Pregled bibliografske jedinice broj: 845596
Standardization of molecular monitoring of bcr-abl fusion transcript according to International Scale
Standardization of molecular monitoring of bcr-abl fusion transcript according to International Scale // Biochemia Medica
Zagreb, 2009. str. 143-143 (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 845596 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Standardization of molecular monitoring of bcr-abl fusion transcript according to International Scale
Autori
Horvat, Ivana ; Radić Antolic, Margareta ; Sertić, Dubravka ; Müller, Martin ; Zadro, Renata
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Biochemia Medica
/ - Zagreb, 2009, 143-143
Skup
6. hrvatski kongres medicinskih biokemičara s međunarnodnim sudjelovanjem
Mjesto i datum
Supetar, Hrvatska, 30.09.2009. - 04.10.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
bcr-abl fusion transcript; International Scale; standardization
Sažetak
Introduction: The most frequent method for monitoring therapy in chronic myeloid leukemia patients was qualitative PCR. Development of quantitative real-time PCR enables nowadays relative bcr-abl quantification. The result depends on the probe and housekeeping gene selection as well as in the standards used. For this reason the subproject “Molecular Monitoring“ within the European Leukemia Net intends to standardize the results obtained in different laboratories. Materials and methods:The aim of the study was to prepare 30 RNA samples that homogenously cover a range of > 3 logs between 0.001 and 10% bcr-abl, to perform the quantification by the method routinely used in laboratory and to send the same samples to the reference laboratory of the Mannheim University Hospital in order to obtain conversion factor for expression of results according to International Scale (IS). The procedure started with the reception of 4 lysates with different dilutions of bcr-abl positive WBC in healthy donors WBC from reference laboratory. Results: Quantification of bcr-abl was performed by the method routinely used in laboratory and the results sent to reference laboratory revealed the preliminary conversion factor of 0.7830. Next, 30 RNA samples were prepared in 6 aliquots, 2 x 107 WBC each. Bcr-abl quantification was performed in 3 aliquots. Other 3 aliquots together with the obtained results were sent to the reference laboratory where the same procedure was repeated. Comparison of results from both centers revealed the final conversion factor of 0.3911 that generates the results according to IS. Conclusion: Standardization enables the expression of results according to IS and comparability of results within institutions. Monitoring of dynamics of the change in bcr-abl fusion transcript quantity enables proper disease monitoring and decision in treatment options.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Medicinski fakultet, Zagreb
Profili:
Renata Zadro
(autor)
Dubravka Sertić
(autor)
Ivana Horvat
(autor)
Margareta Radić Antolic
(autor)