Markey Cancer Center, The University of Kentucky, Lexington, KY 40536, United States; Department of Surgery, The University of Kentucky, Lexington, KY 40536, United States.
Department of Pharmaceutical Sciences, The University of Kentucky, Lexington, KY 40536, United States.
J Control Release. 2018 Apr 10;275:85-91. doi: 10.1016/j.jconrel.2018.02.008. Epub 2018 Feb 6.
Colorectal cancer (CRC) is the second leading cause of cancer deaths in the United States; the predominant cause for mortality is metastasis to distant organs (e.g., lung). A major problem limiting the success of chemotherapy in metastatic CRC is the inability to target tumor tissues selectively and avoid severe side effects to normal tissues and organs. Here, we demonstrate polymeric nanoparticles (PNPs) entrapping chemotherapeutic agents provide a new therapeutic option for treating CRC that has metastasized to the lung. PNPs assembled from FDA approved biocompatible block copolymer accumulated predominantly in lung tissue. PNPs showed negligible accumulation in liver, spleen and kidneys, which was confirmed by fluorescent nanoparticle imaging and analysis of PI3K inhibition in the organs. PNPs entrapping PI3K inhibitors (i.e., wortmannin and PX866) suppressed CRC lung metastasis growth, and SN-38-loaded PNPs completely eliminated CRC lung metastasis. Our results demonstrate that polymer-drug nanoparticles offer a new approach to reduce toxicity of cancer therapy and has the potential to improve outcomes for patients with lung metastasis.
结直肠癌(CRC)是美国癌症死亡的第二大主要原因;主要的死亡原因是转移到远处器官(例如肺)。在转移性 CRC 中,化疗的主要问题是无法选择性地靶向肿瘤组织,并且避免对正常组织和器官产生严重的副作用。在这里,我们证明了包裹化疗药物的聚合物纳米颗粒(PNP)为治疗已转移到肺部的 CRC 提供了新的治疗选择。由 FDA 批准的生物相容性嵌段共聚物组装的 PNP 主要积聚在肺部组织中。PNP 在肝脏、脾脏和肾脏中的积累可以忽略不计,这通过荧光纳米颗粒成像和对器官中 PI3K 抑制的分析得到了证实。包裹 PI3K 抑制剂(即wortmannin 和 PX866)的 PNP 抑制 CRC 肺转移生长,负载 SN-38 的 PNP 完全消除了 CRC 肺转移。我们的结果表明,聚合物-药物纳米颗粒为降低癌症治疗的毒性提供了一种新方法,并有可能改善患有肺转移的患者的治疗效果。