Publication details

CHEK2 gene alterations in the forkhead-associated domain, 1100delC and del5395 do not modify risk of sporadic pancreatic cancer

Authors

MOHELNÍKOVÁ-DUCHOŇOVÁ B. HAVRÁNEK O. HLAVATA I. FORETOVÁ Lenka KLEIBL Zdeněk POHLREICH Petr SOUCEK Pavel

Year of publication 2010
Type Article in Periodical
Magazine / Source Cancer epidemiology
MU Faculty or unit

Faculty of Medicine

Citation
Doi http://dx.doi.org/10.1016/j.canep.2010.06.008
Field Oncology and hematology
Keywords Checkpoint kinase 2; Alterations; Deletion; Pancreatic cancer; Risk
Description 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% Cl = 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.

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