期刊
MOLECULAR PHARMACEUTICS
卷 8, 期 6, 页码 2021-2031出版社
AMER CHEMICAL SOC
DOI: 10.1021/mp200329f
关键词
histone deacetylase inhibitor; resistance; romidepsin; vorinostat; panobinostat
资金
- NIH, National Cancer Institute, Center for Cancer Research
The histone deacetylase inhibitors (HDIs) have shown promise in the treatment of a number of hematologic malignancies, leading to the approval of vorinostat and romidepsin for the treatment of cutaneous T-cell lymphoma and romidepsin for the treatment of peripheral T-cell lymphoma by the U.S. Food and Drug Administration. Despite these promising results, clinical trials with the HDIs in solid tumors have not met with success. Examining mechanisms of resistance to HDIs may lead to strategies that increase their therapeutic potential in solid tumors. However, relatively few examples of drug-selected cell lines exist, and mechanisms of resistance have not been studied in depth. Very few clinical translational studies have evaluated resistance mechanisms. In the current review, we summarize many of the purported mechanisms of action of the HDIs in clinical trials and examine some of the emerging resistance mechanisms.
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