Meng C L, Shklar G, Albright J
Oral Surg Oral Med Oral Pathol. 1982 Feb;53(2):179-89. doi: 10.1016/0030-4220(82)90284-5.
A stable model has been developed for oral mucosal anaplastic epidermoid carcinoma. This model more closely resembles the biologic characteristics of human oral carcinoma than previous models, such as primary epidermoid carcinomas induced in hamster buccal pouches or tongue by chemical carcinogens. This anaplastic oral cancer model was developed by serial abdominal transplantation in neonatal hamsters of original DMBA-induced primary epidermoid carcinomas of hamster buccal pouch. After the second generation, the tumors became stable, maintained an anaplastic appearance histologically, and were biologically aggressive, with rapid growth and metastatic potential. The original DMBA-induced buccal pouch tumors from 42 adult hamsters were transplanted abdominally through five generations in 151 neonatal hamsters. Immunosuppression was crucial in the initial transplantation but became unnecessary in the later serial transplantations. This model can serve as the basis for a variety of future immunologic and biologic studies dealing with oral cancer.
已建立一种口腔黏膜间变性表皮样癌的稳定模型。该模型比先前的模型更接近人类口腔癌的生物学特性,例如化学致癌物诱导的仓鼠颊囊或舌部原发性表皮样癌。这种间变性口腔癌模型是通过在新生仓鼠中对最初由二甲基苯并蒽(DMBA)诱导的仓鼠颊囊原发性表皮样癌进行连续腹部移植而建立的。第二代之后,肿瘤变得稳定,组织学上保持间变外观,并且具有生物学侵袭性,生长迅速且有转移潜能。来自42只成年仓鼠的最初由DMBA诱导的颊囊肿瘤在151只新生仓鼠中进行了五代腹部移植。免疫抑制在初次移植中至关重要,但在后续的连续移植中则不再必要。该模型可作为未来各种口腔癌免疫和生物学研究的基础。