Luteolin and cancer metastasis suppression: focus on the role of epithelial to mesenchymal transition.
Yaseen HussainJing Hao CuiHaroon KhanMichael AschnerGaber El-Saber BatihaPhilippe JeandetPublished in: Medical oncology (Northwood, London, England) (2021)
Epithelial to mesenchymal transition (EMT) is a physiological process that assumes a primary role in the induction of cancer metastasis. This results in increased cell renewal, and resistance to cell death and therapies. EMT, therefore, represents an effective strategy for regulating cancerous cell activity. A need for efficacy and low cytotoxicity epithelial to mesenchymal transition modifying drugs has led to the investigational testing of the efficacy of plethora of different groups of phytonutrients. Luteolin is a natural flavonoid inhibits the growth of cancer cells by various mechanisms, such as the stimulation of cancer cell apoptosis, cell cycle arrest, inhibition of cell replication, tumor growth, improvement of drug resistance, prevention of cancer cell intrusiveness and metastasis. This review article focuses on the anti-cancer and anti-metastatic potential of luteolin targeting various transcription factors, markers and signaling pathways associated with the repression of epithelial to mesenchymal transition.
Keyphrases
- cell death
- papillary thyroid
- cell cycle arrest
- single cell
- squamous cell
- cell therapy
- epithelial mesenchymal transition
- squamous cell carcinoma
- small cell lung cancer
- transcription factor
- cell proliferation
- stem cells
- randomized controlled trial
- childhood cancer
- risk assessment
- cancer therapy
- endoplasmic reticulum stress