Thymoquinone induces apoptosis in oral cancer cells through p38β inhibition

Ehab Abdelfadil1, Ya-Hsin Cheng, Da-Tian Bau

  • 1Graduate Institute of Basic Medical Science, China Medical University, Taichung, Taiwan.

Insights

This study investigated p38 mitogen-activated protein kinase (MAPK) in oral cancer, finding p38β is linked to its development. The anti-cancer compound thymoquinone (TQ) shows promise by downregulating p38β.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cellular Signaling

Background:

  • Oral cancer presents significant morbidity and mortality.
  • The specific roles of p38 MAPK family members in oral cancer remain largely undefined.
  • p38 MAPK signaling pathways regulate crucial cellular processes like proliferation and differentiation.

Purpose of the Study:

  • To investigate the involvement of p38 MAPK family members in oral cancer development.
  • To explore the anti-cancer potential of thymoquinone (TQ) in oral cancer.
  • To elucidate the molecular mechanisms underlying TQ's anti-tumor effects.

Main Methods:

  • Utilized two unique cell lines: chemically induced oral cancer cells (T28) and adjacent non-tumor cells (N28).
  • Screened for the involvement of p38 MAPK in malignant transformation processes.
  • Assessed the anti-cancer activity of thymoquinone (TQ) and its effect on p38 MAPK signaling.

Main Results:

  • Results indicate a significant association between p38β, but not p38α, and oral cancer development.
  • Thymoquinone (TQ) demonstrated anti-cancer activity in the studied oral cancer model.
  • Evidence suggests TQ's anti-tumor effects are mediated through the downregulation of p38β MAPK.

Conclusions:

  • p38β MAPK is implicated in the development of oral cancer.
  • Thymoquinone (TQ) exhibits therapeutic potential against oral cancer.
  • Targeting p38β MAPK with agents like TQ may represent a viable strategy for oral cancer treatment.

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