Short interfering RNA (siRNA) targeting the Lyn kinase induces apoptosis in primary, and drug-resist

Author:  ["Andrzej Ptasznik","Yuji Nakata","Anna Kalota","Stephen G Emerson","Alan M. Gewirtz"]

Publication:  Nature Medicine

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Tags:     Medicine

Abstract

We studied the effects of Lyn ablation on the survival of drug-resistant chronic myelogenous leukemia (CML) blast crisis cells using siRNA. Lyn siRNA reduced Lyn protein in both normal hematopoietic cells and BCR-ABL1-expressing (BCR-ABL1(+)) blasts by 80–95%. Within 48 h, siRNA-treated BCR-ABL1(+) blasts underwent apoptosis, whereas normal cells remained viable. This increased dependence on Lyn signaling for BCR-ABL1(+) blast survival provides the basis for rational treatment of drug-resistant CML blast crisis, particularly when lymphoid in nature.

Cite this article

Ptasznik, A., Nakata, Y., Kalota, A. et al. Short interfering RNA (siRNA) targeting the Lyn kinase induces apoptosis in primary, and drug-resistant, BCR-ABL1(+) leukemia cells. Nat Med 10, 1187–1189 (2004). https://doi.org/10.1038/nm1127

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