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Altered growth properties and cell surface changes in ras transformed mouse bladder epithelium
International Journal of Cancer
|February 15, 1986
Summary
Transfection of the c-Ha-ras-1 oncogene into mouse bladder cells induced tumor formation and anchorage-independent growth. A novel 18 kDa urothelium-specific protein was detected on the cell surface of these ras-transfected cells.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- The c-Ha-ras-1 oncogene plays a critical role in cell proliferation and differentiation.
- Oncogene activation is a key event in the development of various cancers, including bladder cancer.
Purpose of the Study:
- To investigate the effects of c-Ha-ras-1 oncogene transfection on mouse bladder epithelial cells.
- To identify and characterize novel proteins associated with activated ras oncogenes in urothelial cells.
Main Methods:
- Transfection of mouse bladder epithelial cell lines with the c-Ha-ras-1 oncogene.
- Tumorigenicity and anchorage-independent growth assays.
- Immunoprecipitation and immunofluorescence studies to detect and localize specific proteins.
Main Results:
- Transfection led to tumorigenic potential and anchorage-independent growth in most cell lines.
- An 18 kDa protein, specific to urothelial cells expressing activated ras, was identified.
- This 18 kDa protein was localized to the cell surface and not detected in cells transfected with other oncogenes (polyoma middle T, v-myc).
Conclusions:
- Activated c-Ha-ras-1 oncogene confers tumorigenic properties to mouse bladder epithelial cells.
- A novel, urothelium-specific 18 kDa cell surface protein is associated with activated ras gene expression.
- This protein may serve as a biomarker for ras-driven urothelial carcinogenesis.