4,4'‑Bond secalonic acid D targets SP cells and inhibits metastasis in hepatocellular carcinoma

Mol Med Rep. 2020 Jun;21(6):2624-2632. doi: 10.3892/mmr.2020.11055. Epub 2020 Apr 6.

Abstract

The existence of cancer stem cells (CSCs) is considered to be the main reason for chemoresistance, metastasis and the ultimate failure of treatment in hepatocellular carcinoma (HCC). However, there are a few chemical agents that may inhibit CSCs. The present study identified that 4,4'‑bond secalonic acid D (4,4'‑SAD), a compound isolated from the marine‑derived fungus Penicillium oxalicum, inhibited the growth of side population (SP) cells isolated from human liver cancer cell lines PLC/PRF/5 and HuH‑7 by attenuating the expression of ATP‑binding cassette superfamily G member 2. Furthermore, the results of wound healing, Transwell, western blotting and reverse transcription‑quantitative PCR assays demonstrated that 4,4'‑SAD suppressed the invasion and migration of SP cells by downregulating matrix metallopeptidase 9 (MMP‑9) and upregulating the antagonist tissue inhibitor of metalloproteinases 1 in vitro. Moreover, in vivo study results found that 4,4'‑SAD had anti‑lung metastasis efficacy via the decrease of MMP‑9 expression in the H22 HCC model of Kunming mice. Therefore, the present study identified the potential of 4,4'‑SAD as a promising candidate for the treatment of advanced liver cancer.

Keywords: 4,4'‑bond secalonic acid D; SP cells; metastasis; hepatocellular carcinoma; matrix metalloproteinase 9; aTP-binding cassette superfamily G member 2.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2 / metabolism
  • Animals
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / pathology*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Female
  • Humans
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / pathology*
  • Lung Neoplasms / prevention & control
  • Lung Neoplasms / secondary
  • Matrix Metalloproteinase 9 / metabolism
  • Mice
  • Penicillium / chemistry
  • Penicillium / metabolism
  • Side-Population Cells / cytology
  • Side-Population Cells / drug effects*
  • Side-Population Cells / metabolism
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism
  • Transplantation, Heterologous
  • Xanthones / chemistry
  • Xanthones / pharmacology*
  • Xanthones / therapeutic use

Substances

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • TIMP1 protein, human
  • Tissue Inhibitor of Metalloproteinase-1
  • Xanthones
  • secalonic acid
  • Matrix Metalloproteinase 9

Supplementary concepts

  • Penicillium oxalicum