Evidence map›Paper›PMID 32161621›Full record

ArticleCellular & molecular biology letters2020

MicroRNA-125b exerts antitumor functions in cutaneous squamous cell carcinoma by targeting the STAT3 pathway.

Ke Tian, Wanggen Liu, Jing Zhang, Xiaoyi Fan, Jingyuan Liu, Nan Zhao, Chunxia Yao, Guoying Miao

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  9. MiR-134-5p/Life (Basel, Switzerland) · 2022
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  15. Oh, the Mutations You'll Acquire! A Systematic Overview of Cutaneous Squamous Cell Carcinoma.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2021
    Review
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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

8 authors at 2 institutions in 1 country.

Ke Tian1Department of Dermatology, Affiliated Hospital of Hebei University of Engineering, Handan, 056002 China.
Wanggen Liu2Department of Histology and Embryology, Preclinical Medicine College, Xinxiang Medical University, Xinxiang, 453003 China.
Jing Zhang3Department of Pathology, Medical School, Hebei University of Engineering, Handan, 056002 China.
Xiaoyi Fan3Department of Pathology, Medical School, Hebei University of Engineering, Handan, 056002 China.
Jingyuan Liu3Department of Pathology, Medical School, Hebei University of Engineering, Handan, 056002 China.
Nan Zhao3Department of Pathology, Medical School, Hebei University of Engineering, Handan, 056002 China.
Chunxia Yao3Department of Pathology, Medical School, Hebei University of Engineering, Handan, 056002 China.
Guoying Miao1Department of Dermatology, Affiliated Hospital of Hebei University of Engineering, Handan, 056002 China.ORCID 0000-0003-1306-4727
Hebei University of Engineering · CNXinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNA-125b (miR-125b) is downregulated in human cutaneous squamous cell carcinoma (CSCC). However, its function in CSCC has yet to be extensively explored. Here, we analyze the relationship between signal transducer and activator of transcription 3 (STAT3) and miR-125b in CSCC.

methodsWestern blotting and quantitative RT-PCR were used to determine the expression of the miR-125b-STAT3 axis in human CSCC tissues and cell lines. The direct regulatory effect of miR-125b on STAT3 expression was assessed using a luciferase reporter gene assay and RNA immunoprecipitation assay. The MTT assay and flow cytometry were used to determine the role of the miR-125b-STAT3 axis in CSCC cell proliferation and apoptosis.

resultsMiR-125b expression levels were significantly lower in CSCC cell lines and tissues than in normal cell lines and tissues. STAT3 was identified as the direct target of miR-125b. Upregulation of miR-125b and downregulation of STAT3 suppressed cell proliferation and promoted cell apoptosis. Cyclin D1 and Bcl2 were identified as the downstream targets of the miR-125-STAT3 axis.

conclusionsOur findings indicate that miR-125b acts as a tumor suppressor in CSCC by targeting the STAT3 pathway. This observation increases our understanding of the molecular mechanisms of CSCC. Therapies aimed at activating miR-125b or inhibiting STAT3 signaling should be explored as potential treatments for CSCC.

Indexed as

ApoptosisCarcinoma, Squamous CellCell Line, TumorCell ProliferationCyclin D1Gene Expression Regulation, NeoplasticHumansMicroRNAsProto-Oncogene Proteins c-bcl-2Signal TransductionSkin NeoplasmsSTAT3 Transcription FactorBCL2 protein, humanCyclin D1MicroRNAsMIRN125 microRNA, humanProto-Oncogene Proteins c-bcl-2STAT3 protein, humanSTAT3 Transcription FactorCutaneous squamous cell carcinomamicroRNA-125bSignal transducer and activator of transcription (STAT) 3

Identifiers

PMID32161621
PMCPMC7059386
OpenAlexW3012216893

What OpenQuestion holds

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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.