Suppr超能文献

联合射频消融和 IV 脂质体热休克蛋白抑制:在小动物肿瘤模型中减少肿瘤生长并提高动物终点生存率。

Combination radiofrequency (RF) ablation and IV liposomal heat shock protein suppression: reduced tumor growth and increased animal endpoint survival in a small animal tumor model.

机构信息

Laboratory for Minimally Invasive Tumor Therapies, Department of Radiology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA 02215, USA.

出版信息

J Control Release. 2012 Jun 10;160(2):239-44. doi: 10.1016/j.jconrel.2011.12.031. Epub 2011 Dec 30.

Abstract

BACKGROUND

To investigate the effect of IV liposomal quercetin (a known down-regulator of heat shock proteins) alone and with liposomal doxorubicin on tumor growth and end-point survival when combined with radiofrequency (RF) tumor ablation in a rat tumor model.

METHODS

Solitary subcutaneous R3230 mammary adenocarcinoma tumors (1.3-1.5 cm) were implanted in 48 female Fischer rats. Initially, 32 tumors (n=8, each group) were randomized into four experimental groups: (a) conventional monopolar RF alone (70°C for 5 min), (b) IV liposomal quercetin alone (1 mg/kg), (c) IV liposomal quercetin followed 24hr later with RF, and (d) no treatment. Next, 16 additional tumors were randomized into two groups (n=8, each) that received a combined RF and liposomal doxorubicin (15 min post-RF, 8 mg/kg) either with or without liposomal quercetin. Kaplan-Meier survival analysis was performed using a tumor diameter of 3.0 cm as the defined survival endpoint.

RESULTS

Differences in endpoint survival and tumor doubling time among the groups were highly significant (P<0.001). Endpoint survivals were 12.5±2.2 days for the control group, 16.6±2.9 days for tumors treated with RF alone, 15.5±2.1 days for tumors treated with liposomal quercetin alone, and 22.0±3.9 days with combined RF and quercetin. Additionally, combination quercetin/RF/doxorubicin therapy resulted in the longest survival (48.3±20.4 days), followed by RF/doxorubicin (29.9±3.8 days).

CONCLUSIONS

IV liposomal quercetin in combination with RF ablation reduces tumor growth rates and improves animal endpoint survival. Further increases in endpoint survival can be seen by adding an additional anti-tumor adjuvant agent liposomal doxorubicin. This suggests that targeting several post-ablation processes with multi-drug nanotherapies can increase overall ablation efficacy.

摘要

背景

为了研究 IV 脂质体槲皮素(一种已知的热休克蛋白下调剂)单独使用以及与脂质体阿霉素联合应用于射频(RF)肿瘤消融治疗大鼠肿瘤模型时对肿瘤生长和终点生存的影响。

方法

在 48 只雌性 Fischer 大鼠中植入 1.3-1.5cm 的单一皮下 R3230 乳腺腺癌肿瘤。最初,32 个肿瘤(n=8,每组)随机分为四个实验组:(a)单独使用传统的单极 RF(70°C 持续 5 分钟),(b)IV 脂质体槲皮素(1mg/kg),(c)IV 脂质体槲皮素后 24 小时后加用 RF,(d)无治疗。然后,另外 16 个肿瘤随机分为两组(n=8,每组),在 RF 后 15 分钟给予 RF 和脂质体阿霉素(8mg/kg),并分别给予或不给予脂质体槲皮素。使用肿瘤直径为 3.0cm 作为定义的生存终点进行 Kaplan-Meier 生存分析。

结果

各组终点生存和肿瘤倍增时间的差异具有高度显著性(P<0.001)。对照组的终点生存率为 12.5±2.2 天,单独使用 RF 治疗的肿瘤为 16.6±2.9 天,单独使用脂质体槲皮素治疗的肿瘤为 15.5±2.1 天,联合使用 RF 和槲皮素的肿瘤为 22.0±3.9 天。此外,联合使用槲皮素/RF/阿霉素治疗的肿瘤生存时间最长(48.3±20.4 天),其次是 RF/阿霉素(29.9±3.8 天)。

结论

IV 脂质体槲皮素联合 RF 消融可降低肿瘤生长速度并提高动物终点生存率。通过添加额外的抗肿瘤佐剂脂质体阿霉素,可以进一步提高终点生存率。这表明,使用多药物纳米疗法靶向多个消融后过程可以提高整体消融效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5443/3412588/90390495f078/nihms347225f1.jpg

相似文献

引用本文的文献

本文引用的文献

4
Hsp70, a messenger from hyperthermia for the immune system.热休克蛋白 70,高温向免疫系统发出的信使。
Eur J Cell Biol. 2012 Jan;91(1):48-52. doi: 10.1016/j.ejcb.2011.02.001. Epub 2011 Mar 31.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验