Abstract | BACKGROUND AND METHODS: Philadelphia (Ph) positive chronic myeloid leukemia (CML) cannot be induced into a true remission with conventional chemotherapy. Blast cells and precursors obtained from 51 Ph+ CML cases were assayed for expression of the multidrug resistance (MDR)-associated glycoprotein (p170) by immunocytochemistry (APAAP) with the MRK-16 monoclonal antibody. RESULTS AND CONCLUSIONS: Positive cells were found in 11/17 cases in chronic phase (65%), in 4/8 cases in accelerated phase, and in 23/26 cases in blastic phase (89%). The proportion of positive cells, which ranged between less than 1% and 95%, was higher in blastic phase (mean 32 +/- 29.9) than in chronic phase (mean 3 +/- 5.3) (p = 0.006). These findings show that p170 overexpression is common in Ph+ CML, especially after progression to blastic phase, and suggest that p170-related MDR may contribute significantly to treatment failure.
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Authors | A Michelutti, M Michieli, D Damiani, C Melli, A Geromin, D Russo, R Fanin, M Baccarani |
Journal | Haematologica
(Haematologica)
1994 May-Jun
Vol. 79
Issue 3
Pg. 200-4
ISSN: 0390-6078 [Print] Italy |
PMID | 7926967
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- ATP Binding Cassette Transporter, Subfamily B, Member 1
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Topics |
- ATP Binding Cassette Transporter, Subfamily B, Member 1
(biosynthesis)
- Drug Resistance, Multiple
(physiology)
- Humans
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
(blood)
- Molecular Weight
- Retrospective Studies
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