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化疗药物对皮下和原位人肿瘤异种移植模型中肿瘤血管系统的影响。

The effect of chemotherapeutic agents on tumor vasculature in subcutaneous and orthotopic human tumor xenografts.

作者信息

Fung Andrea S, Lee Carol, Yu Man, Tannock Ian F

机构信息

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre and University of Toronto, 610 University Avenue, Toronto, ON, M5G 2 M9, Canada.

出版信息

BMC Cancer. 2015 Mar 10;15:112. doi: 10.1186/s12885-015-1091-6.

Abstract

BACKGROUND

The growth of solid tumors and their regrowth after treatment is dependent upon functional tumor vasculature. Some chemotherapeutic agents have shown anti-angiogenic properties but there are limited studies of the effect of chemotherapy on tumor vasculature. Here we investigate the effect of paclitaxel, 5-fluorouracil (5-FU) and doxorubicin on tumor vasculature in subcutaneous and orthotopic xenografts in mice.

METHODS

The vascular density and percentage of functional blood vessels were evaluated in subcutaneous A431 human vulvar cancer xenografts, and in subcutaneous and orthotopic MCF-7 human breast cancer xenografts, following single doses of paclitaxel, 5-FU or doxorubicin.

RESULTS

There was no significant difference in total (CD31+) blood vessels between untreated ectopic and orthotopic MCF-7 tumors, but there was a significantly lower proportion of functional blood vessels in orthotopic tumors. After paclitaxel treatment, there was a decrease in functional tumor vasculature in A431 subcutaneous xenografts, followed by a subsequent rebound. There was a significant decrease in total vascular density on day 12 in A431 tumors following 5-FU or doxorubicin treatment, but no change in the percentage of functional vessels. An increase in functional blood vessels or percentage of functional vasculature was noted in MCF-7 subcutaneous and orthotopic xenografts following chemotherapy treatment.

CONCLUSIONS

There are differences in the vasculature and microenvironment of ectopic and orthotopic xenografts in mice. Anti-tumor effects of chemotherapy may be due, in part, to effects on tumor vasculature and may vary in different tumor models.

摘要

背景

实体瘤的生长及其治疗后的再生长依赖于功能性肿瘤血管系统。一些化疗药物已显示出抗血管生成特性,但关于化疗对肿瘤血管系统影响的研究有限。在此,我们研究紫杉醇、5-氟尿嘧啶(5-FU)和阿霉素对小鼠皮下和原位异种移植瘤中肿瘤血管系统的影响。

方法

在给予单剂量紫杉醇、5-FU或阿霉素后,评估皮下A431人外阴癌异种移植瘤以及皮下和原位MCF-7人乳腺癌异种移植瘤中的血管密度和功能性血管百分比。

结果

未治疗的异位和原位MCF-7肿瘤之间的总(CD31 +)血管无显著差异,但原位肿瘤中功能性血管的比例显著较低。紫杉醇治疗后,A431皮下异种移植瘤中功能性肿瘤血管系统减少,随后出现反弹。5-FU或阿霉素治疗后第12天,A431肿瘤的总血管密度显著降低,但功能性血管的百分比无变化。化疗治疗后,MCF-7皮下和原位异种移植瘤中功能性血管或功能性血管系统的百分比增加。

结论

小鼠异位和原位异种移植瘤的血管系统和微环境存在差异。化疗的抗肿瘤作用可能部分归因于对肿瘤血管系统的影响,并且在不同的肿瘤模型中可能有所不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa86/4363401/0dbe7fb96b04/12885_2015_1091_Fig1_HTML.jpg

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