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采用血管靶向脂质体药物进行的时辰药理学癌症治疗。

Chronopharmacologic cancer treatment with an angiogenic vessel-targeted liposomal drug.

作者信息

Shimizu Kosuke, Sawazaki Yasuharu, Tanaka Toshiki, Asai Tomohiro, Oku Naoto

机构信息

Department of Medical Biochemistry, University of Shizuoka School of Pharmaceutical Sciences, Suruga-ku, Shizuoka 422-8526, Japan.

出版信息

Biol Pharm Bull. 2008 Jan;31(1):95-8. doi: 10.1248/bpb.31.95.

DOI:10.1248/bpb.31.95
PMID:18175949
Abstract

Antineovascular therapy (ANET), which eradicates angiogenic endothelial cells by specifically delivered anticancer drugs to tumor cells to obtain complete cutoff of blood supply, is an effective modality for cancer treatment. Since the expression of vascular endothelial growth factor (VEGF) in hypoxic tumor cells is known to fluctuate in a circadian oscillation, we investigated the chronopharmacologic treatment of tumors with ANET. Adriamycin-encapsulated liposomes modified with the Ala-Pro-Arg-Pro-Gly (APRPG) peptide (APRPG-LipADM) were prepared, after the APRPG peptide had been shown to have affinity to angiogenic sites. Colon 26 NL-17 tumor-bearing mice were injected three times with APRPG-LipADM at Zeitgeber time (ZT) 2, 8, 14, and 20 where ZT 0 was the time lights were turned on, and tumor growth was monitored. Tumor growth suppression changed with dosing time and was significantly (p<0.01) more potent at ZT 14 compared with ZT 20. The VEGF concentration in the plasma of the tumor-bearing mice was higher in the light phase compared with that in the dark phase, and this circadian oscillation was related to dosing time dependency with ANET. These results indicate that tumor growth suppression is correlated to some extent with the VEGF concentration in the plasma, and that chronopharmacologic treatment of cancer with ANET may enhance the therapeutic efficacy and reduce the side effects.

摘要

抗血管生成疗法(ANET)通过将抗癌药物特异性递送至肿瘤细胞来根除血管生成内皮细胞,从而实现完全切断血液供应,是一种有效的癌症治疗方式。由于已知缺氧肿瘤细胞中血管内皮生长因子(VEGF)的表达会呈昼夜节律性波动,我们研究了ANET对肿瘤的时辰药理学治疗。在已证明丙氨酸-脯氨酸-精氨酸-脯氨酸-甘氨酸(APRPG)肽对血管生成部位具有亲和力后,制备了用APRPG肽修饰的阿霉素包封脂质体(APRPG-LipADM)。给荷Colon 26 NL-17肿瘤的小鼠在授时时间(ZT)2、8、14和20注射三次APRPG-LipADM,其中ZT 0为开灯时间,并监测肿瘤生长情况。肿瘤生长抑制随给药时间而变化,与ZT 20相比,在ZT 14时显著更强(p<0.01)。荷瘤小鼠血浆中的VEGF浓度在光照期高于黑暗期,这种昼夜节律性波动与ANET的给药时间依赖性有关。这些结果表明,肿瘤生长抑制在一定程度上与血浆中的VEGF浓度相关,并且用ANET进行癌症的时辰药理学治疗可能会提高治疗效果并减少副作用。

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