Evidence map›Paper›PMID 31927744›Full record

ArticleJournal of gastrointestinal cancer2021

Prognostic and Diagnostic Values of miR-506 and SPON 1 in Colorectal Cancer with Clinicopathological Considerations.

Rozita Tamjidifar, Morteza Akbari, Saeed Tarzi, Mahsa Sadeghzadeh, Mahsa Abolghasemi, Elham Poursaei, Navid Shomali, Farshad Mahdavi

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Article in Journal of gastrointestinal cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Connecting intermediate phenotypes to disease using multi-omics in heart failure.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2025
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  6. Immune-Related Biomarkers Associated with Lung Metastasis from the Colorectal Cancer Microenvironment.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2022
    Article
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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

8 authors at 2 institutions in 1 country.

Rozita Tamjidifar *Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Morteza Akbari *Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Saeed TarziImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mahsa SadeghzadehTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mahsa AbolghasemiTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Elham PoursaeiTuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Navid ShomaliImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Farshad MahdaviDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Farshadmahdavi48@yahoo.com.
Tabriz University of Medical Sciences · IRIslamic Azad University of Ahar · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOne of the most common cancers in the world is colorectal cancer, which has increased significantly in recent decades. In the carcinogenicity process in the colon, there are genes involved in various cellular processes, such as cell cycle, apoptosis, and cell migration. According to studies carried out, both miR-506 and SPON 1 genes are involved in the process which initiates and promotes cancer. In this study, alterations in the expression of target genes from the viewpoint of carcinogenicity were studied and evaluated.

methodsFifty tumor tissues and normal marginal tissue were collected from patients who were undergoing colorectal cancer surgery. After the extraction of RNA, the real-time PCR method was performed to evaluate the gene expression. Also, alterations of gene expression in response to defined amounts of chemotherapeutic drugs (IC50) were evaluated. P < 0.05 was considered statistically significant.

resultsThe relative expression level of miR-506 in tumor tissues was significantly decreased in comparison with healthy marginal tissues (P = 0.044). On the other hand, the SPON1 gene expression level was decreased too in tumor tissues in comparison with healthy marginal tissues (P = 0.019). There was also a significant relationship between the expression of target genes and clinicopathological involvement. However, there was no significant alteration in these genes along with the chemotherapeutic drug.

conclusionThese findings suggest that the relative expression of miR-506 and SPON 1 gene can be considered as a diagnostic or predictive biomarker for colorectal cancer. However, further studies on protein levels should be conducted.

Indexed as

AdultAgedAntineoplastic AgentsBiomarkers, TumorCarcinogenesisCell Line, TumorChemotherapy, AdjuvantColectomyColonColonoscopyColorectal NeoplasmsDown-RegulationExtracellular Matrix ProteinsFemaleFluorouracilGene Expression Regulation, NeoplasticAntineoplastic AgentsBiomarkers, TumorExtracellular Matrix ProteinsFluorouracilMicroRNAsMIRN506 microRNA, humanOxaliplatinSPON1 protein, humanCRCDiagnosismiR-506PrognosisSPON1Treatment

Identifiers

PMID31927744
OpenAlexW2999567191

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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.