Evidence map›Paper›PMID 33431945›Full record

ArticleScientific reports2021

CircRNA GFRA1 promotes hepatocellular carcinoma progression by modulating the miR-498/NAP1L3 axis.

Shuai Lv, Yingxia Li, Hanbing Ning, Meihui Zhang, Qiaoyu Jia, Xijuan Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The Tumorigenic Role of Circular RNA-MicroRNA Axis in Cancer.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
  12. Journal of gastrointestinal oncology · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

6 authors at 3 institutions in 1 country.

Shuai LvDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450018, Henan Province, China.
Yingxia LiDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450018, Henan Province, China.
Hanbing NingDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450018, Henan Province, China.
Meihui ZhangDepartment of Pediatrics, Henan Provincial People's Hospital; Zhengzhou University People's Hospital; Henan University People's Hospital, No. 7, Weiwu Road, Zhengzhou, 450003, Henan Province, China.
Qiaoyu JiaDepartment of Gastroenterology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450018, Henan Province, China.
Xijuan WangDepartment of Pediatrics, Henan Provincial People's Hospital; Zhengzhou University People's Hospital; Henan University People's Hospital, No. 7, Weiwu Road, Zhengzhou, 450003, Henan Province, China. xijuanwang126@aliyun.com.
First Affiliated Hospital of Zhengzhou University · CNHenan Provincial People's Hospital · CNHenan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs) play essential roles in tumorigenesis and tumor progression. CircRNA GFRA1 (circGFRA1) was dysregulated in many cancer samples and acted as an independent marker for prediction of survivals in various cancer patients. However, the functions and molecular mechanisms of circGFRA1 in hepatocellular carcinoma (HCC) remain unclear. We collected 62 HCC tissues and normal adjacent tissues to evaluate the expression of circGFRA1 and the relationship between circGFRA1 expression and HCC patients' survival. We carried out a list of characterization experiments to investigate the roles and underling mechanisms of circGFRA1 and miR-498 in HCC progressions. CircGFRA1 was greatly increased in HCC tissues and cells, and the over-expression of circGFRA1 was intimately related with the advanced clinical stage and poor survival of HCC patients. The expression of circGFRA1 was negatively correlated with the expression of miR-498, but a positive correlation was found between circGFRA1 and NAP1L3 expression in HCC tissues. Silencing circGFRA1 inhibited the growth and invasion of hepatocellular carcinoma. Moreover, miR-498 over-expression or NAP1L3 inhibition could abrogate the oncogene role of circGFRA1 in HCC in vivo. Our findings indicated that circGFRA1 contributed to HCC progression by modulating the miR-498/NAP1L3 axis in HCC.

Indexed as

AdultAgedAged, 80 and overAnimalsCarcinoma, HepatocellularCell ProliferationCells, CulturedCohort StudiesDisease ProgressionFemaleGlial Cell Line-Derived Neurotrophic Factor ReceptorsHep G2 CellsHumansLiver NeoplasmsMaleMiceGFRA1 protein, humanGlial Cell Line-Derived Neurotrophic Factor ReceptorsMicroRNAsMIRN498 microRNA, humanNAP1L3 protein, humanNerve Tissue ProteinsRNA, Circular

Identifiers

PMID33431945
PMCPMC7801409
OpenAlexW3118559854

What OpenQuestion holds

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LicenceCC BY
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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.