Evidence map›Paper›PMID 31015208›Full record

ArticleBlood advances2019

Rational cotargeting of HDAC6 and BET proteins yields synergistic antimyeloma activity.

Jennifer S Carew, Claudia M Espitia, Weiguo Zhao, Valeria Visconte, Faiz Anwer, Kevin R Kelly, Steffan T Nawrocki

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Enhancer regulation in cancer: from epigenetics to mArchives of pharmacal research · 2025
    Review
  4. [Design, Synthesis, and Efficacy Evaluation of a Novel BRD4/HDAC Dual-Target Small-Molecule Inhibitor in Prostate Cancer].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Article
  5. Review
  6. Article
  7. HDAC6: A unique HDAC family member as a cancer target.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. How metabolism bridles cytotoxic CD8Trends in immunology · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

7 authors at 4 institutions in 1 country.

Jennifer S CarewDivision of Translational and Regenerative Medicine, Department of Medicine, The University of Arizona Comprehensive Cancer Center, Tucson, AZ.
Claudia M EspitiaDivision of Translational and Regenerative Medicine, Department of Medicine, The University of Arizona Comprehensive Cancer Center, Tucson, AZ.
Weiguo ZhaoCancer Therapy and Research Center, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Valeria VisconteDepartment of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Faiz AnwerDivision of Hematology and Oncology, University of Arizona, Tucson AZ; and.ORCID 0000-0001-6914-7439
Kevin R KellyJane Anne Nohl Division of Hematology and Center for the Study of Blood Diseases, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA.
Steffan T NawrockiDivision of Translational and Regenerative Medicine, Department of Medicine, The University of Arizona Comprehensive Cancer Center, Tucson, AZ.
University of Arizona · USCleveland Clinic · USThe University of Texas Health Science Center at San Antonio · USUniversity of Southern California · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Teri L Bankhead · 1985 to 2026
$110.2M
Endoplasmic reticulum stress and oncoviral therapyR01CA190789 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI NAWROCKI, STEFFAN T · 2015 to 2020
$1.6M
Targeting NEDD8-Mediated Protein Turnover in AMLR01CA172443 · NCI · UNIVERSITY OF ARIZONA · PI CAREW, JENNIFER S · 2014 to 2019
$1.5M
Development of lysosome targeted therapeuticsR41CA271967 · NCI · MAJESTIC THERAPEUTICS, LLC · PI CAREW, JENNIFER S, NAWROCKI, STEFFAN T · 2022 to 2022
$258k
NCI NIH HHS P30 CA023074NCI NIH HHS R01 CA172443NCI NIH HHS R01 CA190789NCI NIH HHS R41 CA271967
6 · The paper itself

Abstract

Inhibition of bromodomain and extra terminal (BET) protein family members, including BRD4, decreases the expression of c-MYC and other key oncogenic factors and also significantly induces histone deacetylase 6 (HDAC6) expression. On the basis of the role of HDAC6 in malignant pathogenesis, we hypothesized that rational cotargeting of HDAC6 and BET family proteins may represent a novel approach that yields synergistic antimyeloma activity. We used genetic and pharmacologic approaches to selectively impair HDAC6 and BET function and evaluated the consequential impact on myeloma pathogenesis. These studies identified HDAC6 upregulation as an efficacy reducing mechanism for BET inhibitors because antagonizing HDAC6 activity synergistically enhanced the activity of JQ1 in a panel of multiple myeloma (MM) cell lines and primary CD138

Indexed as

Drug Delivery SystemsAnimalsBromodomain Containing ProteinsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHistone Deacetylase 6HumansHydroxamic AcidsMiceMice, SCIDMultiple MyelomaProteinsProto-Oncogene Proteins c-mycPyrimidinesbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsHDAC6 protein, humanHistone Deacetylase 6Hydroxamic AcidsMYC protein, humanProteinsProto-Oncogene Proteins c-mycPyrimidinesricolinostat

Identifiers

PMID31015208
PMCPMC6482361
OpenAlexW2942170171

What OpenQuestion holds

Textmetadata
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.