Evidence map›Paper›PMID 26722525›Full record

ArticleInternational journal of clinical and experimental pathology2015

Expression of miR-203 is decreased and associated with the prognosis of melanoma patients.

Kai Wang, Zheng-Wen Zhang

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Omics in Cutaneous Melanoma.Asian Pacific journal of cancer prevention : APJCP · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. miRNAs in the Diagnosis and Prognosis of Skin Cancer.Frontiers in cell and developmental biology · 2020
    Review
  16. Observational
  17. Advances in the Application and Impact of MicroRNAs as Therapies for Skin Disease.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2017
    Review
  18. Article
  19. Article
  20. Pivotal MicroRNAs in Melanoma: A Mini-Review.Molecular diagnosis & therapy · 2016
    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

2 authors.

Kai WangDepartment of Plastic Surgery, Henan Provincial People's Hospital Zhengzhou, Henan, China.
Zheng-Wen ZhangDepartment of Plastic Surgery, Henan Provincial People's Hospital Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs or miRs) are a class of small, non-coding RNAs that can regulate the gene expression in various diseases. MicroRNA-203 (miRNA-203 or miR-203) has previously shown significant alteration in a number of cancers. However, the clinical value of miR-203 in melanoma is rarely reported. The present study aimed to clarify the expression pattern and prognostic role of miR-203 in melanoma patients. Quantitative real-time polymerase chain reaction (qRT-PCR) analysis was used to characterize the expression level of miR-203 in 148 cases of melanoma tissues and adjacent non-cancerous tissues. Results showed that miR-203 expression was significantly decreased in melanoma tissues compared with that in adjacent non-cancerous tissues (P<0.05). Additionally, chi-square was performed to analyze the relationship between miR-203 and clinicopathological features and the down-regulation of miR-203 was significantly associated with tumor thickness and tumor stage (P<0.05). Moreover, Kaplan-Meier analysis showed that low miR-203 expression was associated with short overall survival time of patients. Multivariate analysis indicated that miR-203 could be an independent prognostic marker (P=0.003, HR=2.851, 95% CI=1.439-5.650) in melanoma This study for the first time provided evidence that miR-203 could be an independent potential prognostic marker for patients with melanoma, and might even become a new therapeutic target for the treatment of melanoma.

Indexed as

AgedBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMelanomaMicroRNAsMiddle AgedPrognosisSkin NeoplasmsSurvival RateBiomarkers, TumorMicroRNAsMIRN203 microRNA, humanMelanomamir-203prognosis

Identifiers

PMID26722525
PMCPMC4680470

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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.