Ekstedt R D
J Natl Cancer Inst. 1979 Oct;63(4):1065-9.
Weanling BALB/c mice given injections of 300 micrograms concanavalin A (Con A) prior to and at frequent intervals after challenge with Moloney murine sarcoma virus (M-MuSV), 3-methylcholanthrene (MCA), or TEPC-15 plasmacytoma cells showed an enhancement of tumor induction or development. With the M-MuSV and MCA systems, this enhancement was evidenced by larger tumors and, in the MCA system, by more devastating tumors. Regression of the M-MuSV-induced tumors was more prolonged in Con A-treated mice. With the TEPC-15 system, enhancement was evidenced by a more rapid mortality rate in treated animals.
在接受莫洛尼鼠肉瘤病毒(M-MuSV)、3-甲基胆蒽(MCA)或TEPC-15浆细胞瘤细胞攻击之前及之后频繁注射300微克伴刀豆球蛋白A(Con A)的断奶BALB/c小鼠,显示出肿瘤诱导或发展的增强。在M-MuSV和MCA系统中,这种增强表现为肿瘤更大,而在MCA系统中则表现为肿瘤更具破坏性。在Con A处理的小鼠中,M-MuSV诱导肿瘤的消退时间更长。在TEPC-15系统中,处理动物的死亡率更高证明了增强作用。