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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.

DOI:10.1248/bpb.33.216
PMID:20118543
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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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.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。
Biol Pharm Bull. 2010;33(2):216-22. doi: 10.1248/bpb.33.216.
2
CCK-2/gastrin receptor signaling pathway is significant for gemcitabine-induced gene expression of VEGF in pancreatic carcinoma cells.胆囊收缩素-2/胃泌素受体信号通路对吉西他滨诱导胰腺癌 VEGF 基因表达有重要作用。
Life Sci. 2011 Oct 24;89(17-18):603-8. doi: 10.1016/j.lfs.2011.07.019. Epub 2011 Aug 3.
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Effect of Z-360, a novel orally active CCK-2/gastrin receptor antagonist on tumor growth in human pancreatic adenocarcinoma cell lines in vivo and mode of action determinations in vitro.新型口服活性CCK-2/胃泌素受体拮抗剂Z-360对人胰腺腺癌细胞系体内肿瘤生长的影响及体外作用模式的确定
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Z-360 Suppresses Tumor Growth in MIA PaCa-2-bearing Mice Inhibition of Gastrin-induced Anti-Apoptotic Effects.Z-360抑制荷MIA PaCa-2小鼠的肿瘤生长 抑制胃泌素诱导的抗凋亡作用。
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Z-360, a novel therapeutic agent for pancreatic cancer, prevents up-regulation of ephrin B1 gene expression and phosphorylation of NR2B via suppression of interleukin-1 β production in a cancer-induced pain model in mice.Z-360,一种新型胰腺癌治疗药物,通过抑制白细胞介素-1β的产生,防止 Ephrin B1 基因表达上调和 NR2B 磷酸化,在小鼠癌症诱导性疼痛模型中发挥作用。
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Curcumin potentiates antitumor activity of gemcitabine in an orthotopic model of pancreatic cancer through suppression of proliferation, angiogenesis, and inhibition of nuclear factor-kappaB-regulated gene products.姜黄素通过抑制增殖、血管生成以及抑制核因子-κB调节的基因产物,增强吉西他滨在胰腺癌原位模型中的抗肿瘤活性。
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A phase Ib/IIa trial to evaluate the CCK2 receptor antagonist Z-360 in combination with gemcitabine in patients with advanced pancreatic cancer.一项评估 CCK2 受体拮抗剂 Z-360 联合吉西他滨治疗晚期胰腺癌的 Ib/IIa 期临床试验。
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Pre-clinical evaluation of a new orally-active CCK-2R antagonist, Z-360, in gastrointestinal cancer models.新型口服活性CCK-2R拮抗剂Z-360在胃肠道癌模型中的临床前评估
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Gemcitabine sensitivity can be induced in pancreatic cancer cells through modulation of miR-200 and miR-21 expression by curcumin or its analogue CDF.姜黄素或其类似物 CDF 通过调节 miR-200 和 miR-21 的表达可以诱导胰腺癌细胞对吉西他滨敏感。
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RC-3095, a gastrin-releasing peptide receptor antagonist, synergizes with gemcitabine to inhibit the growth of human pancreatic cancer CFPAC-1 in vitro and in vivo.RC-3095,一种胃泌素释放肽受体拮抗剂,与吉西他滨协同抑制人胰腺癌细胞 CFPAC-1 的体外和体内生长。
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