Koyama S, Mukai R, Fukao K, Osuga T
Department of Internal Medicine, University of Tsukuba, Ibaraki.
Jpn J Cancer Res. 1988 Feb;79(2):264-74. doi: 10.1111/j.1349-7006.1988.tb01586.x.
Two murine monoclonal antibodies, SK-930 (isotype IgG2a) and SK-117 (isotype IgG1), were produced from spleen cells of mice immunized against human pancreatic carcinoma cell lines, MIA-PaCa 2 and Panc-1. With the use of the avidin-biotin-immunoperoxidase technique, the SK-930 and SK-117 antibodies detected an antigen found in 24 and 23 formalin-fixed tissue sections, respectively, of tumors obtained from 30 different patients with pancreatic carcinoma. Reactivity was also frequently found with tumors of the gallbladder, bile duct, stomach, colon and esophagus, while a large panel of normal human tissues, including normal pancreatic tissues, displayed little reactivity. These observations suggest that SK-930 and SK-117 are of value in identifying tumor-associated antigen (TAA) expressed in pancreatic carcinoma and other carcinomas of the digestive system. SK-930 antibody immunoprecipitated a 134 kilodalton molecule from extracts of 125I- or [35S]methionine- or [3H]glucosamine-labeled tumor cells. The SK-117-defined antigen corresponds to 152/137 kilodalton molecules. Moreover, cytofluorometric analyses showed that cells treated with periodic acid exhibited greatly decreased reactivity to the two antibodies, but cells treated with neuraminidase, trypsin or pronase showed unchanged reactivity. The findings suggest that the epitopes of the novel TAA expressed on pancreatic carcinoma cells are carbohydrate moieties.
两种鼠源单克隆抗体,SK - 930(同种型IgG2a)和SK - 117(同种型IgG1),是由免疫过人类胰腺癌细胞系MIA - PaCa 2和Panc - 1的小鼠脾细胞产生的。使用抗生物素蛋白 - 生物素 - 免疫过氧化物酶技术,SK - 930和SK - 117抗体分别在取自30例不同胰腺癌患者肿瘤的24份和23份福尔马林固定组织切片中检测到一种抗原。在胆囊、胆管、胃、结肠和食管的肿瘤中也经常发现反应性,而包括正常胰腺组织在内的大量正常人体组织几乎没有反应性。这些观察结果表明,SK - 930和SK - 117在识别胰腺癌和其他消化系统癌症中表达的肿瘤相关抗原(TAA)方面具有价值。SK - 930抗体从125I - 或[35S]甲硫氨酸 - 或[3H]葡糖胺标记的肿瘤细胞提取物中免疫沉淀出一个134千道尔顿的分子。SK - 117识别的抗原对应于152/137千道尔顿的分子。此外,细胞荧光分析表明,经高碘酸处理的细胞对这两种抗体的反应性大大降低,但经神经氨酸酶、胰蛋白酶或链霉蛋白酶处理的细胞反应性未变。这些发现表明,胰腺癌细胞上表达的新型TAA的表位是碳水化合物部分。