Drug Res (Stuttg) 2022; 72(07): 390-395
DOI: 10.1055/a-1842-7545
Original Article

Thymoquinone Potentiates Methotrexate Mediated-Apoptosis in Saos-2 Osteosarcoma Cell Line

Authors

  • Payam Ali khyavi

    1   Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  • Amir Valizadeh

    2   Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran
  • Dariush Shanehbandi

    3   Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  • Bahman Yousefi

    1   Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  • Jafar Soleimanpour

    4   Department of Orthopedic Surgery, School of Medicine and Shohada Educational Hospital, Tabriz University of Medical Sciences, Tabriz, Iran

Abstract

Introduction Recently, various studies have concentrated on the therapeutic potential of thymoquinone (TQ), a natural polyphenol, in various human malignancies, including osteosarcoma. However, the underlying mechanisms in TQ-mediated anti-cancer effects are not yet fully understood. Therefore, the present study investigated the effect of TQ on methotrexate (MTX)-induced apoptosis in Saos-2 cells.

Methods Saos-2 cells were treated with MTX, TQ, and a combination of both, and cell viability was assessed by MTT assay. mRNA expression of apoptotic markers, including Bax, Bcl-2, and caspase-3, was assessed using quantitative real-time polymerase chain reaction (qRT-PCR).

Results MTX resulted in significant inhibition of cell proliferation in a dose-dependent manner. The combination of TQ and MTX inhibited proliferation compared to single treatments (P<0.05). TQ also induced apoptosis by regulating pro-apoptotic markers including Bax and caspase-3 and reducing anti-apoptotic mediators including Bcl-2. In addition, TQ increased MTX-induced apoptosis in Saos-2 cells.

Conclusion The findings of the present study highlight new insights into understanding the role of TQ as a potential therapeutic agent in osteosarcoma by increasing MTX-induced apoptosis.



Publication History

Received: 16 March 2022

Accepted: 03 May 2022

Article published online:
27 June 2022

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