Micallef M, Shibata T, Hosokawa M, Kobayashi H
Laboratory of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.
Anticancer Drugs. 1992 Dec;3(6):659-64. doi: 10.1097/00001813-199212000-00016.
Rat fibrosarcoma (KMT-17) cells and their in vitro clone, 10% FCS A3 cells, shed a tumor-associated antigen (TAA), CE7, from the cell surface under growth-promoting conditions. We treated cells with the antitumor agent bleomycin (BLM) and its analogs peplomycin and liblomycin in vitro and in vivo in an attempt to increase expression of this antigen and induce an antitumor response. Although all three agents enhance antigen expression in vitro, proportionate to their direct antiproliferative effects, only BLM enhances antigen expression in vivo. The in vivo regulation of CE7 expression appears not to be related to the direct cytotoxic effects of the antitumor agents but rather to the immuno-augmenting effects of BLM.
大鼠纤维肉瘤(KMT - 17)细胞及其体外克隆的10%胎牛血清A3细胞,在促进生长的条件下从细胞表面脱落一种肿瘤相关抗原(TAA),即CE7。我们在体外和体内用抗肿瘤药物博来霉素(BLM)及其类似物培洛霉素和利博霉素处理细胞,试图增加这种抗原的表达并诱导抗肿瘤反应。尽管所有三种药物在体外均能增强抗原表达,且与它们的直接抗增殖作用成比例,但只有BLM能在体内增强抗原表达。CE7表达的体内调节似乎与抗肿瘤药物的直接细胞毒性作用无关,而是与BLM的免疫增强作用有关。