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ZD6126抑制人胃癌小鼠模型中原位生长和腹膜癌转移。

ZD6126 inhibits orthotopic growth and peritoneal carcinomatosis in a mouse model of human gastric cancer.

作者信息

McCarty M F, Takeda A, Stoeltzing O, Liu W, Fan F, Reinmuth N, Akagi M, Bucana C, Mansfield P F, Ryan A, Ellis L M

机构信息

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Box 444, Houston, TX 77030-4009, USA.

出版信息

Br J Cancer. 2004 Feb 9;90(3):705-11. doi: 10.1038/sj.bjc.6601490.

Abstract

The purpose of this study was to examine the effects of ZD6126, a novel vascular-targeting agent, on tumour growth and angiogenesis in an orthotopic model of gastric cancer. TMK-1 human gastric adenocarcinoma cells were injected into the gastric wall of nude mice. After the tumours were established (day 14), therapy was initiated. Mice (n=11-12/group) received (a). vehicle, (b). ZD6126 at 100 mg x kg day(-1) i.p. one time per week or (c) ZD6126 at 100 mg x kg day(-1) i.p. five times per week. Tumour mass, volume and the presence or absence of peritoneal carcinomatosis were determined at sacrifice on day 38. Tumours from each group were stained for markers of blood vessels, proliferation and apoptosis. To further define the time frame of the vascular-targeting effects of chronic therapy with ZD6126, TMK-1 cells were again injected into the gastric wall of mice in a second experiment. On day 14, a single i.p. injection of ZD6126 100 mg x kg(-1) mouse(-1) or vehicle was delivered. Groups of three mice each were killed and the tumours harvested at days 1, 3 and 5 post-ZD6126 injection. Tumours were processed and stained for endothelial and tumour cell apoptosis and proliferation. No overt toxicity was observed with ZD6126 therapy. ZD6126 led to a marked inhibition of tumour growth (82% decrease vs control (P<0.001)). ZD6126 also led to a significant decrease in the incidence of peritoneal carcinomatosis (10 out of 12 controls, vs one out of 12 ZD6126) (P<0.01). Histological analysis of tumours revealed large regions of central necrosis in the treated group, as well as a dramatic increase in tumour cell apoptosis (7.4-fold increase (P<0.001)), consistent with the vascular-targeting activity of ZD6126. Mice treated with ZD6126 demonstrated a 59% decrease in PCNA-positive cells (P< 0.02), indicating reduced tumour cell proliferation. In addition, tumours treated with ZD6126 exhibited a 40% decrease in microvessel density (P<0.05). Results from mice treated with a single injection of ZD6126 demonstrated the acute effects this agent has on the tumour vasculature. The ratio of endothelial cell apoptosis to endothelial cell proliferation was increased within 24 h of a single injection. In conclusion, ZD6126 significantly inhibited tumour growth and metastasis in an orthotopic model of human gastric adenocarcinoma, without detectable problematic adverse effects. These data suggest that ZD6126 may be worthy of investigation in the treatment of primary gastric adenocarcinoma.

摘要

本研究旨在探讨新型血管靶向药物ZD6126对胃癌原位模型中肿瘤生长和血管生成的影响。将TMK-1人胃腺癌细胞注射到裸鼠胃壁。肿瘤形成后(第14天)开始治疗。小鼠(每组11 - 12只)接受:(a) 赋形剂;(b) ZD6126,100 mg·kg⁻¹·d⁻¹,腹腔注射,每周1次;或(c) ZD6126,100 mg·kg⁻¹·d⁻¹,腹腔注射,每周5次。在第38天处死时测定肿瘤质量、体积及有无腹膜种植转移。对每组肿瘤进行血管、增殖和凋亡标志物染色。为进一步明确ZD6126长期治疗的血管靶向作用时间框架,在第二个实验中再次将TMK-1细胞注射到小鼠胃壁。在第14天,单次腹腔注射ZD6126 100 mg·kg⁻¹或赋形剂。每组3只小鼠在注射ZD6126后第1、3和5天处死并收获肿瘤。对肿瘤进行处理并染色以检测内皮细胞和肿瘤细胞的凋亡及增殖。ZD6126治疗未观察到明显毒性。ZD6126导致肿瘤生长显著抑制(与对照组相比降低82%,P<0.001)。ZD6126还导致腹膜种植转移发生率显著降低(12只对照组中有10只发生,而12只ZD6126组中只有1只发生)(P<0.01)。肿瘤组织学分析显示治疗组有大片中央坏死区域,以及肿瘤细胞凋亡显著增加(增加7.4倍,P<0.001),这与ZD6126的血管靶向活性一致。用ZD6126治疗的小鼠PCNA阳性细胞减少59%(P<0.02),表明肿瘤细胞增殖减少。此外,用ZD6126治疗的肿瘤微血管密度降低40%(P<0.05)。单次注射ZD6126的小鼠实验结果显示了该药物对肿瘤血管系统的急性作用。单次注射后24小时内,内皮细胞凋亡与内皮细胞增殖的比率增加。总之,ZD6126在人胃腺癌原位模型中显著抑制肿瘤生长和转移,且未检测到有问题的不良反应。这些数据表明ZD6126在原发性胃腺癌治疗中可能值得研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e78/2410155/31b20c79de48/90-6601490f1.jpg

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