Evidence map›Paper›PMID 27049724›Full record

ArticleOncotarget2016

Direct repression of the oncogene CDK4 by the tumor suppressor miR-486-5p in non-small cell lung cancer.

Yang Shao, Yu-Qing Shen, Yan-Li Li, Chen Liang, Bing-Jie Zhang, Sheng-Di Lu, Yan-Yun He, Ping Wang, Qiang-Ling Sun, You-Xin Jin and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.6field-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

42 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. Prospects of microRNAs as therapeutic biomarkers in non-small cell lung cancer.Medical oncology (Northwood, London, England) · 2023
    Review
  4. Insights into the Peritumoural Brain Zone of Glioblastoma:International journal of molecular sciences · 2023
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. MicroRNA-486-5p Suppresses Lung CancerFrontiers in oncology · 2021
    Article
  13. Article
  14. Non-Coding RNAs in Lung Tumor Initiation and Progression.International journal of molecular sciences · 2020
    Review
  15. Article
  16. Regulation of PD-1/PD-L1 Pathway in Cancer by Noncoding RNAs.Pathology oncology research : POR · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Yang ShaoSchool of Life Sciences, Shanghai University, Shanghai, China.
Yu-Qing ShenSchool of Life Sciences, Shanghai University, Shanghai, China.
Yan-Li LiSchool of Life Sciences, Shanghai University, Shanghai, China.
Chen LiangSchool of Life Sciences, Shanghai University, Shanghai, China.
Bing-Jie ZhangSchool of Life Sciences, Shanghai University, Shanghai, China.
Sheng-Di LuShanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Yan-Yun HeSchool of Life Sciences, Shanghai University, Shanghai, China.
Ping WangSchool of Life Sciences, Shanghai University, Shanghai, China.
Qiang-Ling SunCentral Laboratory, Shanghai Chest Hospital, Shanghai Jiaotong University, Shanghai, China.
You-Xin JinSchool of Life Sciences, Shanghai University, Shanghai, China.
Zhong-Liang MaSchool of Life Sciences, Shanghai University, Shanghai, China.
Shanghai University · CNShanghai Chest Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs are a class of non-coding single-stranded RNA, 20-23 nucleotide in length, which can be involved in the regulation of gene expression. Through binding with 3'-untranslated regions (3'-UTR), microRNAs can cause degradation of target mRNAs or inhibition of translation, and thus regulating the expression of genes at the post-transcriptional level. In this study, we found that miR-486-5p was significantly downregulated in non-small cell lung cancer (NSCLC) tissues and cell lines, suggesting that miR-486-5p might function as a tumor suppressor in lung cancer. Additionally, we showed that CDK4, an oncogene that plays an important role in cell cycle G1/S phase progression, was directly targeted by miR-486-5p. Furthermore, our data reveals that knockdown of CDK4 by siRNA can inhibit cell proliferation, promote apoptosis, and impede cell-cycle progression. In epigenetics, the upstream promoter of miR-486-5p was strongly regulated by methylation in NSCLC. Collectively, our results suggest that miR-486-5p could not only inhibit NSCLC by downregulating the expression of CDK4, but also be as a promising and potent therapy in the near future.

Indexed as

A549 CellsApoptosisCarcinoma, Non-Small-Cell LungCell ProliferationCyclin-Dependent Kinase 4DNA MethylationDown-RegulationEpigenesis, GeneticG1 Phase Cell Cycle CheckpointsGene Expression Regulation, NeoplasticHumansLung NeoplasmsMicroRNAsPromoter Regions, GeneticRNA InterferenceSignal TransductionCDK4 protein, humanCyclin-Dependent Kinase 4MicroRNAsMIRN486 microRNA, humanCDK4cell cyclemethylationmiR-486-5pNSCLC

Identifiers

PMID27049724
PMCPMC5085134
OpenAlexW2316119938

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.