Kawai K, Konishi Y, Izumi K, Sato M, Adachi M, Hozumi M
Cellular Technology Institute, Otsuka Pharmaceutical Company, Tokushima, Japan.
Anticancer Res. 1998 Jan-Feb;18(1A):405-12.
Vesnarinone (3,4-dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)- quinolinone), a quinolinone derivative, is an orally active inotropic agent used in Japan for the treatment of chronic heart failure. Recently, it has been reported that vesnarinone induces differentiation and apoptosis in certain types of leukaemia and solid tumour cells, and exhibits antitumour effect on several tumours xenografted in nude mice. In the present study, we examined the antitumour effect of vesnarinone in combination with radiation and conventional anticancer agents in nude mice xenografted with human gastric carcinoma, a poorly-differentiated adenocarcinoma, MKN-45 cell line which has a wild-type p53 gene. Vesnarinone treatment combined with radiation resulted in a higher antitumour activity compared with a single treatment with either vesnarinone or radiation alone. Further, vesnarinone treatment together with radiation and conventional anticancer agents including 5-FU and picibanil (an immunopotentiator) produced the highest antitumour effect compared with any other treatment. Additionally, the combination treatment induced marked differentiation and apoptosis of the tumour cells and an increase in the expression of p53 gene in the treated tumour cells. The results suggest that vesnarinone, in combination with radiation and the conventional antitumour agents, may be of clinical interest for treatment of certain types of gastric tumours.
维司那林(3,4-二氢-6-[4-(3,4-二甲氧基苯甲酰基)-1-哌嗪基]-2(1H)-喹啉酮),一种喹啉酮衍生物,是一种口服有效的强心剂,在日本用于治疗慢性心力衰竭。最近,有报道称维司那林可诱导某些类型的白血病和实体瘤细胞分化和凋亡,并对几种移植到裸鼠体内的肿瘤具有抗肿瘤作用。在本研究中,我们检测了维司那林与放疗及传统抗癌药物联合应用对移植了人胃癌(一种低分化腺癌,MKN-45细胞系,具有野生型p53基因)的裸鼠的抗肿瘤作用。与单独使用维司那林或放疗相比,维司那林与放疗联合治疗具有更高的抗肿瘤活性。此外,与其他任何治疗相比,维司那林与放疗及包括5-氟尿嘧啶和匹克米星(一种免疫增强剂)在内的传统抗癌药物联合治疗产生了最高的抗肿瘤效果。此外,联合治疗诱导了肿瘤细胞的明显分化和凋亡,并使治疗后的肿瘤细胞中p53基因的表达增加。结果表明,维司那林与放疗及传统抗肿瘤药物联合应用可能对某些类型的胃癌治疗具有临床意义。