Pregled bibliografske jedinice broj: 833550
PHARMACOGENOMICS OF ANASTRAZOLE COULD PREDICT INTERPATIENT VARIABILITY IN THE INTENSITY OF ADVERSE EFFECTS
PHARMACOGENOMICS OF ANASTRAZOLE COULD PREDICT INTERPATIENT VARIABILITY IN THE INTENSITY OF ADVERSE EFFECTS // 9th ISABS Conference on Forensic and Anthropologic Genetics and Individualized Medicine
Bol, Hrvatska, 2015. str. 1-1 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 833550 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
PHARMACOGENOMICS OF ANASTRAZOLE COULD PREDICT INTERPATIENT VARIABILITY IN THE INTENSITY OF ADVERSE EFFECTS
Autori
Bojanić, Kristina ; Kizivat, Tomislav ; Kuna, Lucija ; Wagner, Jasenka ; Smolić, Robert ; Božić, Ivana ; Mršo, Margareta ; Raguž-Lučić, Nikola ; Včev, Aleksandar ; Smolić, Martina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
9th ISABS Conference on Forensic and Anthropologic Genetics and Individualized Medicine
Mjesto i datum
Bol, Hrvatska, 22.06.2015. - 26.06.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
anastrozole ; breast cancer ; osteoporosis ; pharmacogenomics
(anastrozole ; breast cancer osteoporosis ; pharmacogenomics)
Sažetak
Anastrozole is a selective competitive aromatase inhibitor (AI) widely used as adjuvant treatment for early stage breast cancer. Phase I metabolism of anastrazole involves N-dealkylation by CYP3A4 and CYP3A5 , whereas phase II predominantly involves glucuronidation by UGT1A4.The most common adverse events of AIs are osteoporosis and musculosceletal events, whereas hepatotoxicity is less frequent.To elucidate genetic polymorphism of enzymes involved in anastrazole metabolism and determine the role of CYP3A4, CYP3A5 and UGT1A4 pharmacogenomics in the interindividual variations in anastrazole metabolism and the intensity of adverse effects. Osteopenia was found in 34% and osteoporosis in 17% of participants. The cumulative incidence of NAFLD was 24.6%in the study group. However, the correlation in the interpatient variability in the intensity of hepatotoxicity or osteoporosis to functional genetic polymorphisms studiedwas not found. The intensity of adverse effects plays an essential part in maintaining patient complience to anastrazole therapy. Functional genetic polymorphisms of enzymes involved in anastrazole metabolism could be correlated to altered aromatase activity, disease prognosis and severity of aromatase inhibitor adverse effects, however large genotyping studies are obligatory.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Osijek
Profili:
Robert Smolić
(autor)
Nikola Raguž-Lučić
(autor)
Ivana Krajina
(autor)
Jasenka Wagner
(autor)
Lucija Kuna Roguljić
(autor)
Tomislav Kizivat
(autor)
Kristina Bojanić
(autor)
Aleksandar Včev
(autor)
Martina Smolić
(autor)