Evidence map›Paper›PMID 35342753›Full record

ArticleBioMed research international2022

hsa-miR-206b Involves in the Development of Papillary Thyroid Carcinoma via Targeting LMX1B.

Hongsheng Lu, Chumeng Zhu, Yanyun Ruan, Lilong Fan, Zhengying Ruan, Qi Chen, Jiuyun Yuan, Yang Xu, Hongwei Wang, Qing Wei

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Hongsheng LuDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, China.ORCID https://orcid.org/0000-0001-6528-4153
Chumeng ZhuPrecision Medicine Center, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang 318000, China.
Yanyun RuanPrecision Medicine Center, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang 318000, China.
Lilong FanDepartment of Pathology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang 318000, China.
Zhengying RuanDepartment of Pathology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang 318000, China.
Qi ChenPrecision Medicine Center, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, Zhejiang 318000, China.ORCID https://orcid.org/0000-0002-0640-6859
Jiuyun YuanNanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.
Yang XuNanjing Geneseeq Technology Inc., Nanjing, Jiangsu, China.
Hongwei WangDepartment of Pathology, People's Hospital, The Affiliated Hospital of Ningbo University, Ningbo, China.ORCID https://orcid.org/0000-0002-3633-0269
Qing WeiDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, China.ORCID https://orcid.org/0000-0002-9990-2535
Taizhou Central Hospital · CNTongji University · CNNingbo University Affiliated Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Papillary thyroid carcinoma (PTC) is the most common endocrine system malignant thyroid cancer, and patients with lymph node metastasis typically exhibit poor prognosis. MicroRNAs (miRNAs) can act as either oncogenes or tumor suppressors in PTC. This study was aimed at using PTC transcriptome data obtained from The Cancer Genome Atlas (TCGA) to identify differentially expressed, survival-related miRNAs and target genes. Methods: We analyzed the TCGA datasets to identify differentially expressed mRNAs/miRNAs in 493 PTC patients with stage I_II group (stages I and II) versus stage III_IV group (stages III and IV) according to TNM staging. The Kaplan-Meier survival analysis, the Cox regression analysis, and the log-rank test were performed to investigate survival-related miRNAs. Results: We identified 36 significantly differentially expressed miRNAs in the stage I_II group versus the stage III_IV group, in which 31 were upregulated and only 5 were downregulated (i.e., hsa-miR-891a-5p, hsa-miR-892a, hsa-miR-888-5p, hsa-miR-891b, and hsa-miR-892b). Additionally, five signature miRNAs (hsa-miR-206, hsa-miR-299-3p, hsa-miR-299-5p, hsa-miR-496, and hsa-miR-509-3-5p) were associated with the overall survival of PTC patients. We also found that Conclusion: hsa-miR-206b might be involved in promoting TNM staging in PTC via targeting of

Indexed as

MicroRNAsThyroid NeoplasmsGene Expression ProfilingHumansLIM-Homeodomain ProteinsPrognosisThyroid Cancer, PapillaryTranscription FactorsLIM homeobox transcription factor 1 betaLIM-Homeodomain ProteinsMicroRNAsMIRN206 microRNA, humanMIRN299 microRNA, humanMIRN496 microRNA, humanTranscription Factors

Identifiers

PMID35342753
PMCPMC8948606
OpenAlexW4220778721

What OpenQuestion holds

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LicenceCC BY
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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.