Evidence map›Paper›PMID 35156716›Full record

ArticleThe EMBO journal2022

Cells on lockdown: long-term consequences of CDK4/6 inhibition.

Alexis R Barr, Sarah E McClelland

Open access · bronzeAbstract readComment
In one paragraph

Article in The EMBO journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Cancer takes many paths through G1/S.Trends in cell biology · 2024
    Review
  5. Review
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Alexis R BarrInstitute of Clinical Sciences, Imperial College London, London, UK.ORCID 0000-0002-6684-8114
Sarah E McClellandBarts Cancer Institute, Queen Mary University of London, London, UK.ORCID 0000-0002-9987-4511
NIHR Imperial Biomedical Research Centre · GBQueen Mary University of London · GB

Funding

Cancer Research UK 25729Medical Research Council MC_UP_1605/8
6 · The paper itself

Abstract

Inhibition of cyclin-dependent kinases Cdk4/6 is emerging as a useful anti-proliferative chemotherapy, but it remains unclear how durable inhibition of cancer cell proliferation is achieved to promote a long-lasting response in patients, or how toxicity is limited to cancer cells with minimal side effects. Two recent papers in The EMBO Journal investigating senescence induction following prolonged Cdk4/6 inhibitor treatment now reveal important insights into ways to increase anti-tumour effects of Cdk4/6 inhibition and to reduce therapy-induced side effects of senescence induction.

Indexed as

Cyclin-Dependent Kinase 6Tumor Suppressor Protein p53Cell Line, TumorCell ProliferationCyclin-Dependent Kinase 4HumansCDK4 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Tumor Suppressor Protein p53

Identifiers

PMID35156716
PMCPMC8922248
OpenAlexW4212834846

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.