High colony‐forming efficiency of primary human tumor cells cultured in the adhesive‐tumor‐cell culture system: Improvements with medium and serum alterations

Fraser L. Baker, Jaffer Ajanf, Gary Spitzer, Barbara J. Tomasovic, Marcia Williams, Margot Finders, William A. Brock

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

The colony‐forming efficiency (CFE) of primary human tumor cells cultured in the adhesive‐tumor‐cell culture system (ATCCS) using Ham's F12 (F12) or Eagle's minimum essential medium, alpha modification (alphaMEM) and culture medium supplemented with either swine, equine or bovine sera were compared. AlphaMEM supplemented with equine serum provided the highest CFE of the combinations. The CFE increase due to the change from F12 to alphaMEM was approximately 5‐fold, and the increase due to the change in serum from swine to equine was approximately 2‐fold. Cytokeratin staining showed that this increase was not due to fibroblast growth. The high‐average CFE with alphaMEM, approximately 3%, means that an inoculum of only 2 × 103 cells is needed to achieve formation of approximately 65 colonies in control cultures, thereby increasing the performance of this system when used in a chemosensitivity assay.

Original languageEnglish (US)
Pages (from-to)95-105
Number of pages11
JournalThe International Journal of Cell Cloning
Volume6
Issue number2
DOIs
StatePublished - 1988

Keywords

  • Adhesive‐tumor‐cell culture system
  • Colony‐forming efficiency
  • Primary human tumor cell cultures

ASJC Scopus subject areas

  • Cell Biology

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