Related Experiment Video
Updated: May 10, 2026

Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry
Published on: July 21, 2017
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.
Aim:
To characterize molecular mechanisms underlying photocatalytic cell death of head and neck squamous cell carcinoma (HNSCC) by zinc oxide nanoparticles (ZnO-NPs).
Materials & Methods:
Human HNSCC-derived FaDu cells were incubated with ZnO-NPs followed by UVA-1 irradiation. Cytotoxicity was assessed by MTT assay and annexin-V propidium iodide test. Autophagy was detected by autophagosome accumulation, conversion of light chain 3 I to II, and lysosomal activity. The generation of reactive oxygen species was measured using the 2',7'-dichlorofluorescein-diacetate test.
Results:
Apoptosis-independent cytotoxic effects were induced by 0.2- and 2-µg/ml ZnO-NPs and UVA-1. FaDu cells promoted autophagosome formation. Significantly elevated light chain 3 II and reactive oxygen species were seen after the combined application of both ZnO-NPs and UVA-1 as photocatalytic treatment. Autophagy probably mediates cell survival under UVA-1 or ZnO-NP exposure alone but induces self-digestive cell death after combined treatment.
Conclusion:
The effect of autophagy on HNSCC viability after nanoparticle-induced photocatalytic treatment seems to depend on the impact of the physicochemical trigger.
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.
Related Concept Videos
Autophagic Cell Death
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and pro-apoptotic...
Autophagy
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
Delivery Pathways to the Lysosome
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
Cellular Injury V: Apoptosis and Autophagy
Phagocytosis of Apoptotic Cells
Normal cells contain receptors that prevent them from being recognized by phagocytes.
Overview of Cell Death
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...

