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Cyclo-oxygenase 2: a pharmacological target for the prevention of cancer
A J Dannenberg1, N K Altorki, J O Boyle
1Department of Medicine, Weill Medical College of Cornell University and Strang Cancer Prevention Center, New York, USA. ajdannen@med.cornell.edu
Abstract:
Understanding the mechanisms underlying carcinogenesis provides insights that are necessary for the development of therapeutic strategies to prevent cancer. Chemoprevention--the use of drugs or natural substances to inhibit carcinogenesis - is an important and rapidly evolving aspect of cancer research. We discuss evidence that cyclooxygenase 2 (COX 2), an inducible form of the enzyme, is a potential pharmacological target to prevent cancer. Key data implicating a causal relation between increased activity of COX 2 and carcinogenesis and possible mechanisms of action of COX 2 in this context are covered. Importantly, selective COX 2 inhibitors appear to be safe enough in human beings to allow large-scale clinical testing in healthy people. Several chemoprevention trials using selective COX 2 inhibitors are underway.
Insights
Cyclooxygenase 2 (COX 2) inhibitors show promise for cancer prevention. Research suggests COX 2 plays a role in cancer development, and selective inhibitors are safe for clinical trials.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Carcinogenesis research is vital for developing cancer prevention strategies.
- Chemoprevention, using drugs or natural substances to inhibit cancer, is a rapidly advancing field.
- Cyclooxygenase 2 (COX 2) is an inducible enzyme implicated in cancer development.
Purpose of the Study:
- To review evidence supporting cyclooxygenase 2 (COX 2) as a pharmacological target for cancer chemoprevention.
- To discuss the role of COX 2 in carcinogenesis and its mechanisms of action.
- To assess the safety and clinical trial readiness of selective COX 2 inhibitors.
Main Methods:
- Literature review of studies on COX 2 and carcinogenesis.
- Analysis of data implicating COX 2 activity in cancer development.
- Evaluation of safety data for selective COX 2 inhibitors in humans.
Main Results:
- Evidence suggests a causal link between increased COX 2 activity and carcinogenesis.
- Potential mechanisms of COX 2 action in cancer development are discussed.
- Selective COX 2 inhibitors demonstrate sufficient safety for large-scale clinical testing.
Conclusions:
- Selective COX 2 inhibitors represent a promising strategy for cancer chemoprevention.
- Ongoing clinical trials are evaluating the efficacy of these inhibitors in healthy individuals.
- Targeting COX 2 offers a viable therapeutic avenue for cancer prevention.
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