Evidence map›Paper›PMID 36175301›Full record

ReviewTrends in cell biology2023

The role of RAS oncogenes in controlling epithelial mechanics.

Agata Nyga, Sushila Ganguli, Helen K Matthews, Buzz Baum

Open access · hybridAbstract readReview
In one paragraph

Review in Trends in cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.0field-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

24 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Clonal effects of thebioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. The significant role of amino acid metabolic reprogramming in cancer.Cell communication and signaling : CCS · 2024
    Review
  16. Mechanotransduction Circuits in Human Pathobiology.International journal of molecular sciences · 2024
    Article
  17. A Hierarchical Mechanotransduction System: From Macro to Micro.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  18. Review
  19. Emerging roles and mechanisms of ERK pathway mechanosensing.Cellular and molecular life sciences : CMLS · 2023
    Review
  20. New insights into RAS in head and neck cancer.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
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

4 authors at 3 institutions in 1 country.

Agata NygaMedical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK. Electronic address: anyga@mrc-lmb.cam.ac.uk.
Sushila GanguliMedical Research Council Laboratory for Molecular Cell Biology, University College London, London, WC1E 6BT, UK.
Helen K MatthewsSchool of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.
Buzz BaumMedical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK; Medical Research Council Laboratory for Molecular Cell Biology, University College London, London, WC1E 6BT, UK; Institute for the Physics of Living Systems, University College London, London, WC1E 6BT, UK.
MRC Laboratory of Molecular Biology · GBMRC Laboratory for Molecular Cell Biology · GBUniversity of Sheffield · GB

Funding

Cancer Research UK 5369923Cancer Research UK C1529/A17343Medical Research Council MC_UP_1201/27Wellcome TrustWellcome Trust 222575/Z/21/Z
6 · The paper itself

Abstract

Mutations in RAS are key oncogenic drivers and therapeutic targets. Oncogenic Ras proteins activate a network of downstream signalling pathways, including extracellular signal-regulated kinase (ERK) and phosphatidylinositol 3-kinase (PI3K), promoting cell proliferation and survival. However, there is increasing evidence that RAS oncogenes also alter the mechanical properties of both individual malignant cells and transformed tissues. Here we discuss the role of oncogenic RAS in controlling mechanical cell phenotypes and how these mechanical changes promote oncogenic transformation in single cells and tissues. RAS activation alters actin organisation and actomyosin contractility. These changes alter cell rheology and impact mechanosensing through changes in substrate adhesion and YAP/TAZ-dependent mechanotransduction. We then discuss how these changes play out in cell collectives and epithelial tissues by driving large-scale tissue deformations and the expansion of malignant cells. Uncovering how RAS oncogenes alter cell mechanics will lead to a better understanding of the morphogenetic processes that underlie tumour formation in RAS-mutant cancers.

Indexed as

Genes, rasNeoplasmsActinsCell Transformation, NeoplasticHumansMechanotransduction, CellularOncogenesPhosphatidylinositol 3-KinasesSignal TransductionActinsPhosphatidylinositol 3-KinasesactinepitheliamechanobiologymechanotransductionmyosinoncogeneRAStissue mechanicsYAP/TAZ signalling

Identifiers

PMID36175301
PMCPMC9850021
OpenAlexW4297369329

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.