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Transformation by the oncogene v-fms: the effects of castanospermine on transformation-related parameters

E J Nichols1, R Manger, S I Hakomori

  • 1Fred Hutchinson Cancer Research Center, Division of Basic Sciences, Seattle, Washington 98104.

Insights

Castanospermine treatment reverted v-fms transformed cells to a normal phenotype, restoring cell morphology and growth control. This suggests castanospermine influences cell surface expression, affecting key transformation parameters.

Area of Science:

  • Cell Biology
  • Biochemistry
  • Molecular Oncology

Background:

  • Viral oncogenes drive cellular transformation, leading to aberrant cell growth and morphology.
  • Castanospermine is an alkaloid known to affect glycoprotein processing.

Purpose of the Study:

  • To investigate the effects of castanospermine on v-fms-transformed Fischer rat embryo (FRE) cells.
  • To determine if castanospermine-induced reversion is specific to the v-fms oncogene.

Main Methods:

  • Treatment of v-fms and v-fgr transformed FRE cells with castanospermine.
  • Analysis of cell morphology, fms protein localization, and fibronectin expression.
  • Assessment of cell growth, contact inhibition, and hexose uptake.

Main Results:

  • Castanospermine treatment induced reversion to normal morphology in v-fms transformed cells, with fms protein accumulation in the endoplasmic reticulum.
  • Reverted cells exhibited restored contact inhibition, fibronectin expression, and actin cytoskeleton.
  • Castanospermine significantly decreased [3H]deoxyglucose uptake in reverted cells, with no effect on v-fgr transformed cells.

Conclusions:

  • Castanospermine induces reversion of v-fms transformed cells, characterized by altered cell morphology and restored growth control.
  • The effects of castanospermine are specific to v-fms transformation, highlighting its role in modulating specific oncogenic pathways.
  • Cell surface expression appears to be a key regulator of anchorage-independent growth, morphology, contact inhibition, and hexose uptake.

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