Evidence map›Paper›PMID 33802849›Full record

ReviewCells2021

Recent Updates on the Significance of KRAS Mutations in Colorectal Cancer Biology.

Loretta László, Anita Kurilla, Tamás Takács, Gyöngyi Kudlik, Kitti Koprivanacz, László Buday, Virag Vas

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  15. Observational
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  20. International journal of molecular sciences · 2023
    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

7 authors at 2 institutions in 1 country.

Loretta LászlóResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
Anita KurillaResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
Tamás TakácsResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
Gyöngyi KudlikResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
Kitti KoprivanaczResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
László BudayResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.
Virag VasResearch Centre for Natural Sciences, Institute of Enzymology, 1051 Budapest, Hungary.ORCID 0000-0001-7249-6816
Institute of Molecular Life Sciences · HUSemmelweis University · HU

Funding

Hungarian Science Foundation FIEK_16-1-2016-0005Hungarian Science Foundation HunProtEx 2018-1.2.1-NKP-2018-00005Hungarian Science Foundation K 124045
6 · The paper itself

Abstract

The most commonly mutated isoform of RAS among all cancer subtypes is KRAS. In this review, we focus on the special role of KRAS mutations in colorectal cancer (CRC), aiming to collect recent data on KRAS-driven enhanced cell signalling, in vitro and in vivo research models, and CRC development-related processes such as metastasis and cancer stem cell formation. We attempt to cover the diverse nature of the effects of KRAS mutations on age-related CRC development. As the incidence of CRC is rising in young adults, we have reviewed the driving forces of ageing-dependent CRC.

Indexed as

Colorectal NeoplasmsGene Expression Regulation, NeoplasticHumansMutationProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)KRAS protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)cancer stem cellscolorectal cancerCRC with ageKRASRAS-driven metastasisRAS signalling

Identifiers

PMID33802849
PMCPMC8002639
OpenAlexW3136119724

What OpenQuestion 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 OpenQuestion graph.