Evidence map›Paper›PMID 28935812›Full record

ArticleCancer research2017

miR-130a Deregulates PTEN and Stimulates Tumor Growth.

Huijun Wei, Ri Cui, Julian Bahr, Nicola Zanesi, Zhenghua Luo, Wei Meng, Guang Liang, Carlo M Croce

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. How MicroRNAs Command the Battle against Cancer.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Cancers · 2023
    Review
  11. Review
  12. Vascular Ageing: Mechanisms, Risk Factors, and Treatment Strategies.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
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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

8 authors at 4 institutions in 2 countries.

Huijun WeiUniversity of Michigan Life Sciences Institute, Ann Arbor, Michigan. huijunw@umich.edu Carlo.Croce@osumc.edu.
Ri CuiDepartment of Cancer Biology and Genetics, and Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Julian BahrUniversity of Michigan Life Sciences Institute, Ann Arbor, Michigan.
Nicola ZanesiDepartment of Cancer Biology and Genetics, and Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Zhenghua LuoDepartment of Cancer Biology and Genetics, and Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Wei MengDepartment of Radiation Oncology, and Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Guang LiangAffiliated Yueqing Hospital and School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Carlo M CroceDepartment of Cancer Biology and Genetics, and Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio. huijunw@umich.edu Carlo.Croce@osumc.edu.
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USUniversity of Michigan · USWenzhou Medical University · CNThe Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Cancer Gene Discovery to Identify Targetable TargetsR35CA197706 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2015 to 2021
$6.4M
NCI NIH HHS P30 CA016058NCI NIH HHS R35 CA197706
6 · The paper itself

Abstract

H-RasV12 oncogene has been shown to promote autophagic cell death. Here, we provide evidence of a contextual role for H-RasV12 in cell death that is varied by its effects on miR-130a. In E1A-immortalized murine embryo fibroblasts, acute expression of H-RasV12 promoted apoptosis, but not autophagic cell death. miRNA screens in this system showed that miR-130a was strongly downregulated by H-RasV12 in this model system. Enforced expression of miR-130a increased cell proliferation in part via repression of PTEN. Consistent with this effect, miR-130a overexpression in human breast cancer cells promoted Akt phosphorylation, cell survival, and tumor growth. In clinical specimens of multiple human cancers, expression of miR-130 family members correlated inversely with PTEN expression. Overall, our results defined miR-130a as an oncogenic miRNA that targets PTEN to drive malignant cell survival and tumor growth.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorCells, CulturedCell SurvivalEmbryo, MammalianFemaleFibroblastsGene Expression ProfilingHEK293 CellsHumansMCF-7 CellsMice, Inbred BALB CMice, NudeMicroRNAsNeoplasmsMicroRNAsMIRN130 microRNA, humanMIRN130 microRNA, mousePTEN Phosphohydrolaseras Proteins

Identifiers

PMID28935812
PMCPMC7081380
OpenAlexW2759401232

What OpenQuestion holds

Textmetadata
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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.