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- Joanne R. Brown
- From the Vanderbilt-Ingram Cancer Center, Nashville, TN
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- Raymond N. DuBois
- From the Vanderbilt-Ingram Cancer Center, Nashville, TN
説明
<jats:p>Cyclooxygenase (COX), a key enzyme in the prostanoid biosynthetic pathway, has received considerable attention due to its role in human cancers. Observational and randomized controlled studies in many different population cohorts and settings have demonstrated protective effects of nonsteroidal anti-inflammatory drugs (NSAIDs; the inhibitors of COX activity) for colorectal cancers (CRCs). COX-2, the inducible isoform of cyclooxygenase, is overexpressed in early and advanced CRC tissues, which portends a poor prognosis. Experimental studies have thus identified important mechanisms and pathways by which COX-2 plays an important role in carcinogenesis. Selective COX-2 inhibitors have been approved for use as adjunctive therapy for patients with familial polyposis. The role of COX-2 inhibitors is currently being evaluated for use in wider populations.</jats:p>
収録刊行物
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- Journal of Clinical Oncology
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Journal of Clinical Oncology 23 (12), 2840-2855, 2005-04-20
American Society of Clinical Oncology (ASCO)
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詳細情報 詳細情報について
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- CRID
- 1360011143968412160
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- NII論文ID
- 30022792018
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- ISSN
- 15277755
- 0732183X
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- データソース種別
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- Crossref
- CiNii Articles