Pregled bibliografske jedinice broj: 62862
CYP2D6 *3 and *4 polymorphism in cancer patients : a study on breast cancer and head and neck cancer
CYP2D6 *3 and *4 polymorphism in cancer patients : a study on breast cancer and head and neck cancer // Clin Chem Lab Med 1999 ; vol 37 : Abstracts volume, Special supplement / Siest, Gerard (ur.).
Milano: Walter de Gruyter, 1999. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 62862 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
CYP2D6 *3 and *4 polymorphism in cancer patients : a study on breast cancer and head and neck cancer
Autori
Štefanović, Mario ; Ivanišević, Ana-Maria ; Topić, Elizabeta ; Petrinović, Rajka ; Orešić, V. ; Turić, Marko ; Čurčić, Ivica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Clin Chem Lab Med 1999 ; vol 37 : Abstracts volume, Special supplement
/ Siest, Gerard - Milano : Walter de Gruyter, 1999
Skup
IFCC-World Lab, 17th International and 13th European congress of Clinical Chemistry and Laboratory Medicine
Mjesto i datum
Firenca, Italija, 06.06.1999. - 11.06.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
CYP2D6 polymorphism; cancer
Sažetak
We investigated the association between the most common Cytochrome P450 CYP2D6 null alleles (CYP2D6*3 and CYP2D6*4) in two different tumor types: breast cancer (BC) and head and neck cancer (HNC). Genotyping was performed in 53 controls, 39 HNC, and 53 BC female patients by PCR-SSCP on whole blood DNA. Study results showed allelic frequencies for *3 and *4 alleles in controls to be 0.9% and 17%, respectively ; among them 1.9% *3 and 29.5% *4 heterozygotes, and 2.3% *4 homozygotes. *3 homozygote was not identified among controls. In HNC patients, allelic frequencies for *3 and *4 alleles were 1.3% and 21.9%, respectively ; out of which 2.6% and 43.8% were heterozygotes for *3 and *4 allele, respectively. We observed no homozygotes. Among BC patients, no *3 allele was found, whereas the frequency of *4 allele was 20.7%. There were 26.8% of heterozygotes and 7.3% of homozygotes for *4 allele. The difference in *4 genotypes comparing the patients to controls was: p=0.05(Chi) for HNC patients and p=0.22(Chi) for BC patients. To confirm our findings suggesting that CYP2D6*4 allele could be a contributory factor for the development of different tumors, further study on larger groups is needed.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
134003
Ustanove:
KBC "Sestre Milosrdnice"
Profili:
Mario Štefanović
(autor)
Ivica Čurčić
(autor)
Elizabeta Topić
(autor)
Rajka Petrinović
(autor)
Marko Turić
(autor)