Evidence map›Paper›PMID 33239613›Full record

ArticleCell death & disease2020

CircCNTNAP3-TP53-positive feedback loop suppresses malignant progression of esophageal squamous cell carcinoma.

Hui Wang, Xuming Song, Yajing Wang, Xuewen Yin, Yingkuan Liang, Te Zhang, Lin Xu, Feng Jiang, Gaochao Dong

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  5. RNA-Binding Proteins (RBPs) and Circular RNA Biogenesis.Advances in experimental medicine and biology · 2025
    Review
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  17. Article
  18. Circular RNAs With Efficacy in PreclinicalCancer genomics & proteomics
    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

9 authors at 2 institutions in 1 country.

Hui WangThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0003-2238-8782
Xuming SongThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
Yajing WangThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
Xuewen YinJiangsu Key Laboratory of Molecular and Translational Cancer Research, Cancer Institute of Jiangsu Province, Nanjing, China.
Yingkuan LiangThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
Te ZhangThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
Lin XuThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China. xulin_83@hotmail.com.ORCID 0000-0001-6490-1471
Feng JiangThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China. fengjiang_nj@njmu.edu.cn.
Gaochao DongThe Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China. ilsyvm@njmu.edu.cn.ORCID 0000-0002-7026-6280
Jiangsu Cancer Hospital · CNNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutation or downregulation of p53 (encoded by TP53) accelerates tumorigenesis and malignant progression in esophageal squamous cell carcinoma (ESCC). However, it is still unknown whether circular RNAs (circRNAs), a novel class of endogenous noncoding RNAs, participate in the regulation of this progress. In this study, we explored the expression profiles of circRNAs in three paired samples of ESCC and identified cCNTNAP3, which is a circRNA that originates from the CNTNAP3 gene transcript and is highly expressed in normal human esophageal tissue. However, we found that the cCNTNAP3 expression level was significantly downregulated in ESCC tissues. In vitro and in vivo studies revealed that cCNTNAP3 inhibited proliferation and increased apoptosis in p53 wild-type ESCC cells, but not in mutant cells. Mechanistically, we found that cCNTNAP3 promotes the expression of p53 by sponging miR-513a-5p. Rescue assay confirmed that the suppressive function of cCNTNAP3 was dependent on miR-513a-5p. We also observed that p53/RBM25 participated in the formation of cCNTNAP3, which implied the existence of a positive feedback loop between cCNTNAP3 and p53. Furthermore, the downregulation of cCNTNAP3 was significantly correlated with later T stage and thus can serve as an independent risk factor for the overall survival of patients with p53 wild-type ESCC. In conclusion, the cCNTNAP3-TP53 positive feedback loop may provide a potential target for the management of ESCC, which also reveals the important role of circRNAs in the regulation of p53.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorDisease ProgressionEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaGene Expression Regulation, NeoplasticHEK293 CellsHeterograftsHumansMembrane ProteinsMiceMice, NudeNerve Tissue ProteinsRNA, CircularTransfectionBiomarkers, TumorCNTNAP3 protein, humanMembrane ProteinsNerve Tissue ProteinsRNA, CircularTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID33239613
PMCPMC7689480
OpenAlexW3108483956

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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.