Evidence map›Paper›PMID 40299934›Full record

ArticlePloS one2025

DERL3 facilitates the progression of clear cell renal cell carcinoma by promoting epithelial-mesenchymal transition via regulation of the TGFB1 pathway.

Chengtao Niu, Haodong Cui, Xintong Sun, Yuchang Yang, Xue Jiang, Zixiang Cong, Yiming Zhang, Zhihong Niu, Wei He

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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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.

Chengtao NiuDepartment of Urology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China.ORCID 0000-0002-5218-7511
Haodong CuiDepartment of Urology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China.
Xintong SunDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Yuchang YangDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Xue JiangShandong Xiehe University, Jinan, China.
Zixiang CongDepartment of Urology, Weihai Municipal Hospital Affiliated to Shandong University, Weihai, China.
Yiming ZhangDepartment of Urology, People's Hospital of Changle County, Weifang, Shandong, China.
Zhihong NiuDepartment of Urology, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China.
Wei HeDepartment of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.ORCID 0000-0002-4272-2891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClear cell renal cell carcinoma (ccRCC) is a highly prevalent malignancy within the urinary system. The intrinsic heterogeneity and resistance to conventional chemotherapy and radiotherapy contribute to the poor prognosis of advanced ccRCC patients. DERL3, part of the Derlin protein family, was first identified for its critical role in endoplasmic reticulum stress. Subsequent studies have revealed its involvement in the progression of multiple tumor types; however, its role in ccRCC remains unclear.

methodsIn this study, we utilized bioinformatics analysis and in vitro experimental approaches to investigate the role of DERL3 expression in the metastasis of renal clear cell carcinoma cells. Additionally, we analyzed the correlation between DERL3 expression and the prognosis of renal clear cell carcinoma patients, while exploring its potential mechanisms of action.

resultsWe demonstrate for the first time that DERL3 promotes tumor progression in ccRCC, showing significantly elevated expression, especially in metastatic ccRCC cell lines. Further studies suggest that this overexpression of DERL3 may promote the epithelial-mesenchymal transition in ccRCC by upregulating TGF-β1, thereby enhancing ccRCC metastasis.

conclusionIn conclusion, our study clarifies the role and potential mechanisms of DERL3 in ccRCC progression, providing promising therapeutic avenues for improving the prognosis of ccRCC patients.

Indexed as

Carcinoma, Renal CellEpithelial-Mesenchymal TransitionKidney NeoplasmsMembrane ProteinsTransforming Growth Factor beta1Cell Line, TumorCell MovementDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMalePrognosisSignal TransductionMembrane ProteinsTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID40299934
PMCPMC12040103

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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.