Evidence map›Paper›PMID 28887744›Full record

ArticleMolecular and cellular biochemistry2018

MicroRNA-203 suppresses proliferation in liver cancer associated with PIK3CA, p38 MAPK, c-Jun, and GSK3 signaling.

Annie Zhang, Jaganathan Lakshmanan, Amirreza Motameni, Brian G Harbrecht

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  7. Review
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  10. Reference Genes for qPCR-Based miRNA Expression Profiling in 14 Human Tissues.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2022
    Review
  11. Article
  12. Article
  13. TRPV4 induces apoptosis via p38 MAPK in human lung cancer cells.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
  14. Article
  15. Article
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  17. [Expression characteristics and clinical significance of microRNA-29a in hepatocellular carcinoma tissues].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2019
    Article
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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

4 authors at 1 institution in 1 country.

Annie ZhangPrice Institute of Surgical Research and Department of Surgery, University of Louisville, Louisville, KY, 40202, USA.
Jaganathan LakshmananPrice Institute of Surgical Research and Department of Surgery, University of Louisville, Louisville, KY, 40202, USA. j0laks01@louisville.edu.
Amirreza MotameniPrice Institute of Surgical Research and Department of Surgery, University of Louisville, Louisville, KY, 40202, USA.
Brian G HarbrechtPrice Institute of Surgical Research and Department of Surgery, University of Louisville, Louisville, KY, 40202, USA.
Rice Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary liver cancer (hepatocellular carcinoma, HCC) is a leading cause of cancer-related deaths, and alternative ways to treat this disease are urgently needed. In recent years, novel approaches to cancer treatment have been based on microRNAs, small non-coding RNA molecules that play a crucial role in cancer progression by regulating gene expression. Overexpression of some microRNAs has shown therapeutic potential, but whether or not this was the case for microRNA-203 (miR-203) in liver cancer was unknown. Therefore, the aim of this study was to investigate the effect of miR-203 overexpression in liver cancer and explore the related mechanisms. Liver cancer cells from the HepG2 and Hep3B cell lines were transfected with either miR-203 mimics or negative control RNA, and then the cells were subjected to cell viability, cell proliferation, and Western blotting assays. As a result of microRNA-203 overexpression, HepG2 and Hep3B cell viability and cell proliferation significantly declined. Furthermore, microRNA-203 overexpression led to inhibited expression of phosphatidylinositol-4,5-bisphosphate 3-kinase (PIK3)/protein kinase B (Akt), c-Jun, and p38 mitogen-activated protein kinases (p38 MAPK), and restored glycogen synthase kinase 3 (GSK 3) activity in HepG2 cells. Our results suggest that c-Jun, p38 MAPK, PIK3CA/Akt, and GSK3 signaling involved in the effect of miR-203 on the proliferation of HCC cells.

Indexed as

MAP Kinase Signaling SystemCarcinoma, HepatocellularCell ProliferationClass I Phosphatidylinositol 3-KinasesGlycogen Synthase KinasesHep G2 CellsHumansLiver NeoplasmsMicroRNAsp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-junRNA, NeoplasmClass I Phosphatidylinositol 3-KinasesGlycogen Synthase KinasesMicroRNAsMIRN203 microRNA, humanp38 Mitogen-Activated Protein KinasesPIK3CA protein, humanProto-Oncogene Proteins c-junRNA, Neoplasmc-JunGSK3Liver cancerMicroRNA-203p38-MAPKPI3K

Identifiers

PMID28887744
OpenAlexW2754481519

What OpenQuestion holds

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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.