Evidence map›Paper›PMID 26369384›Full record

ArticleScientific reports2015

SENP2 regulates MMP13 expression in a bladder cancer cell line through SUMOylation of TBL1/TBLR1.

Mingyue Tan, Hua Gong, Jun Wang, Le Tao, Dongliang Xu, Erdun Bao, Zhihong Liu, Jianxin Qiu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. 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
2.1field-weighted citation impact, top 12% 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, 37 citations in OpenAlex.

  1. SENP1 drives glycolysis and cisplatin resistance in gastric cancer via desumoylating ENO1.Journal of experimental & clinical cancer research : CR · 2025
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  12. PPy@FeFrontiers in chemistry · 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

8 authors at 3 institutions in 1 country.

Mingyue TanDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Hua GongShanghai Tianyou Hospital, Tongji University, Shanghai 200331, China.
Jun WangDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Le TaoDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Dongliang XuDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Erdun BaoDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Zhihong LiuDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Jianxin QiuDepartment of Urology, Shanghai First People's Hospital, Medical College of Shanghai Jiao Tong University, Shanghai 200080, China.
Shanghai First People's Hospital · CNShanghai Jiao Tong University · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BC) is the most popular malignant urinary cancer in China. BC has the highest incidence and mortality among all genitourinary system tumors. Although the early-stage BC could be treated with advanced electron flexible systourethroscope, early metastasis of the BC occur frequently, and often results in poor prognosis. Recently, we reported that small ubiquitin related modifier (SUMO)-specific protease 2 (SENP2) was downregulated in BC specimen. SENP2 appeared to inhibit migration and invasion of bladder cancer cells in vitro, through suppressing MMP13 in BC cells. However, the exact underlying mechanisms remain unknown. Here, we reported that SENP2 inhibited nuclear translocation of β-catenin, which targeted the promotor of MMP13 to activate MMP13 to enhance BC cell metastasis. WNT ligands induced TBL1/TBLR1 SUMOylation to form complexes with β-catenin to facilitate β-catenin nuclear translocation, which could be efficiently inhibited through suppression of SUMOylation of TBL1/TBLR1. Together, our data suggest that SENP2 inhibits MMP13 expression in BC cells through de-SUMOylation of TBL1/TBLR1, which inhibits nuclear translocation of β-catenin. Thus, SENP2 may be a promising therapeutic target for BC.

Indexed as

Gene Expression Regulation, Neoplasticbeta CateninCell Line, TumorCysteine EndopeptidasesHumansMatrix Metalloproteinase 13Models, BiologicalNuclear ProteinsPromoter Regions, GeneticProtein BindingProtein TransportProto-Oncogene ProteinsReceptors, Cytoplasmic and NuclearRepressor ProteinsSumoylationTransducinbeta CateninCysteine EndopeptidasesMatrix Metalloproteinase 13Nuclear ProteinsProto-Oncogene ProteinsReceptors, Cytoplasmic and NuclearRepressor ProteinsSENP2 protein, humanTBL1X protein, humanTBL1XR1 protein, humanTransducinWnt-5a ProteinWNT5A protein, humanWnt Proteins

Identifiers

PMID26369384
PMCPMC4570209
OpenAlexW2405344993

What OpenQuestion holds

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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.