Evidence map›Paper›PMID 35686701›Full record

ArticleMolecular genetics & genomic medicine2022

Effect of KRAS mutations and p53 expression on the postoperative prognosis of patients with colorectal cancer.

Lingfeng Wang, Shengtao Lin, Changshun Yang, Shaoxin Cai, Weihua Li

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

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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

10 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Lingfeng WangShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Shengtao LinShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Changshun YangShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Shaoxin CaiShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Weihua LiShengli Clinical Medical College of Fujian Medical University, Fuzhou, China.ORCID 0000-0003-4581-2240
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the occurrence and development of colorectal cancer, p53 is an important regulator downstream of the MAPK signaling pathway and plays an important role in inhibiting abnormal proliferation signals generated by KRAS mutations. The purpose of this study is to explore the correlation between KRAS mutations and p53 expression and evaluate their prognosis values in colorectal cancer.

methodsPCR technology and immunohistochemical (IHC) staining were used to detect KRAS mutation status and p53 expression level in 266 specimens of colorectal adenocarcinoma. Based on p53 expression level, these were divided into high expression and normal groups. Patients with KRAS mutations were divided into mutant and wild-type groups. The two were combined with each other to analyze the relationship between patients' clinical data and their impact on the prognosis.

resultsKRAS mutations were found in 38.6% of the patients and 40.8% had a high p53 expression. There was no significant difference in the overall survival rate of patients, with or without KRAS gene mutations, and p53 expression level. In the group of patients with KRAS mutations, the survival time of patients with a high p53 expression was significantly lower than that of patients with a normal p53 expression (p = 0.020, log-rank test). Multivariate analysis showed that p53 high expression is an independent risk factor for the overall survival time of patients with KRAS mutations (HR = 2.330, 95% CI = 1.041-5.216, p < 0.05).

conclusionColorectal cancer patients with KRAS mutations with a high p53 expression have a poor prognosis.

Indexed as

AdenocarcinomaColorectal NeoplasmsHumansMutationProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53KRAS protein, humanProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53colorectal adenocarcinomaKRASp53prognosis

Identifiers

PMID35686701
PMCPMC9266597
OpenAlexW4281640393

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.