Human β-defensin-3 inhibits migration of colon cancer cells via downregulation of metastasis-associated 1 family, member 2 expression

Int J Oncol. 2014 Sep;45(3):1059-64. doi: 10.3892/ijo.2014.2507. Epub 2014 Jun 20.

Abstract

The innate immune system plays an important role as the first line of defense against many types of microbes. Accumulating reports suggest that human β-defensins (hBDs) are expressed by and have certain roles in some cancer cells. In this study, we investigated the roles of hBD-3 in colon cancer cells. The expression of hBD-3 was examined by reverse transcriptase-polymerase chain reaction analysis of colon cancer cell lines and immunohistochemical staining of colon cancer tissues. The effect of hBD-3 on proliferation of colon cancer was assessed using the MTT assay and a real-time cell analyzer, and the effect of hBD-3 on the migration of colon cancer cells was also examined. The results showed that hBD-3 is not expressed in colon cancer cells but is produced by tumor-infiltrating monocytes. Migration of colon cancer cells was significantly inhibited by hBD-3 in a dose-dependent manner, although proliferation of colon cancer cells was not affected by administration of hBD-3. Moreover, reduced expression of metastasis-associated 1 family, member 2 (MTA2) mRNA in colon cancer cells was associated with exposure to hBD-3. In conclusion, progression of colon cancer was inhibited by hBD-3 in a paracrine fashion. Therefore, hBD-3 may be a potent new agent for treating colon cancer.

MeSH terms

  • Cell Line, Tumor
  • Cell Proliferation
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / pathology*
  • Gene Expression Regulation, Neoplastic
  • HT29 Cells
  • Histone Deacetylases / genetics*
  • Humans
  • Neoplasm Invasiveness / genetics*
  • Paracrine Communication
  • RNA, Messenger / genetics
  • Repressor Proteins / genetics*
  • beta-Defensins / genetics*
  • beta-Defensins / metabolism*

Substances

  • DEFB103A protein, human
  • RNA, Messenger
  • Repressor Proteins
  • beta-Defensins
  • MTA2 protein, human
  • Histone Deacetylases