Evidence map›Paper›PMID 32094302›Full record

ReviewCancer research2020

Targeting the SAGA and ATAC Transcriptional Coactivator Complexes in MYC-Driven Cancers.

Lisa Maria Mustachio, Jason Roszik, Aimee Farria, Sharon Y R Dent

Open access · greenAbstract readReview
In one paragraph

Review in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Cell state-dependent chromatin targeting in NUT carcinoma.bioRxiv : the preprint server for biology · 2023
    Article
  13. MYC: a complex problem.Trends in cell biology · 2023
    Review
  14. Integrative analysis of histone acetyltransferase KAT2A in human cancer.Cancer biomarkers : section A of Disease markers · 2023
    Article
  15. Genes · 2022
    Article
  16. Article
  17. Review
  18. The biochemical and genetic discovery of the SAGA complex.Biochimica et biophysica acta. Gene regulatory mechanisms · 2021
    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

4 authors at 1 institution in 1 country.

Lisa Maria MustachioDepartments of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jason RoszikMelanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-4561-6170
Aimee FarriaDepartments of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-3524-8730
Sharon Y R DentDepartments of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, Texas. sroth@mdanderson.org.ORCID 0000-0002-4824-3269
The University of Texas MD Anderson Cancer Center · US

Funding

Functions of Mammalian Histone ModifiersR01GM067718 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DENT, SHARON Y. R. · 2003 to 2018
$3.7M
Genetic and Molecular Definition of Histone Modifying Enzyme FunctionsR35GM131678 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DENT, SHARON Y. R. · 2019 to 2023
$2.0M
Defining USP22 Functions During Mammalian DevelopmentR01HD094400 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DENT, SHARON Y. R. · 2018 to 2021
$1.6M
NICHD NIH HHS R01 HD094400NIGMS NIH HHS R01 GM067718NIGMS NIH HHS R35 GM131678
6 · The paper itself

Abstract

Targeting epigenetic regulators, such as histone-modifying enzymes, provides novel strategies for cancer therapy. The GCN5 lysine acetyltransferase (KAT) functions together with MYC both during normal development and in oncogenesis. As transcription factors, MYC family members are difficult to target with small-molecule inhibitors, but the acetyltransferase domain and the bromodomain in GCN5 might provide alternative targets for disruption of MYC-driven functions. GCN5 is part of two distinct multiprotein histone-modifying complexes, SAGA and ATAC. This review summarizes key findings on the roles of SAGA and ATAC in embryo development and in cancer to better understand the functional relationships of these complexes with MYC family members, as well as their future potential as therapeutic targets.

Indexed as

Embryonic DevelopmentNeoplasmsProto-Oncogene Proteins c-mycTranscription FactorsAnimalsHumansp300-CBP-Associated Factorp300-CBP Transcription Factorsp300-CBP-Associated Factorp300-CBP Transcription FactorsProto-Oncogene Proteins c-mycTranscription Factors

Identifiers

PMID32094302
PMCPMC7231639
OpenAlexW3007199821

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.