Evidence map›Paper›PMID 33400243›Full record

ArticleHuman cell2021

Comprehensive upstream and downstream regulatory analyses identify miR-675-3p as a potential prognostic biomarker in melanoma.

Cai-Chou Zhao, Hao Guo, Ying Wang, Jiu-Hong Li

Open access · hybridAbstract read
In one paragraph

Article in Human cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Cells · 2026
    Review
  2. Omics in Cutaneous Melanoma.Asian Pacific journal of cancer prevention : APJCP · 2025
    Review
  3. The functional role of exosomalTranslational cancer research · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. NAR cancer · 2022
    Article
  12. circ_0000567/miR-421/Journal of Cancer · 2022
    Article
  13. 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

4 authors at 2 institutions in 1 country.

Cai-Chou ZhaoDepartment of Dermatology, No. 1 Hospital of China Medical University, 155 North Nanjing Street, Heping Distinct, Shenyang, 110001, Liaoning, China.
Hao GuoDepartment of Dermatology, No. 1 Hospital of China Medical University, 155 North Nanjing Street, Heping Distinct, Shenyang, 110001, Liaoning, China.
Ying WangDepartment of Dermatology, Shengjing Hospital of China Medical University, Heping District, Shenyang, 110004, Liaoning, China.
Jiu-Hong LiDepartment of Dermatology, No. 1 Hospital of China Medical University, 155 North Nanjing Street, Heping Distinct, Shenyang, 110001, Liaoning, China. Pfkl2011@126.com.ORCID http://orcid.org/0000-0001-7261-3664
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

National Outstanding Youth Science Fund Project of National Natural Science Foundation of China (CN) 81903228 HG
6 · The paper itself

Abstract

This study assessed miR-675-3p-related regulatory mechanisms in melanoma and the clinical relevance of such regulatory activities. We downloaded miRNA mature strand expression RNA-Seq, phenotypic, and DNA methylation data pertaining to the TCGA Melanoma cohort. Differentially expressed miRNAs (DEMs) between metastatic and primary melanoma patient tissues were then identified, and miR-675-3p expression in melanoma patient peripheral blood was confirmed using the GSE20994 GEO dataset, while its expression in melanoma cell lines was evaluated via qRT-RCR. The clinical and prognostic implications of miR-675-3p in melanoma were assessed, and miR-675-3p target genes were identified using bioinformatics tools. Functional roles of this miRNA were explored via Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. We identified 3 and 22 miRNAs that were up- and downregulated, respectively, in metastatic melanoma samples relative to primary melanoma samples. Upregulation of miR-675-3p was associated with poorer overall patient survival, tumor histologic grade, and Clark's level. Consistently, miR-675-3p was also overexpressed in the peripheral blood of melanoma patients relative to healthy controls, and in melanoma cell lines relative to control cells. Gene regulatory networks indicated that 32 transcription factors control miR-675-3p expression, and that it, in turn, regulates 10 target genes. KEGG analyses indicated that these genes were associated with cell cycle, transcriptional misregulation in cancer, TGF-beta signaling, and HIF-1 signaling pathways. Gain-of-function assays revealed that miR-675-3p could promote cell proliferation via accelerating cell cycle progression. Western blotting results indicated that miR-675-3p could active TGF-beta and HIF-1 signaling. Through upstream and downstream analyses of miR-675-3p-related regulatory activity, we confirmed that this miRNA participates in key melanoma-related processes and offers value as a prognostic biomarker in melanoma patients.

Indexed as

AgedBiomarkers, TumorCell CycleCell Line, TumorCell ProliferationData AnalysisDatasets as TopicFemaleGene ExpressionGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMelanomaMicroRNAsPrognosisBiomarkers, TumorHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIRN675 microRNA, humanTransforming Growth Factor betaBioinformaticsMelanomamiR-675-3pPrognostic biomarkerSignaling pathways

Identifiers

PMID33400243
PMCPMC7900067
OpenAlexW3120992838

What OpenQuestion holds

Textmetadata
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.