Barium promotes anchorage-independent growth and invasion of human HaCaT keratinocytes via activation of c-SRC kinase

PLoS One. 2011;6(10):e25636. doi: 10.1371/journal.pone.0025636. Epub 2011 Oct 12.

Abstract

Explosive increases in skin cancers have been reported in more than 36 million patients with arsenicosis caused by drinking arsenic-polluted well water. This study and previous studies showed high levels of barium as well as arsenic in the well water. However, there have been no reports showing a correlation between barium and cancer. In this study, we examined whether barium (BaCl(2)) may independently have cancer-related effects on human precancerous keratinocytes (HaCaT). Barium (5-50 µM) biologically promoted anchorage-independent growth and invasion of HaCaT cells in vitro. Barium (5 µM) biochemically enhanced activities of c-SRC, FAK, ERK and MT1-MMP molecules, which regulate anchorage-independent growth and/or invasion. A SRC kinase specific inhibitor, protein phosphatase 2 (PP2), blocked barium-mediated promotion of anchorage-independent growth and invasion with decreased c-SRC kinase activity. Barium (2.5-5 µM) also promoted anchorage-independent growth and invasion of fibroblasts (NIH3T3) and immortalized nontumorigenic melanocytes (melan-a), but not transformed cutaneous squamous cell carcinoma (HSC5 and A431) and malignant melanoma (Mel-ret) cells, with activation of c-SRC kinase. Taken together, our biological and biochemical findings newly suggest that the levels of barium shown in drinking well water independently has the cancer-promoting effects on precancerous keratinocytes, fibroblast and melanocytes in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arsenic / analysis
  • Arsenic / toxicity
  • Bangladesh
  • Barium / analysis
  • Barium / toxicity*
  • CSK Tyrosine-Protein Kinase
  • Cell Adhesion / drug effects
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects
  • Cell Transformation, Neoplastic / pathology
  • Enzyme Activation / drug effects
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Fibroblasts / drug effects
  • Fibroblasts / enzymology
  • Fibroblasts / pathology
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / enzymology*
  • Keratinocytes / pathology*
  • Matrix Metalloproteinase 14 / metabolism
  • Melanocytes / drug effects
  • Melanocytes / enzymology
  • Melanocytes / pathology
  • Mice
  • NIH 3T3 Cells
  • Protein Kinase Inhibitors / pharmacology
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism*
  • Vietnam
  • Water Pollution / analysis
  • Water Wells / chemistry
  • src-Family Kinases

Substances

  • Protein Kinase Inhibitors
  • Barium
  • Protein-Tyrosine Kinases
  • CSK Tyrosine-Protein Kinase
  • Focal Adhesion Protein-Tyrosine Kinases
  • src-Family Kinases
  • CSK protein, human
  • Extracellular Signal-Regulated MAP Kinases
  • Matrix Metalloproteinase 14
  • Arsenic