Evidence map›Paper›PMID 42430378›Full record

ArticlePloS one2026

Could molecular variations be predictive in right and left colon cancer in different gender and age groups?

Hatice Cilem Solak, Nazli Mert, Asim Leblebici, Zerrin Isik, Ender Berat Ellidokuz, Yasemin Basbinar

Abstract read
In one paragraph

Article in PloS one, 2026. 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
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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

6 authors.

Hatice Cilem SolakDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Turkiye.
Nazli MertDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Turkiye.
Asim LeblebiciDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Turkiye.
Zerrin IsikDepartment of Computer Engineering, Faculty of Engineering, Dokuz Eylul University, Izmir, Turkiye.ORCID https://orcid.org/0000-0003-1779-1681
Ender Berat EllidokuzDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Turkiye.
Yasemin BasbinarDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylul University, Izmir, Turkiye.ORCID https://orcid.org/0000-0002-1627-1548

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeft-sided colon-cancer (LCC) and right-sided colon cancer (RCC) harbor different clinical entities and different therapy protocols. Our study aimed to demonstrate genomic expression differences and clarify the clinical differences between LCC and RCC by using in-silico methods.

methodsOur study compares mRNA expression levels between clinical groups to describe variations in molecular characteristics between right-left-sided colon cancer (216 right-141 left) using the TCGA-COAD database. We identified differentially expressed genes and analyzed survival profiles for RCC and LCC. We applied a gene set enrichment analysis and merged the results by group to highlight common and different pathways.

resultsThe results reveal that TG, INSL5, EREG and AIRE were found as age-related genes, and TG, INSL5, EREG, AIRE, HOXB8 and FLT3 were found as gender-related genes for RCC and LCC. We found that high expression of the AIRE gene was linked with poor survival in patients with RCC in males and under 65 age groups. High expression of LEP was correlated with poor survival in patients with RCC, regardless of gender. In addition, low expression of the EREG gene was linked with poor survival in women with RCC.

conclusionsThree genes (AIRE, LEP, EREG), which are effective on the EGFR pathway, would have great predictive and prognostic importance in the context of anti-EGFR therapies.

Indexed as

Colonic NeoplasmsAgedAge FactorsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisSex FactorsTranscription FactorsTranscription Factors

Identifiers

PMID42430378
PMCPMC13353988

What Socratic holds

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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 Socratic graph.