Qi Y, Moyana T, Matte G, Wilkinson A, Bresalier R, Xiang J
Saskatoon Cancer Center, Saskatchewan, Canada.
J Surg Oncol. 1995 May;59(1):3-9. doi: 10.1002/jso.2930590103.
TAG72 is a well-characterized, human tumor-associated antigen present in > 85% of human colonic cancers. In this study, we established an animal model of hepatic metastases of human colonic carcinoma. The high-mucin variant cell line, designated HM7, was derived from the human colonic carcinoma cell line LS174T. Following intrasplenic injection, HM7 was able to induce much greater hepatic metastases in SCID mice compared to its parental cell line LS174T. Numerous hepatic metastases were evident 18 days subsequent to the intrasplenic injection of tumor cells. Using the chimeric anti-TAG72 antibody ccM4, immunohistochemistry demonstrated strong expressions of the TAG72 antigen in these metastases. Our biodistribution and imaging data also showed that the radiolabelled ccM4 antibody was able to localize hepatic metastases in the SCID mice. Based upon these findings, w anticipate that the herein described SCID mouse model will prove most useful in studying hepatic metastases of human colonic carcinoma by using anti-TAG72 therapeutic immunoreagents.
TAG72是一种特征明确的人类肿瘤相关抗原,存在于超过85%的人类结肠癌中。在本研究中,我们建立了人类结肠癌肝转移的动物模型。高黏液素变异细胞系,命名为HM7,源自人类结肠癌细胞系LS174T。脾内注射后,与亲代细胞系LS174T相比,HM7在SCID小鼠中能够诱导出更多的肝转移。脾内注射肿瘤细胞18天后,可见大量肝转移。使用嵌合抗TAG72抗体ccM4,免疫组织化学显示TAG72抗原在这些转移灶中强烈表达。我们的生物分布和成像数据还表明,放射性标记的ccM4抗体能够在SCID小鼠中定位肝转移灶。基于这些发现,我们预计本文所述的SCID小鼠模型将被证明在使用抗TAG72治疗性免疫试剂研究人类结肠癌肝转移方面非常有用。