The combination of reduced MCL-1 and standard chemotherapeutics is tolerable in mice

被引:25
作者
Brinkmann, Kerstin [1 ,2 ]
Grabow, Stephanie [1 ,2 ]
Hyland, Craig D. [1 ]
Teh, Charis E. [1 ,2 ]
Alexander, Warren S. [1 ,2 ]
Herold, Marco J. [1 ,2 ]
Strasser, Andreas [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Canc & Haematol Div, Parkville, Vic, Australia
[2] Univ Melbourne, Mol Genet Canc Div, Dept Med Biol, Melbourne, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
ANTI-APOPTOTIC MCL-1; MANTLE-CELL LYMPHOMA; MYC-DRIVEN MOUSE; HEMATOPOIETIC STEM; BCL-2; FAMILY; TRANSGENIC MICE; SURVIVAL; CANCER; GENE; ANTICANCER;
D O I
10.1038/cdd.2017.125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 similar to 50% reduction in MCL-1 protein in their cells, with abroad 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.
引用
收藏
页码:2032 / 2043
页数:12
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