Pim kinases in hematological malignancies: where are we now and where are we going?

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作者
Patrizia Mondello
Salvatore Cuzzocrea
Michael Mian
机构
[1] University of Messina,Department of Human Pathology
[2] University of Messina,Department of Biological and Environmental Sciences
[3] Hospital S. Maurizio,Department of Hematology
[4] Medical University Innsbruck,Department of Internal Medicine V, Hematology & Oncology
关键词
Pim kinases; Target therapy; Hematologic malignancies; Pim inhibitors;
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摘要
The proviral insertion in murine (PIM) lymphoma proteins are a serine/threonine kinase family composed of three isoformes: Pim-1, Pim-2 and Pim-3. They play a critical role in the control of cell proliferation, survival, homing and migration. Recently, overexpression of Pim kinases has been reported in human tumors, mainly in hematologic malignancies. In vitro and in vivo studies have confirmed their oncogenic potential. Indeed, PIM kinases have shown to be involved in tumorgenesis, to enhance tumor growth and to induce chemo-resistance, which is why they have become an attractive therapeutic target for cancer therapy. Novel molecules inhibiting Pim kinases have been evaluated in preclinical studies, demonstrating to be effective and with a favorable toxicity profile. Given the promising results, some of these compounds are currently under investigation in clinical trials. Herein, we provide an overview of the biological activity of PIM-kinases, their role in hematologic malignancies and future therapeutic opportunities.
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