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Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
Tumor Necrosis Factor-related apoptosis-inducing ligand (TRAIL) Receptor-1 and Receptor-2 agonists for cancer therapy
Norma Lynn Fox1, Robin Humphreys, Troy A Luster
1Human Genome Sciences, Rockville, MD 20850, USA.
Importance Of The Field:
Agents that activate the TNF-related apoptosis-inducing ligand death receptors, TRAIL-R1 and TRAIL-R2, have attracted substantial attention and investment as potential anti-cancer therapies. Preclinical studies of TRAIL-R agonists indicate that they may be efficacious in a wide range of tumor types, especially when combined with chemotherapeutic agents.
Areas Covered In This Review:
The rationale for clinical development of TRAIL-R agonists is described, including the basis for combining these agents with other agents that modulate the 'checks and balances' of the apoptotic pathways. Accruing data that highlight differences between TRAIL-R1 and TRAIL-R2 that could affect the clinical significance of their specific agonists are described. The clinical experience to date with each of the agonists is summarized.
What The Reader Will Gain:
The reader will gain an understanding of the rationale for the clinical development of TRAIL-R agonists, as well as the current status of clinical trials of these interesting new agents.
Take Home Message:
Ongoing clinical trials will provide important information regarding the future development of TRAIL-R agonists.
Insights
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor agonists show promise as anti-cancer therapies, particularly when combined with chemotherapy. Ongoing clinical trials will determine the future development of these agents.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor agonists targeting TRAIL-R1 and TRAIL-R2 are investigated as anti-cancer agents.
- Preclinical data suggest efficacy across various tumor types, especially in combination with chemotherapy.
Purpose of the Study:
- To describe the rationale for clinical development of TRAIL-R agonists.
- To review the basis for combining TRAIL-R agonists with other apoptosis-modulating agents.
- To highlight differences between TRAIL-R1 and TRAIL-R2 and their clinical significance.
Main Methods:
- Review of preclinical and clinical data on TRAIL-R agonists.
- Analysis of combination strategies with chemotherapeutic agents.
- Summarization of current clinical trial experiences.
Main Results:
- Understanding the rationale behind clinical development of TRAIL-R agonists.
- Gaining insight into the current status of clinical trials for these novel agents.
Conclusions:
- Ongoing clinical trials are crucial for determining the future trajectory of TRAIL-R agonist development.
- Further research will elucidate the full potential of TRAIL-R agonists in cancer treatment.
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