Aneuploid colon cancer cells have a robust spindle checkpoint

EMBO Rep. 2001 Jul;2(7):609-14. doi: 10.1093/embo-reports/kve127. Epub 2001 Jul 3.

Abstract

Colon cancer cells frequently display minisatellite instability (MIN) or chromosome instability (CIN). While MIN is caused by mismatch repair defects, the lesions responsible for CIN are unknown. The observation that CIN cells fail to undergo mitotic arrest following spindle damage suggested that mutations in spindle checkpoint genes may account for CIN. However, here we show that CIN cells do undergo mitotic arrest in response to spindle damage. Although the maximum mitotic index achieved by CIN lines is diminished relative to MIN lines, CIN cells clearly have a robust spindle checkpoint. Consistently, mutations in spindle checkpoint genes are rare in human tumours. In contrast, the adenomatous polyposis coli (APC) gene is frequently mutated in CIN cells. Significantly, we show here that expression of an APC mutant in MIN cells reduces the mitotic index following spindle damage to a level observed in CIN cells, suggesting that APC dysfunction may contribute to CIN.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli Protein / genetics
  • Adenomatous Polyposis Coli Protein / metabolism*
  • Aneuploidy*
  • Animals
  • Antineoplastic Agents / pharmacology
  • Cell Cycle / physiology*
  • Chromosomes / metabolism
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / pathology
  • Colonic Neoplasms / physiopathology
  • Flow Cytometry
  • Genes, APC
  • Genes, cdc / physiology*
  • Humans
  • Microscopy, Fluorescence
  • Mitotic Index
  • Nocodazole / pharmacology
  • Spindle Apparatus / drug effects
  • Spindle Apparatus / genetics
  • Spindle Apparatus / physiology*
  • Tumor Cells, Cultured

Substances

  • Adenomatous Polyposis Coli Protein
  • Antineoplastic Agents
  • Nocodazole