Evidence map›Paper›PMID 39682179›Full record

ReviewCancers2024

Oncogenic RAS in Cancers from the DNA Replication Stress and Senescence Perspective.

Hervé Técher, Samira Kemiha, Xieraili Aobuli, Arun Mouli Kolinjivadi

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Elucidating DNA Damage-Dependent Immune System Activation.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Observational
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.

Hervé TécherUniversité Côte d'Azur, Institute for Research on Cancer and Aging of Nice-IRCAN, CNRS, INSERM, 06100 Nice, France.ORCID 0000-0002-4161-0791
Samira KemihaUniversité Côte d'Azur, Institute for Research on Cancer and Aging of Nice-IRCAN, CNRS, INSERM, 06100 Nice, France.ORCID 0000-0001-8405-6957
Xieraili AobuliLee Moffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL 33612, USA.
Arun Mouli KolinjivadiCancer Science Institute of Singapore, National University of Singapore, Singapore 117599, Singapore.ORCID 0000-0003-1172-0866

Funding

Initiative of Excellence Université Côte d'Azur (IdEx) Advanced Research Program 2024Initiative of Excellence Université Côte d'Azur (IdEx) ANR- 15-IDEX-01National Research Agency (ANR) Projet ANR-23-CPJ1-0025-01
6 · The paper itself

Abstract

Rat Sarcoma (RAS)-driven cancers have been one of the main foci in the field of cancer science for over four decades. Despite significant improvement in understanding the biology of RAS oncogene, the method to target RAS-mutated cancers is still unclear. In recent years, the role for RAS beyond its hyperproliferation has been extensively documented. In this review, we systematically address and dwell on the details of the mechanisms of RAS oncogene-mediated alteration in the DNA replication and DNA damage response (DDR) pathways, focusing on lung cancers. We further extend this molecular connection towards cytosolic DNA accumulation, innate immune activation and senescence in RAS-addicted cancers. At the end, we briefly speculate on the potential strategies for targeting RAS mutated lung cancers, considering various approaches targeting DNA replication, DNA repair and the cGAS-STING pro-inflammatory pathway. These new lines of therapy, especially when used in combinations, may enhance treatment efficacy and overcome the challenges associated with these mutations.

Indexed as

cancersDNA damage responseDNA replicationgenomic instabilityRASsenescence

Identifiers

PMID39682179
PMCPMC11640673

What OpenQuestion holds

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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.