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Growth hormone releasing peptide 2 reverses anorexia associated with chemotherapy with 5-fluoruracil in colon cancer cell-bearing mice 被引量:8

Growth hormone releasing peptide 2 reverses anorexia associated with chemotherapy with 5-fluoruracil in colon cancer cell-bearing mice
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摘要 The cancer-associated anorexia-cachexia syndrome is observed in 80% of patients with advanced-stage cancer, and is one of the major obstacles in chemo- therapy. Ghrelin is a orexigenic hormone that has been proposed to prevent anorexia. Aim of the study was to determine whether the addition of the ghrelin agonist growth hormone releasing peptide 2 (GHRP-2) to cytotoxic therapy with 5-fluoruracil (5-FU) prevents the anorexia associated with chemotherapy in cancer cachectic mice. Thirty-three BALB/c female tumourbearing mice were randomized to receive a solution containing: (a) placebo; (b) GHRP-2; (c) 5-FU; or (d) 5-FU + GHRP-2. Ten BALB/c no tumour-bearing mice received placebo solution. Food intake and survival were checked. Six hours after the drug injection the cumulative food intake was signifi cantly increased in mice treated with the combination of 5-FU + GHRP-2 versus the 5-FU alone (P = 0.0096). On day 3, the cumulative food intake of mice treated with GHRP-2,5-FU and 5-FU + GHRP-2 signifi cantly increased com- pared with naive and vehicle groups (P = 0.0007, P = 0.0038 and P = 0.0166, respectively). The median survival time was longer in 5-FU + GHRP-2 treated mice than in those with 5-FU, although it was not signifi cant (18 d versus 15.5 d, P = 0.7). For the fi rst time, we demonstrated that the addition of GHRP-2 to cytotoxic therapy with 5-FU improved appetite in tumour-bearing mice with anorexia/cachexia syndrome in early stage. These data suggest that GHRP-2 may improve the effi cacy of therapy and the quality of life of cancer patients thank to the amelioration of their nutritional state. The cancer-associated anorexia-cachexia syndrome is observed in 80% of patients with advanced-stage cancer, and is one of the major obstacles in chemo- therapy. Ghrelin is a orexigenic hormone that has been proposed to prevent anorexia. Aim of the study was to determine whether the addition of the ghrelin ago- nist growth hormone releasing peptide 2 (GHRP-2) to cytotoxic therapy with 5-fluoruracil (5-FU) prevents the anorexia associated with chemotherapy in cancer cachectic mice. Thirty-three BALB/c female tumour- bearing mice were randomized to receive a solution containing: (a) placebo; (b) GHRP-2; (c) 5-FU; or (d) 5-FU + GHRP-2. Ten BALB/c no tumour-bearing mice received placebo solution. Food intake and survival were checked. Six hours after the drug injection the cumulative food intake was significantly increased in mice treated with the combination of 5-FU + GHRP-2 versus the 5-FU alone (P = 0.0096). On day 3, the cumulative food intake of mice treated with GHRP-2,5-FU and 5-FU + GHRP-2 significantly increased com- pared with naive and vehicle groups (P = 0.0007, P = 0.0038 and P = 0.0166, respectively). The median survival time was longer in 5-FU + GHRP-2 treated mice than in those with 5-FU, although it was not significant (18 d versus 15.5 d, P = 0.7). For the first time, we demonstrated that the addition of GHRP-2 to cytotoxic therapy with 5-FU improved appetite in tumour-bearing mice with anorexia/cachexia syndrome in early stage. These data suggest that GHRP-2 may improve the efficacy of therapy and the quality of life of cancer patients thank to the amelioration of their nutritional state.
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第41期6303-6305,共3页 世界胃肠病学杂志(英文版)
基金 Supported by (in part) A Grant-in-Aid for Scientic Research (B:16390208) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to A.I.)
关键词 GHS 癌症 食欲缺乏 食物摄取 癌细胞 GHS Ghrelin Cancer anorexia-cachexia syndrome Food intake Chemotherapy Colon cancer cell line Murine model
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参考文献6

  • 1[1]Inui A.Cancer anorexia-cachexia syndrome:current issues in research and management.CA Cancer J Clin 2002; 52:72-91
  • 2[2]Bowers CY,Momany FA,Reynolds GA,Hong A.On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone.Endocrinology 1984; 114:1537-1545
  • 3[3]Neary NM,Small CJ,Wren AM,Lee JL,Druce MR,Palmieri C,Frost GS,Ghatei MA,Coombes RC,Bloom SR.Ghrelin increases energy intake in cancer patients with impaired appetite:acute,randomized,placebo-controlled trial.J Clin Endocrinol Metab 2004; 89:2832-2836
  • 4[4]Tschop M,Statnick MA,Suter TM,Heiman ML.GHreleasing peptide-2 increases fat mass in mice lacking NPY:indication for a crucial mediating role of hypothalamic agouti-related protein.Endocrinology 2002; 143:558-568
  • 5[5]Laferrere B,Abraham C,Russell CD,Bowers CY.Growth hormone releasing peptide-2 (GHRP-2),like ghrelin,increases food intake in healthy men.J Clin Endocrinol Metab 2005; 90:611-614
  • 6[6]Seeliger H,Guba M,Koehl GE,Doenecke A,Steinbauer M,Bruns CJ,Wagner C,Frank E,Jauch KW,Geissler EK.Blockage of 2-deoxy-D-ribose-induced angiogenesis with rapamycin counteracts a thymidine phosphorylasebased escape mechanism available for colon cancer under 5-fluorouracil therapy.Clin Cancer Res 2004; 10:1843-1852

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