Evidence map›Paper›PMID 26909600›Full record

ArticleOncotarget2016

Hsa-miR-329 exerts tumor suppressor function through down-regulation of MET in non-small cell lung cancer.

Cheng-Cao Sun, Shu-Jun Li, Feng Zhang, Jing-Yu Pan, Liang Wang, Cui-Li Yang, Yong-Yong Xi, De Jia Li

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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 67 citations in OpenAlex.

  1. The lncRNAsMolecular therapy. Nucleic acids · 2021
    Article
  2. Article
  3. Review
  4. Non-Coding RNAs in Lung Tumor Initiation and Progression.International journal of molecular sciences · 2020
    Review
  5. MicroRNAs and Long Non-coding RNAs in c-Met-Regulated Cancers.Frontiers in cell and developmental biology · 2020
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. miR-206/133b Cluster: A Weapon against Lung Cancer?Molecular therapy. Nucleic acids · 2017
    Review
  19. Article
  20. miR-134: A Human Cancer Suppressor?Molecular therapy. Nucleic acids · 2017
    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

8 authors at 2 institutions in 1 country.

Cheng-Cao SunDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Shu-Jun LiDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Feng ZhangDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Jing-Yu PanDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Liang WangDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Cui-Li YangDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Yong-Yong XiDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
De Jia LiDepartment of Occupational and Environmental Health, School of Public Health, Wuhan University, Wuhan, P. R. China.
Wuhan University · CNWuhan Prevention and Treatment Center for Occupational Diseases · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) act as key regulators of multiple cancers. Hsa-miR-329 (miR-329) functions as a tumor suppressor in some malignancies. However, its role on lung cancer remains poorly understood. In this study, we investigated the role of miR-329 on the development of lung cancer. The results indicated that miR-329 was decreased in primary lung cancer tissues compared with matched adjacent normal lung tissues and very low levels were found in a non-small cell lung cancer (NSCLC) cell lines. Ectopic expression of miR-329 in lung cancer cell lines substantially repressed cell growth as evidenced by cell viability assay, colony formation assay and BrdU staining, through inhibiting cyclin D1, cyclin D2 and up-regulatiing p57(Kip2) and p21(WAF1/CIP1). In addition, miR-329 promoted NSCLC cell apoptosis, as indicated by up-regulation of key apoptosis gene cleaved caspase-3, and down-regulation of anti-apoptosis gene Bcl2. Moreover, miR-329 inhibited cellular migration and invasiveness through inhibiting matrix metalloproteinases (MMP)-7 and MMP-9. Further, oncogene MET was revealed to be a putative target of miR-329, which was inversely correlated with miR-329 expression. Furthermore, down-regulation of MET by siRNA performed similar effects to over-expression of miR-329. Collectively, our results demonstrated that miR-329 played a pivotal role in lung cancer through inhibiting cell proliferation, migration, invasion, and promoting apoptosis by targeting oncogenic MET.

Indexed as

Down-Regulation3' Untranslated RegionsA549 CellsAgedAnimalsApoptosisCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansLung NeoplasmsMaleMice, Inbred BALB C3' Untranslated RegionsMET protein, humanMicroRNAsMIRN329 microRNA, humanProto-Oncogene Proteins c-metapoptosishsa-miRNA-329(miR-329)METnon-small cell lung cancer (NSCLC)proliferation

Identifiers

PMID26909600
PMCPMC5008302
OpenAlexW2337568982

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.