Evidence map›Paper›PMID 30760718›Full record

ArticleNature communications2019

Genomic characterization of genes encoding histone acetylation modulator proteins identifies therapeutic targets for cancer treatment.

Zhongyi Hu, Junzhi Zhou, Junjie Jiang, Jiao Yuan, Youyou Zhang, Xuepeng Wei, Nicki Loo, Yueying Wang, Yutian Pan, Tianli Zhang and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 10% 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.

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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  10. Review
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  14. Article
  15. Review
  16. Identification and Development of BRD9 Chemical Probes.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  17. Article
  18. Article
  19. Article
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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

19 authors at 4 institutions in 2 countries.

Zhongyi HuCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Junzhi ZhouCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Junjie JiangCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Jiao YuanCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Youyou ZhangCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Xuepeng WeiDepartment of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Nicki LooCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Yueying WangCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Yutian PanCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Tianli ZhangCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Xiaomin ZhongCenter for Stem Cell Biology and Tissue Engineering, Department of Biology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510080, China.
Meixiao LongDivision of Hematology, Department of Internal Medicine, Ohio State University, Columbus, 43210, Ohio, USA.
Kathleen T MontoneDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Janos L TanyiDepartment of Obstetrics and Gynecology, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Yi FanDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA.
Tian-Li WangDepartments of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21231, USA.
Ie-Ming ShihDepartments of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21231, USA.
Xiaowen HuCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA. xiaowenh@pennmedicine.upenn.edu.
Lin ZhangCenter for Research on Reproduction and Women's Health, University of Pennsylvania, Philadelphia, Pennsylvania, 19104, USA. linzhang@pennmedicine.upenn.edu.
University of Pennsylvania · USJohns Hopkins Medicine · USSun Yat-sen University · CNThe Ohio State University · US

Funding

Therapeutic Micro RNA Strategies for Ovarian CancerP50CA083638 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GODWIN, ANDREW K., GOLEMIS, ERICA A. · 1999 to 2013
$33.6M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
Endothelial plasticity in glioma vascularization and therapy resistanceR01NS094533 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Yi Fan · 2015 to 2026
$4.3M
Molecular mechanism and preclinical development of BETi and PARPi combination therapyR01CA225929 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2019 to 2023
$1.8M
The epigenetic mechanism of long non-coding RNA in cancerR01CA190415 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2015 to 2019
$1.8M
The role of microRNA, mir-30d, in the initiation and progression of cancerR01CA142776 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2010 to 2014
$1.6M
NCI NIH HHS P50 CA083638NCI NIH HHS P50 CA174523NCI NIH HHS R01 CA142776NCI NIH HHS R01 CA190415NCI NIH HHS R01 CA225929NIH HHS P50CA083638NIH HHS P50CA174523NIH HHS R01CA142776NIH HHS R01CA190415NIH HHS R01CA225929NIH HHS R01NS094533NINDS NIH HHS R01 NS094533
6 · The paper itself

Abstract

A growing emphasis in anticancer drug discovery efforts has been on targeting histone acetylation modulators. Here we comprehensively analyze the genomic alterations of the genes encoding histone acetylation modulator proteins (HAMPs) in the Cancer Genome Atlas cohort and observe that HAMPs have a high frequency of focal copy number alterations and recurrent mutations, whereas transcript fusions of HAMPs are relatively rare genomic events in common adult cancers. Collectively, 86.3% (63/73) of HAMPs have recurrent alterations in at least 1 cancer type and 16 HAMPs, including 9 understudied HAMPs, are identified as putative therapeutic targets across multiple cancer types. For example, the recurrent focal amplification of BRD9 is observed in 9 cancer types and genetic depletion of BRD9 inhibits tumor growth. Our systematic genomic analysis of HAMPs across a large-scale cancer specimen cohort may facilitate the identification and prioritization of potential drug targets and selection of suitable patients for precision treatment.

Indexed as

MutationAcetylationAntineoplastic AgentsBromodomain Containing ProteinsDNA Copy Number VariationsGene Expression Regulation, NeoplasticGenomicsHistone AcetyltransferasesHistonesHumansMolecular Targeted TherapyNeoplasmsTranscription FactorsAntineoplastic AgentsBRD9 protein, humanBromodomain Containing ProteinsHistone AcetyltransferasesHistonesTranscription Factors

Identifiers

PMID30760718
PMCPMC6374416
OpenAlexW2913823173

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.