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Expression of breast cancer resistance protein in blast cells from patients with acute leukemia

Ross, Douglas D., Karp, Judith E., Chen, Tar T., Doyle, L. Austin·2000·Blood

Abstract

Breast cancer resistance protein (BCRP) is a novel member of the adenosine triphosphate–binding cassette superfamily of transport proteins. Transfection and enforced expression of BCRP in drug-sensitive cells confer resistance to mitoxantrone, doxorubicin, daunorubicin, and topotecan. We studied blast cells from 21 acute leukemia patients (20 acute myeloid leukemia, 1 acute lymphocytic leukemia) for the expression of BCRP mRNA using a quantitative reverse-transcription polymerase chain reaction assay. BCRP mRNA expression varied more than 1000-fold among the samples tested, with low or barely detectable expression in half of the samples. Seven samples (33%) had relatively high expression of BCRP mRNA. High expression of BCRP did not correlate strongly with high expression of P-glycoprotein, suggesting that BCRP may cause resistance to certain antileukemic drugs in P-glycoprotein–negative cases. High expression of BCRP mRNA is sufficiently frequent in AML to warrant more extensive investigations to determine the relation of disease subtype and treatment outcome to BCRP expression and function.

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Metadata

Authors
Ross, D. D., Karp, J. E., Chen, T. T., & Doyle, L. A.
Venue
Blood
Published
2000-07-01
Volume
96
Issue
1
Pages
365-368
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2414957002
Cited by
250
References
0
FWCI
9.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Expression of breast cancer resistance protein in blast cells from patients with acute leukemia. https://app.cochat.ai/papers/10.1182/blood.v96.1.365
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Ross, D. D., Karp, J. E., Chen, T. T., & Doyle, L. A. (2000). Expression of breast cancer resistance protein in blast cells from patients with acute leukemia. Blood. https://doi.org/10.1182/blood.v96.1.365

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.