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Published on: August 2, 2024
Functional toll-like receptor 3 expressed by oral squamous cell carcinoma induced cell apoptosis and decreased
Zhifeng He1, Xiaofeng Huang1, Yanhong Ni1
1Central Laboratory of Stomatology, Institute and Hospital of Stomatology, Nanjing University Medical School, Nanjing University, Nanjing, China.
Objective:
The aim of this study was to investigate the expression and function of toll-like receptor 3 (TLR3) in oral squamous cell carcinoma (OSCC).
Study Design:
We first assessed TLR3 expression in 20 cases of primary OSCC tissue. Two OSCC cell lines, SCC4 and CAL27, were used for further study. Lyophilized polyinosinic-polycytidylic acid [Poly(I:C)] was used to activate TLR3 expressed by OSCC. Changes in cytokines expression, cell viability, apoptosis, and migration in OSCC were investigated.
Results:
TLR3 was present in both OSCC tissue and the 2 OSCC cell lines examined. Poly(I:C) stimulated robust responses in OSCC: it upregulated cytokine expression; decreased cell viability by suppressing cell proliferation and inducing apoptosis; and decreased cell migration. Poly(I:C)-TLR3-induced OSCC cell apoptosis was caspase-3-dependent.
Conclusions:
The present study indicated that TLR3 might affect OSCC development and should be considered as a potential target for future OSCC immunotherapy.
Insights
Toll-like receptor 3 (TLR3) is present in oral squamous cell carcinoma (OSCC). Activating TLR3 with Poly(I:C) reduces OSCC cell viability and migration, suggesting TLR3 as a potential immunotherapy target.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Oral squamous cell carcinoma (OSCC) is a prevalent malignancy.
- The role of pattern recognition receptors, such as toll-like receptors (TLRs), in OSCC is not fully understood.
Purpose of the Study:
- To investigate the expression and functional role of toll-like receptor 3 (TLR3) in oral squamous cell carcinoma (OSCC).
Main Methods:
- TLR3 expression was assessed in primary OSCC tissues and cell lines (SCC4, CAL27).
- OSCC cell lines were treated with polyinosinic-polycytidylic acid [Poly(I:C)] to activate TLR3.
- Changes in cytokine expression, cell viability, apoptosis, and migration were analyzed.
Main Results:
- TLR3 was detected in both OSCC tissue and cell lines.
- Poly(I:C) stimulation upregulated cytokine expression in OSCC cells.
- Activation of TLR3 led to decreased cell viability (via suppressed proliferation and induced apoptosis) and reduced cell migration.
- Poly(I:C)-TLR3-induced apoptosis was dependent on caspase-3.
Conclusions:
- TLR3 is expressed in OSCC and its activation influences cancer cell behavior.
- TLR3 may play a role in OSCC development.
- TLR3 represents a potential therapeutic target for OSCC immunotherapy.
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