Antimetastatic Therapies of the Polysulfide Diallyl Trisulfide against Triple-Negative Breast Cancer (TNBC) via Suppressing MMP2/9 by Blocking NF-κB and ERK/MAPK Signaling Pathways

PLoS One. 2015 Apr 30;10(4):e0123781. doi: 10.1371/journal.pone.0123781. eCollection 2015.

Abstract

Background: Migration and invasion are two crucial steps of tumor metastasis. Blockage of these steps may be an effective strategy to reduce the risk. The objective of the present study was to investigate the effects of diallyl trisulfide (DATS), a natural organosulfuric compound with most sulfur atoms found in garlic, on migration and invasion in triple negative breast cancer (TNBC) cells. Molecular mechanisms underlying the anticancer effects of DATS were further investigated.

Methods and results: MDA-MB-231 cells and HS 578t breast cancer cells were treated with different concentrations of DATS. DATS obviously suppressed the migration and invasion of two cell lines and changed the morphological. Moreover, DATS inhibited the mRNA/protein/ enzymes activities of MMP2/9 via attenuating the NF-κB pathway. DATS also inhibited ERK/MAPK rather than p38 and JNK.

Conclusion: DATS inhibits MMP2/9 activity and the metastasis of TNBC cells, and emerges as a potential anti-cancer agent. The inhibitory effects are associated with down-regulation of the transcriptional activities of NF-κB and ERK/MAPK signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allyl Compounds / chemistry
  • Allyl Compounds / pharmacology*
  • Animals
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Drug Screening Assays, Antitumor
  • Female
  • Humans
  • MAP Kinase Signaling System / drug effects*
  • Matrix Metalloproteinase 2 / biosynthesis*
  • Matrix Metalloproteinase 9 / biosynthesis*
  • NF-kappa B / metabolism*
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Neoplasm Proteins / metabolism*
  • Sulfides / chemistry
  • Sulfides / pharmacology*
  • Zebrafish

Substances

  • Allyl Compounds
  • NF-kappa B
  • Neoplasm Proteins
  • Sulfides
  • diallyl trisulfide
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
  • MMP9 protein, human
  • Matrix Metalloproteinase 9

Associated data

  • figshare/10.6084/M9.FIGSHARE.1340468
  • figshare/10.6084/M9.FIGSHARE.1340469
  • figshare/10.6084/M9.FIGSHARE.1340473
  • figshare/10.6084/M9.FIGSHARE.1340477
  • figshare/10.6084/M9.FIGSHARE.1340568
  • figshare/10.6084/M9.FIGSHARE.1340572
  • figshare/10.6084/M9.FIGSHARE.1340574
  • figshare/10.6084/M9.FIGSHARE.1340576
  • figshare/10.6084/M9.FIGSHARE.1340580
  • figshare/10.6084/M9.FIGSHARE.1340581
  • figshare/10.6084/M9.FIGSHARE.1340582
  • figshare/10.6084/M9.FIGSHARE.1340584
  • figshare/10.6084/M9.FIGSHARE.1340585
  • figshare/10.6084/M9.FIGSHARE.1340586
  • figshare/10.6084/M9.FIGSHARE.1340978

Grants and funding

This work was supported by the National Natural Science Foundation of China (No. 81173174, 81403260 and 81202655); The National Key Technology Research & Development Program (No. 2008BAI51B02); Ph.D. Programs Foundation of Ministry of Education of China (No. 20113237110008); Chinese Postdoctoral Science Foundation (2014M551639); Postdoctoral Science Foundation of Jiangsu province (1401138C); Doctoral Innovation Project of Jiangsu Province (KYLX_0977); Jiangsu College graduate research and innovation projects (No. KYLX_0977; CXZZ13_0627). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.