Dieckol inhibits non‐small–cell lung cancer cell proliferation and migration by regulating the PI3K/AKT signaling pathway
Autor: | Yan Zhao, Geng‐Jun Zhu, Xiao‐Feng Li, Chun‐Hong Wang, Wei-Zhang Shen, Li‐Fang Jin |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Lung Neoplasms Cell Survival Health Toxicology and Mutagenesis Apoptosis NSCLC Toxicology Biochemistry Flow cytometry Phosphatidylinositol 3-Kinases 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Annexin Carcinoma Non-Small-Cell Lung Cell Line Tumor medicine Humans PI3K/AKT/mTOR anticancer drug Propidium iodide Molecular Biology Protein kinase B Research Articles PI3K/AKT/mTOR pathway Benzofurans Cell Proliferation A549 cell 030102 biochemistry & molecular biology medicine.diagnostic_test General Medicine Dieckol lung cancer cadherin chemistry 030220 oncology & carcinogenesis dieckol Cancer research Molecular Medicine Proto-Oncogene Proteins c-akt Signal Transduction Research Article |
Zdroj: | Journal of Biochemical and Molecular Toxicology |
ISSN: | 1099-0461 1095-6670 |
DOI: | 10.1002/jbt.22346 |
Popis: | Non‐small–cell lung cancer (NSCLC) is one of the most prevalent type of lung cancers with an increased mortality rate in both developed and developing countries worldwide. Dieckol is one such polyphenolic drug extracted from brown algae which has proven antioxidant and anti‐inflammatory properties. In the present study, we evaluated the anticancer property of dieckol against NSCLC cell line A549. The LC50 value of dieckol was found to be 25 µg/mL by performing 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) assay and the antiapoptotic property of dieckol was analyzed by dual staining technique with acridine orange/propidium iodide (AO/PI) stains. It was further confirmed with flow cytometry analysis with Annexin FITC and JC‐1 staining and the anti‐invasive property was assessed by Transwell assay. The molecular mechanism of dieckol anticancer activity was confirmed by estimating the levels of caspases and by estimating the signaling proteins of Pi3K/AKT/mTOR signaling pathway using the immunoblotting technique. Our data suggest that dieckol is potent anticancer agent, it effectively inhibits the invasive and migratory property A549 cells and it also induces apoptosis via inhibiting Pi3K/AKT/mTOR signaling, activating the tumor suppressor protein E‐cadherin signifying that dieckol is potent natural anticancer drug to treat NSCLC. |
Databáze: | OpenAIRE |
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