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超声介导的空化作用增强了用于三阴性乳腺癌治疗的表皮生长因子受体靶向聚乳酸-聚乙二醇纳米胶束递送

Ultrasound-Mediated Cavitation Enhances EGFR-Targeting PLGA-PEG Nano-Micelle Delivery for Triple-Negative Breast Cancer Treatment.

作者信息

Chen Libin, Zhang Tao, Sun Shan, Ren Wenzhi, Wu Aiguo, Xu Huixiong

机构信息

School of Medicine, Tongji University, Shanghai 200072, China.

Department of Ultrasound in Medicine, Ningbo First Hospital, Ningbo 315010, China.

出版信息

Cancers (Basel). 2021 Jul 6;13(14):3383. doi: 10.3390/cancers13143383.

DOI:10.3390/cancers13143383
PMID:34298600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8304156/
Abstract

Triple-negative breast cancer (TNBC) is highly recurring and metastatic breast cancer with overexpressing epidermal growth factor receptor (EGFR). Herein, a series of in vitro and in vivo analyses were used to explore the therapeutic effect of EGFR-targeting nano-micelles (PLGA-PEG/DOX@anti-EGFR) combined with ultrasound-mediated cavitation (UMC). The prepared nano-micelle drug carriers have good biocompatibility and can greatly increase the drug accumulation in tumor regions, thereby reducing off-target toxicity while enhancing anti-tumor efficacy. Moreover, an in vivo analysis of the practical utility of this treatment modality was conducted by using SonoVue microbubbles to achieve cavitation under different power intensity levels, with an ultrasonic power intensity of 0.5 W/cm maximizing the intra-tumoral blood perfusion. Relative to PLGA-PEG@DOX/anti-EGFR nano-micelles treatment alone, the combination with UMC was better able to suppress tumor growth even at low concentrations. As such, combining actively targeted drug-carrier molecules with UMC represents an effective approach to enhancing therapeutic efficacy while reducing the adverse, systemic effects associated with DOX and other chemotherapeutic drugs, and it can be considered as a promising clinical prospect in the treatment of TNBC.

摘要

三阴性乳腺癌(TNBC)是一种具有高复发性和转移性的乳腺癌,其表皮生长因子受体(EGFR)过表达。在此,我们采用了一系列体外和体内分析方法,以探究靶向EGFR的纳米胶束(PLGA-PEG/DOX@anti-EGFR)联合超声介导空化(UMC)的治疗效果。所制备的纳米胶束药物载体具有良好的生物相容性,能够显著增加药物在肿瘤区域的蓄积,从而降低脱靶毒性,同时增强抗肿瘤疗效。此外,通过使用声诺维微泡在不同功率强度水平下实现空化,对这种治疗方式的实际效用进行了体内分析,超声功率强度为0.5 W/cm²时可使肿瘤内血液灌注最大化。相对于单独使用PLGA-PEG@DOX/anti-EGFR纳米胶束治疗,联合UMC即使在低浓度下也能更好地抑制肿瘤生长。因此,将主动靶向药物载体分子与UMC相结合是一种在提高治疗效果的同时减少与阿霉素及其他化疗药物相关的不良全身效应的有效方法,并且可以被认为是治疗TNBC的一种有前景的临床方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/1a573f783b16/cancers-13-03383-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/193caf3f2b3f/cancers-13-03383-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/2a88632075f8/cancers-13-03383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/639411139f86/cancers-13-03383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/af165d5aa8b7/cancers-13-03383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/f2effb28d766/cancers-13-03383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/8e6abdb05b6e/cancers-13-03383-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/58833e028a1a/cancers-13-03383-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/1a573f783b16/cancers-13-03383-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/193caf3f2b3f/cancers-13-03383-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/2a88632075f8/cancers-13-03383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/639411139f86/cancers-13-03383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/af165d5aa8b7/cancers-13-03383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/f2effb28d766/cancers-13-03383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/8e6abdb05b6e/cancers-13-03383-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/58833e028a1a/cancers-13-03383-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d774/8304156/1a573f783b16/cancers-13-03383-g007.jpg

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