Regional differences in prostaglandin E₂ metabolism in human colorectal cancer liver metastases

BMC Cancer. 2013 Feb 26:13:92. doi: 10.1186/1471-2407-13-92.

Abstract

Background: Prostaglandin (PG) E2 plays a critical role in colorectal cancer (CRC) progression, including epithelial-mesenchymal transition (EMT). Activity of the rate-limiting enzyme for PGE2 catabolism (15-hydroxyprostaglandin dehydrogenase [15-PGDH]) is dependent on availability of NAD+. We tested the hypothesis that there is intra-tumoral variability in PGE2 content, as well as in levels and activity of 15-PGDH, in human CRC liver metastases (CRCLM). To understand possible underlying mechanisms, we investigated the relationship between hypoxia, 15-PGDH and PGE2 in human CRC cells in vitro.

Methods: Tissue from the periphery and centre of 20 human CRCLM was analysed for PGE2 levels, 15-PGDH and cyclooxygenase (COX)-2 expression, 15-PGDH activity, and NAD+/NADH levels. EMT of LIM1863 human CRC cells was induced by transforming growth factor (TGF) β.

Results: PGE2 levels were significantly higher in the centre of CRCLM compared with peripheral tissue (P = 0.04). There were increased levels of 15-PGDH protein in the centre of CRCLM associated with reduced 15-PGDH activity and low NAD+/NADH levels. There was no significant heterogeneity in COX-2 protein expression. NAD+ availability controlled 15-PGDH activity in human CRC cells in vitro. Hypoxia induced 15-PGDH expression in human CRC cells and promoted EMT, in a similar manner to PGE2. Combined 15-PGDH expression and loss of membranous E-cadherin (EMT biomarker) were present in the centre of human CRCLM in vivo.

Conclusions: There is significant intra-tumoral heterogeneity in PGE2 content, 15-PGDH activity and NAD+ availability in human CRCLM. Tumour micro-environment (including hypoxia)-driven differences in PGE2 metabolism should be targeted for novel treatment of advanced CRC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Hypoxia
  • Colorectal Neoplasms / pathology*
  • Dinoprostone / metabolism*
  • Epithelial-Mesenchymal Transition / drug effects
  • Humans
  • Hydroxyprostaglandin Dehydrogenases / metabolism
  • Immunohistochemistry
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / secondary*
  • Microarray Analysis
  • Neoplasm Proteins / metabolism*
  • Transforming Growth Factor beta / pharmacology
  • Tumor Cells, Cultured
  • Tumor Microenvironment

Substances

  • Neoplasm Proteins
  • Transforming Growth Factor beta
  • Hydroxyprostaglandin Dehydrogenases
  • 15-hydroxyprostaglandin dehydrogenase
  • Dinoprostone