Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells.
By PA Marks, V. Richon, R. Rifkind. Journal of the National Cancer Institute, 2000
1,225 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/8b3d0e1dd882f61f156cff9a985b248d266f3bc0
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- PA Marks
- S. Baylin
- Pier Giuseppe Pelicci
- S. Minucci
- Guangdi Wang
- Tien L. Huang
- Madhusoodanan Mottamal
- Shilong Zheng
In Oncology
Citations in the corpus
- Histone Deacetylase Inhibitors in Clinical Studies as Templates for New Anticancer Agents (2015, background): “The balance between acetylation and deacetylation of histones or the reverse activities of HATs and HDACs regulate gene expression through chromatin modifications [4,5].”
- Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells (2001, background): “Several structurally diverse HDAC inhibitors have been identi®ed and their activity in transformed cells in vitro renders them prime candidates for cancer therapy (Marks et al., 2000; KraÈmer et al., 2001).”
- Histone deacetylases and cancer: causes and therapies (2001, background): “Various chemical agents can induce these processes in transformed cell”
- DNA methylation and gene silencing in cancer (2005, background): “A variety of HDAC inhibitors have been shown to inhibit histone deacetylation in human tumor cells, leading to accumulation of acetylated histone proteins”