Evidence map›Paper›PMID 31821686›Full record

ArticleJournal of cellular and molecular medicine2020

Inhibition of bromodomain and extra-terminal proteins increases sensitivity to venetoclax in chronic lymphocytic leukaemia.

Giovanna Carrà, Paolo Nicoli, Marcello Francesco Lingua, Beatrice Maffeo, Antonio Cartellà, Paola Circosta, Mara Brancaccio, Guido Parvis, Valentina Gaidano, Angelo Guerrasio and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 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
1.9field-weighted citation impact, top 14% 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, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Targeting epigenetic mechanisms to overcome venetoclax resistance.Biochimica et biophysica acta. Molecular cell research · 2021
    Review
  12. Review
  13. Co-Operativity between MYC and BCL-2 Pro-Survival Proteins in Cancer.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Enhancing venetoclax activity in hematological malignancies.Expert opinion on investigational drugs · 2020
    Review
  18. 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

13 authors at 2 institutions in 1 country.

Giovanna CarràDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0002-6263-6800
Paolo NicoliDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
Marcello Francesco LinguaDept. of Oncology, University of Turin, Orbassano, Italy.ORCID 0000-0002-0743-2573
Beatrice MaffeoDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.
Antonio CartellàDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0001-7201-141X
Paola CircostaDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0001-8251-6905
Mara BrancaccioDept. of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.ORCID 0000-0003-2327-6846
Guido ParvisDivision of Hematology, Ospedale Mauriziano, Torino, Italy.
Valentina GaidanoDivision of Hematology, Ospedale Mauriziano, Torino, Italy.
Angelo GuerrasioDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0002-1911-795X
Giuseppe SaglioDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0002-1046-3514
Riccardo TaulliDept. of Oncology, University of Turin, Orbassano, Italy.ORCID 0000-0003-1277-6263
Alessandro MorottiDept. of Clinical and Biological Sciences, University of Turin, Orbassano, Italy.ORCID 0000-0002-8407-2903
University of Turin · ITA. O. Ordine Mauriziano di Torino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of drugs able to target BTK, PI3k-delta and BCL2 has dramatically improved chronic lymphocytic leukaemia (CLL) therapies. However, drug resistance to these therapies has already been reported due to non-recurrent changes in oncogenic pathways and genes expression signatures. In this study, we investigated the cooperative role of the BCL2 inhibitor venetoclax and the BRD4 inhibitor JQ1. In particular, we found that JQ1 shows additional activity with venetoclax, in CLL cell lines and in ex vivo isolated primary CD19

Indexed as

AzepinesBridged Bicyclo Compounds, HeterocyclicCell Line, TumorCell ProliferationCell SurvivalDrug SynergismHumansLeukemia, Lymphocytic, Chronic, B-CellSulfonamidesTranscription FactorsTriazolesAzepinesBridged Bicyclo Compounds, Heterocyclic(+)-JQ1 compoundSulfonamidesTranscription FactorsTriazolesvenetoclaxBCL-2BET inhibitorBRD4chronic lymphocytic leukaemiavenetoclax

Identifiers

PMID31821686
PMCPMC6991693
OpenAlexW2995630663

What Socratic 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 Socratic graph.