ADGRD1 promotes bladder cancer progression and angiogenesis via the PI3K/AKT/mTOR-mediated pro-angiogenic secretome - Report - MDSpire

ADGRD1 promotes bladder cancer progression and angiogenesis via the PI3K/AKT/mTOR-mediated pro-angiogenic secretome

  • By

  • Chen Li

  • Zhichao Yang

  • Jialei Zhang

  • Xiaodong Yan

  • Hongwei Su

  • May 28, 2026

  • 0 min

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Clinical Report: ADGRD1 Enhances Bladder Cancer Advancement and Angiogenesis

Overview

ADGRD1 is associated with advanced-stage bladder cancer and may promote tumor growth and angiogenesis through the activation of the PI3K/AKT/mTOR signaling pathway.

Background

Bladder cancer is a leading cause of cancer-related mortality, particularly in advanced stages. Understanding the molecular mechanisms driving tumor progression is crucial.

Data Highlights

FindingDetails
ADGRD1 ExpressionEnriched in advanced-stage and high-grade BLCA
Prognostic ValueAssociated with overall survival and progression-free interval
Functional AssaysPromotes BLCA cell proliferation, migration, invasion, and angiogenesis
Xenograft ModelsEnhanced tumor growth and angiogenesis in vivo
Secretome AnalysisUpregulates VEGF, PDGF, and IL-8
Pathway ActivationIncreased phosphorylation of PI3K/AKT/mTOR components

Key Findings

  • ADGRD1 is significantly upregulated in advanced bladder cancer.
  • High ADGRD1 expression correlates with poor prognosis.
  • ADGRD1 enhances cell proliferation, migration, and invasion in vitro.
  • ADGRD1 promotes angiogenesis through a pro-angiogenic secretome.
  • Activation of the PI3K/AKT/mTOR pathway is mediated by ADGRD1.

Clinical Implications

Further research is needed to explore the potential of ADGRD1 in bladder cancer management.

Conclusion

ADGRD1 is identified as a driver of bladder cancer progression and angiogenesis.

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