Department of Experimental Clinical Oncology, Aarhus University Hospital, Aarhus, Denmark.
Vascul Pharmacol. 2011 Jan-Feb;54(1-2):13-7. doi: 10.1016/j.vph.2010.10.002. Epub 2010 Oct 30.
Combretastatin A-4 phosphate (CA4P) is a promising vascular disrupting agent in cancer treatment, but elicits hypertension in patients. The aim of this study was to use a mouse model to investigate whether hypertension or its modification influenced the treatment efficacy of CA4P in combination with other therapies.
C3H mammary carcinoma bearing or non-bearing CDF1 mice were used. The effects of CA4P alone or in combination with the antihypertensive drug hydralazine (HDZ) on mean arterial blood pressure (MABP), hematocrit (Hct) and hemoglobin concentration ([Hb]) were characterized in non-tumor-bearing animals. Tumor-bearing mice were also treated locally with radiation and/or hyperthermia (41.5 ° C; 60 min) in combination with CA4P alone or CA4P plus HDZ, and TCD50 values (radiation dose that controls 50% of tumors) determined.
Hct, [Hb] and MABP respectively increased from 49.3 ± 0.3%, 9.1 ± 0.1mM and 110 ± 7 mm Hg, to 54.7 ± 0.2%, 10.3 ± 0.1 mM and 127 ± 5 mm Hg, within 1h after injecting 100 mg/kg CA4P. For each parameter the magnitude of the peak increase was largely dose independent within the CA4P dose range tested (10-250 mg/kg). However, high CA4P doses delayed the return to baseline and Hct and [Hb] recovered more slowly than MABP. Co-administration of HDZ (0.2mg/kg) was able to suppress the CA4P-induced increase in MABP for several hours but did not noticeably affect the changes in Hct and [Hb]. The TCD50 value (± 95% confidence interval) for radiation alone was 53 (51-55) Gy. Tumor irradiation followed by injection of either CA4P (100 mg/kg) or CA4P+HDZ 30 min later reduced the TCD50 values to 50 (46-54) Gy and 48 (45-52) Gy, respectively. Heating tumors after irradiating further decreased the TCD50 value to 46 (43-48) Gy. When all treatments were combined the TCD50 was 35 (32-38) Gy, regardless of whether the drugs were CA4P or CA4P+HDZ.
CA4P significantly increased Hct, [Hb] and MABP. Hypertension, but not increases in Hct and [Hb], could be reversed with the antihypertensive drug HDZ. CA4P significantly improved tumor response to radiation or thermoradiation, neither of which was influenced by the addition of HDZ.
Combretastatin A-4 磷酸盐(CA4P)是一种有前途的癌症治疗中的血管破坏剂,但会引起患者高血压。本研究的目的是使用小鼠模型来研究高血压或其修饰是否会影响 CA4P 联合其他疗法的治疗效果。
使用携带或不携带 CDF1 小鼠的 C3H 乳腺肿瘤。在非肿瘤小鼠中,研究 CA4P 单独或与降压药肼屈嗪(HDZ)联合使用对平均动脉血压(MABP)、红细胞压积(Hct)和血红蛋白浓度([Hb])的影响。还对接受局部放射和/或 41.5°C(60 分钟)热疗(CA4P 单独或 CA4P+HDZ)的荷瘤小鼠进行治疗,并确定 TCD50 值(控制 50%肿瘤的辐射剂量)。
在注射 100mg/kg CA4P 后 1 小时内,Hct、[Hb]和 MABP 分别从 49.3±0.3%、9.1±0.1mM 和 110±7mmHg 增加到 54.7±0.2%、10.3±0.1mM 和 127±5mmHg。对于每个参数,在测试的 CA4P 剂量范围内(10-250mg/kg),峰值增加的幅度在很大程度上与剂量无关。然而,高 CA4P 剂量会延迟恢复到基线,Hct 和[Hb]的恢复速度比 MABP 慢。同时给予 HDZ(0.2mg/kg)能够抑制 CA4P 诱导的 MABP 升高数小时,但对 Hct 和[Hb]的变化没有明显影响。单独放射治疗的 TCD50 值(±95%置信区间)为 53(51-55)Gy。肿瘤照射后,无论注射 CA4P(100mg/kg)还是 CA4P+HDZ 30 分钟后,TCD50 值分别降低至 50(46-54)Gy 和 48(45-52)Gy。照射后加热肿瘤可进一步将 TCD50 值降低至 46(43-48)Gy。当所有治疗方法结合使用时,TCD50 为 35(32-38)Gy,无论药物是 CA4P 还是 CA4P+HDZ。
CA4P 显著增加 Hct、[Hb]和 MABP。高血压,但不是 Hct 和[Hb]的增加,可以用降压药 HDZ 逆转。CA4P 显著提高了肿瘤对放射或热放射的反应,HDZ 的加入都没有影响。