Pregled bibliografske jedinice broj: 493738
Low levels of residual disease in CML are associated with low molecular level of oncogene BCR-ABL chimeric genes and low Pgp activity
Low levels of residual disease in CML are associated with low molecular level of oncogene BCR-ABL chimeric genes and low Pgp activity // Annual Meeting of the Austrian Sociezy for Allergology and Immunology (ÖGAI) in co-operation with the national Societies of Croatia, Czech Republic, Hungary, Slovakia and Slovenia
Beč: ÖGAI, Österreichische Gesellschaft für Allergologie und Immunologie, 2010. str. 45-45 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 493738 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Low levels of residual disease in CML are associated with low molecular level of oncogene BCR-ABL chimeric genes and low Pgp activity
Autori
Savić, Ana ; Ajduković, Radmila ; Marušić-Vrsalović, Maruška ; Livun, Ana ; Bendelja, Krešo ; Svoboda-Beusan, Ivna
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Annual Meeting of the Austrian Sociezy for Allergology and Immunology (ÖGAI) in co-operation with the national Societies of Croatia, Czech Republic, Hungary, Slovakia and Slovenia
/ - Beč : ÖGAI, Österreichische Gesellschaft für Allergologie und Immunologie, 2010, 45-45
Skup
Annual Meeting of the Austrian Society for Allergology and Immunology (ŌGAI)
Mjesto i datum
Beč, Austrija, 03.12.2010. - 05.12.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Multidrug resistance; Pgp; CML
Sažetak
Imatinib mesylate (IM) therapy in chronic myelogenous leukemia (CML) patients can induce multidrug resistance (MDR) which is associated with poor treatment outcome. The best known resistance mechanism is associated with activity of P-glycoprotein (Pgp) membrane transporter. Twenty five patients were diagnosed with chronic phase CML at Clinical Hospital Dubrava and were monitored over the period of six years. In order to elucidate the mechanism of MDR induction we evaluated the effect of IM monotherapy by comparing the variations in the activity of Pgp pump with molecular response kinetics. Pgp activity of bone marrow and peripheral blood cells was assessed by flow cytometry and the results were expressed as the ratio of minimal and real pump activity . The kinetics of molecular response was measured by qRT-PCR method and the results were divided in 4 groups: R1= complete molecular remission, R2= major molecular response (MMR), R3= minimal molecular response (mMR) and R4= without response. Nine patients were in R1 (36, 0%), 2 in R2 (8, 0%), 4 in R3 (16, 0%) while 4 patients were in group R4. Two patients entered the study recently and are not evaluable . All R1 patients had low Pgp activity whereas the greatest activity increase was observed in R4 group. These results confirm the link between Pgp activity and molecular response. We conclude that rhodamine test of Pgp activity has clinical value and correlates with the BCR/ABL oncogene changes during therapy with IM, indicating that elevated Pgp activity adds as unfavorable prognostic factor.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
021-0212432-2436 - Rezistencija na lijekove (Svoboda-Beusan, Ivna, MZOS ) ( CroRIS)
Ustanove:
Imunološki zavod d.d.,
Klinička bolnica "Dubrava"
Profili:
Krešo Bendelja
(autor)
Ana Savić Mlakar
(autor)
Ana Livun
(autor)
Maruška Marušić Vrsalović
(autor)
Ivna Svoboda-Beusan
(autor)