Szende B, Schally A V, Lapis K
1st Institute of Pathology and Experimental Cancer Research, Semmelweis University Medical School, Budapest, Hungary.
Acta Morphol Hung. 1991;39(1):53-8.
Tissue transglutaminase (TG) positive tumour cells in MXT mouse mammary cancer were localized by immunohistochemistry. The number of TG-positive tumour cells increased after treatment with analogs of luteinizing hormone-releasing hormone (LH-RH) and somatostatin, which inhibit tumour growth by the enhancement of apoptosis (programmed cell death). TG positivity has been previously reported to be closely linked with apoptosis. In this study, the increase in the number of TG positive tumour cells after hormonal treatment was well correlated with the augmented apoptotic index, i.e. the ratio of tumourous glandular structures which contained tumour cells showing the signs of programmed cell death. TG-positive tumour cells are, therefore, believed to be undergoing programmed cell death.
通过免疫组织化学法对MXT小鼠乳腺癌中组织转谷氨酰胺酶(TG)阳性肿瘤细胞进行定位。用促黄体生成素释放激素(LH-RH)类似物和生长抑素处理后,TG阳性肿瘤细胞数量增加,这两种激素通过增强细胞凋亡(程序性细胞死亡)来抑制肿瘤生长。此前已有报道称TG阳性与细胞凋亡密切相关。在本研究中,激素治疗后TG阳性肿瘤细胞数量的增加与凋亡指数的升高密切相关,凋亡指数即含有显示程序性细胞死亡迹象的肿瘤细胞的肿瘤腺结构的比例。因此,认为TG阳性肿瘤细胞正在经历程序性细胞死亡。