Inhibiting the expression of DNA replication-initiation proteins induces apoptosis in human cancer cells

Cancer Res. 2003 Nov 1;63(21):7356-64.

Abstract

DNA replication-initiation proteins are expressed in cancer cells, whereas some of these proteins are not expressed in nonproliferating normal cells. Therefore, replication-initiation proteins may present attractive targets for anticancer therapy. Using selected antisense oligodeoxynucleotides and small interfering RNA molecules targeted to the mRNA encoding the DNA replication-initiation proteins hCdc6p, hMcm2p, and hCdc45p, we show that the target genes could be effectively and specifically silenced and that, consequently, DNA replication and cell proliferation were inhibited in cultured human cells. In addition, silencing of these genes resulted in apoptosis in both p53-positive and -negative cancer cells but not in normal cells: cancer cells entered an abortive S-phase, whereas normal cells arrested mainly in G(1) phase. Our studies are the first to suggest that inhibiting the expression of selective replication-initiation proteins is a novel and effective anticancer strategy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Cell Cycle Proteins / antagonists & inhibitors*
  • Cell Cycle Proteins / biosynthesis
  • Cell Cycle Proteins / genetics
  • Cell Division / genetics
  • DNA Replication / genetics*
  • Gene Silencing
  • HeLa Cells
  • Humans
  • Mice
  • Mice, Nude
  • Minichromosome Maintenance Complex Component 2
  • Neoplasms / genetics*
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Nuclear Proteins / antagonists & inhibitors*
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics
  • Oligonucleotides, Antisense / genetics
  • RNA, Messenger / antagonists & inhibitors
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • Transfection
  • Tumor Suppressor Protein p53 / physiology
  • Xenograft Model Antitumor Assays

Substances

  • CDC45 protein, human
  • CDC6 protein, human
  • Cdc45 protein, mouse
  • Cell Cycle Proteins
  • Nuclear Proteins
  • Oligonucleotides, Antisense
  • RNA, Messenger
  • RNA, Small Interfering
  • Tumor Suppressor Protein p53
  • Minichromosome Maintenance Complex Component 2