Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Potomac Affinity Proteins, LLC, North Potomac, MD 20878, USA.
J Control Release. 2024 Jun;370:614-625. doi: 10.1016/j.jconrel.2024.05.015. Epub 2024 May 14.
Mutations in RAS, a family of proteins found in all human cells, drive a third of cancers, including many pancreatic, colorectal, and lung cancers. However, there is a lack of clinical therapies that can effectively prevent RAS from causing tumor growth. Recently, a protease was engineered that specifically degrades active RAS, offering a promising new tool for treating these cancers. However, like many other intracellularly acting protein-based therapies, this protease requires a delivery vector to reach its site of action within the cell. In this study, we explored the incorporation of cationic lipids into ionizable lipid nanoparticles (LNPs) to develop a RAS protease delivery platform capable of inhibiting cancer cell proliferation in vitro and in vivo. A library of 13 LNPs encapsulating RAS protease was designed, and each formulation was evaluated for in vitro delivery efficiency and toxicity. A subset of four top-performing LNP formulations was identified and further evaluated for their impact on cancer cell proliferation in human colorectal cancer cells with mutated KRAS in vitro and in vivo, as well as their in vivo biodistribution and toxicity. In vivo, both the concentration of cationic lipid and type of cargo influenced LNP and cargo distribution. All lead candidate LNPs showed RAS protease functionality in vitro, and the top-performing formulation achieved effective intracellular RAS protease delivery in vivo, decreasing cancer cell proliferation in an in vivo xenograft model and significantly reducing tumor growth and size. Overall, this work demonstrates the use of LNPs as an effective delivery platform for RAS proteases, which could potentially be utilized for cancer therapies.
RAS 是一种存在于所有人类细胞中的蛋白质家族,其突变驱动了三分之一的癌症,包括许多胰腺癌、结直肠癌和肺癌。然而,目前缺乏能够有效阻止 RAS 引发肿瘤生长的临床疗法。最近,一种能够特异性降解活性 RAS 的蛋白酶被设计出来,为治疗这些癌症提供了一种有前途的新工具。然而,像许多其他细胞内作用的蛋白质基疗法一样,这种蛋白酶需要一个输送载体才能到达细胞内的作用部位。在这项研究中,我们探索了将阳离子脂质纳入可离子化脂质纳米颗粒 (LNP) 中,以开发一种能够抑制体外和体内癌细胞增殖的 RAS 蛋白酶输送平台。设计了一个包含 RAS 蛋白酶的 13 个 LNP 的文库,并对每种制剂的体外输送效率和毒性进行了评估。确定了四个表现最佳的 LNP 制剂子集,并进一步评估了它们对体外具有突变 KRAS 的人结直肠癌细胞增殖以及体内生物分布和毒性的影响。在体内,阳离子脂质的浓度和货物的类型都影响 LNP 和货物的分布。所有候选 LNP 都表现出体外的 RAS 蛋白酶功能,表现最佳的制剂在体内实现了有效的细胞内 RAS 蛋白酶输送,减少了体内异种移植模型中的癌细胞增殖,并显著减少了肿瘤的生长和大小。总体而言,这项工作证明了 LNP 可作为 RAS 蛋白酶的有效输送平台,这可能可用于癌症治疗。