Evidence map›Paper›PMID 33177705›Full record

ReviewNature reviews. Cancer2021

Equivocal, explicit and emergent actions of PKC isoforms in cancer.

Peter J Parker, Sophie J Brown, Veronique Calleja, Probir Chakravarty, Mathias Cobbaut, Mark Linch, Jacqueline J T Marshall, Silvia Martini, Neil Q McDonald, Tanya Soliman and 1 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The chordoid gliomaScience signaling · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  14. PKCActa pharmaceutica Sinica. B · 2024
    Article
  15. Article
  16. Article
  17. Apoptosis and eryptosis: similarities and differences.Apoptosis : an international journal on programmed cell death · 2024
    Review
  18. Article
  19. Article
  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

11 authors at 3 institutions in 1 country.

Peter J ParkerProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK. peter.parker@crick.ac.uk.ORCID http://orcid.org/0000-0002-6218-2933
Sophie J BrownProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.
Veronique CallejaProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.
Probir ChakravartyBioinformatics, The Francis Crick Institute, London, UK.
Mathias CobbautProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0003-0279-0336
Mark LinchUCL Cancer Institute, University College London, London, UK.
Jacqueline J T MarshallProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0001-5491-2919
Silvia MartiniProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.
Neil Q McDonaldSignalling and Structural Biology Laboratory, Francis Crick Institute, London, UK.
Tanya SolimanCentre for Cancer Genomics and Computational Biology, Bart's Cancer Institute, London, UK.ORCID http://orcid.org/0000-0002-4687-629X
Lisa WatsonProtein Phosphorylation Laboratory, Francis Crick Institute, London, UK.
The Francis Crick Institute · GBCRUK Lung Cancer Centre of Excellence · GBKing's College London · GB

Funding

Cancer Research UK FC001130Department of HealthMedical Research Council FC001130Wellcome Trust FC001130
6 · The paper itself

Abstract

The maturing mutational landscape of cancer genomes, the development and application of clinical interventions and evolving insights into tumour-associated functions reveal unexpected features of the protein kinase C (PKC) family of serine/threonine protein kinases. These advances include recent work showing gain or loss-of-function mutations relating to driver or bystander roles, how conformational constraints and plasticity impact this class of proteins and how emergent cancer-associated properties may offer opportunities for intervention. The profound impact of the tumour microenvironment, reflected in the efficacy of immune checkpoint interventions, further prompts to incorporate PKC family actions and interventions in this ecosystem, informed by insights into the control of stromal and immune cell functions. Drugging PKC isoforms has offered much promise, but when and how is not obvious.

Indexed as

AnimalsHumansIsoenzymesMutationNeoplasmsPhosphorylationPromoter Regions, GeneticProtein Kinase CTumor MicroenvironmentIsoenzymesProtein Kinase C

Identifiers

PMID33177705
OpenAlexW3100551133

What Socratic 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 Socratic graph.