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Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
Cytochrome P450 Eicosanoid Signaling Pathway in Colorectal Tumorigenesis
Weicang Wang1, Katherine Z Sanidad2, Guodong Zhang3,4
1Department of Food Science, University of Massachusetts, Amherst, MA, USA.
Abstract:
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of cancer-related death in the United States. It is important to discover novel cellular targets which are crucial in the pathogenesis of CRC, which could facilitate development of mechanism-based strategies to reduce the risks of CRC. Emerging studies support that the cytochrome P450 (CYP) monooxygenase/soluble epoxide hydrolase (sEH) pathway and their eicosanoid metabolites play critical roles in colonic inflammation and CRC, and could be therapeutically explored for treating or preventing CRC. Here in this review, we discuss recent studies about the roles of the CYP/sEH eicosanoid pathway in the pathogenesis of colonic inflammation and CRC.
Insights
Discovering new targets for colorectal cancer (CRC) is vital. The cytochrome P450/soluble epoxide hydrolase (CYP/sEH) pathway and its metabolites are key players in colon inflammation and CRC development.
Area of Science:
- Biomedical Science
- Oncology
- Molecular Biology
Background:
- Colorectal cancer (CRC) is a leading cause of cancer death in the US.
- Novel therapeutic targets are needed to combat CRC.
- The cytochrome P450 (CYP)/soluble epoxide hydrolase (sEH) pathway is implicated in inflammation and cancer.
Purpose of the Study:
- To review recent studies on the role of the CYP/sEH eicosanoid pathway in CRC pathogenesis.
- To highlight the potential of this pathway as a therapeutic target for CRC.
Main Methods:
- Literature review of recent studies.
- Analysis of the role of CYP/sEH pathway metabolites in colonic inflammation and CRC.
Main Results:
- The CYP/sEH pathway and its eicosanoid metabolites are critical in colonic inflammation.
- These pathways play significant roles in the development of CRC.
- Evidence suggests therapeutic potential for targeting the CYP/sEH pathway in CRC.
Conclusions:
- The CYP/sEH eicosanoid pathway is a promising area for CRC research.
- Targeting this pathway could lead to new strategies for CRC prevention and treatment.
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