The Root Bark of Morus alba L. Suppressed the Migration of Human Non-Small-Cell Lung Cancer Cells through Inhibition of Epithelial⁻Mesenchymal Transition Mediated by STAT3 and Src.
Tae-Rin MinHyun-Ji ParkMoon Nyeo ParkBonlgee KimShin-Hyung ParkPublished in: International journal of molecular sciences (2019)
The root bark of Morus alba L. (MA) has been traditionally used for the treatment of various lung diseases in Korea. Although recent research has demonstrated its anticancer effects in several cancer cells, it is still unclear whether MA inhibits the migratory ability of lung cancer cells. The present study investigated the effects of MA on the migration of lung cancer cells and explored the underlying mechanism. Results from a transwell assay and wound-healing assay demonstrated that methylene chloride extracts of MA (MEMA) suppressed the migration and invasion of H1299, H460, and A549 human non-small-cell lung cancer (NSCLC) cells in a concentration-dependent manner. Results from Western blot analyses showed that MEMA reduced the phosphorylation of STAT3 and Src. In addition, MEMA downregulated the expression of epithelial-mesenchymal transition (EMT) marker proteins including Slug, Snail, Vimentin, and N-cadherin, while upregulating the expression of Occludin-a tight-junction protein. The regulation of EMT markers and the decrease of migration by MEMA treatment were reversed once phospho-mimetic STAT3 (Y705D) or Src (Y527F) was transfected into H1299 cells. In conclusions, MEMA inhibited the migratory activity of human NSCLC cells through blocking Src/STAT3-mediated EMT.
Keyphrases
- epithelial mesenchymal transition
- induced apoptosis
- transforming growth factor
- signaling pathway
- endothelial cells
- cell cycle arrest
- cell proliferation
- tyrosine kinase
- small cell lung cancer
- poor prognosis
- high throughput
- endoplasmic reticulum stress
- pluripotent stem cells
- wound healing
- cell death
- mesenchymal stem cells
- binding protein
- small molecule
- blood brain barrier
- bone marrow
- long non coding rna
- smoking cessation
- single molecule
- cell adhesion