Evidence map›Paper›PMID 31501407›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

KIAA1199, a Target of MicoRNA-486-5p, Promotes Papillary Thyroid Cancer Invasion by Influencing Epithelial-Mesenchymal Transition (EMT).

Xuehua Jiao, Jiandong Ye, Xiujie Wang, Xueyan Yin, Guodong Zhang, Xingbo Cheng

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 50 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 3 institutions in 1 country.

Xuehua JiaoDepartment of Endocrinology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China (mainland).
Jiandong YeDepartment of General Surgery, The First People's Hospital of Wujiang District, Suzhou, Jiangsu, China (mainland).
Xiujie WangDepartment of Endocrinology, The First People's Hospital of Wujiang District, Suzhou, Jiangsu, China (mainland).
Xueyan YinDepartment of Endocrinology, The First People's Hospital of Wujiang District, Suzhou, Jiangsu, China (mainland).
Guodong ZhangDepartment of Endocrinology, Suzhou Yongding Hospital, Suzhou, Jiangsu, China (mainland).
Xingbo ChengDepartment of Endocrinology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China (mainland).
Wujiang District People's Hospital · CNSoochow University · CNSuzhou Yongding Hospital

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND KIAA1199 has been reported to be associated with malignant progression and poor clinical outcomes in various human malignancies. However, its clinical role and molecular function remain unknown in papillary thyroid cancer (PTC). MATERIAL AND METHODS The Cancer Genome Atlas (TCGA) was used to investigate the expression profiles of KIAA1199 and miR-486-5p in PTC. Immunohistochemistry was used to validate the protein expression of KIAA1199 in PTC. The Weighted Gene Co-expression Network Analysis (WGCNA) and Gene Set Enrichment Analysis (GSEA) were used to explore the potential pathway underling KIAA1199 in PTC. In vitro and in vivo experiments were performed to investigate the biological role of KIAA1199 in PTC progression. Luciferase reporter assays and Western blot analysis were performed to determine whether KIAA1199 is a downstream target of miR-486-5p. RESULTS We found that KIAA1199 was aberrantly elevated in PTC tissues compared with normal tissues, and upregulation of KIAA1199 was positively correlated with more advanced clinical variables. Additionally, bioinformatic analysis indicated that KIAA1199 was involved in cell migration and invasion. KIAA1199 silencing inhibited the invasive ability of PTC cells by affecting epithelial-mesenchymal transition (EMT) in vitro and in vivo. Furthermore, miR-486-5p was identified as an upstream microRNA that directly targets the 3'-UTR region of KIAA1199. CONCLUSIONS The miR-486-5p/KIAA1199/EMT axis might play a critical role in PTC invasion and metastasis and offers a potential therapeutic strategy for PTC.

Indexed as

AnimalsBase SequenceCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansHyaluronoglucosaminidaseMaleMice, Inbred BALB CMice, NudeMicroRNAsNeoplasm InvasivenessThyroid Cancer, PapillaryUp-RegulationCEMIP protein, humanHyaluronoglucosaminidaseMicroRNAsMIRN486 microRNA, human

Identifiers

PMID31501407
PMCPMC6752488
OpenAlexW2973057232

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.