Unknown

Dataset Information

0

Histone deacetylase inhibitors in the treatment of hematological malignancies and solid tumors.


ABSTRACT: The human genome is epigenetically organized through a series of modifications to the histone proteins that interact with the DNA. In cancer, many of the proteins that regulate these modifications can be altered in both function and expression. One example of this is the family of histone deacetylases (HDACs), which as their name implies remove acetyl groups from the histone proteins, allowing for more condensed nucleosomal structure. HDACs have increased expression in cancer and are also believed to promote carcinogenesis through the acetylation and interaction with key transcriptional regulators. Given this, small molecule histone deacetylases inhibitors have been identified and developed, which not only inhibit HDACs, but can also lead to growth arrest, differentiation, and/or apoptosis in tumors both in vitro and in vivo. Here, we will discuss some of the recent developments in clinical trials utilizing HDACs inhibitors for the treatment of both hematological malignancies as well as solid tumors.

SUBMITTER: Federico M 

PROVIDER: S-EPMC3004414 | biostudies-literature | 2011

REPOSITORIES: biostudies-literature

altmetric image

Publications

Histone deacetylase inhibitors in the treatment of hematological malignancies and solid tumors.

Federico Mario M   Bagella Luigi L  

Journal of biomedicine & biotechnology 20101206


The human genome is epigenetically organized through a series of modifications to the histone proteins that interact with the DNA. In cancer, many of the proteins that regulate these modifications can be altered in both function and expression. One example of this is the family of histone deacetylases (HDACs), which as their name implies remove acetyl groups from the histone proteins, allowing for more condensed nucleosomal structure. HDACs have increased expression in cancer and are also believ  ...[more]

Similar Datasets

| S-EPMC3365365 | biostudies-literature
| S-EPMC3795372 | biostudies-literature
| S-EPMC4361776 | biostudies-literature
| S-EPMC3054015 | biostudies-literature
| S-EPMC7870522 | biostudies-literature
| S-EPMC6212943 | biostudies-literature
| S-EPMC5422942 | biostudies-literature
| S-EPMC5854188 | biostudies-other
| S-EPMC8162746 | biostudies-literature
| S-EPMC8779837 | biostudies-literature