Results 81 to 90 of about 24,005 (199)
Aim: Due to extensive treatment switching in the MAVORIC trial, lack of UK regulatory licence for the comparator, overall survival (OS) with mogamulizumab was compared with patients with previously treated advanced mycosis fungoides/S ´ ezary syndrome (
Neil Hawkins +4 more
doaj +1 more source
Decitabine-Vorinostat combination treatment in acute myeloid leukemia activates pathways with potential for novel triple therapy [PDF]
Despite advancements in cancer therapeutics, acute myeloid leukemia patients over 60 years old have a 5-year survival rate of less than 8%. In an attempt to improve this, epigenetic modifying agents have been combined as therapies in clinical studies. In
Clarke, Kathryn M. +4 more
core +1 more source
We integrated four omics to build a breast cancer immunotherapy predictor. Survival‐associated biomarkers were compressed into 200 latent features via an autoencoder, then refined using three survival models. K‐means defined two subgroups (C1, high‐risk and C2, low‐risk).
Houda Bendani +3 more
wiley +1 more source
Suberoylanilide hydroxamic acid (SAHA) or vorinostat (VOR) is a potent inhibitor of class I histone deacetylases (HDACs) that is approved for the treatment of cutaneous T-cell lymphoma.
Anand Kumar Meka +7 more
doaj +1 more source
A pharmacogenetic study of vorinostat glucuronidation [PDF]
High interindividual pharmacokinetic variability was observed in phase 1 studies of vorinostat (suberoylanilide hydroxamic acid), an oral histone deacetylase inhibitor. Thus, we hypothesized that the variability can be explained by genetic variants of the uridine 5'-diphosphate-glucuronosyltransferases (UGTs) involved in vorinostat metabolism ...
Soonmo Peter, Kang +7 more
openaire +2 more sources
Development of a novel cell-based assay system EPISSAY for screening epigenetic drugs and liposome formulated decitabine [PDF]
Extent: 11 p.BACKGROUND: Despite the potential of improving the delivery of epigenetic drugs, the subsequent assessment of changes in their epigenetic activity is largely dependent on the availability of a suitable and rapid screening bioassay.
Akkamsetty, Y. +9 more
core +2 more sources
DNTTIP1 drives leukaemogenesis through MiDAC‐mediated epigenetic silencing of BMF
DNTTIP1 cooperates with SP1 to recruit HDAC1/2, leading to BMF silencing and reduced competitive binding of BMF to BCL2.This suppresses autophagy and apoptosis, promoting leukaemic cell survival. Targeting the DNTTIP1‐HDAC1/2‐BMF axis reactivates BMF and induces anti‐leukaemic effects.
Ruolin Xiu +12 more
wiley +1 more source
Reversion of epigenetically mediated BIM silencing overcomes chemoresistance in Burkitt lymphoma [PDF]
In Burkitt lymphoma/leukemia (BL), achievement of complete remission with first-line chemotherapy remains a challenging issue, as most patients who respond remain disease-free, whereas those refractory have few options of being rescued with salvage ...
Agirre-Ena, X. (Xabier) +12 more
core +1 more source
This study employs an integrative in silico approach combining network pharmacology, molecular docking, and molecular dynamics simulations to explore the molecular association between trigonelline and ovarian aging, identifying five hub proteins (MMP9, JAK2, PARP1, HDAC1, and CYP3A4) and three major mechanistic axes related to extracellular matrix ...
Woon Shin Yong +4 more
wiley +1 more source
Histone deacetylase inhibitors – molecular mechanisms of actions and clinical applications [PDF]
Histone deacetylases (HDACs) play an important role in the epigenetic regulation of gene expression implicated in cancer pathogenesis. Inhibitors of HDACs (HDI) are under investigation as novel anti-cancer drugs, which induce histone hyperacetylation ...
Andrzej Stepulak +3 more
core +1 more source

