Evidence map›Paper›PMID 42436778›Full record

ArticleTranslational andrology and urology2026

MAGI3 inhibits renal clear cell carcinoma progression through the JAK-STAT3 pathway.

Xiangqiu Chen, Tao Wu, Weifei Liang, Ming Huang, Shaohua Zeng, Qingchun Zhou, Hao Lin, Xichun Zheng, Qizhi Xu, Jing Wang and 5 more

Abstract read
In one paragraph

Article in Translational andrology and urology, 2026. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Xiangqiu Chen *Department of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Tao Wu *Department of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Weifei Liang *Center for Cancer and Immunology Research, State Key Laboratory of Respiratory Disease, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.
Ming Huang *Department of Cardiovascular Intensive Care Unit, The Seventh Affiliated Hospital Sun Yat-sen University, Shenzhen, China.
Shaohua ZengDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Qingchun ZhouDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Hao LinDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Xichun ZhengDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Qizhi XuDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jing WangLaboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Wenwu LiuSchool of Nursing, University of South China, Hengyang, China.
Qingyou ZhengDepartment of Urology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Qishan LongDepartment of Urology, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, Shenzhen, China.
Zhuohui NingDepartment of Pain Medicine, First Hospital of Shanxi Medical University, Taiyuan, China.
Xinyi CaoLaboratory Medicine, Shenzhen Hospital, Southern Medical University, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Clear cell renal cell carcinoma (ccRCC) is the most common kidney cancer subtype. While localized disease is treated surgically, therapeutic options for advanced cases remain limited. This highlights an urgent need for reliable prognostic markers and novel therapeutic targets. Therefore, this study aimed to clarify the clinical significance and functional role of MAGI3 in ccRCC. Methods: We analyzed MAGI3 expression in ccRCC and normal tissues using public datasets and clinical samples. Its correlation with clinicopathological features and patient survival was evaluated. The biological role of MAGI3 and its underlying mechanism were investigated through in vitro and Results: MAGI3 expression was significantly downregulated in tumor tissues compared with adjacent normal kidney specimens. Lower MAGI3 levels correlated positively with advanced tumor stage, higher Fuhrman nuclear grade, lymph node metastasis, increased infiltration of immunosuppressive cell populations, and poorer overall patient prognosis. Functional experiments further demonstrated that MAGI3 overexpression effectively suppressed ccRCC cell proliferation, migration, and invasion in vitro and in vivo by inhibiting STAT3 signaling phosphorylation and downstream transcriptional activity. Conclusions: Our study identifies MAGI3 as a novel tumor suppressor in ccRCC that constrains cancer progression via the STAT3 pathway. These results firmly establish MAGI3 as a potential prognostic biomarker for ccRCC.

Indexed as

Clear cell renal cell carcinoma (ccRCC)differentially expressed genes (DEGs)JAK-STAT3MAGI3

Identifiers

PMID42436778
PMCPMC13355252

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