Balasenthil Seetharaman, Rao Kunchala S, Nagini Siddavaram
Department of Biochemistry, Faculty of Science, Annamalai University, Annamalainagar-608 002, Tamil Nadu, India.
Pol J Pharmacol. 2003 Sep-Oct;55(5):793-8.
We examined the effect of S-allylcysteine (SAC), a water-soluble garlic constituent, on cytokeratin expression, a sensitive and specific marker for differentiation status during 7,12-dimethylbenz[a]anthracene (DMBA)-induced hamster buccal pouch (HBP) carcinogenesis in male Syrian hamsters. Hamsters were divided into four groups of six animals each. Animals in group 1 were painted with a 0.5% solution of DMBA in liquid paraffin on the right buccal pouches three times a week for 14 weeks. Group 2 animals were painted with DMBA as in group I, and in addition they received orally 200 mg/kg of SAC on days alternate to DMBA application. Group 3 animals received SAC as in group 2. Group 4 animals received neither DMBA nor SAC and served as the control. The hamsters were killed after an experimental period of 14 weeks. Cytokeratin expression was detected by Western blot analysis using monoclonal antibodies AE1 and AE3. In DMBA-induced HBP tumors, the decreased expression of high molecular weight cytokeratins of molecular mass between 55-70 kDa was observed. Administration of SAC (200 mg/kg) to animals painted with DMBA suppressed the incidence of DMBA-induced carcinomas and was associated with restoration of normal cytokeratin expression. The results of the present study suggest that inhibition of HBP tumorigenesis by SAC may be due to its regulatory effects on differentiation, tumor invasiveness, and its ability to migrate and form metastases.
我们研究了水溶性大蒜成分S-烯丙基半胱氨酸(SAC)对细胞角蛋白表达的影响,细胞角蛋白是在7,12-二甲基苯并[a]蒽(DMBA)诱导的雄性叙利亚仓鼠颊囊(HBP)癌变过程中分化状态的敏感且特异的标志物。仓鼠被分为四组,每组六只动物。第1组动物每周三次在右侧颊囊涂抹0.5% DMBA的液体石蜡溶液,持续14周。第2组动物如第1组那样涂抹DMBA,此外,在与涂抹DMBA交替的日子里口服200 mg/kg的SAC。第3组动物如第2组那样接受SAC。第4组动物既不接受DMBA也不接受SAC,作为对照。在14周的实验期后处死仓鼠。使用单克隆抗体AE1和AE3通过蛋白质印迹分析检测细胞角蛋白表达。在DMBA诱导的HBP肿瘤中,观察到分子量在55 - 70 kDa之间的高分子量细胞角蛋白表达降低。给涂抹DMBA的动物施用SAC(200 mg/kg)可抑制DMBA诱导的癌的发生率,并与正常细胞角蛋白表达的恢复相关。本研究结果表明,SAC对HBP肿瘤发生的抑制作用可能归因于其对分化、肿瘤侵袭性以及迁移和形成转移能力的调节作用。