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