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Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
TRAIL in cancer therapy: present and future challenges
Delphine Mérino1, Najoua Lalaoui, Alexandre Morizot
1INSERM, U866, Dijon, F-21079, France.
Abstract:
Since its identification in 1995, TNF-related apoptosis-inducing ligand (TRAIL) has sparked growing interest in oncology due to its reported ability to selectively trigger cancer cell death. In contrast to other members of the TNF superfamily, TRAIL administration in vivo is safe. The relative absence of toxic side effects of this naturally occurring cytokine, in addition to its antitumoural properties, has led to its preclinical evaluation. However, despite intensive investigations, little is known in regards to the mechanisms underlying TRAIL selectivity or efficiency. An appropriate understanding of its physiological relevance, and of the mechanisms controlling cancer cells escape from TRAIL-induced cell death, will be required to optimally use the cytokine in clinics. The present review focuses on recent advances in the understanding of TRAIL signal transduction and discusses the existing and future challenges of TRAIL-based cancer therapy development.
Insights
TNF-related apoptosis-inducing ligand (TRAIL) shows promise for selective cancer cell death induction with minimal toxicity. Further research into TRAIL mechanisms and cancer cell resistance is crucial for effective clinical application.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- TNF-related apoptosis-inducing ligand (TRAIL) identified in 1995.
- TRAIL selectively induces cancer cell death with low in vivo toxicity.
- Preclinical evaluations highlight TRAIL's antitumoural potential.
Purpose of the Study:
- To review recent advances in TRAIL signal transduction.
- To discuss challenges in TRAIL-based cancer therapy.
- To understand mechanisms of TRAIL selectivity and cancer cell resistance.
Main Methods:
- Literature review of TRAIL signal transduction pathways.
- Analysis of preclinical and clinical TRAIL therapy data.
- Discussion of cancer cell escape mechanisms from TRAIL-induced apoptosis.
Main Results:
- TRAIL exhibits selective cancer cell apoptosis induction.
- Understanding TRAIL mechanisms and cancer resistance is limited.
- TRAIL's safety profile supports its therapeutic interest.
Conclusions:
- Further elucidation of TRAIL signaling is needed.
- Overcoming cancer cell resistance is key for clinical success.
- TRAIL-based therapies require optimized strategies for effective cancer treatment.
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