Pregled bibliografske jedinice broj: 31209
Detection of TCR-gamma gene rearrangement in acute lymphoblastic leukemia by multiplex PCR
Detection of TCR-gamma gene rearrangement in acute lymphoblastic leukemia by multiplex PCR // V. seminar New Trends in the Treatment of Acute Leukemia / Mrsić, Mirando ; Labar, Boris (ur.).
Zagreb: University Hospital Rebro Zagreb and European School of Oncology, 1998. str. 21-21 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 31209 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Detection of TCR-gamma gene rearrangement in acute lymphoblastic leukemia by multiplex PCR
Autori
Selak, Nives ; Zadro, Renata ; Aurer, Igor ; Mrsić, Mirando ; Labar, Boris ; Stavljenić-Rukavina, Ana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
V. seminar New Trends in the Treatment of Acute Leukemia
/ Mrsić, Mirando ; Labar, Boris - Zagreb : University Hospital Rebro Zagreb and European School of Oncology, 1998, 21-21
Skup
V. seminar New Trends in the Treatment of Acute Leukemia
Mjesto i datum
Dubrovnik, Hrvatska, 06.09.1998. - 09.09.1998
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
PCR; TCR-gamma; acute leukemia
Sažetak
Detection of clonal antigen receptor gene rearrangement can be used to determine lineage of lymphoproliferation. As in T-cell malignancies there is no immunopathological equivalent to monoclonal surface immunoglobulin like in B-cell neoplasms, molecular genetic studies are especially important. In our study we have tested a series of patients with the diagnosis of acute lymphoblastic leukemia (ALL) as well as normal individuals for the T-cell receptor gamma-chain gene rearrangement. Genomic DNA was isolated from peripheral blood or bone marrow of 20 ALL patients as well as from peripheral blood of 20 healthy individuals according to standard procedures. Four out of seven patients showed the exclusive presence of a single TCR-gamma gene rearrangement. Two patients exhibited two rearranged TCR-gamma genes, while in one patient positive reaction was obtained with three VJ primer combinations producing only two bands on agarose gels. Molecular analysis of rearranged T-cell receptor genes by multiplex PCR represents a useful and rapid tool for confirming diagnosis, to determine the extent of disease and to monitor the response to therapy.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti