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Toll-like receptor-guided therapeutic intervention of human cancers: molecular and immunological perspectives
Suprabhat Mukherjee1, Ritwik Patra1, Payam Behzadi2
1Integrative Biochemistry & Immunology Laboratory, Department of Animal Science, Kazi Nazrul University, Asansol, West Bengal, India.
Abstract:
Toll-like receptors (TLRs) serve as the body's first line of defense, recognizing both pathogen-expressed molecules and host-derived molecules released from damaged or dying cells. The wide distribution of different cell types, ranging from epithelial to immune cells, highlights the crucial roles of TLRs in linking innate and adaptive immunity. Upon stimulation, TLRs binding mediates the expression of several adapter proteins and downstream kinases, that lead to the induction of several other signaling molecules such as key pro-inflammatory mediators. Indeed, extraordinary progress in immunobiological research has suggested that TLRs could represent promising targets for the therapeutic intervention of inflammation-associated diseases, autoimmune diseases, microbial infections as well as human cancers. So far, for the prevention and possible treatment of inflammatory diseases, various TLR antagonists/inhibitors have shown to be efficacious at several stages from pre-clinical evaluation to clinical trials. Therefore, the fascinating role of TLRs in modulating the human immune responses at innate as well as adaptive levels directed the scientists to opt for these immune sensor proteins as suitable targets for developing chemotherapeutics and immunotherapeutics against cancer. Hitherto, several TLR-targeting small molecules (e.g., Pam3CSK4, Poly (I:C), Poly (A:U)), chemical compounds, phytocompounds (e.g., Curcumin), peptides, and antibodies have been found to confer protection against several types of cancers. However, administration of inappropriate doses of such TLR-modulating therapeutics or a wrong infusion administration is reported to induce detrimental outcomes. This review summarizes the current findings on the molecular and structural biology of TLRs and gives an overview of the potency and promises of TLR-directed therapeutic strategies against cancers by discussing the findings from established and pipeline discoveries.
Insights
Toll-like receptors (TLRs) are key immune sensors. This review explores TLRs
Area of Science:
- Immunology and Molecular Biology
- Cancer Therapeutics
Background:
- Toll-like receptors (TLRs) are crucial pattern recognition receptors, acting as the first line of defense against pathogens and damaged self-cells.
- TLRs bridge innate and adaptive immunity, mediating inflammatory responses through complex signaling pathways involving adapter proteins and kinases.
- Dysregulation of TLRs is implicated in various diseases, including inflammatory and autoimmune conditions, microbial infections, and cancer.
Purpose of the Study:
- To review the molecular and structural biology of Toll-like receptors (TLRs).
- To provide an overview of TLR-directed therapeutic strategies for cancer treatment.
- To discuss the potential and challenges of using TLR modulators in oncology.
Main Methods:
- Comprehensive literature review of existing research on TLRs and their therapeutic applications.
- Analysis of preclinical and clinical findings related to TLR agonists and antagonists in cancer.
- Examination of various TLR-targeting agents, including small molecules, phytocompounds, peptides, and antibodies.
Main Results:
- TLRs play a significant role in immune surveillance and response modulation.
- Various TLR-targeting agents have demonstrated efficacy in preclinical and clinical settings for cancer therapy.
- Potential risks associated with inappropriate administration of TLR modulators necessitate careful dose and infusion management.
Conclusions:
- Toll-like receptors are promising targets for developing novel chemotherapeutics and immunotherapeutics against cancer.
- Further research into TLR biology and therapeutic strategies is essential for optimizing cancer treatment outcomes.
- Careful consideration of administration parameters is critical to maximize therapeutic benefits and minimize adverse effects of TLR modulators.
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