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CG100649, a novel COX-2 inhibitor, inhibits colorectal adenoma and carcinoma growth in mouse models

  • Sun Hee Kim
  • , Ofer Margalit
  • , Hiroshi Katoh
  • , Dingzhi Wang
  • , Hong Wu
  • , Dianren Xia
  • , Vijaykumar R. Holla
  • , Peiying Yang
  • , Raymond N. Dubois

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Pages (from-to)1105-1112
Number of pages8
JournalInvestigational New Drugs
Volume32
Issue number6
DOIs
StatePublished - Dec 1 2014

Keywords

  • CG100649
  • COX-2
  • Carbonic anhydrase-I/-II
  • Celecoxib
  • Colorectal cancer
  • PGE

ASJC Scopus subject areas

  • Oncology
  • Pharmacology
  • Pharmacology (medical)

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