Recent advances in targeting COX-2 for cancer therapy: a review
1Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Cairo University Kasr El-Aini Street, P.O. Box 11562 Cairo Egypt asmaa.kassab@pharma.cu.edu.eg +20 2023635140 +20 2023639307.
Abstract:
Cyclooxygenase-2 (COX-2) is involved in the production of prostaglandins and thromboxanes, which control biological processes like inflammation, angiogenesis, and cell division. Numerous premalignant tissues and many human malignant tumors overexpress COX-2. Metabolites from COX-2 may support tumor growth, transformation, invasion, metastatic dissemination, premalignant hyperproliferation, downregulation of apoptosis, and tumor survival. COX-2 also triggers activity like cancer stem cells (CSCs). Populations of CSCs isolated from many cancer types are linked to overexpression of COX-2. Using nonsteroidal anti-inflammatory drugs (NSAIDs) reduces the risk of solid tumors, including colon, stomach, and esophageal malignancies. The anticancer potential of NSAIDs is mediated via COX-2 dependent or COX-2 independent pathways. For cancer patients, COX-2 may be a crucial target for therapeutic and chemoprotective measures. This review introduces the involvement of COX-2 in cancer via different pathways and provides a comprehensive review of the most recent updates on COX-2 inhibitors as potential anticancer candidates. This review aims to spark fresh thinking in the pursuit of more logical COX-2 inhibitor designs that may effectively treat cancer.
Insights
Cyclooxygenase-2 (COX-2) promotes cancer progression and is linked to cancer stem cells. COX-2 inhibitors, including NSAIDs, show anticancer potential and are key therapeutic targets.
Area of Science:
- Biochemistry
- Oncology
- Pharmacology
Background:
- Cyclooxygenase-2 (COX-2) regulates prostaglandins and thromboxanes, influencing inflammation, angiogenesis, and cell division.
- Overexpression of COX-2 is observed in premalignant tissues and various human cancers, potentially driving tumor growth, invasion, and survival.
- COX-2 activity is implicated in cancer stem cell (CSC) functions, with CSC populations often exhibiting elevated COX-2 levels.
Purpose of the Study:
- To review the multifaceted role of COX-2 in cancer development and progression.
- To provide a comprehensive overview of current research on COX-2 inhibitors as anticancer agents.
- To stimulate novel strategies for designing effective COX-2 inhibitors for cancer therapy.
Main Methods:
- Literature review of scientific articles on COX-2, cancer, and nonsteroidal anti-inflammatory drugs (NSAIDs).
- Analysis of pathways involved in COX-2-mediated cancer progression.
- Evaluation of the therapeutic and chemoprotective potential of COX-2 inhibitors.
Main Results:
- COX-2 metabolites contribute to tumor growth, metastasis, and apoptosis evasion.
- NSAIDs demonstrate anticancer effects through COX-2 dependent and independent mechanisms.
- COX-2 is identified as a critical target for cancer treatment and prevention.
Conclusions:
- Targeting COX-2 offers a promising strategy for cancer therapy and chemoprevention.
- Further research into COX-2 inhibitor design is crucial for developing more effective cancer treatments.
- Understanding COX-2's role in cancer stem cells may lead to new therapeutic approaches.
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