Wei Weijun, Rosenkrans Zachary T, Luo Quan-Yong, Lan Xiaoli, Cai Weibo
Department of Nuclear Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, 600 Yishan Road, Shanghai 200233, China.
Department of Radiology, University of Wisconsin - Madison, Madison, Wisconsin 53705, United States.
Small Methods. 2019 Feb 13;3(2). doi: 10.1002/smtd.201800365. Epub 2018 Nov 15.
Autophagy is a conserved process that is critical for sequestering and degrading proteins, damaged or aged organelles, and for maintaining cellular homeostasis under stress conditions. Despite its dichotomous role in health and diseases, autophagy usually promotes growth and progression of advanced cancers. In this context, clinical trials using chloroquine and hydroxychloroquine as autophagy inhibitors have suggested that autophagy inhibition is a promising approach for treating advanced malignancies and/or overcoming drug resistance of small molecule therapeutics (i.e., chemotherapy and molecularly targeted therapy). Efficient delivery of autophagy inhibitors may further enhance the therapeutic effect, reduce systemic toxicity, and prevent drug resistance. As such, nanocarriers-based drug delivery systems have several distinct advantages over free autophagy inhibitors that include increased circulation of the drugs, reduced off-target systemic toxicity, increased drug delivery efficiency, and increased solubility and stability of the encapsulated drugs. With their versatile drug encapsulation and surface-functionalization capabilities, nanocarriers can be engineered to deliver autophagy inhibitors to tumor sites in a context-specific and/or tissue-specific manner. This review focuses on the role of nanomaterials utilizing autophagy inhibitors for cancer therapy, with a focus on their applications in different cancer types.
自噬是一个保守的过程,对于隔离和降解蛋白质、受损或老化的细胞器以及在应激条件下维持细胞稳态至关重要。尽管自噬在健康和疾病中具有双重作用,但它通常会促进晚期癌症的生长和进展。在这种情况下,使用氯喹和羟氯喹作为自噬抑制剂的临床试验表明,抑制自噬是治疗晚期恶性肿瘤和/或克服小分子疗法(即化疗和分子靶向治疗)耐药性的一种有前景的方法。自噬抑制剂的有效递送可能会进一步提高治疗效果、降低全身毒性并预防耐药性。因此,基于纳米载体的药物递送系统相对于游离自噬抑制剂具有几个明显的优势,包括药物循环增加、脱靶全身毒性降低、药物递送效率提高以及封装药物的溶解度和稳定性增加。凭借其多功能的药物封装和表面功能化能力,纳米载体可以被设计成以特定背景和/或组织特异性的方式将自噬抑制剂递送至肿瘤部位。本综述重点关注利用自噬抑制剂的纳米材料在癌症治疗中的作用,重点是它们在不同癌症类型中的应用。