Maruo K, Ueyama Y, Hioki K, Saito M, Nomura T, Tamaoki N
Exp Cell Biol. 1982;50(2):115-9. doi: 10.1159/000163136.
Human gastric carcinoma showed different growth in nude mice depending on their genetic backgrounds which included BALB/cA-nu (nude mice with a BALB/cA genetic background), CBA/N-nu, NFS/N-nu, NIH(s)-nu, C3H/HeN+-nu, C57BL/6N-nu and lasat mice (BALB/cA-nu, Dh). Rapid growth of human carcinoma was observed in CBA/N-nu, NFS/N-nu and NIH(s)-nu. The human carcinoma in NIH(s)-nu showed the widest deviation in tumor weight. These data suggest that NFS/N-nu and CBA/N-nu are strains which are more recommended for anticancer agent screening systems than BALB/cA-nu, NIH(s)-nu, C3H/HeN+-nu, C57BL/6N-nu and lasat mice, although many other factors including productivity of the mice, strain differences in drug metabolism and drug toxicity must be considered.
人类胃癌在裸鼠中的生长情况因遗传背景而异,这些遗传背景包括BALB/cA-nu(具有BALB/cA遗传背景的裸鼠)、CBA/N-nu、NFS/N-nu、NIH(s)-nu、C3H/HeN+-nu、C57BL/6N-nu和lasat小鼠(BALB/cA-nu,Dh)。在CBA/N-nu、NFS/N-nu和NIH(s)-nu中观察到人类癌的快速生长。NIH(s)-nu中的人类癌在肿瘤重量上表现出最大的偏差。这些数据表明,与BALB/cA-nu、NIH(s)-nu、C3H/HeN+-nu、C57BL/6N-nu和lasat小鼠相比,NFS/N-nu和CBA/N-nu是更推荐用于抗癌药物筛选系统的品系,尽管必须考虑许多其他因素,包括小鼠的繁殖力、药物代谢的品系差异和药物毒性。