Evidence map›Paper›PMID 27599530›Full record

ReviewCold Spring Harbor perspectives in medicine2016

HDACs and HDAC Inhibitors in Cancer Development and Therapy.

Yixuan Li, Edward Seto

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 759 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
759citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

759 citing papers in PubMed, 1 synthesis or guideline pooled it.

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699 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

2 authors.

Yixuan LiGeorge Washington University Cancer Center, Department of Biochemistry and Molecular Medicine, George Washington University, Washington, DC 20037.
Edward SetoGeorge Washington University Cancer Center, Department of Biochemistry and Molecular Medicine, George Washington University, Washington, DC 20037.

Funding

Targeting SIRT1 in Mantle Cell LymphomaR01CA187040 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI SETO, EDWARD · 2014 to 2018
$1.6M
The Basic and Translational Implication of SIRT1 and DNMT1 in CancerR01CA169210 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI SETO, EDWARD · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA169210NCI NIH HHS R01 CA187040
6 · The paper itself

Abstract

Over the last several decades, it has become clear that epigenetic abnormalities may be one of the hallmarks of cancer. Posttranslational modifications of histones, for example, may play a crucial role in cancer development and progression by modulating gene transcription, chromatin remodeling, and nuclear architecture. Histone acetylation, a well-studied posttranslational histone modification, is controlled by the opposing activities of histone acetyltransferases (HATs) and histone deacetylases (HDACs). By removing acetyl groups, HDACs reverse chromatin acetylation and alter transcription of oncogenes and tumor suppressor genes. In addition, HDACs deacetylate numerous nonhistone cellular substrates that govern a wide array of biological processes including cancer initiation and progression. This review will discuss the role of HDACs in cancer and the therapeutic potential of HDAC inhibitors (HDACi) as emerging drugs in cancer treatment.

Indexed as

Protein Processing, Post-TranslationalAcetylationApoptosisCell CycleDNA DamageHistone AcetyltransferasesHistone Deacetylase InhibitorsHistone DeacetylasesHumansNeoplasmsHistone AcetyltransferasesHistone Deacetylase InhibitorsHistone Deacetylases

Identifiers

PMID27599530
PMCPMC5046688

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.