| Literature DB >> 25085205 |
Sun-Hee Kim1, Ofer Margalit1, Hiroshi Katoh1, Dingzhi Wang1, Hong Wu1, Dianren Xia1, Vijaykumar R Holla1, Peiying Yang1, Raymond N DuBois1.
Abstract
Nonsteroidal anti-inflammatory drugs (NSAIDs) and selective cyclooxygenase-2 (COX-2) inhibitors (COXIBs) can reduce the risk of developing colorectal cancer (CRC) and are being considered for use as adjuvant therapy for treatment of CRC patients. However, long-term use of most NSAIDs, except aspirin, increases cardiovascular risk, hampering use of these drugs in CRC prevention and possibly for treatment. CG100649 is a new member of the COXIB family, which is proposed to inhibit both COX-2 and carbonic anhydrase-I/-II (CA-I/-II) activity. Using mouse models, we show here that CG100649 inhibits premalignant and malignant colorectal lesions in mouse models, partly through inhibiting tumor cell proliferation. These pre-clinical findings suggest a need for further exploration of CG100649 for CRC prevention and treatment. The long-term safety profile of CG100649, particularly regarding its effect on cardiovascular risk, is yet to be determined.Entities:
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Year: 2014 PMID: 25085205 PMCID: PMC4356209 DOI: 10.1007/s10637-014-0144-z
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850