Evidence map›Paper›PMID 41361160›Full record

ArticleDiscover oncology2025

Investigating the expression of hsa_circ_0036722/hsa-miR-503-5p/PDCD4 axis in esophageal cancer.

Shayan Marhamati, Roghayeh Abbasalipourkabir, Zeinab Seyedkhan, Nasrin Ziamajidi, Fatemeh Bahreini, Amirnader Emami Razavi, Mahdi Bahmani

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

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4 · The record

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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

7 authors.

Shayan MarhamatiDepartment of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Roghayeh AbbasalipourkabirDepartment of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Zeinab SeyedkhanDepartment of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Nasrin ZiamajidiDepartment of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Fatemeh BahreiniDepartment of Molecular Medicine and Genetics, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Amirnader Emami RazaviIran National Tumor Bank, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Mahdi BahmaniDepartment of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. M.bahmani@umsha.ac.ir.

Funding

Vice Chancellor for Research and Technology, Hamadan University of Medical Sciences 140305164029
6 · The paper itself

Abstract

backgroundEsophageal cancer (EC) is the ninth most common cancer globally. Circular RNAs (circRNAs), including hsa_circ_0036722, are important in various cancers, but their specific role in EC remains unclear. Therefore, this study investigates the roles of hsa_circ_0036722 in EC.

methodsWe analyzed circRNAs sequencing from Gene Expression Omnibus (GEO). On the other hand, analyzed miRNAs and mRNAs sequencing related to EC from The Cancer Genome Atlas (TCGA). Then, the hsa_circ_0036722/hsa-mir-503-5p/PDCD4 axis was identified using online tools for detecting circRNA-associated miRNAs and target mRNAs. Gene expression levels in 20 EC tissue pairs were assessed using RT-qPCR, while PDCD4 protein expression was evaluated by Western blot. A receiver operating characteristic (ROC) analysis was performed to evaluate their diagnostic potential.

resultsRT-qPCR results demonstrated decreased expression of hsa_circ_0036722 and PDCD4, alongside increased hsa-miR-503-5p expression in EC tissues. A reduction in PDCD4 protein expression was also noted. Correlations showed that hsa_circ_0036722 and PDCD4 expressions were positively correlated, while hsa_circ_0036722 and hsa-miR-503-5p were negatively correlated. In addition, a significant negative correlation was observed between hsa-miR-503-5p and PDCD4 expression. Elevated levels of hsa-miR-503-5p were detected in early stages of EC. The ROC curve reflected a significant area under the curve for the axis genes.

conclusionThis study identified a novel regulatory axis, hsa_circ_0036722/hsa-mir-503-5p/PDCD4, for regulating EC, which may be a potential target for treating patients with this cancer.

Indexed as

DiagnosisEsophageal cancerhsa_circ_0036722hsa-mir-503-5pPDCD4

Identifiers

PMID41361160
PMCPMC12796057

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