Quercetin suppresses the metastatic ability of lung cancer through inhibiting Snail-dependent Akt activation and Snail-independent ADAM9 expression pathways

Biochim Biophys Acta Mol Cell Res. 2017 Oct;1864(10):1746-1758. doi: 10.1016/j.bbamcr.2017.06.017. Epub 2017 Jun 23.

Abstract

Metastasis is the major cause of death from lung cancer. Quercetin, a widely distributed bioflavonoid, is well known to induce growth inhibition in a variety of human cancer cells, but how it affects lung cancer cell invasion and metastasis is unclear. Herein, we found that quercetin inhibited the migration/invasion of non-small cell lung cancer (NSCLC) cell lines and bone metastasis in an orthotopic A549 xenograft model by suppressing the Snail-mediated epithelial-to-mesenchymal transition (EMT). Moreover, survival times of animals were also prolonged after quercetin treatment. Mechanistic investigations found that quercetin suppressed Snail-dependent Akt activation by upregulating maspin and Snail-independent a disintegrin and metalloproteinase (ADAM) 9 expression pathways to modulate the invasive ability of NSCLC cells. In clinical samples, we observed that patients with Snailhigh/p-Akthigh tumors had the shortest survival times. In addition, a lower survival rate was also found in ADAM9high patients than in ADAM9low patients. Overall, our results provide new insights into the role of quercetin-induced molecular regulation in suppressing NSCLC metastasis and suggest that quercetin has potential therapeutic applications for metastatic NSCLC.

Keywords: A disintegrin and metalloprotease 9; Akt; Invasion; Non-small cell lung cancer; Quercetin; Snail.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • ADAM Proteins / genetics*
  • Animals
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Epithelial-Mesenchymal Transition / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Membrane Proteins / genetics*
  • Mice
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology
  • Oncogene Protein v-akt / genetics*
  • Quercetin / administration & dosage*
  • Serpins / genetics*
  • Signal Transduction / drug effects
  • Snail Family Transcription Factors / genetics*
  • Xenograft Model Antitumor Assays

Substances

  • Membrane Proteins
  • SERPIN-B5
  • Serpins
  • Snail Family Transcription Factors
  • Quercetin
  • Oncogene Protein v-akt
  • ADAM Proteins
  • ADAM9 protein, human