Evidence map›Paper›PMID 33130965›Full record

ReviewMolecular biology reports2020

MiR-196: emerging of a new potential therapeutic target and biomarker in colorectal cancer.

Peyman Pourdavoud, Bahram Pakzad, Meysam Mosallaei, Zahra Saadatian, Emran Esmaeilzadeh, Asma Alimolaie, Alireza Shaygannejad

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Hypermethylation ofAdvanced biomedical research · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. The roles of ING5 in cancer: A tumor suppressor.Frontiers in cell and developmental biology · 2022
    Review
  11. Article
  12. Article
  13. 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 at 6 institutions in 1 country.

Peyman PourdavoudIranian Red Crescent Society, Tehran, Iran.
Bahram PakzadDepartment of Internal Medicine, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Meysam MosallaeiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Zahra SaadatianGonabad University of Medical Sciences, Gonabad, Iran.
Emran EsmaeilzadehFaculty of Medicine, AJA University of Medical Science, Tehran, Iran.
Asma AlimolaieDepartment of Biology, Faculty of Science, Shahid Bahonar University of Kerman, Kerman, Iran.
Alireza ShaygannejadDepartment of Internal Medicine (Gastrointestinal Division), Faculty of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran. a_shaygannejad@yahoo.com.ORCID http://orcid.org/0000-0002-6206-8428
Aja University of Medical Sciences · IRArdabil University of Medical Sciences · IRGonabad University of Medical Sciences · IRIsfahan University of Medical Sciences · IRShahid Bahonar University of Kerman · IRUniversity of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deregulation of microRNAs, as key elements in colorectal cancer (CRC) pathogenesis, is correlated with various stages of this cancer. miR-196 is involved in the initiation and progression of a verity of malignances, especially CRC. miR-196 in CRC cells could target different types of genes with oncogenic and/or tumor suppressor function such as HOX genes, GATA6, SOCS1, SOCS3, ANXA1, DFFA, PDCD4, ZG16 and ING5. Therefore, these genes could be up or down-regulated in cells and subsequently change the capacity of CRC cells in terms of tumor development, progression and, response to therapy. Comprehension of miR-196-associated aberrations underlying the CRC pathogenesis might introduce promising targets for therapy. Additionally, it seems that miR-196 expression profiling, especially circulatory exosomal miR-196, might be useful for diagnosis and prognosis determination of the CRC patients. In this review, at first, we summarize the roles of miR-196 in different types of cancers. After that, a detailed discussion about this miRNA and also their targets in CRC pathogenesis, progression, and response to treatment are represented. Moreover, we highlight the potential utilization of miR-196 and its targets as therapeutic targets and novel biomarkers in early detection and prediction of prognosis in CRC patients.

Indexed as

AnimalsBiomarkers, TumorCarcinogenesisCell Line, TumorColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansMicroRNAsPrognosisBiomarkers, TumorMicroRNAsMIRN196 microRNA, humanBiomarkerColorectal cancer (CRC)MicroRNA-196Therapy

Identifiers

PMID33130965
OpenAlexW3097376250

What OpenQuestion holds

Textmetadata
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.