Dkk-3 induces apoptosis through mitochondrial and Fas death receptor pathways in human mucinous ovarian cancer cells

Int J Gynecol Cancer. 2015 Mar;25(3):372-9. doi: 10.1097/IGC.0000000000000340.

Abstract

Objective: Dkk-3 is a Wnt signaling inhibitor that is frequently inactivated in human cancers. Dkk-3 possesses an antiproliferative activity and induces apoptosis in tumor cells, suggesting that it functions as a tumor suppressor. In this study, we investigated the molecular function of Dkk-3 in human ovarian cancer cells.

Methods: We assessed the levels of Dkk-3 protein expression in human mucinous and clear cell ovarian cancer cells, and compared cell viabilities between cell lines that expressed Dkk-3 and those that did not, as well as between cells that expressed Dkk-3 and those whose expression of Dkk-3 was reduced by small interfering RNA. We also evaluated the characteristic fragmentation of DNA to detect apoptosis in Dkk-3-deficient cells. To further investigate the molecular mechanisms of apoptosis, we assessed the expression of molecules involved in apoptosis signaling pathways in Dkk-3-deficient cells.

Results: The expression of the Dkk-3 protein was observed in most of the ovarian cancer cell lines tested. Dkk-3-deficient cells showed faster growth than Dkk-3-replete cells. The characteristic fragmentation of DNA was not observed in Dkk-3-deficient cells, which showed decreased levels of expression in caspase-3, activated caspase-9, Bax, p53, activated caspase-8, and Fas/CD95, as well as an increase in Bcl-2 expression.

Conclusions: Although Dkk-3 expression was observed in most of human ovarian cancer cell lines, Dkk-3 has a tumor-suppressive function and a proapoptotic effect, inducing apoptosis through mitochondrial and Fas death receptor pathways in human mucinous ovarian cancer MCAS cells.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adenocarcinoma, Mucinous / metabolism*
  • Apoptosis
  • Caspase 1 / metabolism
  • Caspase 8 / metabolism
  • Caspase 9 / metabolism
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Survival
  • Chemokines
  • DNA Fragmentation
  • DNA, Neoplasm / metabolism*
  • Death Domain Receptor Signaling Adaptor Proteins / metabolism*
  • Female
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Mitochondria / metabolism*
  • Ovarian Neoplasms / metabolism*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • RNA, Small Interfering
  • Tumor Suppressor Protein p53 / metabolism
  • Wnt Signaling Pathway
  • bcl-2-Associated X Protein / metabolism
  • fas Receptor / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Chemokines
  • DKK3 protein, human
  • DNA, Neoplasm
  • Death Domain Receptor Signaling Adaptor Proteins
  • FAS protein, human
  • Intercellular Signaling Peptides and Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Small Interfering
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • fas Receptor
  • Caspase 8
  • Caspase 9
  • Caspase 1