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Differential tissue regulation of the insulin-like growth factors in rats bearing the MStT/W15 pituitary tumor

  • Marie C. Gelato
  • , Joseph Vassalotti
  • , Elizabeth Spatola
  • , Carol Rutherford
  • , Kenneth Marsh
  • , Harold E. Carlson
  • Stony Brook University
  • VA Medical Center

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

The content of insulin-like growth factors, IGF-I and IGF-II, was measured in tissues of rats bearing a transplantable mammosomatotrophic tumor. MStT/WIS. Serum IGF-I was elevated in tumor-implanted rats [2, 557 ± (SE) 419 vs. 891 ± 100 ng/ml], and tumor tissue concentrations of IGF-I were increased (321 ± 16 ng/g) in comparison to control liver tissue (160 ± 5ng/g) or control pituitary (80 ± 3 ng/g). The IGF-I levels were significantly increased in most peripheral tissues in the tumor-bearing rats with the exception of the liver. In support of this finding, messenger RNA for prepro IGF-I was likewise not increased in the livers of tumor-bearing rats, nor was there an increase in the growth hormone-dependent IGF-binding protein, BP-3, in the liver or serum of these animals. All tumors had detectable levels of prepro IGF-I mRNA which was, however, less than 50% of that noted in normal control liver. The tumors also expressed an IGF-BP which was identified as IGF-BP-2 by immunoblotting. Serum concentrations of IGF-II were similar in control and tumor-bearing animals (| 70 ng/ml). IGF-II levels in the tumor (90 ± 5 ng/g) were significantly higher than levels in control liver (34 ± 2 ng/g), but similar to those found in normal pituitary (165 ± 24 ng/g). In peripheral tissues, IGF-II concentrations were selectively increased in skeletal muscle and heart of tumor-bearing rats. These data demonstrate tissue-specific regulation of IGF-1 and IGF-II. Paradoxically, the liver does not appear to be stimulated over control levels by high serum growth hormone levels, since neither IGF-I peptide, IGF-I mRNA, nor 1GF-BP-3 levels are increased in livers of tumor-bearing rats. This suggests that the increase in serum IGF-I in these animals is due to increased production of IGF-I by the tumors themselves and by nonhepatic peripheral tissues and further that hepatic responsiveness to growth hormone is diminished in these tumor-bearing animals.

Original languageEnglish
Pages (from-to)765-774
Number of pages10
JournalNeuroendocrinology
Volume56
Issue number6
DOIs
StatePublished - 1992

Keywords

  • Growth hormone
  • Insulin-like growth factors
  • Pituitary tumor
  • Prolactin
  • Rat

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