CD44+/CD24- ovarian cancer cells demonstrate cancer stem cell properties and correlate to survival

Clin Exp Metastasis. 2012 Dec;29(8):939-48. doi: 10.1007/s10585-012-9482-4. Epub 2012 May 18.

Abstract

Cancer cells with the surface marker profile CD44+/CD24- have previously been described to possess cancer stem cell-like properties. This manuscript evaluates those properties in ovarian cancer cell lines. The proportion of CD44+/CD24- cells corresponded to the clinical aggressiveness of each ovarian cancer cell line histologic subtype. CD44+/CD24- cells demonstrated enhanced progressive differentiation as well as showing a 60-fold increase in Matrigel invasion in both SKOV3 and OV90 cell lines (p < 0.001 each) compared to other phenotypes. CD44+/CD24- demonstrated significant resistance to all chemotherapy agents used in all cell lines, with a 71-93 % increase in resistance compared with baseline. Using a threshold of 25 % CD44+/CD24- ovarian cancer cells found in ascites, patients with >25 % CD44+/CD24- were significantly more likely to recur (83 vs. 14 %, p = 0.003) and had shorter median progression-free survival (6 vs. 18 months, p = 0.01). In conclusion, the CD44+/CD24- phenotype in ovarian cancer cells demonstrate cancer stem cell-like properties of enhanced differentiation, invasion, and resistance to chemotherapy. This CD44+/CD24- phenotype correlates to clinical endpoints with increased risk of recurrence and shorter progression-free survival in patients with ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Surface / metabolism
  • Biomarkers, Tumor / metabolism
  • CD24 Antigen / immunology
  • CD24 Antigen / metabolism*
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • Disease-Free Survival
  • Female
  • Humans
  • Hyaluronan Receptors / immunology
  • Hyaluronan Receptors / metabolism*
  • Neoplasm Invasiveness
  • Neoplastic Stem Cells / pathology*
  • Neoplastic Stem Cells / physiology*
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / metabolism*
  • Ovarian Neoplasms / pathology*
  • Phenotype
  • Receptors, Cell Surface / biosynthesis
  • Receptors, Cell Surface / metabolism

Substances

  • Antigens, Surface
  • Biomarkers, Tumor
  • CD24 Antigen
  • Hyaluronan Receptors
  • Receptors, Cell Surface