Department of Obstetrics and Gynecology, School of Medicine, Fukuoka University, Fukuoka, Japan.
Cancer Sci. 2010 Apr;101(4):984-90. doi: 10.1111/j.1349-7006.2009.01479.x. Epub 2009 Dec 19.
The purpose of the present study was to develop a new method of chemoembolization to improve the therapeutic effectiveness and safety profile of cancer treatment. A chemoembolization approach was designed for human solid tumors using resorbable calcium-phosphate ceramic microspheres loaded with an agent anti-angiogenic to tumor vasculature in vivo. The human uterine sarcoma cell line FU-MMT-3 was used in this study because this tumor is aggressive and also exhibits a poor response to radiotherapy or any chemotherapy currently used. The calcium-phosphate ceramic microspheres loaded with TNP-470, an anti-angiogenic agent, were injected into FU-MMT-3 xenografts in nude mice three times per week for 8 weeks. The treatment using TNP-470-loaded microspheres suppressed tumor growth, compared to treatment with TNP-470 alone, microspheres alone, and the control. The mean tumor weight after treatment using TNP-470-loaded microspheres was significantly lower than that after treatment with microspheres alone. These ceramic microspheres were remarkably embolized in tumor microvessels as well as in the feeding arteries and a significant reduction of intratumoral vascularity was also demonstrated following treatment with TNP-470-loaded microspheres. Severe loss of body weight was not observed in any mice treated with the TNP-470-loaded microspheres, compared to treatment with TNP-470 alone. These results suggest that targeting tumor vasculature in human uterine sarcoma using calcium-phosphate microspheres might be more effective and safer than the treatment that employs anti-angiogenic agent alone. This new chemoembolization method incorporating an anti-angiogenic agent may contribute to the effective treatment of locally advanced or recurrent solid tumors.
本研究旨在开发一种新的化疗栓塞方法,以提高癌症治疗的疗效和安全性。设计了一种使用可吸收的磷酸钙陶瓷微球负载抗血管生成剂治疗人类实体肿瘤的化疗栓塞方法,该方法在体内靶向肿瘤血管。本研究使用人子宫肉瘤细胞系 FU-MMT-3,因为该肿瘤侵袭性强,对目前使用的放疗或任何化疗均反应不佳。将负载 TNP-470 的磷酸钙陶瓷微球每周三次注入裸鼠 FU-MMT-3 异种移植物中,共 8 周。与单独使用 TNP-470、单独使用微球和对照组相比,负载 TNP-470 的微球治疗抑制了肿瘤生长。负载 TNP-470 的微球治疗后的平均肿瘤重量明显低于单独使用微球治疗后的肿瘤重量。这些陶瓷微球在肿瘤微血管以及供血动脉中均有明显栓塞作用,并且负载 TNP-470 的微球治疗后也明显减少了肿瘤内血管生成。与单独使用 TNP-470 相比,使用负载 TNP-470 的微球治疗的小鼠体重没有明显下降。这些结果表明,使用磷酸钙微球靶向人类子宫肉瘤的肿瘤血管可能比单独使用抗血管生成剂的治疗更有效和更安全。这种新的化疗栓塞方法结合抗血管生成剂可能有助于有效治疗局部晚期或复发性实体肿瘤。