Evidence map›Paper›PMID 29246957›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2018

Chemoprevention of Preclinical Breast and Lung Cancer with the Bromodomain Inhibitor I-BET 762.

Di Zhang, Ana S Leal, Sarah Carapellucci, Kayla Zydeck, Michael B Sporn, Karen T Liby

Open access · greenAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
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  5. Review
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  7. The circadian rhythm key geneFrontiers in immunology · 2023
    Article
  8. Article
  9. Article
  10. The BET family in immunity and disease.Signal transduction and targeted therapy · 2021
    Review
  11. Article
  12. Article
  13. The emerging role of BET inhibitors in breast cancer.Breast (Edinburgh, Scotland) · 2020
    Review
  14. The application of histone deacetylases inhibitors in glioblastoma.Journal of experimental & clinical cancer research : CR · 2020
    Review
  15. Review
  16. Review
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Di ZhangDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
Ana S LealDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
Sarah CarapellucciDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
Kayla ZydeckDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
Michael B SpornDepartment of Pharmacology, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire.
Karen T LibyDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan. liby.kare@msu.edu.
Michigan State University · USDartmouth College · US

Funding

Integrative Training in the Pharmacological SciencesT32GM092715 · NIGMS · MICHIGAN STATE UNIVERSITY · PI NEUBIG, RICHARD R · 2011 to 2020
$1.5M
NIGMS NIH HHS T32 GM092715
6 · The paper itself

Abstract

Breast cancer and lung cancer remain the top two leading causes of cancer-related deaths in women. Because of limited success in reducing the high mortality of these diseases, new drugs and approaches are desperately needed. Cancer prevention is one such promising strategy that is effective in both preclinical and clinical studies. I-BET 762 is a new bromodomain inhibitor that reversibly targets BET (bromodomain and extraterminal) proteins and impairs their ability to bind to acetylated lysines on histones, thus interrupting downstream transcription. This inhibitor has anti-inflammatory effects and induces growth arrest in many cancers and is currently under clinical trials for treatment of cancer. However, few studies have investigated the chemopreventive effects of bromodomain inhibitors. Here, we found that I-BET 762 significantly delayed tumor development in preclinical breast and lung cancer mouse models. This drug not only induced growth arrest and downregulated c-Myc, pSTAT3, and pERK protein expression in tumor cells

Indexed as

A549 CellsAnimalsBenzodiazepinesChemopreventionFemaleHumansLung NeoplasmsMammary Neoplasms, ExperimentalMiceMice, Inbred StrainsTumor Cells, CulturedXenograft Model Antitumor AssaysBenzodiazepinesmolibresib

Identifiers

PMID29246957
PMCPMC10265586
OpenAlexW2771430225

What OpenQuestion 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 OpenQuestion graph.