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Cancer's epigenetic drugs: where are they in the cancer medicines?
- Source :
- The Pharmacogenomics Journal. 20:367-379
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- Epigenetic modulation can affect the characteristics of cancers. Because it is likely to manipulate epigenetic genes, they can be considered as potential targets for cancer treatment. In this comprehensive study, epigenetic drugs are categorized according to anticancer mechanisms and phase of therapy. The relevant articles or databases were searched for epigenetic approaches to cancer therapy. Epigenetic drugs are divided according to their mechanisms and clinical phases that have been approved by the FDA or are undergoing evaluation phases. DNA methylation agents, chromatin remodelers specially HDACs, and noncoding RNAs especially microRNAs are the main epi-drugs for cancer. Despite many challenges, combination therapy using epi-drugs and routine therapies such as chemotherapy in various approaches have exhibited beneficial effects compared with each treatment alone. Cancer stem cell targeting and epigenetic editing have been confirmed as definitive pathways for cancer treatment. This paper reviewed the available epigenetic approaches to cancer therapy.
- Subjects :
- 0301 basic medicine
Combination therapy
Antineoplastic Agents
Bioinformatics
030226 pharmacology & pharmacy
Epigenesis, Genetic
03 medical and health sciences
0302 clinical medicine
Cancer stem cell
Neoplasms
microRNA
Genetics
Animals
Humans
Medicine
Cancer epigenetics
Epigenetics
Epigenomics
Pharmacology
business.industry
Cancer
DNA Methylation
medicine.disease
Gene Expression Regulation, Neoplastic
030104 developmental biology
Drug Resistance, Neoplasm
DNA methylation
Molecular Medicine
business
Subjects
Details
- ISSN :
- 14731150 and 1470269X
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- The Pharmacogenomics Journal
- Accession number :
- edsair.doi.dedup.....1cbcb7081e2b3256b75b166f54f56b5f
- Full Text :
- https://doi.org/10.1038/s41397-019-0138-5