Insulin-like growth factor binding protein-6 activates programmed cell death in non-small cell lung cancer cells

Naoko Sueoka, Ho Young Lee, Sandra Wiehle, Richard J. Cristiano, Bing Liang Fang, Lin Ji, Jack A. Roth, Waun Ki Hong, Pinchas Cohen, Jonathan M. Kurie

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

Insulin-like growth factor binding proteins (IGFBPs) are secreted into the extra-cellular matrix and inhibit cell growth through IGF-dependent and -independent mechanisms. In this study, we investigated the role of IGFBP-6, a relatively unexplored member of the IGFBP family, in the proliferation of non-small cell lung cancer (NSCLC) cells. Infection of NSCLC cell lines in vitro with an adenovirus expressing human IGFBP-6 under the control of a CMV promoter (Ad5CMV-BP6) reduced NSCLC cell number through activation of programmed cell death, as shown by cell staining with Hoechst 33342 or DNA end-labeling with bromodeoxyuridine triphosphate. The growth regulatory effect of IGFBP-6 was investigated in vivo by intratumoral injection of Ad5CMV-BP6 in NSCLC xenografts established in nu/nu mice. A single injection of Ad5CMV-BP6 reduced the size of NSCLC xenografts by 45%. These findings indicate that IGFBP-6 is a potent inducer of programmed cell death in cancer cells and support investigations into IGFBP-6 as a potential target in cancer therapeutics.

Original languageEnglish (US)
Pages (from-to)4432-4436
Number of pages5
JournalOncogene
Volume19
Issue number38
DOIs
StatePublished - Sep 7 2000

Keywords

  • Apoptosis
  • Growth inhibition
  • Tumor

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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