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.
Original language | English |
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Pages (from-to) | 1746-1758 |
Number of pages | 13 |
Journal | Biochimica et Biophysica Acta - Molecular Cell Research |
Volume | 1864 |
Issue number | 10 |
DOIs | |
Publication status | Published - Oct 1 2017 |
Keywords
- A disintegrin and metalloprotease 9
- Akt
- Invasion
- Non-small cell lung cancer
- Quercetin
- Snail
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology