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Tumor Biology

Human Osteosarcoma Cell Lines Are Dependent on Insulin-like Growth Factor I for in Vitro Growth

Cynthia Chavez Kappel, Maria C. Velez-Yanguas, Steven Hirschfeld and Lee J. Helman
Cynthia Chavez Kappel
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Maria C. Velez-Yanguas
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Steven Hirschfeld
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Lee J. Helman
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DOI:  Published May 1994
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Abstract

Osteogenic sarcoma is the most common bone tumor of childhood and typically occurs during the adolescent growth spurt when growth hormone and insulin-like growth factor I (IGF-I) may be at their lifetime highest levels. Since IGF-I is involved in normal bone growth and differentiation, we have evaluated the possible role of IGF-I signaling in the growth of human osteogenic sarcoma cell lines. In this study, we demonstrate that in vitro survival of cells is dependent on exogenously supplied IGF-I. Furthermore, we show that these cells display functional IGF-I receptors on their surface and that in vitro growth is inhibited by blocking these receptors either by monoclonal antibodies or by antisense oligonucleotides. These data demonstrate that human osteogenic sarcoma cell lines are dependent on signaling through the IGF-I receptor for in vitro survival and proliferation. Furthermore, they suggest that modulation of the growth hormone/IGF-I axis may affect the growth of these tumors in vivo.

Footnotes

  • ↵1 To whom requests for reprints should be addressed, at Molecular Oncology Section, Pediatric Branch, National Cancer Institute, Building 10/13N240, Bethesda, MD 20892.

  • Received December 13, 1993.
  • Accepted March 15, 1994.
  • ©1994 American Association for Cancer Research.
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May 1994
Volume 54, Issue 10
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Human Osteosarcoma Cell Lines Are Dependent on Insulin-like Growth Factor I for in Vitro Growth
Cynthia Chavez Kappel, Maria C. Velez-Yanguas, Steven Hirschfeld and Lee J. Helman
Cancer Res May 15 1994 (54) (10) 2803-2807;

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Human Osteosarcoma Cell Lines Are Dependent on Insulin-like Growth Factor I for in Vitro Growth
Cynthia Chavez Kappel, Maria C. Velez-Yanguas, Steven Hirschfeld and Lee J. Helman
Cancer Res May 15 1994 (54) (10) 2803-2807;
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