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Updated: May 24, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
The interrelationships between Src, Cav-1 and RhoGD12 in transitional cell carcinoma of the bladder
1Institute of Cancer, College of MVLS, University of Glasgow, Western Infirmary, Glasgow G11 6NT, UK.
Activated Src family kinases and downstream proteins indicate a good prognosis in bladder cancer, unlike other tumors. This activation positively correlates with RhoGD12 expression, suggesting a favorable outcome for patients.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Investigating signaling pathways in bladder cancer is crucial for understanding tumor progression.
- Src family kinases (SFKs), focal adhesion kinase (FAK), caveolin-1 (Cav-1), and RhoGD12 are implicated in various cancers.
Purpose of the Study:
- To evaluate the expression and activity of SFKs, FAK, Cav-1, and RhoGD12 in bladder cancer patients.
- To determine the prognostic significance of these molecules in transitional cell carcinoma of the bladder.
Main Methods:
- Immunohistochemical staining was performed on tumor samples from 58 bladder cancer patients.
- Expression levels of c-Src, phosphorylated Src (Y419), dephosphorylated Src (Y527), phosphorylated FAK (Y861), Cav-1, and RhoGD12 were quantified using the weighted histoscore method.
Main Results:
- High membrane expression of dephosphorylated Src (Y527) and phosphorylated Src (Y419) correlated with increased cancer-specific survival.
- Elevated phosphorylated FAK (Y861) at the membrane also showed association with better survival.
- Membrane Src Y419 expression was an independent prognostic factor in multivariate analysis.
Conclusions:
- Contrary to findings in other solid tumors, activated SFKs and downstream signaling proteins are associated with a favorable prognosis in bladder cancer.
- Activated Src demonstrates a positive relationship with RhoGD12 expression, suggesting a potential interplay in bladder tumor biology.
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