Recent developments in epigenetic cancer therapeutics: clinical advancement and emerging trends

被引:108
作者
Nepali, Kunal [1 ]
Liou, Jing-Ping [1 ,2 ]
机构
[1] Taipei Med Univ, Coll Pharm, Sch Pharm, 250 Wuxing St, Taipei 11031, Taiwan
[2] Taipei Med Univ, Biomed Commercializat Ctr, Taipei 11031, Taiwan
关键词
Epigenetics; Cancer; PROTACS; Multitargeting; Scaffolds; Inhibitors; Mechanisms; CRISPR; Cas9; HISTONE-DEACETYLASE INHIBITOR; ACUTE MYELOID-LEUKEMIA; SMALL-MOLECULE INHIBITOR; TUMOR-SUPPRESSOR GENES; DNA METHYLTRANSFERASE INHIBITORS; SELECTIVE BROMODOMAIN BRD; PHASE-I; 1ST-IN-HUMAN; LABEL SINGLE-AGENT; CELL LUNG-CANCER; HDAC INHIBITOR;
D O I
10.1186/s12929-021-00721-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epigenetic drug discovery field has evidenced significant advancement in the recent times. A plethora of small molecule inhibitors have progressed to clinical stage investigations and are being explored exhaustively to ascertain conclusive benefits in diverse malignancies. Literature precedents indicates that substantial amount of efforts were directed towards the use of epigenetic tools in monotherapy as well as in combination regimens at the clinical level, however, the preclinical/preliminary explorations were inclined towards the identification of prudent approaches that can leverage the anticancer potential of small molecule epigenetic inhibitors as single agents only. This review article presents an update of FDA approved epigenetic drugs along with the epigenetic inhibitors undergoing clinical stage investigations in different cancer types. A detailed discussion of the pragmatic strategies that are expected to steer the progress of the epigenetic therapy through the implementation of emerging approaches such as PROTACS and CRISPR/Cas9 along with logical ways for scaffold fabrication to selectively approach the enzyme isoforms in pursuit of garnering amplified antitumor effects has been covered. In addition, the compilation also presents the rational strategies for the construction of multi-targeting scaffold assemblages employing previously identified pharmacophores as potential alternatives to the combination therapy.
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页数:58
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