Evidence map›Paper›PMID 37835512›Full record

ArticleCancers2023

Unraveling the Role of Molecular Profiling in Predicting Treatment Response in Stage III Colorectal Cancer Patients: Insights from the IDEA International Study.

Ippokratis Messaritakis, Eleni Psaroudaki, Konstantinos Vogiatzoglou, Maria Sfakianaki, Pantelis Topalis, Ioannis Iliopoulos, Dimitrios Mavroudis, John Tsiaoussis, Nikolaos Gouvas, Maria Tzardi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
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

11 authors at 3 institutions in 2 countries.

Ippokratis MessaritakisLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.ORCID 0000-0003-1877-500X
Eleni PsaroudakiLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.
Konstantinos VogiatzoglouLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.
Maria SfakianakiLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.
Pantelis TopalisInstitute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, 70013 Heraklion, Greece.ORCID 0000-0002-1635-4810
Ioannis IliopoulosLaboratory of Computational Biology, Division of Basic Sciences, School of Medicine, University of Crete, 71003 Heraklion, Greece.
Dimitrios MavroudisLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.
John TsiaoussisDepartment of Anatomy, School of Medicine, University of Crete, 70013 Heraklion, Greece.ORCID 0000-0002-9892-1048
Nikolaos GouvasMedical School, University of Cyprus, 99010 Nicosia, Cyprus.ORCID 0000-0002-6541-4226
Maria TzardiLaboratory of Pathology, Medical School, University of Crete, 70013 Heraklion, Greece.
John SouglakosLaboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.ORCID 0000-0002-1642-1147
University of Crete · GRFoundation for Research and Technology Hellas · GRUniversity of Cyprus · CY

Funding

Gastrointestinal cancer study group N/AHellenic Society of Medical Oncology N/A
6 · The paper itself

Abstract

backgroundThis study aimed to investigate the molecular profiles of 237 stage III CRC patients from the international IDEA study. It also sought to correlate these profiles with Toll-like and vitamin D receptor polymorphisms, clinicopathological and epidemiological characteristics, and patient outcomes.

methodsWhole Exome Sequencing and PCR-RFLP on surgical specimens and blood samples, respectively, were performed to identify molecular profiling and the presence of Toll-like and vitamin D polymorphisms. Bioinformatic analysis revealed mutational status.

resultsAmong the enrolled patients, 63.7% were male, 66.7% had left-sided tumors, and 55.7% received CAPOX as adjuvant chemotherapy. Whole exome sequencing identified 59 mutated genes in 11 different signaling pathways from the Kyoto Encyclopedia of Genes and Genomes (KEGG) CRC panel. On average, patients had 8 mutated genes (range, 2-21 genes). Mutations in

conclusionsMolecular characterization of tumor cells can enhance our understanding of the disease course. Mutations may serve as promising prognostic biomarkers, offering improved treatment options. Confirming these findings will require larger patient cohorts and international collaborations to establish correlations between molecular profiling, clinicopathological and epidemiological characteristics and clinical outcomes.

Indexed as

bioinformaticscolorectal cancerIDEA studymolecular profilingstage IIIwhole exome sequencing

Identifiers

PMID37835512
PMCPMC10571744
OpenAlexW4387264484

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.