Thymoquinone potentiates anti‐cancer effects of cisplatin in oral squamous cell carcinoma via targeting oxidative stress

Author:

Fath Mohsen Karami1,Nasiri Kamyar2,Ghasemzadeh Shabnam3,Nejati Seyedeh Tabasom4,Ghafari Nima2,Masouleh Sahand Saeidpour5,Dadgar Esmaeel5,Kazemi Kimia Sadat6,Esfahaniani Mahla7

Affiliation:

1. Department of Cellular and Molecular Biology, Faculty of Biological Sciences Kharazmi University Tehran Iran

2. Faculty of Dentistry Islamic Azad University of Medical Sciences Tehran Iran

3. Faculty of Dentistry Qazvin University of Medical Sciences Qazvin Iran

4. School of Dentistry Hormozgan University of Medical Sciences Bandar Abbas Iran

5. Faculty of Dentistry Tabriz University of Medical Sciences Tabriz Iran

6. Faculty of Dentistry Shahid Beheshti University of Medical Sciences Tehran Iran

7. Faculty of Dentistry Golestan University of Medical Sciences Gorgan Iran

Abstract

AbstractRecent evidence has proved that thymoquinone as a natural polyphenol has great anticancer and anti‐proliferative effects in cancer cells. In this study, we aimed to examine the effects of thymoquinone on increasing cisplatin‐induced apoptosis human oral squamous cell carcinoma cells and its underlying molecular mechanisms. SCC‐25 cancer cells treated by thymoquinone and cisplatin with different concentrations. Cell viability will determine by using MTT assay. The concentrations of reactive oxygen species (ROS) and antioxidant activities were determined using specific related kits. DNA damage, lipid, and protein oxidation were assessed. Real‐time PCR and Western blot analysis will be used to determine the expression of apoptosis‐related proteins including Bax, Bcl‐2, and caspase‐3. Combination of thymoquinone and cisplatin suppressed synergistically SCC‐25 cancer cell viability and induced apoptosis in dose‐depended manner. Cell treatment with combination of thymoquinone and cisplatin led to accumulation of ROS within cells and increase in the intracellular levels of DNA damage, protein and lipid peroxidation. In addition, the combination of thymoquinone and cisplatin modulated the mRNA and protein expression levels of apoptosis‐related proteins including Bax, Bcl‐2, and caspase‐3. Thymoquinone potentiated cisplatin anti‐cancer effect on OSCC by inducing oxidative stress in cells.

Publisher

Wiley

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