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精心设计了一种用于HER2阳性乳腺癌增强生物光热协同治疗的HER2特异性巨噬细胞仿生多功能纳米平台。

Ingenious designed a HER2-Specific macrophage biomimetic multifunctional nanoplatform for enhanced bio-photothermal synergistic therapy in HER2 positive breast cancer.

作者信息

Yang Peng, Du Fuyu, Zhang Weijie, Liu Weijing, Ye Zixuan, Fan Hongyu, Yu Jie, von Deneen Karen M, Wang Zhongliang, Ning Pengbo

机构信息

School of Life Science and Technology, Xidian University, Xi'an, Shaanxi, 710071, PR China.

Engineering Research Center of Molecular & Neuroimaging, Ministry of Education, Xi'an, Shaanxi, 710071, PR China.

出版信息

Mater Today Bio. 2024 May 20;26:101095. doi: 10.1016/j.mtbio.2024.101095. eCollection 2024 Jun.

Abstract

Photothermal therapy (PTT) has garnered extensive attention as an efficient strategy for cancer therapy. Unfortunately, there are currently no suitable photothermal agents (PTAs) capable of effectively treating HER2-positive breast cancer (HER2 BC) due to the challenges in addressing blood circulation and tumor accumulation. Here, we propose a HER2-specific macrophage biomimetic nanoplatform IR820@ZIF-8@EM (AMBP) for enhanced bio-photothermal therapy of HER2 BC. An anti-HER2 antibody was expressed in engineered macrophages using the transmembrane expression technique. As an efficient PTAs, IR820 dyes were assembled into ZIF-8 as to develop a "nano-thermal-bomb". Homology modeling methods support that the expressed anti-HER2 antibody can specifically recognize the HER2 receptor. Moreover, antibody-dependent cell-mediated cytotoxicity can also be induced in HER2 BC cells by AMBP. fluorescence confocal imaging showed that AMBP promoted the uptake of HER2 cancer cells while anti-tumor experiments demonstrated that AMBP efficiently accumulates in the tumor regions. Finally, under spatiotemporally controlled near-infrared (NIR) irradiation, three of the six tumors were eradicated in AMBP-treated mice, demonstrating a safe and effective strategy. In conclusion, our research opens a new paradigm for antibody-specific macrophage, and it is expected that these characteristics will have substantial clinical translation potential for BC treatment.

摘要

光热疗法(PTT)作为一种有效的癌症治疗策略已引起广泛关注。不幸的是,由于在解决血液循环和肿瘤蓄积方面存在挑战,目前尚无能够有效治疗人表皮生长因子受体2阳性乳腺癌(HER2 BC)的合适光热剂(PTA)。在此,我们提出一种用于增强HER2 BC生物光热治疗的HER2特异性巨噬细胞仿生纳米平台IR820@ZIF-8@EM(AMBP)。使用跨膜表达技术在工程化巨噬细胞中表达抗HER2抗体。作为一种有效的PTA,IR820染料被组装到ZIF-8中以开发一种“纳米热炸弹”。同源建模方法支持所表达的抗HER2抗体能够特异性识别HER2受体。此外,AMBP还可在HER2 BC细胞中诱导抗体依赖性细胞介导的细胞毒性。荧光共聚焦成像显示AMBP促进了HER2癌细胞的摄取,而抗肿瘤实验表明AMBP在肿瘤区域有效蓄积。最后,在时空控制的近红外(NIR)照射下,AMBP治疗的小鼠中有六只肿瘤中的三只被根除,证明了该策略的安全性和有效性。总之,我们的研究开创了抗体特异性巨噬细胞的新范例,预计这些特性在BC治疗中具有巨大的临床转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d47/11152651/ebcd7b70b2d0/ga1.jpg

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