Evidence map›Paper›PMID 21345145›Full record

ReviewFuture oncology (London, England)2011

Rational therapeutic combinations with histone deacetylase inhibitors for the treatment of cancer.

K Ted Thurn, Scott Thomas, Amy Moore, Pamela N Munster

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06930118 (An Exploratory Study Investigating the Combination of Chidamide, Regorafenib, Plus Iparomlimab and Tuvonralimab for the Treatment of Drug-esistant and Efractory Dvanced Colorectal Cancer), which is not on this map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
8.0field-weighted citation impact, top 2% 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.

NCT06930118 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

An Exploratory Study Investigating the Combination of Chidamide, Regorafenib, Plus Iparomlimab and Tuvonralimab for the Treatment of Drug-esistant and Efractory Dvanced Colorectal Cancer

TypeinterventionalSponsorShanghai Changzheng HospitalRan2025 to 2027Enrolled60ConditionsAdvanced Colorectal Cancer in the Third-line Treatment and Beyond, pMMR/MSS Advanced Colorectal CancerArmschidamide, regorafenib, and iparomlimab/tuvonralimab
3 · Its place in the literature

Who cites it

111 citing papers in PubMed, 243 citations in OpenAlex.

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51 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

K Ted ThurnDepartment of Medicine, Hematology/Oncology Division. University of California-San Francisco, 1600 Divisadero Street, San Francisco, CA 94115, USA.
Scott Thomas
Amy Moore
Pamela N Munster
University of California, San Francisco · US

Funding

The role of HDAC2 in hormone therapy resistanceR01CA152989 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MUNSTER, PAMELA N. · 2011 to 2015
$1.6M
The Role of Selective HDAC Enzymes in Drug SensitivityR01CA122657 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MUNSTER, PAMELA N. · 2007 to 2010
$1.1M
Potentiation of Topo Inhibitors by HDAC InhibitorsR21CA105875 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI MUNSTER, PAMELA N · 2004 to 2005
$504k
Potentiation of Topo Inhibitors by the HDACi, SAHAR21CA112913 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI MUNSTER, PAMELA N. · 2006 to 2007
$427k
NCI NIH HHS 5R01CA122657NCI NIH HHS R01 CA122657NCI NIH HHS R01 CA152989NCI NIH HHS R21 CA105875NCI NIH HHS R21CA105875NCI NIH HHS R21 CA112913NCI NIH HHS R21CA112913
6 · The paper itself

Abstract

Histone deacetylases (HDACs) regulate the acetylation of a variety of histone and nonhistone proteins, controlling the transcription and regulation of genes involved in cell cycle control, proliferation, survival, DNA repair and differentiation. Unsurprisingly, HDAC expression is frequently altered in hematologic and solid tumor malignancies. Two HDAC inhibitors (vorinostat and romidepsin) have been approved by the US FDA for the treatment of cutaneous T-cell lymphoma. As single agents, treatment with HDAC inhibitors has demonstrated limited clinical benefit for patients with solid tumors, prompting the investigation of novel treatment combinations with other cancer therapeutics. In this article, the rationales and clinical progress of several combinations with HDAC inhibitors are presented, including DNA-damaging chemotherapeutic agents, radiotherapy, hormonal therapies, DNA methyltransferase inhibitors and various small-molecule inhibitors. The future application of HDAC inhibitors as a treatment for cancer is discussed, examining current hurdles to overcome before realizing the potential of this new approach.

Indexed as

AcetylationAntineoplastic AgentsChromatinDNA RepairGene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsHistone DeacetylasesHumansMicrotubulesMolecular Targeted TherapyNeoplasmsAntineoplastic AgentsChromatinHistone Deacetylase InhibitorsHistone Deacetylases

Identifiers

PMID21345145
PMCPMC3127396
OpenAlexW2105906697

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.