Adipocytes reprogram prostate cancer stem cell machinery.
Fabrizio FontanaMartina AnselmiPatrizia LimontaPublished in: Journal of cell communication and signaling (2023)
It is now well-established that an obese condition correlates with a higher risk of prostate cancer (PCa). A crosstalk between adipose tissue and PCa has been observed but is still poorly characterized. Herein, we demonstrated that 3T3-L1 adipocyte conditioned media (CM) could endow PC3 and DU145 PCa cells with stemness properties, by stimulating their sphere formation ability and promoting CD133 and CD44 expression. Moreover, after exposure to adipocyte CM both PCa cell lines underwent partial epithelial-to-mesenchymal transition (EMT), with E-/N-cadherin switch and Snail upregulation. Specifically, these changes in PC3 and DU145 cell phenotype were accompanied by increased tumor clonogenic activity and survival, as well as by enhanced invasion, anoikis resistance and matrix metalloproteinase (MMP) production. Finally, adipocyte CM-treated PCa cells exhibited reduced responsiveness to both docetaxel and cabazitaxel, demonstrating greater chemoresistance. Overall, these data indicate that adipose tissue can effectively contribute to PCa aggressiveness by reprogramming the cancer stem cell (CSC) machinery. Adipocytes endow prostate cancer cells with stem-like properties and mesenchymal traits, increasing their tumorigenicity, invasion and chemoresistance.
Keyphrases
- adipose tissue
- cancer stem cells
- prostate cancer
- insulin resistance
- high fat diet
- cell migration
- induced apoptosis
- epithelial mesenchymal transition
- cell cycle arrest
- poor prognosis
- stem cells
- radical prostatectomy
- bone marrow
- gene expression
- genome wide
- cell proliferation
- squamous cell carcinoma
- cell therapy
- single cell
- cell death
- machine learning
- oxidative stress
- skeletal muscle
- nk cells
- mesenchymal stem cells
- deep learning