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用于时空可控信号放大分子成像和组合肿瘤治疗的内源性酶激活的球形核酸。

Endogenous Enzyme-Activatable Spherical Nucleic Acids for Spatiotemporally Controlled Signal Amplification Molecular Imaging and Combinational Tumor Therapy.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.

Yueyang Central Hospital, Yueyang 414020, China.

出版信息

Anal Chem. 2023 Oct 3;95(39):14710-14719. doi: 10.1021/acs.analchem.3c02831. Epub 2023 Sep 20.

Abstract

Due to the adjustable hybridization activity, antinuclease digestion stability, and superior endocytosis, spherical nucleic acids (SNAs) have been actively developed as probes for molecular imaging and the development of noninvasive diagnosis and image-guided surgery. However, since highly expressed biomarkers in tumors are not negligible in normal tissues, an inevitable background signal and the inability to precisely release probes at the chosen region remain a challenge for SNAs. Herein, we proposed a rationally designed, endogenous enzyme-activatable functional SNA (Ep-SNA) for spatiotemporally controlled signal amplification molecular imaging and combinational tumor therapy. The self-assembled amphiphilic polymer micelles (SM-ASO), which were obtained by a simple and rapid copper-free strain-promoted azide-alkyne cycloaddition click reaction between dibenzocyclooctyne-modified antisense oligonucleotide and azide-containing aliphatic polymer polylactic acid, were introduced as the core elements of Ep-SNA. This Ep-SNA was then constructed by connecting two apurinic/apyrimidinic (AP) site-containing trailing DNA hairpins, which could occur via a hybridization chain reaction in the presence of low-abundance survivin mRNA to SM-ASO through complementary base pairing. Notably, the AP site-containing trailing DNA hairpins also empowered the SNA with the feasibility of drug delivery. Once this constructed intelligent Ep-SNA nanoprobe was specifically cleaved by the highly expressed cytoplasmic human apurinic/apyrimidinic endonuclease 1 in tumor cells, three key elements (trailing DNA hairpins, antisense oligonucleotide, and doxorubicin) could be released to enable subsequent high-sensitivity survivin mRNA imaging and combinational cancer therapy (gene silencing and chemotherapy). This strategy shows great application prospects of SNAs as a precise platform for the integration of disease diagnosis and treatment and can contribute to basic biomedical research.

摘要

由于可调杂交活性、抗核酸酶消化稳定性和优越的内吞作用,球形核酸 (SNA) 已被积极开发为分子成像探针,并用于开发非侵入性诊断和图像引导手术。然而,由于肿瘤中高表达的生物标志物在正常组织中不可忽视,因此不可避免地会出现背景信号,并且无法在所选区域精确释放探针,这仍然是 SNA 的一个挑战。在此,我们提出了一种合理设计的、内源性酶激活功能 SNA (Ep-SNA),用于时空控制信号放大的分子成像和联合肿瘤治疗。自组装两亲聚合物胶束 (SM-ASO) 通过二苯并环辛炔修饰的反义寡核苷酸与含叠氮的脂肪族聚合物聚乳酸之间的简单快速的铜促进叠氮-炔环加成点击反应获得,作为 Ep-SNA 的核心元素。然后,通过连接两个含有无嘌呤/无嘧啶 (AP) 位点的尾随 DNA 发夹构建了 Ep-SNA,在低丰度生存素 mRNA 的存在下,通过杂交链反应,可以通过互补碱基配对将 Ep-SNA 连接到 SM-ASO。值得注意的是,含有 AP 位点的尾随 DNA 发夹还使 SNA 具有药物递送的可行性。一旦这种构建的智能 Ep-SNA 纳米探针被肿瘤细胞中高表达的细胞质人嘌呤/嘧啶内切核酸酶 1 特异性切割,三个关键元素(尾随 DNA 发夹、反义寡核苷酸和阿霉素)就可以被释放,从而实现随后的高灵敏度生存素 mRNA 成像和联合癌症治疗(基因沉默和化学疗法)。该策略展示了 SNA 作为疾病诊断和治疗整合的精确平台的巨大应用前景,并有助于基础生物医学研究。

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