Gasperi-Campani A, Roncuzzi L, Zoli W, Amadori D
Department of Experimental Pathology, University of Bologna, Italy.
Anticancer Drug Des. 1997 Mar;12(2):91-8.
Lonidamine (LND) is a potential chemotherapeutic agent which can positively modulate the efficacy of several antineoplastic agents. The ribosome-inactivating protein Saporin 6 (SO 6), which acts as a rRNA N-glycosidase and a DNA nuclease, has recently attracted interest as a novel potential anticancer and antiviral agent. Synergism between LND and SO 6 was previously demonstrated by us in the human metastatic MAST breast cancer cell line in vitro. In the present study, the antiproliferative effect of the drugs, either alone or in combination, was investigated in vitro at various concentrations in 17 primary cell cultures established from patients carrying infiltrating ductal carcinomas of the breast. Results indicate a strong synergistic effect in 11/17 cases, when LND was administered as a second drug. This is in agreement with previous results in the MAST cell line. Synergism was evident at SO 6 concentrations between 3.3 x 10(-10) and 1.7 x 10(-9) M.
氯尼达明(LND)是一种潜在的化疗药物,它可以积极调节几种抗肿瘤药物的疗效。核糖体失活蛋白皂草素6(SO 6)作为一种rRNA N-糖苷酶和DNA核酸酶,最近作为一种新型潜在的抗癌和抗病毒药物引起了人们的关注。我们之前在人转移性MAST乳腺癌细胞系中证实了LND和SO 6之间的协同作用。在本研究中,在由患有浸润性导管癌的患者建立的17种原代细胞培养物中,以不同浓度体外研究了单独或联合使用这些药物的抗增殖作用。结果表明,当LND作为第二种药物给药时,11/17的病例中有很强的协同作用。这与之前在MAST细胞系中的结果一致。在SO 6浓度为3.3×10(-10)至1.7×10(-9)M之间时,协同作用明显。