Primary cilia presence and implications in bladder cancer progression and invasiveness.
Pablo IruzubietaTomás CastiellaEva MonleónCarmen BergaGuillermo MuñozMª Concepción JunqueraPublished in: Histochemistry and cell biology (2021)
Urothelial bladder cancer is the tenth most common cancer worldwide. It is divided into muscle and non-muscle invading bladder cancer. Primary cilia have been related to several cancer hallmarks such as proliferation, epithelial-to-mesenchymal transition (EMT) or tumoral progression mainly through signaling pathways as Hedgehog (Hh). In the present study, we used immunohistochemical and ultrastructural techniques in human tissues of healthy bladder, non-muscle-invasive bladder cancer (NMIBC) and muscle-invasive bladder cancer (MIBC) to study and clarify the activation of epithelial-to-mesenchymal transition and Hedgehog signaling pathway and the presence of primary cilia. Thus, we found a clear correlation between EMT and Hedgehog activation and bladder cancer stage and progression. Moreover, we identified the presence of primary cilia in these tissues. Interestingly, we found that in NMIBC, some ciliated cells cross the basement membrane and localized in lamina propria, near blood vessels. These results show a correlation between EMT beginning from urothelial basal cells and primary cilia assembly and suggest a potential implication of this structure in tumoral migration and invasiveness (likely in a Hh-dependent way). Hence, primary cilia may play a fundamental role in urothelial bladder cancer progression and suppose a potential therapeutic target.
Keyphrases
- muscle invasive bladder cancer
- signaling pathway
- induced apoptosis
- epithelial mesenchymal transition
- high grade
- endothelial cells
- gene expression
- papillary thyroid
- pi k akt
- squamous cell carcinoma
- skeletal muscle
- cell cycle arrest
- risk assessment
- cell proliferation
- squamous cell
- young adults
- endoplasmic reticulum stress
- lymph node metastasis
- oxidative stress
- childhood cancer
- pluripotent stem cells
- drug induced