| Literature DB >> 28800129 |
Kerstin Brinkmann1,2, Stephanie Grabow1,2, Craig D Hyland1, Charis E Teh1,2, Warren S Alexander1,2, Marco J Herold1,2, Andreas Strasser1,2.
Abstract
A common therapeutic strategy to combat human cancer is the use of combinations of drugs, each targeting different cellular processes or vulnerabilities. Recent studies suggest that addition of an MCL-1 inhibitor to such anticancer drug treatments could be an attractive therapeutic strategy. Thus, it is of great interest to understand whether combinations of conventional anticancer drugs with an MCL-1 inhibitor will be tolerable and efficacious. In order to mimic the combination of MCL-1 inhibition with other cancer therapeutics, we treated Mcl-1+/- heterozygous mice, which have a ~50% reduction in MCL-1 protein in their cells, with a broad range of chemotherapeutic drugs. Careful monitoring of treated mice revealed that a wide range of chemotherapeutic drugs had no significant effect on the general well-being of Mcl-1+/- mice with no overt damage to a broad range of tissues, including the haematopoietic compartment, heart, liver and kidney. These results indicate that MCL-1 inhibition may represent a tolerable strategy in cancer therapy, even when combined with select cytotoxic drugs.Entities:
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Year: 2017 PMID: 28800129 PMCID: PMC5686343 DOI: 10.1038/cdd.2017.125
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828