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评价多机制抗血管生成联合治疗增强胰腺癌细胞毒治疗反应。

Evaluation of poly-mechanistic antiangiogenic combinations to enhance cytotoxic therapy response in pancreatic cancer.

机构信息

Division of Surgical Oncology, Department of Surgery, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

PLoS One. 2012;7(6):e38477. doi: 10.1371/journal.pone.0038477. Epub 2012 Jun 18.

Abstract

Gemcitabine (Gem) has limited clinical benefits in pancreatic ductal adenocarcinoma (PDAC). The present study investigated combinations of gemcitabine with antiangiogenic agents of various mechanisms for PDAC, including bevacizumab (Bev), sunitinib (Su) and EMAP II. Cell proliferation and protein expression were analyzed by WST-1 assay and Western blotting. In vivo experiments were performed via murine xenografts. Inhibition of in vitro proliferation of AsPC-1 PDAC cells by gemcitabine (10 µM), bevacizumab (1 mg/ml), sunitinib (10 µM) and EMAP (10 µM) was 35, 22, 81 and 6 percent; combination of gemcitabine with bevacizumab, sunitinib or EMAP had no additive effects. In endothelial HUVECs, gemcitabine, bevacizumab, sunitinib and EMAP caused 70, 41, 86 and 67 percent inhibition, while combination of gemcitabine with bevacizumab, sunitinib or EMAP had additive effects. In WI-38 fibroblasts, gemcitabine, bevacizumab, sunitinib and EMAP caused 79, 58, 80 and 29 percent inhibition, with additive effects in combination as well. Net in vivo tumor growth inhibition in gemcitabine, bevacizumab, sunitinib and EMAP monotherapy was 43, 38, 94 and 46 percent; dual combinations of Gem+Bev, Gem+Su and Gem+EMAP led to 69, 99 and 64 percent inhibition. Combinations of more than one antiangiogenic agent with gemcitabine were generally more effective but not superior to Gem+Su. Intratumoral proliferation, apoptosis and microvessel density findings correlated with tumor growth inhibition data. Median animal survival was increased by gemcitabine (26 days) but not by bevacizumab, sunitinib or EMAP monotherapy compared to controls (19 days). Gemcitabine combinations with bevacizumab, sunitinib or EMAP improved survival to similar extent (36 or 37 days). Combinations of gemcitabine with Bev+EMAP (43 days) or with Bev+Su+EMAP (46 days) led to the maximum survival benefit observed. Combination of antiangiogenic agents improves gemcitabine response, with sunitinib inducing the strongest effect. These findings demonstrate advantages of combining multi-targeting agents with standard gemcitabine therapy for PDAC.

摘要

吉西他滨(Gem)在胰腺导管腺癌(PDAC)中的临床获益有限。本研究探讨了吉西他滨与各种机制的抗血管生成药物联合应用于 PDAC 的效果,这些药物包括贝伐单抗(Bev)、舒尼替尼(Su)和 EMAP II。通过 WST-1 检测和 Western blot 分析细胞增殖和蛋白表达。通过鼠异种移植进行体内实验。吉西他滨(10 μM)、贝伐单抗(1 mg/ml)、舒尼替尼(10 μM)和 EMAP(10 μM)对 AsPC-1 PDAC 细胞体外增殖的抑制率分别为 35%、22%、81%和 6%;吉西他滨与贝伐单抗、舒尼替尼或 EMAP 的联合应用无相加作用。在血管内皮细胞 HUVEC 中,吉西他滨、贝伐单抗、舒尼替尼和 EMAP 分别抑制 70%、41%、86%和 67%,而吉西他滨与贝伐单抗、舒尼替尼或 EMAP 的联合应用具有相加作用。在 WI-38 成纤维细胞中,吉西他滨、贝伐单抗、舒尼替尼和 EMAP 分别抑制 79%、58%、80%和 29%,联合应用也具有相加作用。吉西他滨、贝伐单抗、舒尼替尼和 EMAP 单药治疗的体内肿瘤生长抑制率分别为 43%、38%、94%和 46%;吉西他滨与贝伐单抗、舒尼替尼或 EMAP 的双重联合治疗抑制率分别为 69%、99%和 64%。多种抗血管生成药物与吉西他滨的联合应用通常更有效,但并不优于吉西他滨+舒尼替尼。肿瘤内增殖、凋亡和微血管密度的发现与肿瘤生长抑制数据相关。与对照组(19 天)相比,吉西他滨(26 天)可延长中位动物生存期,但贝伐单抗、舒尼替尼或 EMAP 单药治疗不能延长生存期。吉西他滨联合贝伐单抗、舒尼替尼或 EMAP 可延长至相似程度的生存期(36 或 37 天)。吉西他滨联合贝伐单抗+EMAP(43 天)或联合贝伐单抗+舒尼替尼+EMAP(46 天)可获得最长的生存获益。联合应用抗血管生成药物可提高吉西他滨的反应,其中舒尼替尼诱导作用最强。这些发现表明,联合使用多靶点药物与标准吉西他滨治疗 PDAC 具有优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e6/3377661/d5c8e64fc958/pone.0038477.g001.jpg

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