Nanoparticle-induced photocatalytic head and neck squamous cell carcinoma cell death is associated with autophagy

Stephan Hackenberg1, Agmal Scherzed, Antje Gohla

  • 1Department of Oto-Rhino-Laryngology, Plastic, Aesthetic & Reconstructive Head & Neck Surgery, University Hospital of Wuerzburg, Germany.

Abstract

Insights

Zinc oxide nanoparticles (ZnO-NPs) combined with UVA-1 irradiation induce photocatalytic cell death in head and neck squamous cell carcinoma (HNSCC). Autophagy plays a dual role, mediating survival or cell death depending on the treatment specifics.

Area of Science:

  • Nanomedicine
  • Photocatalysis
  • Cancer Biology

Background:

  • Head and neck squamous cell carcinoma (HNSCC) remains a significant health challenge.
  • Developing novel therapeutic strategies for HNSCC is crucial.
  • Zinc oxide nanoparticles (ZnO-NPs) show potential in cancer treatment.

Purpose of the Study:

  • To elucidate the molecular mechanisms of photocatalytic cell death in HNSCC induced by ZnO-NPs.
  • To investigate the role of autophagy in ZnO-NP-mediated photodynamic therapy.

Main Methods:

  • FaDu cells (HNSCC-derived) were treated with ZnO-NPs and UVA-1 irradiation.
  • Cytotoxicity assessed via MTT assay and Annexin-V/propidium iodide staining.
  • Autophagy markers (autophagosome accumulation, LC3-I/II conversion) and reactive oxygen species (ROS) generation were quantified.

Main Results:

  • ZnO-NPs and UVA-1 induced apoptosis-independent cytotoxicity.
  • Combined treatment significantly increased autophagosome formation, LC3-II levels, and ROS generation.
  • Autophagy appeared to promote cell survival under individual treatments but mediated cell death under combined photocatalytic treatment.

Conclusions:

  • Photocatalytic treatment with ZnO-NPs and UVA-1 triggers HNSCC cell death.
  • Autophagy's role in HNSCC viability is context-dependent, influenced by the photocatalytic trigger.
  • These findings offer insights into nanoparticle-based photodynamic therapy for HNSCC.

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