Evidence map›Paper›PMID 39810224›Full record

ReviewEpigenetics & chromatin2025

Crosstalk between non-coding RNAs and programmed cell death in colorectal cancer: implications for targeted therapy.

Seyed Reza Taha, Mehdi Karimi, Bahar Mahdavi, Milad Yousefi Tehrani, Ali Bemani, Shahriar Kabirian, Javad Mohammadi, Sina Jabbari, Meysam Hushmand, Alireza Mokhtar and 1 more

Abstract readReview
In one paragraph

Review in Epigenetics & chromatin, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Food science & nutrition · 2026
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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

11 authors.

Seyed Reza TahaDepartment of Pathology and Immunology, Washington University School of Medicine, St. LouisWashington, MO, USA.
Mehdi KarimiFaculty of Medicine, Bogomolets National Medical University (NMU), Kiev, Ukraine. Karimi9010@gmail.com.ORCID 0009-0006-4388-0214
Bahar MahdaviDepartment of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Milad Yousefi TehraniStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Ali BemaniStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Shahriar KabirianStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Javad MohammadiStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Sina JabbariStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Meysam HushmandStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Alireza MokhtarStudent Research Committee, Kashan University of Medical Sciences, Kashan, Iran.
Mohammad Hossein PourhanifehResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran. mhph.lord.1996@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) remains one of the most common causes of cancer-related mortality worldwide. Its progression is influenced by complex interactions involving genetic, epigenetic, and environmental factors. Non-coding RNAs (ncRNAs), including microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), have been identified as key regulators of gene expression, affecting diverse biological processes, notably programmed cell death (PCD).

objectiveThis review aims to explore the relationship between ncRNAs and PCD in CRC, focusing on how ncRNAs influence cancer cell survival, proliferation, and treatment resistance.

methodsA comprehensive literature analysis was conducted to examine recent findings on the role of ncRNAs in modulating various PCD mechanisms, including apoptosis, autophagy, necroptosis, and pyroptosis, and their impact on CRC development and therapeutic response.

resultsncRNAs were found to significantly regulate PCD pathways, impacting tumor growth, metastasis, and treatment sensitivity in CRC. Their influence on these pathways highlights the potential of ncRNAs as biomarkers for early CRC detection and as targets for innovative therapeutic interventions.

conclusionUnderstanding the involvement of ncRNAs in PCD regulation offers new insights into CRC biology. The targeted modulation of ncRNA-PCD interactions presents promising avenues for personalized cancer treatment, which may improve patient outcomes by enhancing therapeutic effectiveness and reducing resistance.

Indexed as

ApoptosisColorectal NeoplasmsRNA, UntranslatedGene Expression Regulation, NeoplasticHumansMicroRNAsRNA, CircularRNA, Long NoncodingMicroRNAsRNA, CircularRNA, Long NoncodingRNA, UntranslatedCancerColorectal cancerGeneticNon-coding RNAsOncologyProgrammed cell death

Identifiers

PMID39810224
PMCPMC11734566

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.