Evidence map›Paper›PMID 31334580›Full record

ArticleCell proliferation2019

MicroRNA-191 promotes hepatocellular carcinoma cell proliferation by has_circ_0000204/miR-191/KLF6 axis.

Fang Tian, Chengtao Yu, Min Wu, Xiaoyu Wu, Lingfeng Wan, Xuejun Zhu

Abstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed.

  1. Article
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  4. Review
  5. Review
  6. Review
  7. Circular RNAs in Cell Cycle Regulation of Cancers.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Circ_0005918 Sponges miR-622 to Aggravate Intervertebral Disc Degeneration.Frontiers in cell and developmental biology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  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

6 authors.

Fang TianAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0002-8409-8812
Chengtao YuSchool of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Min WuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.
Xiaoyu WuLife Science and Technology Institute, China Pharmaceutical University, Nanjing, China.
Lingfeng WanAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.
Xuejun ZhuAffiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-8885-5924

Funding

Research Project of Affiliated Hospital of Nanjing University of Chinese Medicine Y17014Research project of Jiangsu Provincial Health and Family Planning Committee LGY2017077"Six Talent Projects" of Jiangsu Province 2015-WSN-047the Priority Academic Program Development of Jiangsu Higher Education Institutions 035062002003c
6 · The paper itself

Abstract

objectivesMicroRNAs are powerful regulators in hepatocellular carcinoma (HCC) tumorigenesis. MicoRNA-191 (miR-191) has been reported to play an important role in HCC, However, the regulatory mechanism is still unclear. In this study, we investigated the role of miR-191 in HCC and studied its underlying mechanisms of action. MATERIALS AND

methodsThe expression of miR-191 in HCC tissues was determined by quantitative real-time PCR (qRT-PCR). The role of miR-191 in HCC cells was examined by using both in vitro and in vivo assays. Downstream targets of miR-191 were determined by qRT-PCR and Western blot analysis. Dual-luciferase assays were performed to validate the interaction between miR-191 and its targets.

resultsThe expression of miR-191 was significantly higher in HCC patients and a higher miR-191 expression predicted poorer prognosis. Analysis of The Cancer Genome Atlas data sets suggested that miR-191 positively correlated with cell cycle progression. Gain and loss of function assays showed that miR-191 promoted cell cycle progression and proliferation. Luciferase reporter assay showed that miR-191 directly targeted the 3'-untranslated region of KLF6 mRNA. Furthermore, circular RNA has_circ_0000204 could sponge with miR-191, resulting in inactivation of miR-191.

conclusionsOur study sheds light on the novel underlying mechanism of miR-191 in HCC, which may accelerate the development of cancer therapy.

Indexed as

3' Untranslated RegionsAnimalsAntagomirsCarcinoma, HepatocellularCell Line, TumorCell ProliferationDatabases, FactualDisease ProgressionFemaleG1 Phase Cell Cycle CheckpointsHumansKruppel-Like Factor 6Liver NeoplasmsMaleMiceMicroRNAs3' Untranslated RegionsAntagomirsKLF6 protein, humanKruppel-Like Factor 6MicroRNAsMIRN191 microRNA, humanRNARNA, Circularcell cyclehas_circ_0000204Hepatocellular carcinomaKLF6miR-191

Identifiers

PMID31334580
PMCPMC6797514

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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.