek

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Checkpoint kinase 2 gene (CHEK2) alterations increase risk of several cancer types. We analyzed selected CHEK2 alterations in 270 Czech pancreatic cancer patients and in 683 healthy controls. The pancreatic cancer risk was higher in individuals who inherited rare alterations in CHEK2 region involving forkhead-associated domain other than I157T (OR. = 5.14; 95% CI. = 0.94-28.23) but the observed association was non-significant (p= 0.057). The most frequent I157T mutation did not alter the pancreatic cancer risk and neither the followed deletion of 5395 bp nor c.1100delC were found in any of pancreatic cases. We conclude that the I157T, other alterations in its proximity, del5395 and c.1100delC in CHEK2 do not predispose to pancreatic cancer risk in the Czech population.

Original languageEnglish (US)
Pages (from-to)656-658
Number of pages3
JournalCancer Epidemiology
Volume34
Issue number5
DOIs
StatePublished - Oct 2010

Keywords

  • Alterations
  • Checkpoint kinase 2
  • Deletion
  • Pancreatic cancer
  • Risk

ASJC Scopus subject areas

  • Epidemiology
  • Oncology
  • Cancer Research

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