Materials and Interfaces Center, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Medical Oncology, Shenzhen People's Hospital, the Second Clinical Medical College of Jinan University, Shenzhen 518055, China.
Theranostics. 2020 Mar 26;10(11):4720-4736. doi: 10.7150/thno.43092. eCollection 2020.
: Although inorganic nanomaterials have been widely used in multimodal cancer therapies, the intrinsic contributions of the materials are not well understood and sometimes underestimated. In this work, bioactive phospho-therapy with black phosphorus nanosheets (BPs) for tumor suppression is studied. : Orthotopic liver tumor and acute myeloid leukemia are chosen as the models for the solid tumor and hematological tumor, respectively. BPs are injected into mice through the tail vein and tumor growth is monitored by IVIS bioluminescence imaging. Tumor tissues and serum samples are collected to determine the suppression effect and biosafety of BPs after treatment. : The studies show that BPs with high intracellular uptake produce apoptosis- and autophagy-mediated programmed cell death of human liver carcinoma cells but do not affect normal cells. BPs passively accumulate in the tumor site at a high concentration and inhibit tumor growth. The tumor weight is much less than that observed from the doxorubicin (DOX)-treated group. The average survival time is extended by at least two months and the survival rate is 100% after 120 days. Western bolt analysis confirms that BPs suppress carcinoma growth the apoptosis and autophagy pathways. In addition, administration of BPs into mice suffering from leukemia results in tumor suppression and long survival. : This study reveals that BPs constitute a type of bioactive anti-cancer agents and provides insights into the application of inorganic nanomaterials to cancer therapy.
尽管无机纳米材料已广泛应用于多模态癌症治疗中,但人们对其内在贡献的认识还不够清楚,有时甚至低估了这些贡献。在这项工作中,研究了具有生物活性的黑磷纳米片(BPs)进行肿瘤抑制的磷酸治疗。
选择原位肝癌和急性髓性白血病分别作为实体瘤和血液系统肿瘤模型。通过尾静脉将 BPs 注射到小鼠体内,并通过 IVIS 生物发光成像监测肿瘤生长。收集肿瘤组织和血清样本,以确定治疗后 BPs 的抑制效果和生物安全性。
研究表明,具有高细胞内摄取率的 BPs 会导致人肝癌细胞发生凋亡和自噬介导的程序性细胞死亡,但不会影响正常细胞。BPs 被动地在肿瘤部位积聚到高浓度,从而抑制肿瘤生长。肿瘤重量明显低于多柔比星(DOX)治疗组观察到的重量。平均存活时间至少延长了两个月,120 天后存活率为 100%。Western bolt 分析证实 BPs 通过凋亡和自噬途径抑制癌的生长。此外,将 BPs 施用于患有白血病的小鼠中可抑制肿瘤生长并延长生存期。
这项研究揭示了 BPs 构成了一种具有生物活性的抗癌药物,并为将无机纳米材料应用于癌症治疗提供了新的思路。