Human malignant fibrous histiocytomas in vitro: growth characteristics and their association with expression of mRNA for platelet-derived growth factor, transforming growth factor-alpha and their receptors

Eur J Cancer. 1998 Dec;34(13):2094-100. doi: 10.1016/s0959-8049(98)00247-0.

Abstract

Eight human malignant fibrous histiocytomas were examined in vitro, in order to relate their growth properties to mRNA expression for platelet-derived growth factor (PDGF), PDGF receptor (PDGF-R), transforming growth factor-alpha (TGF-alpha) and the epidermal growth factor receptor (EGF-R). Reverse transcriptase-polymerase chain reaction (RT-PCR) showed that all cell lines expressed mRNA for PDGF-R alpha and/or PDGF-R beta; six cell lines expressed mRNA for the PDGF-A chain, with one cell line coexpressing PDGF-B chain mRNA; seven cell lines expressed mRNA for TGF-alpha whereas six cell lines expressed EGF-R mRNA. Conditioned medium from three cell lines contained PDGF; none of the cell lines released TGF-alpha. Two cell lines grew without serum requirements; whereas both expressed mRNA for PDGF, PDGF-R, TGF-alpha and EGF-R, other cell lines, unable to grow without serum, showed the same combination of growth factor/growth factor receptor expression. The two cell lines able to grow without serum were also shown to be stimulated by the addition of PDGF-BB. These findings show that simultaneous expression of mRNA for a growth factor and its receptor does not necessarily imply an autocrine or paracrine loop. However, two of our cell lines fulfil the requirements of possible PDGF-related autocrine and paracrine regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cell Division
  • ErbB Receptors / metabolism
  • Female
  • Histiocytoma, Benign Fibrous / metabolism*
  • Histiocytoma, Benign Fibrous / pathology*
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Platelet-Derived Growth Factor / metabolism*
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / metabolism
  • Receptors, Platelet-Derived Growth Factor / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Transforming Growth Factor alpha / metabolism*
  • Tumor Cells, Cultured

Substances

  • Platelet-Derived Growth Factor
  • RNA, Messenger
  • RNA, Neoplasm
  • Transforming Growth Factor alpha
  • ErbB Receptors
  • Receptors, Platelet-Derived Growth Factor