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Blood Cancer J. 2015 Jul 17;5:e325. doi: 10.1038/bcj.2015.46.

Targeting the Pim kinases in multiple myeloma.

Author information

1
Apoptosis Research Centre, National University of Ireland Galway and Department of Haematology, Galway University Hospital, Galway, Ireland.
2
Apoptosis Research Centre, National University of Ireland Galway, Galway, Ireland.
3
Max-Eder Unit "Experimental Therapies for Hematologic Malignancies", Department of Medicine V, Heidelberg University Medical Center, Im Neuenheimer Feld 410 and German Cancer Research Centre (DKFZ), Heidelberg, Germany.

Abstract

Multiple myeloma (MM) is a plasma cell malignancy that remains incurable. Novel treatment strategies to improve survival are urgently required. The Pims are a small family of serine/threonine kinases with increased expression across the hematological malignancies. Pim-2 shows highest expression in MM and constitutes a promising therapeutic target. It is upregulated by the bone marrow microenvironment to mediate proliferation and promote MM survival. Pim-2 also has a key role in the bone destruction typically seen in MM. Additional putative roles of the Pim kinases in MM include trafficking of malignant cells, promoting oncogenic signaling in the hypoxic bone marrow microenvironment and mediating resistance to therapy. A number of Pim inhibitors are now under development with lead compounds entering the clinic. The ATP-competitive Pim inhibitor LGH447 has recently been reported to have single agent activity in MM. It is anticipated that Pim inhibition will be of clinical benefit in combination with standard treatments and/or with novel drugs targeting other survival pathways in MM.

PMID:
26186558
PMCID:
PMC4526774
DOI:
10.1038/bcj.2015.46
[Indexed for MEDLINE]
Free PMC Article

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