Histone deacetylase inhibitors as anticancer drugs

T Eckschlager, J Plch, M Stiborova… - International journal of …, 2017 - mdpi.com
Carcinogenesis cannot be explained only by genetic alterations, but also involves
epigenetic processes. Modification of histones by acetylation plays a key role in epigenetic …

Recent progress on tubulin inhibitors with dual targeting capabilities for cancer therapy

W Shuai, G Wang, Y Zhang, F Bu, S Zhang… - Journal of Medicinal …, 2021 - ACS Publications
Microtubules play a crucial role in multiple cellular functions including mitosis, cell signaling,
and organelle trafficking, which makes the microtubule an important target for cancer …

Rational design of multitarget-directed ligands: strategies and emerging paradigms

J Zhou, X Jiang, S He, H Jiang, F Feng… - Journal of medicinal …, 2019 - ACS Publications
Due to the complexity of multifactorial diseases, single-target drugs do not always exhibit
satisfactory efficacy. Recently, increasing evidence indicates that simultaneous modulation …

Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas

Y Jiao, TM Pawlik, RA Anders, FM Selaru… - Nature …, 2013 - nature.com
Through exomic sequencing of 32 intrahepatic cholangiocarcinomas, we discovered
frequent inactivating mutations in multiple chromatin-remodeling genes (including BAP1 …

Cancer epigenetics reaches mainstream oncology

M Rodríguez-Paredes, M Esteller - Nature medicine, 2011 - nature.com
Epigenetics is one of the most promising and expanding fields in the current biomedical
research landscape. Since the inception of epigenetics in the 1940s, the discoveries …

Epigenetic modifications as therapeutic targets

TK Kelly, DD De Carvalho, PA Jones - Nature biotechnology, 2010 - nature.com
Epigenetic modifications work in concert with genetic mechanisms to regulate transcriptional
activity in normal tissues and are often dysregulated in disease. Although they are …

Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group

M Lobera, KP Madauss, DT Pohlhaus… - Nature chemical …, 2013 - nature.com
In contrast to studies on class I histone deacetylase (HDAC) inhibitors, the elucidation of the
molecular mechanisms and therapeutic potential of class IIa HDACs (HDAC4, HDAC5 …

The epigenetic effects of butyrate: potential therapeutic implications for clinical practice

R Berni Canani, M Di Costanzo, L Leone - Clinical epigenetics, 2012 - Springer
Butyrate is a short chain fatty acid derived from the microbial fermentation of dietary fibers in
the colon. In the last decade, multiple beneficial effects of butyrate at intestinal and …

Histone deacetylase inhibitors (HDACIs): multitargeted anticancer agents

K Ververis, A Hiong, TC Karagiannis… - Biologics: Targets and …, 2013 - Taylor & Francis
Histone deacetylase (HDAC) inhibitors are an emerging class of therapeutics with potential
as anticancer drugs. The rationale for developing HDAC inhibitors (and other chromatin …

Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair

JH Lee, ML Choy, L Ngo, SS Foster… - Proceedings of the …, 2010 - National Acad Sciences
Histone deacetylase inhibitors (HDACi) developed as anti-cancer agents have a high
degree of selectivity for killing cancer cells. HDACi induce acetylation of histones and …