Silva Renata N, Ribeiro Daniel A, Salvadori Daisy M F, Marques Mariângela E A
Department of Pathology, Botucatu Medical School, Sao Paulo State University, UNESP, São Paulo, Brazil.
Exp Toxicol Pathol. 2007 Sep;59(1):61-8. doi: 10.1016/j.etp.2007.02.010. Epub 2007 Jun 26.
Taking into consideration that glutatione S-transferase (GST) and cellular proliferation play a crucial role during carcinogenesis, the goal of this study was to investigate the expression of placental GST, called GST-P, and proliferating cellular nuclear antigen (PCNA) by means of immunohistochemistry during rat tongue carcinogenesis induced by 4-nitroquinoline 1-oxide (4NQO). This is a useful model for studying oral squamous cell carcinoma phase by phase. Male Wistar rats were distributed into three groups of 10 animals each and treated with 50 ppm 4NQO solution by drinking water for 4, 12 or 20 weeks. Ten animals were used as negative control. GST-P positive foci were detected in non-neoplastic oral cells at 4 weeks of 4NQO administration. In the same way, GST-P positive cells were detected in pre-neoplastic lesions and squamous cell carcinomas induced after 12 and 20 weeks-treatment, respectively. None of the control animals expressed GST-P positive cells. Regarding cellular proliferation, PCNA positive nuclei were higher at 12 and 20 weeks following 4NQO exposure (p<0.05) when compared to negative control. These results suggest that the expression of GST-P is correlated with cellular proliferation, in which GST-P is associated with risk and progression of oral cancer, whereas PCNA is closely involved during neoplastic conversion.
考虑到谷胱甘肽S-转移酶(GST)和细胞增殖在致癌过程中起着关键作用,本研究的目的是通过免疫组织化学方法,研究在4-硝基喹啉1-氧化物(4NQO)诱导的大鼠舌癌发生过程中,胎盘型GST即GST-P和增殖细胞核抗原(PCNA)的表达情况。这是一个逐阶段研究口腔鳞状细胞癌的有用模型。将雄性Wistar大鼠分为三组,每组10只,通过饮用含50 ppm 4NQO的溶液处理4周、12周或20周。10只动物作为阴性对照。在给予4NQO 4周时,在非肿瘤性口腔细胞中检测到GST-P阳性灶。同样,在分别经过12周和20周处理后诱导的癌前病变和鳞状细胞癌中也检测到GST-P阳性细胞。对照动物均未表达GST-P阳性细胞。关于细胞增殖,与阴性对照相比,4NQO暴露后12周和20周时PCNA阳性核更高(p<0.05)。这些结果表明,GST-P的表达与细胞增殖相关,其中GST-P与口腔癌的风险和进展相关,而PCNA在肿瘤转化过程中密切相关。