Evidence map›Paper›PMID 25712263›Full record

ArticleBritish journal of haematology2015

Entinostat, a novel histone deacetylase inhibitor is active in B-cell lymphoma and enhances the anti-tumour activity of rituximab and chemotherapy agents.

Sarah Frys, Zachary Simons, Qiang Hu, Matthew J Barth, Juan J Gu, Cory Mavis, Joseph Skitzki, Liu Song, Myron S Czuczman, Francisco J Hernandez-Ilizaliturri

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in British journal of haematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02733380 (The Efficacy and Safety of Chidamide Combined With VDDT Regimen(Vinorelbine,Liposomal Doxorubicin,Dexamethasone and Thalidomide) in Relapse and Refractory Patients With Diffuse Large B Cell Lymphoma), which is not on this map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02733380 phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

The Efficacy and Safety of Chidamide Combined With VDDT Regimen(Vinorelbine,Liposomal Doxorubicin,Dexamethasone and Thalidomide) in Relapse and Refractory Patients With Diffuse Large B Cell Lymphoma

TypeinterventionalSponsorHenan Cancer HospitalRan2016 to 2021Enrolled20ConditionsDiffuse Large B-cell LymphomaArmsChidamide, Vinorelbine, Liposomal Doxorubicin or mitoxantrone, Dexamethasone, Thalidomide
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
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  8. Article
  9. Entinostat Enhances the Efficacy of Chemotherapy in Small Cell Lung Cancer Through S-phase Arrest and Decreased Base Excision Repair.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  10. Article
  11. Review
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  15. Article
  16. Article
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  18. Article
  19. Can we use epigenetics to prime chemoresistant lymphomas?Hematology. American Society of Hematology. Education Program · 2020
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Sarah FrysDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA; Department of Immunology, Roswell Park Cancer Institute, Buffalo, NY, USA.
Zachary Simons
Qiang Hu
Matthew J Barth
Juan J Gu
Cory Mavis
Joseph Skitzki
Liu Song
Myron S Czuczman
Francisco J Hernandez-Ilizaliturri
Roswell Park Comprehensive Cancer Center · US

Funding

Targeting the proteasome to overcome therapy resistance in B-NHLR01CA136907 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI CZUCZMAN, MYRON S · 2009 to 2013
$1.8M
NCI NIH HHS 5R01CA136907-02NCI NIH HHS R01 CA136907
6 · The paper itself

Abstract

Histone deacetylases (HDACs) inhibitors are active in T-cell lymphoma and are undergoing pre-clinical and clinical testing in other neoplasms. Entinostat is an orally bioavailable class I HDAC inhibitor with a long half-life, which is under evaluation in haematological and solid tumour malignancies. To define the activity and biological effects of entinostat in B-cell lymphoma we studied its anti-tumour activity in several rituximab-sensitive or -resistant pre-clinical models. We demonstrated that entinostat is active in rituximab-sensitive cell lines (RSCL), rituximab-resistant cell lines (RRCL) and primary tumour cells isolated from lymphoma patients (n = 36). Entinostat exposure decreased Bcl-XL (BCL2L1) levels and induced apoptosis in cells. In RSCL and RRCL, entinostat induced p21 (CDKN1A) expression leading to G1 cell cycle arrest and exhibited additive effects when combined with bortezomib or cytarabine. Caspase inhibition diminished entinostat activity in some primary tumour cells suggesting that entinostat has dual mechanisms-of-action. In addition, entinostat increased the expression of CD20 and adhesion molecules. Perhaps related to these effects, we observed a synergistic activity between entinostat and rituximab in a lymphoma-bearing severe combined immunodeficiency (SCID) mouse model. Our data suggests that entinostat is an active HDAC inhibitor that potentiates rituximab activity in vivo and supports its further clinical development in B-cell lymphoma.

Indexed as

AnimalsAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsApoptosisbcl-X ProteinBenzamidesBoronic AcidsBortezomibCell Line, TumorCyclin-Dependent Kinase Inhibitor p21CytarabineDrug Resistance, NeoplasmFemaleG1 Phase Cell Cycle CheckpointsHistone Deacetylase InhibitorsHumansAntibodies, Monoclonal, Murine-DerivedBCL2L1 protein, humanbcl-X ProteinBenzamidesBoronic AcidsBortezomibCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21CytarabineentinostatHistone Deacetylase InhibitorsPyrazinesPyridinesRituximabentinostathistone deacetylase inhibitorslymphomarituximab

Identifiers

PMID25712263
PMCPMC5802357
OpenAlexW2092971169

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.