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铁-乳铁蛋白纳米制剂靶向survivin以杀死结肠癌干细胞,并维持铁、钙和锌的吸收。

Fe-bLf nanoformulation targets survivin to kill colon cancer stem cells and maintains absorption of iron, calcium and zinc.

作者信息

Kanwar Jagat R, Mahidhara Ganesh, Roy Kislay, Sasidharan Sreenivasan, Krishnakumar Subramanian, Prasad Neerati, Sehgal Rakesh, Kanwar Rupinder K

机构信息

Nanomedicine, Laboratory of Immunology & Molecular Biomedical Research (LIMBR), School of Medicine (SoM), Faculty of Health, Deakin University, Waurn Ponds, Victoria 3217, Australia.

出版信息

Nanomedicine (Lond). 2015 Jan;10(1):35-55. doi: 10.2217/nnm.14.132. Epub 2014 Jul 14.

Abstract

AIM

To validate the anticancer efficacy of alginate-enclosed, chitosan-conjugated, calcium phosphate, iron-saturated bovine lactoferrin (Fe-bLf) nanocarriers/nanocapsules (NCs) with improved sustained release and ability to induce apoptosis by downregulating survivin, as well as cancer stem cells.

MATERIALS & METHODS: The stability, nanotoxicity of the modified nanoformulation was evaluated and their anticancer efficacy was re-examined. Their mechanism of internalization was studied and we identified the role of various miRNAs in absorption of these NCs/iron in various body parts of mice. We determined the effect of these NCs on survivin, stem cell markers, red blood cell count, iron, calcium and zinc concentration in mice, determined the antiangiogenic properties of these NCs and studied their effect on cancer stem-like cells.

RESULTS

Spherical NCs (396.1 ± 27.2 nm) exceedingly reduced viability of Caco-2 cells (32 ± 2.83%). The NCs also showed effective internalization and reduction of cancer stem cell markers in triple-positive CD133, survivin and CD44 cancer stem-like cells. Mice treated with the NCs showed no nanotoxicity and did not develop any tumors in xenograft colon cancer models. We found that the serum iron, zinc and calcium absorption were increased. DMT1, LRP, transferrin and lactoferrin receptors were responsible for internalization of the NCs. Different miRNAs were responsible for iron regulation in different organs. Interestingly, NCs inhibited survivin and its different isoforms.

CONCLUSION

Our results confirmed that NCs internalized and changed the expression of selected miRNAs that further enhanced their uptake. The NCs activated both extrinsic, as well as intrinsic apoptotic pathways to induce apoptosis by targeting survivin in cancer cells and cancer stem cells, without inducing any nonspecific nanotoxicity. Apart from inhibiting angiogenesis and stem cell markers, NCs also maintained iron and calcium levels.

摘要

目的

验证海藻酸盐包裹、壳聚糖共轭、磷酸钙、铁饱和牛乳铁蛋白(Fe-bLf)纳米载体/纳米胶囊(NCs)的抗癌功效,其具有改善的缓释性能以及通过下调生存素和癌症干细胞来诱导细胞凋亡的能力。

材料与方法

评估修饰后的纳米制剂的稳定性、纳米毒性,并重新检查其抗癌功效。研究其内化机制,我们确定了各种微小RNA(miRNA)在小鼠不同身体部位对这些NCs/铁吸收中的作用。我们测定了这些NCs对小鼠生存素、干细胞标志物、红细胞计数、铁、钙和锌浓度的影响,确定了这些NCs的抗血管生成特性,并研究了它们对癌症干细胞样细胞的作用。

结果

球形NCs(396.1±27.2纳米)极大地降低了Caco-2细胞的活力(32±2.83%)。NCs还显示出在三阳性CD133、生存素和CD44癌症干细胞样细胞中有效内化并降低癌症干细胞标志物。用NCs处理的小鼠在异种移植结肠癌模型中未显示出纳米毒性且未发生任何肿瘤。我们发现血清中铁、锌和钙的吸收增加。二价金属离子转运体1(DMT1)、低密度脂蛋白受体相关蛋白(LRP)、转铁蛋白和乳铁蛋白受体负责NCs的内化。不同的miRNA在不同器官中负责铁的调节。有趣的是,NCs抑制生存素及其不同异构体。

结论

我们的结果证实,NCs被内化并改变了所选miRNA的表达,这进一步增强了它们的摄取。NCs通过靶向癌细胞和癌症干细胞中的生存素来激活外源性和内源性凋亡途径以诱导细胞凋亡,而不诱导任何非特异性纳米毒性。除了抑制血管生成和干细胞标志物外,NCs还维持了铁和钙的水平。

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