Evidence map›Paper›PMID 39441422›Full record

SynthesisJournal of cancer research and clinical oncology2024

Epigenetic modulation of autophagy pathway by small molecules in colorectal cancer: a systematic review.

Mozhdeh Zamani, Farima Safari, Morvarid Siri, Somayeh Igder, Niloofar Khatami, Sanaz Dastghaib, Pooneh Mokarram

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of cancer research and clinical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

7 authors.

Mozhdeh ZamaniAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Farima SafariAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Morvarid SiriAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Somayeh IgderDepartment of Clinical Biochemistry, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Niloofar KhatamiAutophagy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Sanaz DastghaibEndocrinology and Metabolism Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. suny.respina@gmail.com.ORCID http://orcid.org/0000-0001-8553-9221
Pooneh MokarramAutophagy Research Center, Department of Biochemistry, Shiraz University of Medical Sciences, Shiraz, Iran. mokaram2@gmail.com.ORCID http://orcid.org/0000-0002-9717-0473

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeColorectal cancer (CRC) remains a global health challenge with limited treatment success due to drug resistance. Recent research highlights the potential of small molecules to modulate CRC by targeting epigenetics or autophagy pathways. This systematic review explores the epigenetic effect of small molecules on autophagy in CRC, aiming to identify novel therapeutic strategies.

methodsFollowing PRISMA guidelines, we systematically reviewed 508 studies from PubMed, Scopus, and Web of Science databases until August 13, 2023.

resultsEight studies met inclusion criteria, examining the role of small molecules as epigenetic modulators (Histone acetylation/deacetylation, DNA methylation/demethylation and gene expression regulation by miRNAs) influencing the autophagy pathway in CRC. The studies encompassed in vitro and animal model in vivo studies. Small molecules exhibited diverse effects on autophagy in CRC. For instance, panobinostat promoted autophagy leading to CRC cell death, while aspirin inhibited autophagy flux, reducing aspirin-mediated CRC cell death. The epigenetic modulation of autophagy by various small molecules differently affects their anticancer effect, which underscores the complexity of therapeutic interventions.

conclusionUnderstanding the intricate dynamics among small molecules, epigenetic modifications, and autophagy in CRC is crucial for developing targeted therapeutic strategies. Considering the dual role of autophagy in tumorigenesis and tumor suppression, administration of these small molecules may differently affect the cancer cell fate and drug response or resistance based on their effect on the autophagy pathway. Therefore, recognition of the epigenetics mechanism of anticancer small molecules on autophagy may contribute to deciding how to prescribe them for better CRC treatment.

Indexed as

Antineoplastic AgentsAutophagyColorectal NeoplasmsEpigenesis, GeneticAnimalsDNA MethylationGene Expression Regulation, NeoplasticHumansSmall Molecule LibrariesAntineoplastic AgentsSmall Molecule LibrariesAutophagyColorectal cancerDNA methylationHistone acetylationmiRNASmall molecules

Identifiers

PMID39441422
PMCPMC11499346

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.