Adiponectin suppresses colorectal carcinogenesis under the high-fat diet condition

被引:144
作者
Fujisawa, T. [1 ]
Endo, H. [1 ]
Tomimoto, A. [1 ]
Sugiyama, M. [1 ]
Takahashi, H. [1 ]
Saito, S. [1 ]
Inamori, M. [1 ]
Nakajima, N. [2 ]
Watanabe, M. [3 ]
Kubota, N. [4 ]
Yamauchi, T. [4 ]
Kadowaki, T. [4 ]
Wada, K. [5 ]
Nakagama, H. [6 ]
Nakajima, A. [1 ]
机构
[1] Yokohama City Univ, Sch Med, Div Gastroenterol, Yokohama, Kanagawa 232, Japan
[2] Natl Inst Infect Dis, Dept Pathol, Tokyo, Japan
[3] Yokohama Natl Univ, Med Engn Lab, Grad Sch Engn, Yokohama, Kanagawa 240, Japan
[4] Univ Tokyo, Dept Internal Med, Grad Sch Med, Tokyo, Japan
[5] Osaka Univ, Dept Pharmacol, Grad Sch Dent, Osaka, Japan
[6] Natl Canc Ctr, Res Inst, Div Biochem, Tokyo 104, Japan
关键词
D O I
10.1136/gut.2008.159293
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aims: The effect of adiponectin on colorectal carcinogenesis has been proposed but not fully investigated. We investigated the effect of adiponectin deficiency on the development of colorectal cancer. Methods: We generated three types of gene-deficient mice ( adiponectin-deficient, adiponectin receptor 1-deficient, and adiponectin receptor 2-deficient) and investigated chemical-induced colon polyp formation and cell proliferation in colon epithelium. Western blot analysis was performed to elucidate the mechanism which affected colorectal carcinogenesis by adiponectin deficiency. Results: The numbers of colon polyps were significantly increased in adiponectin-deficient mice compared with wild-type mice fed a high-fat diet. However, no difference was observed between wild-type and adiponectin-deficient mice fed a basal diet. A significant increase in cell proliferative activity was also observed in the colonic epithelium of the adiponectin-deficient mice when compared with wild-type mice fed a high-fat diet; however, no difference was observed between wild-type and adiponectin-deficient mice fed a basal diet. Similarly, an increase in epithelial cell proliferation was observed in adiponectin receptor 1-deficient mice, but not in adiponectin receptor 2-deficient mice. Western blot analysis revealed activation of mammalian target of rapamycin, p70 S6 kinase, S6 protein and inactivation of AMP-activated protein kinase in the colon epithelium of adiponectin-deficient mice fed with high-fat diet. Conclusions: Adiponectin suppresses colonic epithelial proliferation via inhibition of the mammalian target of the rapamycin pathway under a high-fat diet, but not under a basal diet. These studies indicate a novel mechanism of suppression of colorectal carcinogenesis induced by a Western-style high-fat diet.
引用
收藏
页码:1531 / 1538
页数:8
相关论文
共 39 条
[1]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[2]   When translation meets transformation: the mTOR story [J].
Averous, J. ;
Proud, C. G. .
ONCOGENE, 2006, 25 (48) :6423-6435
[3]  
Avruch J, 2001, Prog Mol Subcell Biol, V26, P115
[4]   ACRP30/adiponectin: an adipokine regulating glucose and lipid metabolism [J].
Berg, AH ;
Combs, TP ;
Scherer, PE .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (02) :84-89
[5]   The adipocyte-secreted protein Acrp30 enhances hepatic insulin action [J].
Berg, AH ;
Combs, TP ;
Du, XL ;
Brownlee, M ;
Scherer, PE .
NATURE MEDICINE, 2001, 7 (08) :947-953
[6]   Overweight, obesity, and cancer risk [J].
Bianchini, F ;
Kaaks, R ;
Vainio, H .
LANCET ONCOLOGY, 2002, 3 (09) :565-574
[7]   Regulation of adiponectin and its receptors in response to development of diet-induced obesity in mice [J].
Bullen, John W., Jr. ;
Bluher, Susann ;
Kelesidis, Theodoros ;
Mantzoros, Christos S. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2007, 292 (04) :E1079-E1086
[8]   Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults [J].
Calle, EE ;
Rodriguez, C ;
Walker-Thurmond, K ;
Thun, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (17) :1625-1638
[9]   Upstream of the mammalian target of rapamycin: do all roads pass through mTOR? [J].
Corradetti, M. N. ;
Guan, K-L .
ONCOGENE, 2006, 25 (48) :6347-6360
[10]   Leptin treatment markedly increased plasma adiponectin but barely decreased plasma resistin of ob/ob mice [J].
Delporte, ML ;
El Mkadem, SA ;
Quisquater, M ;
Brichard, SM .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 287 (03) :E446-E453