Evidence map›Paper›PMID 35682560›Full record

ReviewInternational journal of molecular sciences2022

Potential of the miR-200 Family as a Target for Developing Anti-Cancer Therapeutics.

Hyein Jo, Kyeonghee Shim, Dooil Jeoung

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Do Metastatic Cells Arise from PD-L1International journal of molecular sciences · 2026
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  15. Genetic variations in tumor-suppressor miRNA-encoding genes and their target genes: focus on breast cancer development and possible therapeutic strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

3 authors at 1 institution in 1 country.

Hyein JoDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Kyeonghee ShimDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Dooil JeoungDepartment of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Kangwon National University · KR

Funding

National Research Foundation of Korea 2017M3A9G7072417National Research Foundation of Korea 2017R1A2A2A05001029National Research Foundation of Korea BK21 plus program
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs (18-24 nucleotides) that play significant roles in cell proliferation, development, invasion, cancer development, cancer progression, and anti-cancer drug resistance. miRNAs target multiple genes and play diverse roles. miRNAs can bind to the 3'UTR of target genes and inhibit translation or promote the degradation of target genes. miR-200 family miRNAs mostly act as tumor suppressors and are commonly decreased in cancer. The miR-200 family has been reported as a valuable diagnostic and prognostic marker. This review discusses the clinical value of the miR-200 family, focusing on the role of the miR-200 family in the development of cancer and anti-cancer drug resistance. This review also provides an overview of the factors that regulate the expression of the miR-200 family, targets of miR-200 family miRNAs, and the mechanism of anti-cancer drug resistance regulated by the miR-200 family.

Indexed as

Antineoplastic AgentsMicroRNAsNeoplasms3' Untranslated RegionsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumans3' Untranslated RegionsAntineoplastic AgentsMicroRNAsMIRN200 microRNA, humananti-cancer drug resistancecancer/testis antigen CAGEclinical valuemechanismmicroRNA 200 familymicroRNA mimicsmolecular networkPD-L1

Identifiers

PMID35682560
PMCPMC9180509
OpenAlexW4281563996

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.