Increased tumorigenicity of fibronectin receptor deficient Chinese hamster ovary cell variants

C Schreiner1, M Fisher, S Hussein

  • 1Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill 27599.

Cancer Research
|March 15, 1991
PubMed

Insights

Altered expression of the alpha 5/beta 1 integrin fibronectin receptor in Chinese hamster ovary cells impacts tumor growth rates in mice. Higher receptor levels correlate with slower tumor progression, suggesting a role in cancer development.

Area of Science:

  • Cell Biology
  • Oncology
  • Biochemistry

Background:

  • Integrins are crucial cell surface receptors involved in cell adhesion and signaling.
  • The alpha 5/beta 1 integrin, a fibronectin receptor, plays a role in various cellular processes, including cell migration and proliferation.

Purpose of the Study:

  • To investigate the effect of varying alpha 5/beta 1 integrin fibronectin receptor expression levels on tumor growth.
  • To determine if altered fibronectin receptor expression influences the tumorigenic potential of Chinese hamster ovary (CHO) cells.

Main Methods:

  • Development of Chinese hamster ovary (CHO) cell sublines with deficient or altered expression of the alpha 5/beta 1 integrin fibronectin receptor.
  • Subcutaneous injection of these variant cell sublines into nude mice to assess tumor growth rates.
  • Analysis of fibronectin receptor expression levels in recovered tumor cells to confirm phenotype stability.

Main Results:

  • Significant differences in tumor growth rates were observed among the variant cell sublines.
  • Clones with very low fibronectin receptor expression exhibited the most rapid tumor growth.
  • Clones with elevated fibronectin receptor expression showed slower tumor growth compared to wild-type cells.

Conclusions:

  • The level of alpha 5/beta 1 fibronectin receptor expression is inversely correlated with tumor growth rate.
  • The alpha 5/beta 1 fibronectin receptor may act as a suppressor of rapid tumor progression.
  • Stable expression phenotypes suggest the receptor's role is intrinsic to the cells' tumorigenic behavior.

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