Tumors secreting human TNF/cachectin induce cachexia in mice

Cell. 1987 Aug 14;50(4):555-63. doi: 10.1016/0092-8674(87)90028-6.

Abstract

Anorexia and weight loss are serious complications that adversely effect the prognosis of cancer patients. It has been suggested that TNF/cachectin may cause cachexia. To determine if TNF/cachectin can induce progressive weight loss in tumor-bearing animals, a clone of the human TNF/cachectin gene was isolated and inserted into a mammalian expression vector. This construct was transfected into CHO cells, and a cell line (CHO/TNF-20) that secretes TNF/cachectin was isolated. A cell line (CHO/CMV-Neo) that contains the same expression vector without the TNF/cachectin gene was also isolated. Nude mice injected intraperitoneally with CHO/TNF-20 cells died more quickly than mice injected with CHO/CMV-Neo cells. Eighty-seven percent of mice inoculated intramuscularly with CHO/TNF-20 cells developed severe cachexia and weight loss. All mice bearing CHO/CMV-Neo tumors maintained or increased their body weight. We conclude that mice bearing tumors that secrete TNF/cachectin develop progressive wasting and die more quickly than mice bearing control tumors.

MeSH terms

  • Animals
  • Body Weight
  • Cachexia / etiology*
  • Cell Line
  • Cricetinae
  • Female
  • Fibroblasts
  • Glycoproteins / metabolism*
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Neoplasms, Experimental / complications
  • Neoplasms, Experimental / metabolism*
  • Ovary
  • Recombinant Proteins / metabolism
  • Tumor Necrosis Factor-alpha

Substances

  • Glycoproteins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha