Institute of Biomaterials and Biomedical Engineering, University of Toronto, Ontario M5G 1L7, Canada.
Acc Chem Res. 2011 Oct 18;44(10):1105-13. doi: 10.1021/ar200017e. Epub 2011 May 10.
Over hundreds of millions of years, animals have evolved endogenous lipoprotein nanoparticles for shuttling hydrophobic molecules to different parts of the body. In the last 70 years, scientists have developed an understanding of lipoprotein function, often in relationship to lipid transport and heart disease. Such biocompatible, lipid-protein complexes are also ideal for loading and delivering cancer therapeutic and diagnostic agents, which means that lipoprotein and lipoprotein-inspired nanoparticles also offer opportunities for cancer theranostics. By mimicking the endogenous shape and structure of lipoproteins, the nanocarrier can remain in circulation for an extended period of time, while largely evading the reticuloendothelial cells in the body's defenses. The small size (less than 30 nm) of the low-density (LDL) and high-density (HDL) classes of lipoproteins allows them to maneuver deeply into tumors. Furthermore, lipoproteins can be targeted to their endogenous receptors, when those are implicated in cancer, or to other cancer receptors. In this Account, we review the field of lipoprotein-inspired nanoparticles related to the delivery of cancer imaging and therapy agents. LDL has innate cancer targeting potential and has been used to incorporate diverse hydrophobic molecules and deliver them to tumors. Nature's method of rerouting LDL in atherosclerosis provides a strategy to extend the cancer targeting potential of lipoproteins beyond its narrow purview. Although LDL has shown promise as a drug nanocarrier for cancer imaging and therapy, increasing evidence indicates that HDL, the smallest lipoprotein, may also be of use for drug targeting and uptake into cancer cells. We also discuss how synthetic HDL-like nanoparticles, which do not include human or recombinant proteins, can deliver molecules directly to the cytoplasm of certain cancer cells, effectively bypassing the endosomal compartment. This strategy could allow HDL-like nanoparticles to be used to deliver drugs that have increased activity in the cytoplasm. Lipoprotein nanoparticles have evolved to be ideal delivery vehicles, and because of that specialized function, they have the potential to improve cancer theranostics.
数亿年来,动物进化出内源性脂蛋白纳米颗粒,以将疏水分子运送到身体的不同部位。在过去的 70 年中,科学家们已经了解了脂蛋白的功能,通常与脂质运输和心脏病有关。这种生物相容性的脂质-蛋白复合物也非常适合装载和输送癌症治疗和诊断剂,这意味着脂蛋白和受其启发的纳米颗粒也为癌症治疗和诊断提供了机会。通过模拟脂蛋白的内源性形状和结构,纳米载体可以在体内循环系统中延长停留时间,同时很大程度上逃避机体防御系统中的网状内皮细胞。低密脂蛋白(LDL)和高密脂蛋白(HDL)的纳米载体的尺寸较小(小于 30nm),可以深入肿瘤内部。此外,当内源性受体参与癌症时,脂蛋白可以靶向其内源受体,或者靶向其他癌症受体。在本综述中,我们回顾了与癌症成像和治疗剂递送相关的脂蛋白启发型纳米颗粒领域。LDL 具有固有的癌症靶向潜力,并已被用于结合多种疏水分子并将其递送至肿瘤。在动脉粥样硬化中重新引导 LDL 的自然方法为延长脂蛋白的癌症靶向潜力提供了一种策略,使其超越了其狭窄的范围。尽管 LDL 已显示出作为癌症成像和治疗的药物纳米载体的潜力,但越来越多的证据表明,最小的脂蛋白 HDL 也可能用于药物靶向和摄取癌细胞。我们还讨论了如何使用不含人类或重组蛋白的合成 HDL 样纳米颗粒将分子直接递送至某些癌细胞的细胞质中,有效地绕过内体区室。这种策略可以使 HDL 样纳米颗粒能够用于递送至细胞质中活性增加的药物。脂蛋白纳米颗粒已经进化为理想的递药载体,并且由于这种特殊功能,它们有可能改善癌症治疗和诊断。