Combination Chemoprevention for Colon Cancer Targeting Polyamine Synthesis and Inflammation
被引:70
作者:
Gerner, Eugene W.
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h-index: 0
机构:
Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
Canc Prevent Pharmaceut, Tucson, AZ USAUniv Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
Gerner, Eugene W.
[1
,2
]
Meyskens, Frank L., Jr.
论文数: 0引用数: 0
h-index: 0
机构:
Canc Prevent Pharmaceut, Tucson, AZ USA
Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Irvine, CA USAUniv Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
Meyskens, Frank L., Jr.
[2
,3
]
机构:
[1] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[2] Canc Prevent Pharmaceut, Tucson, AZ USA
[3] Univ Calif Irvine, Chao Family Comprehens Canc Ctr, Irvine, CA USA
Increased polyamine synthesis and inflammation have long been associated with colon carcinogenesis in both preclinical models and in humans. Recent experimental studies suggest that polyamines may be mechanistically involved in colonic inflammatory processes. Genetic epidemiology results indicate that a single nucleotide polymorphism influencing the expression of a polyamine biosynthetic gene is associated with both risk of colon polyp occurrence and recurrence, and the response to aspirin as a polyp preventive agent. A prospective, randomized, placebo-controlled clinical trial of combination difluoromethylomithine, a selective inhibitor of polyamine synthesis, and sulindac, a nonsteroidal anti-inflammatory drug, found that the 3-year treatment was associated with a 70% reduction of recurrence of all adenomas, and over a 90% reduction of recurrence of advanced and/or multiple adenomas, without evidence of serious toxicities. This proof-of-principle trial indicates that targeting polyamine synthesis and inflammation can be an effective strategy for preventing the occurrence of the advanced and/or multiple adenomas that are most closely associated with the development of colon cancers in humans.