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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
Cox-2 and cancer chemoprevention: picking up the pieces
1Brigham and Women's Hospital, Dana Farber Cancer Institute, Boston, MA 02115, USA.
Abstract:
Inhibitors of prostaglandin synthesis show great promise as cancer chemopreventive agents, with efficacy demonstrated in randomized clinical trials. Unfortunately, these agents also cause toxicity in susceptible individuals. The recent reports of cardiovascular adverse events in patients treated with selective Cox-2 inhibitors for colorectal adenoma prevention remind us that all therapies carry risks as well as benefits. This article will discuss the biologic rationale for using selective Cox-2 inhibitors in cancer chemoprevention, and outline new avenues of research necessary to allow their successful use in patients at risk for colorectal cancer.
Insights
Selective Cox-2 inhibitors show promise for cancer chemoprevention but carry risks. Further research is needed to safely use these agents in patients at risk for colorectal cancer.
Area of Science:
- Oncology
- Pharmacology
Background:
- Prostaglandin synthesis inhibitors are effective cancer chemopreventive agents.
- Selective cyclooxygenase-2 (Cox-2) inhibitors have shown efficacy in clinical trials for colorectal adenoma prevention.
- However, these agents can cause toxicity, including cardiovascular adverse events.
Purpose of the Study:
- To discuss the biologic rationale for using selective Cox-2 inhibitors in cancer chemoprevention.
- To outline new research directions for the safe application of these agents.
Main Methods:
- Review of existing literature on prostaglandin synthesis inhibitors and Cox-2 inhibitors.
- Analysis of reported adverse events and clinical trial data.
- Discussion of biological mechanisms and potential therapeutic strategies.
Main Results:
- Selective Cox-2 inhibitors offer a promising strategy for cancer chemoprevention.
- Cardiovascular risks associated with selective Cox-2 inhibitors necessitate careful patient selection and monitoring.
- Understanding the balance between benefits and risks is crucial for therapeutic success.
Conclusions:
- Selective Cox-2 inhibitors have a strong biologic basis for cancer chemoprevention.
- Mitigating toxicity and managing risks are essential for widespread clinical adoption.
- Future research should focus on identifying patient populations who can benefit most while minimizing adverse events.
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