Hematology Xagena

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Xagena Newsletter
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Chronic myelogenous leukaemia: activation of LYN kinase is associated with resistance to Glivec

Activation of LYN kinase is associated with resistance to Imatinib ( Gleevec, Glivec ) in patients with chronic myelogenous leukemia ( CML ).

Imatinib is the standard therapy for newly diagnosed CML patients. However, some patients develop resistance to the drug over time. In some patients, resistance develops in response to mutations in the BCR-ABL gene. In other cases, though, researchers find no mutations to explain the resistance. Previous work by Nicholas Donato, of the University of Michigan Comprehensive Cancer Center in Ann Arbor and others suggested that one possible mechanism of this mutation-negative resistance is the activation of LYN kinase, which is normally controlled by BCR-ABL in CML cells.

In the current study, Donato and colleagues have expanded that work and examined the impact of overexpression and gene silencing of LYN kinase in CML cell lines treated with Imatinib. They also determined the level of LYN activation in samples from 12 Imatinib-resistant patients who lacked BCR-ABL mutations and 6 patients whose tumor cells were sensitive to the drug but who were unable to tolerate its side effects.

They found that overexpression and activation of LYN kinase was associated with Imatinib resistance in both cell lines and patient samples. Moreover, when they treated these cells with Imatinib, they saw that BCR-ABL activity was suppressed as happens in CML cells sensitive to the drug, but LYN activation was not suppressed. When the researchers blocked expression of the LYN gene in the resistant cells, they restored Imatinib responsiveness and triggered cell death.

These studies expand the spectrum of cellular changes that occur during Imatinib therapy beyond outgrowth of cells with BCR-ABL point mutations and support the use of other tyrosine kinase inhibitors to treat a broad spectrum of Imatinib-resistant CML patients. ( Xagena )

Source: Journal of the National Cancer Institute, 2008