Evidence map›Paper›PMID 35876041›Full record

ArticleClinical and translational medicine2022

Circular RNA circ-TNPO3 inhibits clear cell renal cell carcinoma metastasis by binding to IGF2BP2 and destabilizing SERPINH1 mRNA.

Xiaojuan Pan, Bo Huang, Qiang Ma, Junwu Ren, Yuying Liu, Cong Wang, Dawei Zhang, Jian Fu, Lingyu Ran, Ting Yu and 10 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

54 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Deltacoronavirus Modulates circRNA cGLIS3 Metabolism to Evade Host Antiviral Response.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

20 authors at 4 institutions in 1 country.

Xiaojuan PanCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Bo HuangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Qiang MaCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Junwu RenCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Yuying LiuCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Cong WangDepartment of Urology, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Dawei ZhangDepartment of Urology, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Jian FuDepartment of Urology, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Lingyu RanDepartment of Kidney, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Ting YuDepartment of Clinical Laboratory, The 89th Hospital of The People's Liberation Army, Weifang, P. R. China.
Haiping LiCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Xiaolin WangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Feifei YangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Ce LiangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Yuying ZhangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Shimin WangCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Jingjing RenDepartment of Clinical Laboratory, The 89th Hospital of The People's Liberation Army, Weifang, P. R. China.
Wei LiDepartment of Pharmacy, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Yongquan WangDepartment of Urology, Southwest Hospital, Army Medical University, Chongqing, P. R. China.
Bin XiaoCollege of Pharmacy, Chongqing Medical University, Chongqing, P. R. China.
Chongqing Medical University · CNArmy Medical University · CN117th Hospital of People's Liberation Army · CNSouthwest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClear cell renal cell carcinoma (ccRCC) is a common malignant tumour of the urinary tract. The major causes of poor prognosis are the lack of early diagnosis and metastasis. Accumulating research reveals that circular RNAs (circRNAs) can play key roles in the development and the progression of cancer. However, the role of circRNAs in ccRCC is still uncertain.

methodsThe circRNAs microarray (n = 4) was performed to investigate the circRNAs with differential expression in ccRCC tissues. The candidate circRNA was selected based on the cut-off criteria, such as circRNA expression abundance, circRNA size and the design of divergent primers. The circ-transportin-3 (TNPO3) levels in ccRCC tissues were tested by quantitative real-time (qRT)-PCR (n = 110). The characteristics and subcellular localization of circ-TNPO3 were identified via RNase R assay, qRT-PCR and fluorescence in situ hybridization (FISH). Then, we explored the biological roles of circ-TNPO3 in ccRCC via the function experiments in vitro and in vivo. RNA pull-down, RNA immunoprecipitation, bioinformatic analysis, RNA-FISH assays and rescue assays were applied to validate the interactions between circ-TNPO3, insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) and serpin family H member 1 (SERPINH1) to uncover the underlying molecular mechanisms of circ-TNPO3.

resultsWe detected the obvious downregulation of circ-TNPO3 in ccRCC compared to matched adjacent normal tissues (n = 110). The lower circ-TNPO3 expression was found in ccRCC patients with distant metastasis, higher World Health Organization/International Society of Urologic Pathologists (WHO/ISUP) grade and more advanced tumour T stage. In vitro and in vivo, circ-TNPO3 significantly suppressed the proliferation and migration of ccRCC cells. Mechanistically, we elucidated that circ-TNPO3 directly bound to IGF2BP2 protein and then destabilized SERPINH1 mRNA. Moreover, IGF2BP2/SERPINH1 axis was responsible for circ-TNPO3's function of inhibiting ccRCC metastasis. Epithelial splicing regulatory protein 1 (ESRP1) was probably involved in the biogenesis of circ-TNPO3.

conclusionsCirc-TNPO3 can suppress ccRCC progression and metastasis via directly binding to IGF2BP2 protein and destabilizing SERPINH1 mRNA. Circ-TNPO3 may act as a potential target for ccRCC treatment.

Indexed as

Carcinoma, Renal CellKidney Neoplasmsbeta KaryopherinsCell Line, TumorGene Expression Regulation, NeoplasticHSP47 Heat-Shock ProteinsHumansIn Situ Hybridization, FluorescenceRNARNA-Binding ProteinsRNA, CircularRNA, Messengerbeta KaryopherinsHSP47 Heat-Shock ProteinsIGF2BP2 protein, humanRNARNA-Binding ProteinsRNA, CircularRNA, MessengerSERPINH1 protein, humanTNPO3 protein, humancirc-TNPO3clear cell renal cell carcinomaIGF2BP2SERPINH1

Identifiers

PMID35876041
PMCPMC9309750
OpenAlexW4287221835

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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.