Evidence map›Paper›PMID 32090490›Full record

ArticleFEBS open bio2020

miR-21-5p promotes cell proliferation and G1/S transition in melanoma by targeting CDKN2C.

Zhaohui Yang, Bo Liao, Xiaoyan Xiang, Sha Ke

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. Article
  6. miR-21-5p Targets PIK3R1 to Regulate the NF-International journal of endocrinology · 2025
    Article
  7. Article
  8. Review
  9. HNRNPA2B1-mediated mJournal of translational medicine · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. High-LevelOphthalmology science · 2022
    Article
  14. Article
  15. Review
  16. Review
  17. Review
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  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Zhaohui YangDepartment of Burns and Plastic Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Bo LiaoDepartment of Urology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Xiaoyan XiangDepartment of Burns and Plastic Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Sha KeDepartment of Neurology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.ORCID 0000-0002-6009-5262
Affiliated Hospital of North Sichuan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human melanoma is a highly malignant tumor originating from cutaneous melanocytes. The noncoding RNA microRNA (miR)-21-5p has been reported to be expressed at high levels in malignant melanocytic skin tissues, but its potential functional role in melanoma remains poorly understood. Here, we explored the cellular effects of miR-21-5p on melanoma in vitro and the underlying mechanisms. Quantitative real-time PCR was used to show that miR-21-5p is significantly up-regulated in clinical samples from patients with melanoma as compared with adjacent noncancerous tissues. Overexpression of miR-21-5p significantly enhanced, whereas knockdown attenuated, cell proliferation and G1/S transition in melanoma cell lines (A375 and M14). Luciferase reporter assays were used to show that the cyclin-dependent kinase inhibitor 2C (CDKN2C) is a downstream target of miR-21-5p. Furthermore, miR-21-5p mimics resulted in a decrease in CDKN2C expression, and CDKN2C expression was observed to be inversely correlated with miR-21-5p expression in melanoma tissues. Rescue experiments were performed to show that overexpression of CDKN2C partially reversed the effects of miR-21-5p up-regulation on A375 cells. Consistently, knockdown of CDKN2C abolished the effects of miR-21-5p down-regulation on A375 cells. Overall, our studies demonstrate that miR-21-5p can promote the growth of melanoma cells by targeting CDKN2C, which may induce G0/G1 phase arrest of melanoma cells.

Indexed as

AdultAgedApoptosisCell CycleCell Line, TumorCell MovementCell ProliferationChinaCyclin-Dependent Kinase Inhibitor p18FemaleG1 Phase Cell Cycle CheckpointsGene ExpressionGene Expression Regulation, NeoplasticHumansMaleMelanomaCDKN2C protein, humanCyclin-Dependent Kinase Inhibitor p18MicroRNAsMIRN21 microRNA, humanCDKN2CG0/G1 phase arrestmelanomamiR-21-5pproliferation

Identifiers

PMID32090490
PMCPMC7193168
OpenAlexW3007264026

What OpenQuestion holds

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LicenceCC BY
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.