Bergamo A, Masi A, Jakupec M A, Keppler B K, Sava G
Callerio Foundation Onlus, Via A. Fleming 22-31, 34127 Trieste, Italy.
Met Based Drugs. 2009;2009:681270. doi: 10.1155/2009/681270. Epub 2009 Sep 17.
The effects of indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (KP1019, or FFC14A), the second ruthenium compound that entered clinical trials, in an in vitro model of tumour invasion and metastasis show that the antitumour effects of this compound might include also the modulation of cell behaviour although its cytotoxicity appears to be predominant over these effects. The comparison with its imidazole analogue KP418 shows however its superiority, being able to control in vitro cell growth and in some instances also in vivo tumour development. These results suggest that the activity of KP1019 is predominantly due to direct cytotoxic effects for tumour cells, evident also in vivo on primary tumour growth and that the effects on modulation of the biological behaviour of the cancer cell can be present but might have only a partial role.
吲唑鎓反式-四氯双(1H-吲唑)钌(III)是进入临床试验的第二种钌化合物,其在肿瘤侵袭和转移体外模型中的作用表明,该化合物的抗肿瘤作用可能还包括对细胞行为的调节,尽管其细胞毒性似乎比这些作用更为显著。然而,与咪唑类似物KP418相比,它具有优势,能够控制体外细胞生长,在某些情况下还能控制体内肿瘤发展。这些结果表明,KP1019的活性主要归因于对肿瘤细胞的直接细胞毒性作用,在体内对原发性肿瘤生长也很明显,并且对癌细胞生物学行为的调节作用可能存在,但可能只起部分作用。