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PhotoImmunoNanoTherapy reveals an anticancer role for sphingosine kinase 2 and dihydrosphingosine-1-phosphate

机译:PhotoImmunoNano疗法揭示了鞘氨醇激酶2和磷酸二氢鞘氨醇的抗癌作用

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Tumor-associated inflammation mediates the development of a systemic immunosuppressive milieu that is a major obstacle to effective treatment of cancer. Inflammation has been shown to promote the systemic expansion of immature myeloid cells which have been shown to exert immunosuppressive activity in laboratory models of cancer as well as cancer patients. Consequentially, significant effort is underway toward the development of therapies that decrease tumor-associated inflammation and immunosuppressive cells. The current study demonstrated that a previously described deep tissue imaging modality, which utilized indocyanine green-loaded calcium phosphosilicate nanoparticles (ICG-CPSNPs), could be utilized as an immunoregulatory agent. The theranostic application of ICG-CPSNPs as photosensitizers for photodynamic therapy was shown to block tumor growth in murine models of breast cancer, pancreatic cancer, and metastatic osteosarcoma by decreasing inflammation-expanded immature myeloid cells. Therefore, this therapeutic modality was termed PhotoImmunoNanoTherapy. As phosphorylated sphingolipid metabolites have been shown to have immunomodulatory roles, it was hypothesized that the reduction of immature myeloid cells by PhotoImmunoNanoTherapy was dependent upon bioactive sphingolipids. Mechanistically, PhotoImmunoNanoTherapy induced a sphingosine kinase 2-dependent increase in sphingosine-1-phosphate and dihydrosphingosine-1- phosphate. Furthermore, dihydrosphingosine-1-phosphate was shown to selectively abrogate myeloid lineage cells while concomitantly allowing the expansion of lymphocytes that exerted an antitumor effect. Collectively, these findings revealed that PhotoImmunoNanoTherapy, utilizing the novel nontoxic theranostic agent ICG-CPSNP, can decrease tumor-associated inflammation and immature myeloid cells in a sphingosine kinase 2-dependent manner. These findings further defined a novel myeloid regulatory role for dihydrosphingosine-1-phosphate. PhotoImmunoNanoTherapy holds the potential to be a revolutionary treatment for cancers with inflammatory and immunosuppressive phenotypes.
机译:肿瘤相关的炎症介导了全身免疫抑制环境的发展,这是有效治疗癌症的主要障碍。炎症已显示出促进未成熟髓样细胞的系统性扩张,在癌症以及癌症患者的实验室模型中,炎症细胞已显示出发挥免疫抑制活性。因此,正在致力于减少肿瘤相关炎症和免疫抑制细胞的疗法的开发。当前的研究表明,利用吲哚菁绿负载的磷酸硅酸钙纳米颗粒(ICG-CPSNPs)的先前描述的深层组织成像方式可以用作免疫调节剂。 ICG-CPSNPs作为光敏剂在光动力疗法中的治疗学应用已证明可通过减少炎症扩大的未成熟髓样细胞来阻止乳腺癌,胰腺癌和转移性骨肉瘤小鼠模型中的肿瘤生长。因此,这种治疗方式被称为光免疫纳米疗法。由于已显示磷酸化的鞘脂代谢物具有免疫调节作用,因此可以假设通过PhotoImmunoNanoTherapy减少未成熟髓样细胞取决于生物活性鞘脂。从机理上讲,PhotoImmunoNanoTherapy诱导了鞘氨醇-1-磷酸和二氢鞘氨醇-1-磷酸的鞘氨醇激酶2依赖性增加。此外,显示了磷酸二氢鞘氨醇-1-酯选择性地消除了髓系谱系细胞,同时伴随着淋巴细胞的扩展而发挥了抗肿瘤作用。总的来说,这些发现表明,利用新型无毒治疗药物ICG-CPSNP,PhotoImmunoNano疗法可以以鞘氨醇激酶2依赖性方式减少肿瘤相关的炎症和未成熟的髓样细胞。这些发现进一步定义了二氢鞘氨醇-1-磷酸的新型髓样调节作用。 PhotoImmunoNano疗法有潜力成为具有炎症和免疫抑制表型的癌症的革命性疗法。

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