Evidence map›Paper›PMID 40483365›Full record

ReviewDiscover oncology2025

Elucidating Ras protein as a dual therapeutic target for inflammation and cancer: a review.

Parmar Keshri Nandan, Jayanthi Sivaraman

Abstract readReview
In one paragraph

Review in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Parmar Keshri NandanSchool of Biosciences and Technology, Vellore Institute of Technology, Vellore, India.
Jayanthi SivaramanSchool of Biosciences and Technology, Vellore Institute of Technology, Vellore, India. jayanthi.s@vit.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer, one of the most dreadful diseases of the twenty-first century develops as a result of unregulated inflammatory responses and mutations of genes. In human cancers, among various mutated genes, the Ras gene is one of the most commonly mutated oncogenes. However, when it comes to inflammation, oncogenic Ras mutants can induce tumorigenesis without tumour suppression loss driven by inflammatory responses. Ras protein is a membrane-bound protein with inbuilt GTPase activity which is activated by a variety of extracellular stimuli, converting from an inactive form to an active form. Oncogenic Ras mutants is continuously activated in cancer, thereby enhancing aberrant downstream signalling that leads to tumorigenesis. So, to highlight the significance of Ras protein in cancer and inflammation, this review discussed the signalling pathway for the activation of Ras protein, the role of Ras in immunity and inflammation, downstream regulators of Ras protein and their inhibitors epigenetic regulation of Ras protein. Moreover, we have also done a database-based search using the Database of Cancer Mutant Protein Domains (DCMP) to find out the single nucleotide polymorphism (SNP) level of the Ras gene in different types of cancer. In terms of future perspective, this review discussed emerging strategies to target Ras protein.

Indexed as

ApoptosisCytokinesGTPasesMalignanciesMutation

Identifiers

PMID40483365
PMCPMC12145382

What Socratic holds

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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.