Human lung cancers growing on extracellular matrix: expression of oncogenes and growth factors

Anticancer Res. 1992 Nov-Dec;12(6B):2191-6.

Abstract

The goal of this study was to evaluate the extracellular matrix (ECM) as a model for growing human lung cancers and to study the feasibility of its application for cellular and molecular studies of tumor biology. Bovine corneal endothelial cell ECM coated dishes were evaluated as a growth substrate for tumor cultures. Growth success, morphology and oncoprotein/growth factor expression for 74 different lung cancers (adenocarcinoma, epidermoid carcinoma and small cell carcinoma) were compared after seeding fresh surgical explants onto bovine corneal endothelial cell ECM and plastic culture substrate. Nineteen out of 74 tumors (26%) plated on ECM demonstrated measurable growth. Growth on ECM was superior to growth on plastic for the lung tumors. All 19 tumor cultures showed malignant morphology and functions. They were examined under the light microscope, and in all cases pre- and post-cytology confirmed malignancy. Tumor cells seeded on ECM retained their malignant phenotype in comparison to tumors grown on plastic. Several oncoproteins (c-myc, c-Ha-ras, c-erbB-2) and growth factors/receptors (EGF, EGF-R, TGF alpha) were immunostained. These analyses were performed immediately after disaggregation of tumor cells obtained surgically and after seeding on ECM or plastic. Strong expression of oncoproteins/growth factors was detected in tumor cells immediately after surgery or when the cells were plated on ECM. On the other hand, moderate or no expression was observed in the same type of cells on plastic.

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / pathology
  • Biomarkers, Tumor / analysis*
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Small Cell / pathology
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / pathology
  • Cell Aggregation
  • Cell Division
  • Epidermal Growth Factor / analysis*
  • Epidermal Growth Factor / biosynthesis
  • ErbB Receptors / analysis*
  • ErbB Receptors / biosynthesis
  • Extracellular Matrix / physiology
  • Genes, myc
  • Genes, ras
  • Humans
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology*
  • Ploidies
  • Proto-Oncogene Proteins / analysis*
  • Proto-Oncogene Proteins c-myc / analysis*
  • Proto-Oncogene Proteins p21(ras) / analysis*
  • Proto-Oncogenes*
  • Receptor, ErbB-2
  • Transforming Growth Factor alpha / analysis*
  • Transforming Growth Factor alpha / biosynthesis
  • Tumor Cells, Cultured

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-myc
  • Transforming Growth Factor alpha
  • Epidermal Growth Factor
  • ErbB Receptors
  • Receptor, ErbB-2
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)