Transforming growth factor-beta 1, beta 2, and beta 3, urokinase and parathyroid hormone-related peptide expression in 8701-BC breast cancer cells and clones

Differentiation. 1993 Dec;55(1):73-80. doi: 10.1111/j.1432-0436.1993.tb00034.x.

Abstract

8701-BC is a recently characterized cell line isolated from a primary ductal infiltrating carcinoma of the breast (d.i.c.), showing some pleomorphism in cell microanatomy at an ultrastructural level. We have obtained different sublines of 8701-BC cells by cloning in soft agar at different concentrations (0.3% and 0.6%), and we have characterized the cloned lines by some morphological and growth parameters. 8701-BC cells and clones have been submitted to analysis by reverse transcriptase-linked polymerase chain reaction to detect mRNAs of various cytokines (transforming growth factor-beta s, tumour necrosis factors, interleukin 1s, interleukin 6, parathyroid hormone-related peptide, gamma interferon) and of urokinase, which are bioactive molecules commonly involved in cell-cell and cell-stroma interactions at primary and/or secondary sites of invasion. The aims of the present investigation were to determine: (a) if the corresponding genes are active in 8701-BC cell line and (b) if the sublines tested exhibit transcriptional heterogeneity. The results obtained show that 8701-BC cells express transcripts of transforming growth factor-beta s, urokinase and parathyroid hormone-related peptide (PTHrP), the latter product being responsible for the cancer-associated humoral hypercalcemic syndrome. Moreover, while the first two mRNAs are detectable in all the sublines tested, PTHrP is expressed almost uniquely by the clones isolated in 0.6% agar which exhibit a peculiar morphological appearance, a higher growth rate and a more active invasive behaviour in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Biomarkers, Tumor / analysis
  • Breast Neoplasms / chemistry*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology*
  • Carcinoma, Ductal, Breast / chemistry*
  • Carcinoma, Ductal, Breast / genetics
  • Carcinoma, Ductal, Breast / pathology*
  • Clone Cells
  • Humans
  • Interleukin-1 / analysis
  • Interleukin-1 / genetics
  • Interleukin-6 / analysis
  • Interleukin-6 / genetics
  • Molecular Sequence Data
  • Parathyroid Hormone-Related Protein
  • Phenotype
  • Polymerase Chain Reaction
  • Proteins / analysis*
  • Proteins / genetics
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Transforming Growth Factor beta / analysis*
  • Transforming Growth Factor beta / genetics
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / analysis
  • Tumor Necrosis Factor-alpha / genetics
  • Urokinase-Type Plasminogen Activator / analysis*
  • Urokinase-Type Plasminogen Activator / genetics

Substances

  • Biomarkers, Tumor
  • Interleukin-1
  • Interleukin-6
  • PTHLH protein, human
  • Parathyroid Hormone-Related Protein
  • Proteins
  • RNA, Messenger
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Urokinase-Type Plasminogen Activator