Evidence map›Paper›PMID 32428871›Full record

ArticleAging2020

PIWI-interacting RNAs piR-13643 and piR-21238 are promising diagnostic biomarkers of papillary thyroid carcinoma.

Zhengyan Chang, Guo Ji, Runzhi Huang, Hong Chen, Yaohui Gao, Weifeng Wang, Xuechen Sun, Jie Zhang, Jiayi Zheng, Qing Wei

Abstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Emerging functions of piwi-interacting RNAs in diseases.Journal of cellular and molecular medicine · 2021
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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

10 authors.

Zhengyan ChangDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.
Guo JiDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.
Runzhi HuangDivision of Spine, Department of Orthopedics, Tongji Hospital Affiliated to Tongji University School of Medicine, Shanghai, China.
Hong ChenCenter for Difficult and Complicated Abdominal Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
Yaohui GaoDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.
Weifeng WangCentral Laboratory, Shanghai Tenth People's Hospital, Shanghai, China.
Xuechen SunDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.
Jie ZhangKey Laboratory of Spine and Spinal Cord Injury Repair and Regeneration (Tongji University), Ministry of Education, Shanghai, China.
Jiayi ZhengDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.
Qing WeiDepartment of Pathology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging studies demonstrate that PIWI-interacting RNAs (piRNAs) participate in the development of cancers. 75 pairs of papillary thyroid carcinoma (PTC) samples and 31 benign thyroid nodule samples were included in this three-phase biomarker identifying study. First, piRNA expression profiles of five pairs of PTC samples were acquired piRNA sequencing. The expression of all upregulated piRNAs were further validated by RT-qPCR. Paired t and nonparametric test were used to evaluate the association between all upregulated piRNAs and clinic stage. The expression levels of key piRNAs were corrected by demographic data to construct a multivariate model to distinguish malignant nodules from benign. Additionally, the intersection between target genes of key piRNAs and differentially expressed genes in The Cancer Genome Atlas (TCGA) PTC samples were used to perform enrichment analysis. Only piR-13643 and piR-21238 were significantly upregulated in PTC and associated with clinic stage. Moreover, both piR-13643 (Area Under Curve (AUC): 0.821) and piR-21238 (AUC: 0.823) showed better performance in distinguishing malignant nodules from benign than currently used biomarkers HBME1 (AUC: 0.590). Based on our findings, piR-13643 and piR-21238 were observed to be significantly upregulated in human PTC. PIWI-interacting RNAs could serve as promising novel biomarkers for accurate detection of PTC.

Indexed as

Thyroid Cancer, PapillaryThyroid NeoplasmsArgonaute ProteinsBiomarkers, TumorDiagnosis, DifferentialFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasmsNeoplasm StagingNomogramsRNA InterferenceRNA, Small InterferingUp-RegulationArgonaute ProteinsBiomarkers, TumorPIWIL1 protein, humanRNA, Small InterferingbiomarkersdiagnosisnomogramPIWI-interacting RNAsthyroid cancer

Identifiers

PMID32428871
PMCPMC7288952

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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.