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采用车兵组合策略的实体瘤治疗

Solid Tumor Therapy Using a Cannon and Pawn Combination Strategy.

作者信息

Song Wantong, Tang Zhaohui, Zhang Dawei, Wen Xue, Lv Shixian, Liu Zhilin, Deng Mingxiao, Chen Xuesi

机构信息

1. Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, PR China;

2. Department of Chemistry, Northeast Normal University, Changchun, 130021, PR China;

出版信息

Theranostics. 2016 Apr 28;6(7):1023-30. doi: 10.7150/thno.14741. eCollection 2016.

Abstract

Nanocarrier-based anti-tumor drugs hold great promise for reducing side effects and improving tumor-site drug retention in the treatment of solid tumors. However, therapeutic outcomes are still limited, primarily due to a lack of drug penetration within most tumor tissues. Herein, we propose a strategy using a nanocarrier-based combination of vascular disrupting agents (VDAs) and cytotoxic drugs for solid tumor therapy. Specifically, combretastatin A-4 (CA4) serves as a "cannon" by eradicating tumor cells at a distance from blood vessels; concomitantly, doxorubicin (DOX) serves as a "pawn" by killing tumor cells in close proximity to blood vessels. This "cannon and pawn" combination strategy acts without a need to penetrate every tumor cell and is expected to eliminate all tumor cells in a solid tumor. In a murine C26 colon tumor model, this strategy proved effective in eradicating greater than 94% of tumor cells and efficiently inhibited tumor growth with a weekly injection. In large solid tumor models (C26 and 4T1 tumors with volumes of approximately 250 mm(3)), this strategy also proved effective for inhibiting tumor growth. These results showing remarkable inhibition of tumor growth provide a valuable therapeutic choice for solid tumor therapy.

摘要

基于纳米载体的抗肿瘤药物在实体瘤治疗中对于减少副作用和提高肿瘤部位药物滞留具有巨大潜力。然而,治疗效果仍然有限,主要原因是大多数肿瘤组织内药物渗透不足。在此,我们提出一种策略,即使用基于纳米载体的血管破坏剂(VDA)和细胞毒性药物联合用于实体瘤治疗。具体而言,康普瑞汀A-4(CA4)作为“大炮”,通过在远离血管的部位消除肿瘤细胞;同时,阿霉素(DOX)作为“卒子”,通过杀死靠近血管的肿瘤细胞。这种“大炮与卒子”联合策略无需穿透每个肿瘤细胞即可发挥作用,有望消除实体瘤中的所有肿瘤细胞。在小鼠C26结肠肿瘤模型中,该策略被证明在每周注射一次的情况下能够有效根除超过94%的肿瘤细胞并有效抑制肿瘤生长。在大型实体瘤模型(体积约为250立方毫米的C26和4T1肿瘤)中,该策略也被证明对抑制肿瘤生长有效。这些显示出显著肿瘤生长抑制效果的结果为实体瘤治疗提供了一种有价值的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d6c/4876626/6746c965a679/thnov06p1023g001.jpg

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