De Paula A M, Gomez R S
Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Rua Conde de Linhares, Belo Horizonte, Brazil.
Anticancer Res. 2001 Jan-Feb;21(1A):379-85.
The purpose of the present study was to evaluate the relationship between histological epithelial dysplasia, the immunolocalization of p53 and glutathione S-transferase pi on the immunolocalization of the CD57 antigen.
Seventy biopsies were included in the study and the streptavidin-biotin-peroxidase method was used to detect the antigens.
The results demonstrated a significant relationship between p53, GST-pi positive staining with moderate/severe epithelial dysplasia. There was no relationship between p53 and GST-pi. The mean number of CD57+ lymphoid cells was higher in the lesions with increased epithelial dysplasia and positive for GST-pi. No difference was found regarding CD57 immunolocalization in leukoplakias positive and negative for p53.
As the presence of CD57+ lymphoid cells are indicative of immunosuppression, our study suggests that the severity of epithelial dysplasia and positive immunolabelling for GST-pi are associated with local immune response alterations in oral leukoplakias. Our data also give support to the idea that GST-pi and p53 are not time-point related during oral cancer development.
本研究旨在评估组织学上皮发育异常、p53和谷胱甘肽S-转移酶π的免疫定位与CD57抗原免疫定位之间的关系。
本研究纳入70份活检标本,采用链霉亲和素-生物素-过氧化物酶法检测抗原。
结果显示,p53、GST-π阳性染色与中/重度上皮发育异常之间存在显著关系。p53与GST-π之间无关联。上皮发育异常增加且GST-π呈阳性的病变中,CD57+淋巴细胞的平均数量更高。p53阳性和阴性的白斑在CD57免疫定位方面未发现差异。
由于CD57+淋巴细胞的存在表明免疫抑制,我们的研究表明,上皮发育异常的严重程度和GST-π免疫标记阳性与口腔白斑局部免疫反应改变有关。我们的数据也支持以下观点,即在口腔癌发生过程中,GST-π和p53与时间点无关。