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化疗预刺激胰腺肿瘤微环境促进静脉注射低分子肝素包裹脂质-siRNA 复合物的递送和抗转移疗效。

Chemotherapy priming of the Pancreatic Tumor Microenvironment Promotes Delivery and Anti-Metastasis Efficacy of Intravenous Low-Molecular-Weight Heparin-Coated Lipid-siRNA Complex.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery Systems, West China School of Pharmacy, Sichuan University, No. 17, Block 3, Southern Renmin Road, Chengdu 610041, China.

出版信息

Theranostics. 2019 Jan 1;9(2):355-368. doi: 10.7150/thno.29137. eCollection 2019.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a type of malignant tumor with high lethality. Its high tumor cell-density and large variety of extracellular matrix (ECM) components present major barriers for drug delivery. Paclitaxel-loaded PEGylated liposomes (PTX-Lip) were used as a tumor-priming agent to induce tumor cell apoptosis and decrease the abundance of ECM to promote cellular uptake and tumor delivery of nanodrugs. Paclitaxel exerts anti-cancer effects but, paradoxically, exacerbates cancer metastasis and drug resistance by increasing the expression of apoptotic B-cell lymphoma-2 protein (BCL-2). Thus, low-molecular-weight heparin-coated lipid-siRNA complex (LH-Lip/siBCL-2) was constructed to inhibit cancer metastasis and silence BCL-2 by BCL-2 siRNA (siBCL-2). Significant tumor growth inhibition efficacy was observed, accompanied by obvious inhibition of cancer metastasis . These results suggested our sequential delivery of PTX-Lip and LH-Lip/siBCL-2 might provide a practical approach for PDAC or other ECM-rich tumors.

摘要

胰腺导管腺癌(PDAC)是一种致死率很高的恶性肿瘤。其高肿瘤细胞密度和大量细胞外基质(ECM)成分构成了药物输送的主要障碍。载紫杉醇的聚乙二醇化脂质体(PTX-Lip)被用作肿瘤引发剂,以诱导肿瘤细胞凋亡并减少 ECM 的丰度,从而促进纳米药物的细胞摄取和肿瘤传递。紫杉醇发挥抗癌作用,但通过增加凋亡 B 细胞淋巴瘤-2 蛋白(BCL-2)的表达,反而会加剧癌症转移和耐药性。因此,构建了低分子量肝素包被的脂质-siRNA 复合物(LH-Lip/siBCL-2),通过 BCL-2 siRNA(siBCL-2)抑制癌症转移和沉默 BCL-2。观察到显著的肿瘤生长抑制效果,同时明显抑制癌症转移。这些结果表明,我们对 PTX-Lip 和 LH-Lip/siBCL-2 的序贯递药可能为 PDAC 或其他富含 ECM 的肿瘤提供一种实用的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8740/6376180/cbed9ba66c5a/thnov09p0355g001.jpg

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