Salsbury A J, Burrage K, Hellmann K
Br Med J. 1970 Nov 7;4(5731):344-6. doi: 10.1136/bmj.4.5731.344.
Treatment with I.C.R.F. 159 completely inhibited metastasis formation in mice implanted with Lewis lung carcinoma at doses having little influence on the rate of growth of the primary implant. This inhibition was due to the effect of I.C.R.F. 159 on the development of blood vessels of the invading margins of the primary tumour. So far as is known, this is the first time a drug has induced a specific loss of the malignant characteristic of blood-borne tumour cell dissemination.
用I.C.R.F. 159进行治疗,在对原发性植入瘤生长速率影响很小的剂量下,能完全抑制接种Lewis肺癌的小鼠体内转移灶的形成。这种抑制作用是由于I.C.R.F. 159对原发性肿瘤侵袭边缘血管生成的影响。就目前所知,这是首次有药物诱导血行性肿瘤细胞播散这一恶性特征的特异性丧失。