Human cytomegalovirus infection is correlated with enhanced cyclooxygenase-2 and 5-lipoxygenase protein expression in breast cancer

J Cancer Res Clin Oncol. 2019 Aug;145(8):2083-2095. doi: 10.1007/s00432-019-02946-8. Epub 2019 Jun 15.

Abstract

Purpose: While enhanced expression of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LO) and their derived metabolites is associated with breast cancer (BC) risk, the precise link between BC carcinogenesis and enhanced inflammatory activity remains to be clarified. Human Cytomegalovirus (HCMV) may induce expression of COX-2 and 5-LO and is frequently found in breast cancer biopsies. Thus, we investigated whether there is an association between HCMV proteins and expression of COX-2 and 5-LO in human BC tissue and BC cell lines.

Materials and methods: Paraffin embedded biopsies obtained from 49 patients with breast cancer and 26 tissue samples from adjacent, benign breast tissues were retrospectively examined for HCMV-immediate early (IE), HCMV-Late (LA), COX-2, and 5-LO proteins by immunohistochemistry. In vitro, uninfected and HCMV-infected BC cell lines were examined for COX-2 and 5-LO transcripts and proteins by PCR and flow cytometry.

Results: Extensive expression of COX-2, 5-LO and HCMV-IE proteins were preferentially detected in BC samples. We found a statistically significant concordant correlation between extensive HCMV-IE and COX-2 (P < 0.0001) as well as with HCMV-IE and 5-LO (P = 0.0003) in infiltrating BC. In vitro, HCMV infection induced COX-2 and 5-LO transcripts and COX-2 proteins in MCF-7 cells (P =0.008, P =0.018, respectively). In MDA-MB-231 cells that already had high base line levels of COX-2 expression, HCMV induced both COX-2 and 5-LO proteins but not transcripts.

Conclusion: Our findings demonstrate a significant correlation between extensive HCMV-IE protein expression and overexpression of COX-2 and 5-LO in human breast cancer.

Keywords: 5-LO; Breast cancer; COX-2; Human cytomegalovirus; MCF-7; MDA-MB-231.

MeSH terms

  • Arachidonate 5-Lipoxygenase / metabolism*
  • Breast Neoplasms / complications*
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / virology
  • Cells, Cultured
  • Cyclooxygenase 2 / metabolism*
  • Cytomegalovirus Infections / complications*
  • Cytomegalovirus Infections / metabolism*
  • Female
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • MCF-7 Cells
  • Middle Aged
  • Retrospective Studies
  • Tissue Array Analysis

Substances

  • Arachidonate 5-Lipoxygenase
  • Cyclooxygenase 2
  • PTGS2 protein, human