Human ovarian cancer and cisplatin resistance: possible role of inhibitor of apoptosis proteins

Endocrinology. 2001 Jan;142(1):370-80. doi: 10.1210/endo.142.1.7897.


The inhibitor of apoptosis proteins (IAPs) constitutes a family of highly conserved apoptosis suppressor proteins that were originally identified in baculoviruses. Although IAP homologs have recently been demonstrated to suppress apoptosis in mammalian cells, their expression and role in human ovarian epithelial cancer and chemotherapy resistance are unknown. In the present study we used cisplatin-sensitive and -resistant human ovarian surface epithelial (hOSE) cancer cell lines and adenoviral antisense and sense complementary DNA expression to examine the role of IAP in the regulation of apoptosis in human ovarian cancer cells and chemoresistance. Antisense down-regulation of X-linked inhibitor of apoptosis protein (Xiap), but not human inhibitor of apoptosis protein-2 (Hiap-2), induced apoptosis in cisplatin-sensitive and, to a lesser extent, in -resistant cells. Cisplatin consistently decreased Xiap content and induced apoptosis in the cisplatin-sensitive, but not cisplatin-resistant, cells. Hiap-2 expression was either unaffected or inhibited to a lesser extent. The inhibition of IAP protein expression and induction of apoptosis by cisplatin was time and concentration dependent. Infection of cisplatin-sensitive cells with adenoviral sense Xiap complementary DNA resulted in overexpression of Xiap and markedly attenuated the ability of cisplatin to induce apoptosis. Immunohistochemical localization of the IAPs in hOSE tumors demonstrated the presence of Xiap and Hiap-2, with their levels being highest in proliferative, but not apoptotic, epithelial cells. These studies indicate that Xiap is an important element in the control of ovarian tumor growth and may be a point of regulation for cisplatin in the induction of apoptosis. These results suggest that the ability of cisplatin to down-regulate Xiap content may be an important determinant of chemosensitivity in hOSE cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Carcinoma / pathology
  • Cell Survival / drug effects
  • Cisplatin / toxicity*
  • Drug Resistance, Neoplasm*
  • Female
  • Humans
  • Mice
  • Middle Aged
  • Oligodeoxyribonucleotides, Antisense / toxicity
  • Ovarian Neoplasms / pathology
  • Proteins / genetics
  • Proteins / physiology*
  • Rats
  • Recombinant Proteins / metabolism
  • Transfection
  • Tumor Cells, Cultured
  • X-Linked Inhibitor of Apoptosis Protein


  • Oligodeoxyribonucleotides, Antisense
  • Proteins
  • Recombinant Proteins
  • X-Linked Inhibitor of Apoptosis Protein
  • XIAP protein, human
  • Cisplatin