Evidence map›Paper›PMID 39449908›Full record

ArticleCureus2024

Impact of Suppressor of Mothers Against Decapentaplegic (SMAD) 7 Gene Single Nucleotide Polymorphisms on Colorectal Cancer Risk and Prognosis.

Maurício Peixoto, Marta Viana-Pereira, Maria Júlia Amorim, Ana D Marques, Diana Freitas, Joana Cunha, Filipa Pereira, Rui Reis, Elisabete Couto

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Maurício PeixotoMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Marta Viana-PereiraMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Maria Júlia AmorimMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Ana D MarquesMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Diana FreitasMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Joana CunhaMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Filipa PereiraMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.
Rui ReisOncology, School of Medicine and the Life and Health Sciences Research Institute, University of Minho, Braga, PRT.
Elisabete CoutoMedical Oncology, Unidade Local de Saúde de Braga, Braga, PRT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a prevalent diagnosis worldwide with significant associated mortality. Single nucleotide polymorphic (SNP) variants have been identified as being associated with CRC risk. Although SMAD7 SNPs have been associated with the risk of developing CRC, their prognostic effect is still unclear. We carried out a case-control study to establish an association between genotypes of the suppressor of mothers against decapentaplegic (SMAD) 7 SNP rs4464148, rs4939827, and rs12953717 and CRC risk. Furthermore, we retrospectively assessed whether these SNPs had prognostic implications in CRC patients by evaluating survival with Kaplan-Meier curves and Cox regression. Only the CT genotype of the rs4939827 variant showed an association with CRC risk, and no genotype (CC, CT, or TT) of any of the three SNPs was shown to have prognostic implications in overall survival. Our study failed to show an association between certain SNP genotypes and the risk of CRC, which has already been well documented in two meta-analyses. Furthermore, it showed no prognostic relevance for these SNPs. More studies are needed to understand whether there are population variations or haplotype effects that could disturb the evaluation of these results.

Indexed as

colon cancercolorectal cancerprognosisrectal cancerrisksmad7

Identifiers

PMID39449908
PMCPMC11500270

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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.