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Z-360,一种新型的胆囊收缩素 2/胃泌素受体拮抗剂,可抑制吉西他滨诱导的人胰腺癌细胞血管内皮生长因子基因的表达。

Z-360, a novel cholecystokinin-2/gastrin receptor antagonist, inhibits gemcitabine-induced expression of the vascular endothelial growth factor gene in human pancreatic cancer cells.

机构信息

Central Research Laboratories, Zeria Pharmaceutical Co., Ltd, 2512-1 Oshikiri, Kumagaya, Saitama 360-0111, Japan.

出版信息

Biol Pharm Bull. 2010;33(2):216-22. doi: 10.1248/bpb.33.216.

Abstract

Z-360 is a novel cholecystokinin (CCK)-2/gastrin receptor antagonist that is being developed for the treatment of pancreatic adenocarcinoma in combination with gemcitabine. A previous study shows that the co-administration of Z-360 with gemcitabine significantly prolonged the survival of mice with orthotopically implanted human pancreatic adenocarcinoma cell lines. To clarify the therapeutic effects of Z-360 in combined with gemcitabine, we analyzed gene expression. When gemcitabine was administered, CCK-2/gastrin receptor expression was induced in an orthotropic xenograft model; the result indicating that Z-360 could act on gemcitabine-sensitive cells. Both in vitro and in vivo studies showed that gemcitabine increased the expression of vascular endothelial growth factor A (VEGFA), a prognostic factor for survival in pancreatic cancer, while Z-360 suppressed this induction of VEGFA gene expression. These results help to explain how Z-360 prolongs survival when used in combination with gemcitabine.

摘要

Z-360 是一种新型的胆囊收缩素 (CCK)-2/胃泌素受体拮抗剂,正在开发用于联合吉西他滨治疗胰腺腺癌。先前的研究表明,Z-360 与吉西他滨联合使用可显著延长原位植入人胰腺腺癌细胞系的小鼠的存活期。为了阐明 Z-360 联合吉西他滨的治疗效果,我们分析了基因表达。在原位异种移植模型中,当给予吉西他滨时,CCK-2/胃泌素受体表达被诱导;结果表明 Z-360 可以作用于吉西他滨敏感细胞。体外和体内研究均表明,吉西他滨增加了血管内皮生长因子 A(VEGFA)的表达,VEGFA 是胰腺癌生存的预后因素,而 Z-360 抑制了这种 VEGFA 基因表达的诱导。这些结果有助于解释 Z-360 与吉西他滨联合使用时如何延长生存时间。

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