Abstract
Smac mimetics (SMs), a class of drugs that can promote tumor cell death, represent a potential therapeutic strategy for the treatment of cancer. In this issue of Cancer Cell, Lalaoui et al. (2016) report that SM efficacy can be potently increased by inhibition of the p38α MAPK/MK2 signaling pathway.
Copyright © 2016 Elsevier Inc. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Comment
MeSH terms
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Animals
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Antineoplastic Agents / therapeutic use*
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Humans
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Intracellular Signaling Peptides and Proteins / antagonists & inhibitors*
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Intracellular Signaling Peptides and Proteins / physiology*
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Leukemia / drug therapy*
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Mitochondrial Proteins / physiology*
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Molecular Mimicry*
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Protein Serine-Threonine Kinases / antagonists & inhibitors*
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p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors*
Substances
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Antineoplastic Agents
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Intracellular Signaling Peptides and Proteins
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Mitochondrial Proteins
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Protein Serine-Threonine Kinases
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p38 Mitogen-Activated Protein Kinases