| Literature DB >> 28648644 |
Jer-Hwa Chang1, Shu-Leung Lai2, Wan-Shen Chen3, Wen-Yueh Hung4, Jyh-Ming Chow5, Michael Hsiao6, Wei-Jiunn Lee7, Ming-Hsien Chien8.
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.Entities:
Keywords: A disintegrin and metalloprotease 9; Akt; Invasion; Non-small cell lung cancer; Quercetin; Snail
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Year: 2017 PMID: 28648644 DOI: 10.1016/j.bbamcr.2017.06.017
Source DB: PubMed Journal: Biochim Biophys Acta Mol Cell Res ISSN: 0167-4889 Impact factor: 4.739