Luteolin attenuates migration and invasion of lung cancer cells via suppressing focal adhesion kinase and non-receptor tyrosine kinase signaling pathway

• Published in: Nutrition research and practice 2020, 14(2), , pp.127-133
• Main Authors: Masraksa, Wuttipong, Tanasawet, Supita, Hutamekalin, Pilaiwanwadee, Wongtawatchai, Tulaporn, Sukketsiri, Wanida
• Format: Article
• Language: English
• Subjects: Botulinum toxin; Cdc42 protein; Cell division; Cell migration; Cell viability; Chemoresistance; Cytotoxicity; Filopodia; Focal adhesion kinase; Immunofluorescence; Kinases; Lung cancer; Metastases; Metastasis; Non-small cell lung carcinoma; Original Research; Protein-tyrosine kinase receptors; Rac1 protein; Ras protein; RhoA protein; Signal transduction; Small cell lung carcinoma; Wound healing; 생활과학
• ISSN: 1976-1457; 2005-6168
• DOI: 10.4162/nrp.2020.14.2.127

Non-small cell lung cancer is mostly recognized among other types of lung cancer with a poor prognosis by cause of chemotherapeutic resistance and increased metastasis. Luteolin has been found to decrease cell metastasis. However, its underlying mechanisms remain unresolved. The objective of this study was to examine the effect (and its mechanism) of luteolin on the migration and invasion of human non-small cell lung cancer A549 cells. Cell viability was investigated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Wound healing and transwell assays were evaluated to assess migration and invasion, respectively. Western blot analysis and immunofluorescence were further performed to investigate the role of luteolin and its mechanisms of action. Administration with up to 40 µM luteolin showed no cytotoxic activity on lung cancer A549 cells or non-cancer MRC-5 cells. Additionally, luteolin at 20-40 µM significantly suppressed A549 cells' migration, invasion, and the formation of filopodia in a concentration-dependent manner at 24 h. This is similar with western blot analysis, which revealed diminished the phosphorylated focal adhesion kinase (pFAK), phosphorylated non-receptor tyrosine kinase (pSrc), Ras-related C3 botulinum toxin substrate 1 (Rac1), cell division control protein 42 (Cdc42), and Ras homolog gene family member A (RhoA) expression levels. Overall, our data indicate that luteolin plays a role in controlling lung cancer cells' migration and invasion via Src/FAK and its downstream Rac1, Cdc42, and RhoA pathways. Luteolin might be considered a promising candidate for suppressing invasion and metastasis of lung cancer cells.