Evidence map›Paper›PMID 34326893›Full record

ArticleComputational and mathematical methods in medicine2021

A Comprehensive Evaluation of miR-144-3p Expression and Its Targets in Laryngeal Squamous Cell Carcinoma.

Bin-Yu Mo, Jin-Shu Pang, Wen-Bin Dai, Ya-Si Su, Wei Jiang, Su-Ning Huang

Open access · hybridAbstract read
In one paragraph

Article in Computational and mathematical methods in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 53% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

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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 1 institution in 1 country.

Bin-Yu MoDepartment of Otolaryngology, Liuzhou People's Hospital of Guangxi, No. 8 Wenchang Rd., Liuzhou, Guangxi Zhuang Autonomous Region, 545006, China.ORCID https://orcid.org/0000-0001-8969-6152
Jin-Shu PangDepartment of Radiotherapy, Guangxi Medical University Cancer Hospital, No. 71 Hedi Rd., Nanning, Guangxi Zhuang Autonomous Region, 530021, China.ORCID https://orcid.org/0000-0002-1919-4859
Wen-Bin DaiDepartment of Pathology, Liuzhou People's Hospital of Guangxi, No. 8 Wenchang Rd., Liuzhou, Guangxi Zhuang Autonomous Region, 545006, China.ORCID https://orcid.org/0000-0003-4190-6805
Ya-Si SuDepartment of Pathology, Liuzhou People's Hospital of Guangxi, No. 8 Wenchang Rd., Liuzhou, Guangxi Zhuang Autonomous Region, 545006, China.ORCID https://orcid.org/0000-0003-4890-4116
Wei JiangDepartment of Educational Administration, Guangxi Medical University Cancer Hospital, No. 71 Hedi Rd., Nanning, Guangxi Zhuang Autonomous Region, 530021, China.ORCID https://orcid.org/0000-0003-4564-8356
Su-Ning HuangDepartment of Radiotherapy, Guangxi Medical University Cancer Hospital, No. 71 Hedi Rd., Nanning, Guangxi Zhuang Autonomous Region, 530021, China.ORCID https://orcid.org/0000-0001-9911-9084
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laryngeal squamous cell carcinoma (LSCC) is an aggressive type of head and neck squamous cell carcinoma (HNSCC) with a relatively high rate of morbidity and mortality. An altered miR-144-3p level in LSCC with a small number of patients has been previously reported. However, the clinical implication of miR-144-3p and its involved mechanism underlying this disease is not clearly elucidated. In this work, we aimed to confirm the expression of miR-144-3p with larger samples and also to identify target genes for the investigation of the underlying mechanism of miR-144-3p in LSCC. The levels of miR-144-3p were downregulated in 155 samples of LSCC tissues as compared to 26 non-LSCC samples (SMD: -0.78; 95% confidence interval (CI): -1.23, -0.32). The AUC of 0.90 in the summarized ROC curve also indicated a potential ability to differentiate LSCC from non-LSCC tissues, with a sensitivity of 0.78 and a specificity of 0.88. With respect to the molecular mechanism, we predicted the potential targets from online-based prediction, peer-reviewed publications, and RNA-seq and microarray data. In particular, the genes influenced by transfection with miR-144-3p in the LSCC FaDu cell line were collected from the microarray GSE56243. Lastly, 12 novel targets for miR-144-3p in LSCC were obtained by different algorithms. In conclusion, our study confirmed the loss or downregulation of miR-144-3p in LSCC, which might contribute to the LSCC tumorigenesis and progression via regulation of the 12 novel targets, such as IL24, ITGA6, and CEP55. In the future, further investigations are required to validate the present results.

Indexed as

Cell Cycle ProteinsCell Line, TumorComputational BiologyDisease ProgressionDown-RegulationFemaleGene Expression Regulation, NeoplasticGene OntologyHumansIntegrin alpha6Interleukin-24InterleukinsLaryngeal NeoplasmsMaleMicroRNAsMiddle AgedCell Cycle ProteinsCep55 protein, humanIntegrin alpha6Interleukin-24InterleukinsITGA6 protein, humanMicroRNAsMIRN144 microRNA, humanTenascinTNC protein, human

Identifiers

PMID34326893
PMCPMC8302387
OpenAlexW3184532576

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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.