Evidence map›Paper›PMID 31534138›Full record

ArticleCell death & disease2019

Epigenetic re-wiring of breast cancer by pharmacological targeting of C-terminal binding protein.

Jung S Byun, Samson Park, Dae Ik Yi, Jee-Hye Shin, Sara Gil Hernandez, Stephen M Hewitt, Marc C Nicklaus, Megan L Peach, Laura Guasch, Binwu Tang and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. 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

21 authors at 8 institutions in 2 countries.

Jung S ByunNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA.
Samson ParkGenetics Branch, National Cancer Institute, Bethesda, MD, 20892, USA.
Dae Ik YiGenetics Branch, National Cancer Institute, Bethesda, MD, 20892, USA.
Jee-Hye ShinLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD, 20892, USA.
Sara Gil HernandezGenetics Branch, National Cancer Institute, Bethesda, MD, 20892, USA.
Stephen M HewittLaboratory of Pathology, National Cancer Institute, Bethesda, MD, 20892, USA.
Marc C NicklausChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 20892, USA.
Megan L PeachBasic Science Program, Chemical Biology Laboratory, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.
Laura GuaschChemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD, 20892, USA.
Binwu TangLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD, 20892, USA.
Lalage M WakefieldLaboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD, 20892, USA.
Tingfen YanNational Human Genome Institute, Bethesda, MD, 20892, USA.
Ambar CabanNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA.
Alana JonesNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0003-3827-2426
Mohamed KabboutNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA.
Nasreen VohraBrody School of Medicine at East Carolina University, Greenville, NC, 27834, USA.
Anna María NápolesNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA.
Sandeep SinghalDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, 10032, USA.
Ryan YanceyDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, 10032, USA.
Adriana De SierviLaboratorio de Oncologıa Molecular y Nuevos Blancos Terapeuticos, Instituto de Biologıa y Medicina Experimental (IBYME), CONICET, Buenos Aires, Argentina.
Kevin GardnerNational Institute on Minority Health and Health Disparities, Bethesda, MD, 20892, USA. Klg2160@cumc.columbia.edu.
National Cancer Institute · USNational Institute on Minority Health and Health Disparities · USColumbia University Irving Medical Center · USFrederick National Laboratory for Cancer Research · USConsejo Nacional de Investigaciones Científicas y Técnicas · AREast Carolina University · USLeidos (United States) · USNational Human Genome Research Institute · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
NIMHD DIR TransitionZIAMD000005 · NIMHD · NATIONAL INSTITUTE ON MINORITY HEALTH AND HEALTH DISPARITIES · PI NAPOLES, ANNA MARIA · 2016 to 2018
$7.1M
Mechanisms of Transcriptional Control by p300ZIABC010846 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GARDNER, KEVIN · 2009 to 2017
$4.8M
Intramural NIH HHS ZIA BC010846Intramural NIH HHS ZIA MD000005NCI NIH HHS HHSN261200800001ENCI NIH HHS P30 CA013696
6 · The paper itself

Abstract

The C-terminal binding protein (CtBP) is an NADH-dependent dimeric family of nuclear proteins that scaffold interactions between transcriptional regulators and chromatin-modifying complexes. Its association with poor survival in several cancers implicates CtBP as a promising target for pharmacological intervention. We employed computer-assisted drug design to search for CtBP inhibitors, using quantitative structure-activity relationship (QSAR) modeling and docking. Functional screening of these drugs identified 4 compounds with low toxicity and high water solubility. Micro molar concentrations of these CtBP inhibitors produces significant de-repression of epigenetically silenced pro-epithelial genes, preferentially in the triple-negative breast cancer cell line MDA-MB-231. This epigenetic reprogramming occurs through eviction of CtBP from gene promoters; disrupted recruitment of chromatin-modifying protein complexes containing LSD1, and HDAC1; and re-wiring of activating histone marks at targeted genes. In functional assays, CtBP inhibition disrupts CtBP dimerization, decreases cell migration, abolishes cellular invasion, and improves DNA repair. Combinatorial use of CtBP inhibitors with the LSD1 inhibitor pargyline has synergistic influence. Finally, integrated correlation of gene expression in breast cancer patients with nuclear levels of CtBP1 and LSD1, reveals new potential therapeutic vulnerabilities. These findings implicate a broad role for this class of compounds in strategies for epigenetically targeted therapeutic intervention.

Indexed as

Alcohol OxidoreductasesBreast NeoplasmsDNA-Binding ProteinsEpigenesis, GeneticFemaleHumansAlcohol OxidoreductasesC-terminal binding proteinDNA-Binding Proteins

Identifiers

PMID31534138
PMCPMC6751206
OpenAlexW2974652651

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.