Combination Chemoprevention for Colon Cancer Targeting Polyamine Synthesis and Inflammation

被引:67
|
作者
Gerner, Eugene W. [1 ,2 ]
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
关键词
FAMILIAL ADENOMATOUS POLYPOSIS; ORNITHINE-DECARBOXYLASE; DIAMINE EXPORTER; MOUSE MODEL; ASPIRIN; CELLS; CARCINOGENESIS; PREVENTION; IDENTIFICATION; COLITIS;
D O I
10.1158/1078-0432.CCR-08-2235
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:758 / 761
页数:4
相关论文
共 50 条
  • [1] Rationale for, and design of, a clinical trial targeting polyamine metabolism for colon cancer chemoprevention
    Gerner, E. W.
    Meyskens, F. L., Jr.
    Goldschmid, S.
    Lance, P.
    Pelot, D.
    AMINO ACIDS, 2007, 33 (02) : 189 - 195
  • [2] Rationale for, and design of, a clinical trial targeting polyamine metabolism for colon cancer chemoprevention
    E. W. Gerner
    F. L. Meyskens
    S. Goldschmid
    P. Lance
    D. Pelot
    Amino Acids, 2007, 33 : 189 - 195
  • [3] Targeting Inflammation for Bladder Cancer Chemoprevention
    Madka V.
    Asch A.S.
    Rao C.V.
    Current Pharmacology Reports, 2017, 3 (6) : 447 - 457
  • [4] Roles of prostanoids in colon carcinogenesis and their potential targeting for cancer chemoprevention
    Mutoh, M
    Takahashi, M
    Wakabayashi, K
    CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (19) : 2375 - 2382
  • [5] Chemoprevention with Phytonutrients and Microalgae Products in Chronic Inflammation and Colon Cancer
    Talero, Elena
    Avila-Roman, Javier
    Motilva, Virginia
    CURRENT PHARMACEUTICAL DESIGN, 2012, 18 (26) : 3939 - 3965
  • [6] Emerging concepts in targeting the polyamine metabolic pathway in epithelial cancer chemoprevention and chemotherapy
    Basuroy, UK
    Gerner, EW
    JOURNAL OF BIOCHEMISTRY, 2006, 139 (01): : 27 - 33
  • [7] Polyamine metabolism as target for cancer chemoprevention
    Seiler, N
    Atanassov, CL
    Raul, F
    INTERNATIONAL JOURNAL OF ONCOLOGY, 1998, 13 (05) : 993 - 1006
  • [8] CHEMOPREVENTION OF COLON CANCER
    WINN, RJ
    LEVIN, B
    HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1989, 3 (01) : 65 - 73
  • [9] Chemoprevention of colon cancer
    Choi, SW
    Mason, JB
    CURRENT OPINION IN GASTROENTEROLOGY, 1998, 14 (02) : 173 - 178
  • [10] Cancer pharmacoprevention: Targeting polyamine metabolism to manage risk factors for colon cancer
    Gerner, Eugene W.
    Bruckheimer, Elizabeth
    Cohen, Alfred
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (48) : 18770 - 18778