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Updated: Aug 10, 2026

Focus Formation: A Cell-based Assay to Determine the Oncogenic Potential of a Gene
Published on: December 31, 2014
Production of transforming growth factors by simian sarcoma virus-transformed cells
Abstract:
Cellular transformation of normal rat kidney (NRK) cells by simian sarcoma virus (SSV) results in a complete loss of the cellular requirement of externally added polypeptide growth factors for proliferation. Moreover, SSV-transformed NRK cells have a strongly reduced ability to bind both external platelet-derived growth factor and epidermal growth factor, when compared to nontransformed NRK cells. Analysis of serum-free medium conditioned by SSV-transformed NRK cells shows that this cell line secretes both types alpha and beta transforming growth factor (TGF). The level of TGF alpha production (300 ng/liter conditioned medium) by SSV-transformed NRK is among the highest described to date. Since addition of TGF alpha and beta in combination is sufficient to induce phenotypic transformation of NRK cells, it is concluded that although expression of the sis oncogene is essential for transformation, expression of additional genes may be required for the phenotypic alterations accompanying complete cellular transformation.
Insights
Simian sarcoma virus (SSV) transformation of rat kidney cells causes loss of growth factor dependence and reduced growth factor binding. These SSV-transformed cells secrete high levels of transforming growth factor alpha (TGF-α) and TGF-β, inducing phenotypic transformation.
Area of Science:
- Cell Biology
- Virology
- Molecular Biology
Background:
- Normal rat kidney (NRK) cells require external polypeptide growth factors for proliferation.
- Simian sarcoma virus (SSV) is known to cause cellular transformation.
Purpose of the Study:
- To investigate the effects of SSV transformation on NRK cell growth factor requirements and production.
- To determine the role of transforming growth factors (TGFs) in SSV-induced cellular transformation.
Main Methods:
- Comparison of growth factor binding and proliferation in SSV-transformed versus non-transformed NRK cells.
- Analysis of conditioned medium from SSV-transformed NRK cells for secreted growth factors.
- Assessment of TGF-α and TGF-β's ability to induce phenotypic transformation in NRK cells.
Main Results:
- SSV-transformed NRK cells exhibit a complete loss of requirement for external growth factors.
- SSV-transformed NRK cells show significantly reduced binding of platelet-derived growth factor and epidermal growth factor.
- SSV-transformed NRK cells secrete high levels of both TGF-α and TGF-β.
- Combined TGF-α and TGF-β are sufficient to induce phenotypic transformation in NRK cells.
Conclusions:
- While sis oncogene expression is crucial for SSV-induced transformation, additional gene expression may be necessary for complete phenotypic alterations.
- Secreted TGFs play a significant role in the phenotypic transformation of NRK cells by SSV.
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