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Celecoxib: a specific COX-2 inhibitor with anticancer properties
Alane T Koki1, Jaime L Masferrer
1Pharmacia Corporation, Chesterfield, MO 63017, USA. alane.t.koki@pharmacia.com
Abstract:
In addition to the well-established pathophysiological role that COX-2 plays in inflammation, recent evidence implies that this isoform may also be involved in multiple biologic events throughout the tumorigenic process. Many epidemiological studies demonstrate that nonsteroidal anti-inflammatory drugs (NSAIDs) reduce the risk of a wide range of tumors. Further, COX-2 is chronically overexpressed in many premalignant, malignant, and metastatic human cancers, and levels of overexpression have been shown to significantly correlate to invasiveness, prognosis, and survival in some cancers. Pharmacological studies consistently demonstrate that COX-2 inhibitors dose-dependently inhibit tumor growth and metastasis in various relevant animal models of cancer. Importantly, several investigators have also shown COX-2 inhibitors may act additively or synergistically with currently used cytotoxics and molecularly targeted agents. Here we present a broad overview of the growing evidence that COX-2 plays a pivotal role throughout oncogenesis and summarize the rationale to explore the use of COX-2 inhibitors for the prevention and/or treatment of cancer as a single agent or in combination with current anticancer modalities.
Insights
Cyclooxygenase-2 (COX-2) is implicated in cancer development and progression. COX-2 inhibitors show promise for cancer prevention and treatment, alone or with other therapies.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Cyclooxygenase-2 (COX-2) is known for its role in inflammation.
- Emerging evidence suggests COX-2 involvement in tumorigenesis.
- COX-2 overexpression correlates with cancer invasiveness and prognosis.
Purpose of the Study:
- To review the role of COX-2 in oncogenesis.
- To summarize the rationale for using COX-2 inhibitors in cancer.
- To explore combination therapies with COX-2 inhibitors.
Main Methods:
- Review of epidemiological studies on NSAIDs and cancer risk.
- Analysis of pharmacological studies on COX-2 inhibitors in cancer models.
- Examination of studies on COX-2 inhibitor synergy with anticancer agents.
Main Results:
- Epidemiological studies link NSAIDs to reduced cancer risk.
- COX-2 is overexpressed in various human cancers.
- COX-2 inhibitors inhibit tumor growth and metastasis in animal models.
- COX-2 inhibitors show potential synergy with existing cancer treatments.
Conclusions:
- COX-2 plays a significant role throughout the process of cancer development.
- COX-2 inhibitors represent a potential strategy for cancer prevention and treatment.
- Further exploration of COX-2 inhibitors as single agents or in combination therapies is warranted.