Drug Res (Stuttg) 2025; 75(09): 386-391
DOI: 10.1055/a-2713-0136
Original Article

Diosgenin Enhances the Sensitivity to Methotrexate Through Oxidative DNA Damage in Saos-2 Osteosarcoma Cancer Cells

Autor*innen

  • Hadi Ghobadi

    1   Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
  • Amir Valizadeh

    2   Clinical Biochemistry and Laboratory Medicine, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
    3   Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
  • Mohsen Dashti

    2   Clinical Biochemistry and Laboratory Medicine, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
    4   Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
  • Afsaneh Ghasemzadeh

    2   Clinical Biochemistry and Laboratory Medicine, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
    4   Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
  • Bahman Yousefi

    2   Clinical Biochemistry and Laboratory Medicine, Tabriz University of Medical Sciences, Tabriz, Iran (the Islamic Republic of)
    5   Department of Orthopedic Surgery, School of Medicine and Shohada Educational Hospital, Tabriz University of Medical Sciences Tabriz, Iran (the Islamic Republic of)

Gefördert durch: Tabriz University of Medical Sciences 67064

Abstract

Background

Previously, diosgenin, a steroidal saponin, has demonstrated therapeutic potential for osteosarcoma. However, the underlying mechanisms still remain unknown.

Objectives

This study was designed to investigate the impact of diosgenin on methotrexate-mediated apoptosis in Saos-2 cells, specifically related to DNA damage.

Methods

To assess the cell vitality of Saos-2 cells, we treated them with methotrexate, diosgenin, and a mixture of both, then performed the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide technique. Western blot was used to evaluate DNA damage by measuring the expression of γ-H2AX protein. The ELISA method was also applied to find the quantity of 8-oxo-2′-deoxyguanosine, and flow cytometry was used to analyze apoptosis.

Results

Combining methotrexate with diosgenin led to a major reduction in cell proliferation rate compared to monotreatments (p<0.05). This combination significantly increased apoptosis, measured by flow cytometry, and increased levels of γ-H2AX protein and 8-oxo-2′-deoxyguanosine.

Conclusion

Diosgenin significantly augmented methotrexate-mediated apoptosis in Saos-2 cells through enhanced DNA damage mechanisms. These findings suggest that diosgenin could serve as a promising adjuvant therapeutic agent to improve the efficacy of current methotrexate-based chemotherapy regimens in osteosarcoma treatment, potentially reducing required drug doses and minimizing associated toxicity while maintaining therapeutic effectiveness.



Publikationsverlauf

Eingereicht: 02. Juli 2025

Angenommen nach Revision: 23. September 2025

Artikel online veröffentlicht:
18. November 2025

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