Ono M, Tanaka N
First Department of Surgery, Okayama University Medical School 2-5-1, Japan.
In Vivo. 1997 May-Jun;11(3):233-41.
Cepharanthin (CE), a bisbenzylisoquinoline alkaloid drug, was tested in vitro and in vivo with chemotherapeutic agents, vincristine (VCR), vinblastine (VLB), and vindesine (VDS). The activity of these agents alone or in combination was tested against a human colon cancer cell line (RPMI 4788) or a human uterine cervical cancer cell line (HeLa), using a modified microcytotoxicity-viable cell staining assay. In the in vitro study, the antiproliferative activities of each vinca alkaloid were enhanced additively or synergistically by combination with CE in RPMI 4788 cells as well as HeLa cells. The sequential exposure of the RPMI 4788 cells or HeLa cells to both CE and each vinca alkaloid agent showed evidence of a more significant potentiation. The antiproliferative activity of the combination of each vinca alkaloid agent(VCR, VLB, or VDS) with CE was almost equivalent to the effect of each vinca alkaloid agent alone which was potentiated by CE tenfold through several hundredfold. In an experimental model of tumor growth and survival, in which RPMI 4788 cells were transplanted subcutaneously or intraperitoneally into BALB/c nu/nu mice respectively, CE (1 mg/kg) alone exerted not significant inhibitory activity against tumor growth or survival, and VCR (0.25 mg/kg) alone partially inhibited these antitumor activities. Furthermore, the antitumor effects of VCR were elevated synergistically by the simultaneous administration of CE. These studies indicate that due to their therapeutic potential, combinations of vinca alkaloid agent with CE might be a promising therapy for some human cancers.
千金藤素(CE)是一种双苄基异喹啉生物碱药物,在体外和体内与化疗药物长春新碱(VCR)、长春碱(VLB)和长春地辛(VDS)进行了测试。使用改良的微细胞毒性-活细胞染色试验,测试了这些药物单独或联合使用对人结肠癌细胞系(RPMI 4788)或人子宫颈癌细胞系(HeLa)的活性。在体外研究中,在RPMI 4788细胞和HeLa细胞中,每种长春花生物碱与CE联合使用时,其抗增殖活性呈相加或协同增强。RPMI 4788细胞或HeLa细胞先后暴露于CE和每种长春花生物碱药物,显示出更显著的增强作用。每种长春花生物碱药物(VCR、VLB或VDS)与CE联合使用的抗增殖活性几乎等同于每种长春花生物碱药物单独使用的效果,而CE单独使用时可使其增强10倍至数百倍。在肿瘤生长和存活的实验模型中,将RPMI 4788细胞分别皮下或腹腔注射到BALB/c nu/nu小鼠体内,单独使用CE(1 mg/kg)对肿瘤生长或存活没有显著的抑制活性,单独使用VCR(0.25 mg/kg)部分抑制了这些抗肿瘤活性。此外,同时给予CE可协同提高VCR的抗肿瘤作用。这些研究表明,由于其治疗潜力,长春花生物碱药物与CE联合使用可能是治疗某些人类癌症的一种有前景的疗法。