IS P-GLYCOPROTEIN A SUFFICIENT MARKER FOR MULTIDRUG-RESISTANCE IN-VIVO - IMMUNOHISTOCHEMICAL STAINING FOR P-GLYCOPROTEIN IN CHILDREN AND ADULT LEUKEMIA - CORRELATION WITH CLINICAL OUTCOME

Citation
S. Kaczorowski et al., IS P-GLYCOPROTEIN A SUFFICIENT MARKER FOR MULTIDRUG-RESISTANCE IN-VIVO - IMMUNOHISTOCHEMICAL STAINING FOR P-GLYCOPROTEIN IN CHILDREN AND ADULT LEUKEMIA - CORRELATION WITH CLINICAL OUTCOME, Leukemia & lymphoma, 20(1-2), 1995, pp. 143-152
Citations number
52
Categorie Soggetti
Hematology
Journal title
ISSN journal
10428194
Volume
20
Issue
1-2
Year of publication
1995
Pages
143 - 152
Database
ISI
SICI code
1042-8194(1995)20:1-2<143:IPASMF>2.0.ZU;2-3
Abstract
Seventy-eight patients: 45 children, 33 adults and 27 normal healthy d onors were enrolled in the study. Expression of P-glycoprotein (P-gp) was evaluated with three monoclonal antibodies (MAb's) directed to int ra-(C219, JSB-1) and extra-cellular (MRK-16) epitopes of P-gp and immu nocytochemical (IC) APAAP staining method, Twenty-seven healthy donors peripheral blood mononuclear cells (PBMC) were investigated by means of IC and FACScan analysis. Positive staining for P-gp was detected in 31% children's and 33% adults' leukemia samples. No reactivity of thr ee MAb's was observed with peripheral blood mononuclear cells (PBMC) b y means of IC. Flow cytometry analysis with C219 MAb revealed staining for P-gp present on sub-population of lymphocytes and monocytes. P-gp (+) as well as P-gp (-) cases were compared in respect to clinical ou tcome, FAB classification and blood group. Complete remission (CR) was achieved in 12/14 (85%) children's and 9/11 (81%) adults' P-gp (+) le ukemia cases. Within the P-gp (-) leukemia cases CR was observed in 24 /29 (82%) and 18/22 (81%), respectively. Partial remission, relapse, r esistance and death were noticed in 14% children's and 18% adults' P-g p (+) samples. In P-gp (-) cases these parameters were observed in 17% and 18%, respectively. These results raise the question whether the e xpression of P-gp can be used as single prognostic marker to detect mu ltidrug resistance (MDR phenomenon) in vivo?