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Targeting DAMPs by Aspirin Inhibits Head and Neck Cancer Stem Cells and Stimulates Radio-Sensitization to Proton
Tea Vasiljevic1, Emilija Zapletal1, Marko Tarle2,3
1Laboratory for Personalized Medicine, Division of Molecular Medicine, Rudjer Boskovic Institute, Bijenicka 54, 10000 Zagreb, Croatia.
Background:
Cancer stem cells (CSCs) are a subpopulation of cancer cells known for their self-renewal capacity, tumorigenicity, and resistance to treatment. Toll-like receptor 3 (TLR3) plays a complex role in cancer, exhibiting both pro-apoptotic and pro-tumorigenic effects. This study investigates the pro-tumorigenic role of TLR3, specifically its impact on CSCs in head and neck cancer.
Methods:
We have investigated Detroit 562, FaDu and SQ20B cell lines, the latter being stably transfected with a plasmid containing inducible shRNA for TLR3, by cultivating them to form tumor spheres in order to study CSCs.
Results:
Our findings demonstrate that TLR3 activation promotes stemness in head and neck cancer cell lines. This is evidenced by increased tumor sphere formation, promotion of epithelial-to-mesenchymal transition (EMT), upregulated stemness gene expression, and elevated aldehyde dehydrogenase (ALDH) activity. Conditional TLR3 knockdown abolished tumor sphere formation, confirming its important role. Furthermore, TLR3 activation triggers the secretion of damage-associated molecular patterns (DAMPs) into the tumor microenvironment, leading to increased cancer cell migration. This was inhibited by DAMP inhibitors. In patient tissue samples, we observed co-localization of TLR3 with stemness markers CD133 and ALDH1, as well as with heat shock protein 70 (HSP70) and receptor for advanced glycation end products (RAGE). We then explored potential CSC-targeted therapies, initially combining the apoptosis inducer poly (I:C) with DAMP inhibitors and γ-irradiation. While this combination proved effective in adherent cells, it failed to eliminate tumor spheres. Nevertheless, we discovered that proton radiotherapy, particularly when combined with aspirin (HMGB1 inhibitor) and poly (I:C), effectively eliminates CSCs.
Conclusions:
This novel combination holds promise for the development of new therapeutic strategies for head and neck cancers, particularly given the promising results of proton therapy in treating this disease.
Insights
Toll-like receptor 3 (TLR3) promotes cancer stem cell (CSC) stemness in head and neck cancer. A novel proton radiotherapy combination effectively eliminates CSCs, offering new therapeutic hope.
Area of Science:
- Oncology
- Immunology
Background:
- Cancer stem cells (CSCs) drive tumor growth and treatment resistance.
- Toll-like receptor 3 (TLR3) has a dual role in cancer, potentially promoting tumor progression.
- This study focuses on TLR3's pro-tumorigenic effects on CSCs in head and neck cancer.
Purpose of the Study:
- To investigate the role of TLR3 in promoting stemness in head and neck cancer stem cells.
- To identify potential therapeutic strategies targeting CSCs in head and neck cancer.
Main Methods:
- Utilized head and neck cancer cell lines (Detroit 562, FaDu, SQ20B) and tumor sphere formation assays to study CSCs.
- Employed inducible shRNA for TLR3 knockdown and assessed stemness markers (EMT, gene expression, ALDH activity).
- Analyzed patient tissue samples for co-localization of TLR3 with stemness and microenvironment markers (CD133, ALDH1, HSP70, RAGE).
Main Results:
- TLR3 activation significantly enhanced CSC stemness, evidenced by increased tumor sphere formation, EMT, stemness gene expression, and ALDH activity.
- TLR3 knockdown inhibited tumor sphere formation, confirming its critical role.
- TLR3 triggered DAMP secretion, promoting cancer cell migration, which was blocked by DAMP inhibitors.
- Patient samples showed co-localization of TLR3 with CSC and microenvironment markers.
- A combination of proton radiotherapy, aspirin, and poly (I:C) effectively eliminated CSCs.
Conclusions:
- TLR3 plays a crucial pro-tumorigenic role in head and neck cancer stem cells.
- Proton radiotherapy combined with aspirin and poly (I:C) presents a promising therapeutic strategy for head and neck cancers by targeting CSCs.
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