Evidence map›Paper›PMID 32596961›Full record

ArticleJournal of cellular and molecular medicine2020

The oncogenic role of MUC12 in RCC progression depends on c-Jun/TGF-β signalling.

Sheng-Lin Gao, Rui Yin, Li-Feng Zhang, Si-Min Wang, Jia-Sheng Chen, Xing-Yu Wu, Chuang Yue, Li Zuo, Min Tang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  7. The Role of the PAX Genes in Renal Cell Carcinoma.International journal of molecular sciences · 2024
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  8. Prognostic role ofHeliyon · 2024
    Article
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  17. Article
  18. Analysis of mRNA mFrontiers in genetics · 2023
    Article
  19. Article
  20. 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 4 institutions in 1 country.

Sheng-Lin GaoDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.ORCID 0000-0002-8557-0218
Rui YinCenter for Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Li-Feng ZhangDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.
Si-Min WangChangzhou Third People's Hospital, Changzhou, China.
Jia-Sheng ChenDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.
Xing-Yu WuDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.
Chuang YueDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.
Li ZuoDepartment of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, Changzhou, China.
Min TangDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Changzhou No.2 People's Hospital · CNChangzhou Third People's Hospital · CNJiangsu Province Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) is a common kidney cancer worldwide. Even though current treatments show promising therapeutic effectiveness, metastatic RCC still has limited therapeutic options so that novel treatments were urgently needed. Here, we identified that MUC12 was overexpressed in RCC patients and served as poor prognostic factor for RCC progression. Overexpression of MUC12 increased RCC cell growth and cell invasion while deficiency of MUC12 exerted opposite effects on RCC cells. Mechanistic dissection demonstrated that MUC12-mediated RCC cell growth and cell invasion were dependent of TGF-β1 signalling because they could be blocked in the presence of TGF-β1 inhibitor. Moreover, the regulation of TGF-β1 by MUC12 relied on the transactivation of c-Jun. MUC12 promoted the recruitment of c-Jun on the promoter of TGF-β1, leading to its transcription. Importantly, knockdown of c-Jun also attenuated MUC12-mediated TGF-β1 induction and RCC cell invasion. In summary, our study defines the role of MUC12 in RCC progression and provides rational to develop novel targeted therapy to battle against RCC.

Indexed as

OncogenesSignal TransductionBiomarkers, TumorCarcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationComputational BiologyDatabases, GeneticEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMucinsPrognosisProto-Oncogene Proteins c-junBiomarkers, TumorMUC12 protein, humanMucinsProto-Oncogene Proteins c-junTransforming Growth Factor betac-JuninvasionMUC12renal cell carcinomaTGF-β1

Identifiers

PMID32596961
PMCPMC7412406
OpenAlexW3038037653

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.