Evidence map›Paper›PMID 39527690›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

STAMBPL1/TRIM21 Balances AXL Stability Impacting Mesenchymal Phenotype and Immune Response in KIRC.

Shiyu Huang, Xuke Qin, Shujie Fu, Juncheng Hu, Zhengyu Jiang, Min Hu, Banghua Zhang, Jiachen Liu, Yujie Chen, Minghui Wang and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Upregulation ofTranslational andrology and urology · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. PTPN9 dephosphorylates IGF1RJournal of experimental & clinical cancer research : CR · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Role of Ubiquitin-regulated EMT in Cancer Metastasis and Chemoresistance.International journal of biological sciences · 2025
    Review
  15. Article
  16. Review
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

13 authors.

Shiyu HuangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Xuke QinDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Shujie FuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Juncheng HuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Zhengyu JiangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Min HuDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Banghua ZhangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Jiachen LiuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Yujie ChenDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Minghui WangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Xiuheng LiuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.
Zhiyuan ChenDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.ORCID 0000-0002-6820-3678
Lei WangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, 430060, China.

Funding

National Natural Science Foundation of China 82203258National Natural Science Foundation of China 82372200
6 · The paper itself

Abstract

Kidney renal clear cell carcinoma (KIRC) is recognized as an immunogenic tumor, and immunotherapy is incorporated into its treatment landscape for decades. The acquisition of a tumor mesenchymal phenotype through epithelial-to-mesenchymal transition (EMT) is associated with immune evasion and can contribute to immunotherapy resistance. Here, the involvement of STAM Binding Protein Like 1 (STAMBPL1) is reported in the development of mesenchymal and immune evasion phenotypes in KIRC cells. Mechanistically, STAMBPL1 elevated protein abundance and surface accumulation of TAM Receptor AXL through diminishing the TRIM21-mediated K63-linked ubiquitination and subsequent lysosomal degradation of AXL, thereby enhancing the expression of mesenchymal genes while suppressing chemokines CXCL9/10 and HLA/B/C. In addition, STAMBPL1 enhanced PD-L1 transcription via facilitating nuclear translocation of p65, and knockdown (KD) of STAMBPL1 augmented antitumor effects of PD-1 blockade. Furthermore, STAMBPL1 silencing and the tyrosine kinase inhibitor (TKI) sunitinib also exhibited a synergistic effect on the suppression of KIRC. Collectively, targeting the STAMBPL1/TRIM21/AXL axis can decrease mesenchymal phenotype and potentiate anti-tumor efficacy of cancer therapy.

Indexed as

Axl Receptor Tyrosine KinaseCarcinoma, Renal CellEpithelial-Mesenchymal TransitionKidney NeoplasmsPhenotypeReceptor Protein-Tyrosine KinasesAnimalsCell Line, TumorDisease Models, AnimalHumansMiceProto-Oncogene ProteinsRibonucleoproteinsAXL protein, humanAxl Receptor Tyrosine KinaseProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRibonucleoproteinsimmunotherapy resistancekidney renal clear cell carcinomamesenchymal phenotypeSTAM binding protein like 1ubiquitination

Identifiers

PMID39527690
PMCPMC11714167

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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.