Overexpression of CC10 modifies neoplastic potential in lung cancer cells

Cell Growth Differ. 1998 Jun;9(6):475-85.

Abstract

CC10 is infrequently expressed in non-small cell lung cancer cell lines, despite being abundantly produced by progenitor cells for normal and neoplastic airway epithelium. We overexpressed CC10 cDNA in the non-small cell lung cancer cell line A549 to determine its effect on the neoplastic phenotype. A549 cells transfected with CC10 demonstrated a marked reduction in invasiveness that was paralleled by diminished 92-kDa and absent 72-kDa metalloproteinase activity by zymography. Western analysis revealed the near absence of the corresponding matrix metalloproteinases (MMPs) MMP-2 and MMP-9 in the CC10-transfected cell lines, but not in the vector-transfected cell lines. The CC10-transfected cell lines also demonstrated decreased adhesiveness to fibronectin compared with the controls. CC10 expression was associated with decreased anchorage-independent growth but not with decreased anchorage-dependent growth. These data suggest that loss of CC10 may contribute to carcinogenesis, because CC10 antagonizes the neoplastic phenotype.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / metabolism
  • Animals
  • Carcinoma, Non-Small-Cell Lung / enzymology
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Cell Communication / physiology
  • Cell Division / physiology
  • Cricetinae
  • Enzyme Inhibitors / metabolism*
  • Extracellular Matrix Proteins / metabolism
  • Humans
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / metabolism*
  • Mesocricetus
  • Metalloendopeptidases / metabolism
  • Neoplasm Invasiveness / pathology
  • Neoplastic Processes
  • Proteins / metabolism*
  • RNA, Messenger / analysis
  • Transfection
  • Tumor Cells, Cultured
  • Uteroglobin*

Substances

  • Enzyme Inhibitors
  • Extracellular Matrix Proteins
  • Proteins
  • RNA, Messenger
  • SCGB1A1 protein, human
  • Uteroglobin
  • Metalloendopeptidases