Autocrine stimulation of interleukin-1 in the growth of human thyroid carcinoma cell line NIM 1

J Clin Endocrinol Metab. 1993 Jan;76(1):127-33. doi: 10.1210/jcem.76.1.8421076.

Abstract

We reported first in this study that human thyroid cell line NIM 1 established from a patient with papillary adenocarcinoma of the thyroid associated with hypercalcemia and peripheral neutrocytosis produced interleukin (IL)-1 alpha and IL-1 beta in the culture supernatant and cell lysate as detected by murine thymocyte proliferative response and enzyme-linked immunosorbent assay. Production of IL-1 alpha and IL-1 beta was further confirmed by the demonstration of IL-1 alpha and IL-1 beta messenger ribonucleic acid expression with Northern blot hybridization analysis. The in vitro growth of NIM 1 cells was inhibited by the addition of anti-IL-1 alpha and IL-1 beta antibody. The growth of NIM 1 cells was further enhanced by the addition of recombinant human IL-1 alpha and IL-1 beta, whereas this enhancement was also inhibited by the addition of anti-IL-1 antibody. IL-1 receptors were expressed on NIM 1 cells. These results suggest that IL-1 plays a regulatory role in the growth of NIM 1 cells by an autocrine mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / immunology
  • Adenocarcinoma / pathology*
  • Animals
  • Antibodies / pharmacology
  • Cell Division / drug effects*
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Humans
  • Interleukin-1 / genetics
  • Interleukin-1 / immunology
  • Interleukin-1 / pharmacology*
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • RNA, Messenger / analysis
  • Receptors, Interleukin-1 / analysis
  • Receptors, Interleukin-1 / metabolism
  • Recombinant Proteins / pharmacology
  • T-Lymphocytes / immunology
  • Thyroid Neoplasms / genetics
  • Thyroid Neoplasms / immunology
  • Thyroid Neoplasms / pathology*
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

Substances

  • Antibodies
  • Interleukin-1
  • RNA, Messenger
  • Receptors, Interleukin-1
  • Recombinant Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor