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Targeting DNA methylation for treating triple-negative breast cancer.
- Source :
-
Pharmacogenomics [Pharmacogenomics] 2019 Nov; Vol. 20 (16), pp. 1151-1157. - Publication Year :
- 2019
-
Abstract
- Triple-negative breast cancer (TNBC) accounts for 15-20% of all invasive breast cancers and tends to have aggressive histological features and poor clinical outcomes. Unlike, estrogen receptor- or HER2-positive diseases, TNBC patients currently lack the US FDA-approved targeted therapies. DNA methylation is a critical mechanism of epigenetic modification. It is well known that aberrant DNA methylation contributes to the malignant transformation of cells by silencing critical tumor suppressor genes. DNA methyltransferase inhibitors reactivate silenced tumor suppressor genes and result in tumor growth arrest, with therapeutic effects observed in patients with hematologic malignancies. The antitumor effect of these DNA methyltransferase inhibitors has also been explored in solid tumors, especially in TNBC that currently lacks targeted therapies.
- Subjects :
- Animals
Azacitidine adverse effects
Azacitidine pharmacology
Cell Line, Tumor
DNA Methylation drug effects
DNA Methyltransferase 3A
Decitabine adverse effects
Decitabine pharmacology
Epigenesis, Genetic genetics
Female
Gene Expression Regulation, Neoplastic drug effects
Humans
Mice
Promoter Regions, Genetic
Triple Negative Breast Neoplasms genetics
Triple Negative Breast Neoplasms pathology
Tumor Suppressor Proteins
Xenograft Model Antitumor Assays
DNA Methyltransferase 3B
DNA (Cytosine-5-)-Methyltransferase 1 genetics
DNA (Cytosine-5-)-Methyltransferases genetics
Triple Negative Breast Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1744-8042
- Volume :
- 20
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Pharmacogenomics
- Publication Type :
- Academic Journal
- Accession number :
- 31755366
- Full Text :
- https://doi.org/10.2217/pgs-2019-0078