Nanomedicine as an emerging platform for metastatic lung cancer therapy

被引:60
作者
Landesman-Milo, Dalit [1 ,2 ,3 ]
Ramishetti, Srinivas [1 ,2 ,3 ]
Peer, Dan [1 ,2 ,3 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Cell Res & Immunol, Lab NanoMed, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Iby & Aladar Fleischman Fac Engn, Dept Mat Sci & Engn, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Ctr Nanosci & Nanotechnol, IL-69978 Tel Aviv, Israel
关键词
Lipid nanoparticles; Polymers; Drug delivery; siRNA and lung metastasis; RNAI-BASED NANOMEDICINES; MULTIDRUG-RESISTANCE; LIPID NANOPARTICLES; BREAST-CANCER; IMMUNE-RESPONSE; SIRNA DELIVERY; IN-VIVO; TUMOR; DRUG; INHIBITION;
D O I
10.1007/s10555-015-9554-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic lung cancer is one of the most common cancers leading to mortality worldwide. Current treatment includes chemo- and pathway-dependent therapy aiming at blocking the spread and proliferation of these metastatic lesions. Nanomedicine is an emerging multidisciplinary field that offers unprecedented access to living cells and promises the state of the art in cancer detection and treatment. Development of nanomedicines as drug carriers (nanocarriers) that target cancer for therapy draws upon principles in the fields of chemistry, medicine, physics, biology, and engineering. Given the zealous activity in the field as demonstrated by more than 30 nanocarriers already approved for clinical use and given the promise of recent clinical results in various studies, nanocarrier-based strategies are anticipated to soon have a profound impact on cancer medicine and human health. Herein, we will detail the latest innovations in therapeutic nanomedicine with examples from lipid-based nanoparticles and polymer-based approaches, which are engineered to deliver anticancer drugs to metastatic lung cells. Emphasis will be placed on the latest and most attractive delivery platforms, which are developed specifically to target lung metastatic tumors. These novel nanomedicines may open new avenues for therapeutic intervention carrying new class of drugs such as RNAi and mRNA and the ability to edit the genome using the CRISPER/Cas9 system. Ultimately, these strategies might become a new therapeutic modality for advanced-stage lung cancer.
引用
收藏
页码:291 / 301
页数:11
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