Cellular transformation and the 'morphologic phenotype' of transformed cells

Nature
|August 17, 1978
PubMed

Insights

The expression of the Rous sarcoma virus (RSV) transforming gene (src) alters fibroblast cell properties, primarily by reducing cell-to-substratum adhesion. These changes in the morphologic phenotype resemble effects seen with peptide hormones like insulin.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Virology

Background:

  • The transforming gene (src) product from RNA tumor viruses influences cell growth and characteristics.
  • Transformed cells exhibit altered adhesion, appearance, and surface properties, collectively termed the 'morphologic phenotype'.
  • Diminished cell-to-substratum adhesion is a key factor in the morphologic phenotype of src-expressing cells.

Purpose of the Study:

  • To investigate the impact of src gene expression on cultured fibroblasts.
  • To explore the underlying mechanisms contributing to the morphologic phenotype of transformed cells.
  • To compare the effects of src expression with those of peptide hormones.

Main Methods:

  • Analysis of gene expression in cultured fibroblasts.
  • Observation and characterization of cellular morphology and adhesion properties.
  • Investigation of the roles of cyclic AMP and cell surface proteins (CSP).

Main Results:

  • Src expression promotes fibroblast growth.
  • Src expression significantly alters cell adhesion, appearance, and surface properties.
  • The observed changes in the morphologic phenotype are largely attributed to reduced cell-to-substratum adhesion.

Conclusions:

  • Src gene product expression profoundly affects fibroblast characteristics.
  • The morphologic phenotype induced by src is primarily mediated by decreased cell adhesion.
  • The cellular responses to src expression share similarities with peptide hormone actions, such as insulin.

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