Tatsuta M, Iishi H, Baba M, Hirasawa R, Iseki K, Yano H, Sakai N, Uehara H, Nakaizumi A
Department of Gastrointestinal Oncology, Osaka Medical Centre for Cancer and Cardiovascular Diseases, Japan.
Br J Cancer. 1998 Oct;78(7):857-61. doi: 10.1038/bjc.1998.593.
The effect of prolonged administration of transforming growth factor (34-43)-alpha, an antagonist of TGF-alpha, on gastric carcinogenesis induced by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) and on the labelling and apoptotic indices and TGF-alpha immunoreactivity of gastric mucosa and gastric cancers was examined in Wistar rats. The rats received intraperitoneal injections of 10 or 20 microg kg(-1) body weight of TGF(34-43)-alpha every other day after oral treatment with MNNG for 25 weeks. Long-term administration of TGF(34-43)-alpha at both doses significantly reduced the incidence of gastric cancers at the end of the experiment in week 52. However, TGF(34-43)-alpha had no significant effect on the number, histological type or depth of involvement of gastric cancers. Administration of TGF(34-43)-alpha also significantly decreased the bromodeoxyuridine labelling index and TGF-alpha immunoreactivity, and significantly increased the apoptotic index of antral mucosa and gastric cancers. These findings indicate that TGF(34-43)-alpha inhibits gastric carcinogenesis, and that its effects are mediated through decreased cell proliferation and TGF-alpha immunoreactivity and increased apoptosis induction in the gastric cancers.
在Wistar大鼠中,研究了转化生长因子(34 - 43)-α(一种TGF-α拮抗剂)长期给药对N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的胃癌发生、胃黏膜和胃癌的标记及凋亡指数以及TGF-α免疫反应性的影响。在用MNNG口服治疗25周后,大鼠每隔一天接受腹腔注射10或20微克/千克体重的TGF(34 - 43)-α。在第52周实验结束时,两种剂量的TGF(34 - 43)-α长期给药均显著降低了胃癌的发生率。然而,TGF(34 - 43)-α对胃癌的数量、组织学类型或浸润深度没有显著影响。给予TGF(34 - 43)-α还显著降低了溴脱氧尿苷标记指数和TGF-α免疫反应性,并显著增加了胃窦黏膜和胃癌的凋亡指数。这些发现表明,TGF(34 - 43)-α抑制胃癌发生,其作用是通过降低细胞增殖和TGF-α免疫反应性以及增加胃癌中的凋亡诱导来介导的。