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Cimetidine inhibits in vivo growth of human colon cancer and reverses histamine stimulated in vitro and in vivo growth.

机译:西咪替丁抑制人结肠癌的体内生长并逆转组胺刺激的体外和体内生长。

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摘要

The effect of histamine and cimetidine on the growth of four human colon cancer cell lines was studied. Histamine significantly stimulated the uptake of tritiated thymidine in vitro in a dose dependent manner, to a maximum of 120% and 116% of controls for C170 and LIM2412, respectively. This effect was antagonised by cimetidine, but not diphenhydramine. Histamine also stimulated a dose dependent increase in cyclic adenosine monophosphate accumulation in C170 cells, antagonised by cimetidine. When grown as subcutaneous xenografts in Balb/c nuu mice, cimetidine had a significant inhibitory effect on the same two cell lines. The final volume of C170 tumours in animals given cimetidine was 44% of controls. This response was dose dependent, plateauing at a cimetidine dose of 50 mg/kg/day. The final volume of LIM2412 tumours in animals given cimetidine was 60% of controls. Histamine administered locally by a mini-osmotic pump stimulated C170 tumour growth to 164% of controls, was antagonised by cimetidine at a dose of 200 mg/kg/day, but not by lower concentrations. Histamine has a trophic effect on at least two colorectal cancer cell lines in vivo and in vitro. As this effect is antagonised by cimetidine, it may be mediated via tumour histamine type 2 receptors.
机译:研究了组胺和西咪替丁对四种人结肠癌细胞系生长的影响。组胺在体外以剂量依赖性方式显着刺激of化胸腺嘧啶核苷的摄取,最大分别为C170和LIM2412的对照的120%和116%。西咪替丁可拮抗这一作用,但苯海拉明则不能。组胺还刺激了西咪替丁拮抗的C170细胞中环状单磷酸腺苷积累的剂量依赖性增加。当在Balb / c nu / nu小鼠中作为皮下异种移植物生长时,西咪替丁对相同的两种细胞系具有明显的抑制作用。给予西咪替丁的动物体内C170肿瘤的最终体积为对照组的44%。该反应是剂量依赖性的,在西咪替丁剂量为50 mg / kg / day时达到平稳。给予西咪替丁的动物中LIM2412肿瘤的最终体积为对照组的60%。由微型渗透泵局部给药的组胺刺激了C170肿瘤生长至对照组的164%,被西咪替丁以200 mg / kg / day的剂量拮抗,但没有降低浓度。组胺在体内和体外对至少两种结直肠癌细胞系具有营养作用。由于该作用被西咪替丁拮抗,它可能是通过肿瘤组胺2型受体介导的。

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