Evidence map›Paper›PMID 26254100›Full record

ReviewTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

MicroRNA-224: as a potential target for miR-based therapy of cancer.

Wei Chen, Xue-Mei Fan, Ling Mao, Jun-Ying Zhang, Jian Li, Jian-Zhong Wu, Jin-Hai Tang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. LDL Receptor Pathway Regulation by miR-224 and miR-520d.Frontiers in cardiovascular medicine · 2020
    Article
  7. Article
  8. Bta-miR-124a Affects Lipid Metabolism by RegulatingBioMed research international · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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 5 institutions in 1 country.

Wei ChenGraduate School, Xuzhou Medical College, Xuzhou, Jiangsu, China. jsszlyypw@163.com.
Xue-Mei FanNanjing Maternity and Child Health Care Hospital, Nanjing, Jiangsu, China.
Ling MaoDepartment of General Surgery, Huaian Second People's Hospital, Huaian, China.
Jun-Ying ZhangNanjing Medical University Affiliated Cancer Hospital, Cancer Institute of Jiangsu Province, Nanjing, Jiangsu, China.
Jian LiNanjing Medical University Affiliated Cancer Hospital, Cancer Institute of Jiangsu Province, Nanjing, Jiangsu, China.
Jian-Zhong WuNanjing Medical University Affiliated Cancer Hospital, Cancer Institute of Jiangsu Province, Nanjing, Jiangsu, China.
Jin-Hai TangNanjing Medical University Affiliated Cancer Hospital, Cancer Institute of Jiangsu Province, Nanjing, Jiangsu, China. tjh_doctor@163.com.
Nanjing Medical University · CNJiangsu Cancer Hospital · CNNanjing Maternity and Child Health Care Hospital · CNXian Yang Central Hospital · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small noncoding RNA molecules which regulate the target gene expression posttranscriptionally. Increasing studies have shown that microRNAs play important roles in multiple biological pathways. For instance, aberrant expression of microRNA-224 (miR-224) plays a vital role in tumor biology in various types of human cancer. Here, we aim to summarize the molecular mechanisms that lead to the overexpression of miR-224 in cancers, analyze the effect of miR-224 on tumor biology, and reveal the clinical significance of miR-224. MiR-224 regulates its targets by modulating messenger RNA (mRNA) stability and/or protein translation, and it would provide new insight into molecular targeting cancer treatment.

Indexed as

Genetic TherapyBiomarkers, TumorCarcinogenesisGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasmsBiomarkers, TumorMicroRNAsMIRN224 microRNA, humanBiomakerCancerMicroRNAMicroRNA-224Therapy

Identifiers

PMID26254100
OpenAlexW2198066582

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.