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凋亡级联反应激发的脂质纳米囊泡与包裹的紫杉醇在耐化疗结肠癌中显示出协同作用。

Apoptotic cascade inspired lipid nanovesicles show synergism with encapsulated paclitaxel in chemoresistant colon carcinoma.

作者信息

Joshi Nitin, Shanmugam Thanigaivel, Deshmukh Atul, Banerjee Rinti

机构信息

Department of Biosciences & Bioengineering, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.

出版信息

Nanomedicine (Lond). 2014;9(12):1789-805. doi: 10.2217/nnm.13.182. Epub 2014 Apr 4.

Abstract

UNLABELLED

Inspired from the apoptotic cascade, we developed phosphatidylserine (PS)-based proapoptotic lipid nanovesicles, capable of bypassing drug resistance and exhibiting synergistic anticancer activity with encapsulated paclitaxel in chemoresistant human colon adenocarcinoma (HCT-15).

MATERIALS & METHODS: Nanovesicles were developed and evaluated both in vitro and in vivo for their proapoptotic activity, synergism with encapsulated paclitaxel and ability to bypass drug resistance.

RESULTS

110 ± 7 nm sized nanovesicles were found to be proapoptotic and synergistic with paclitaxel, and bypassed drug resistance. The formulation, with synergistic inputs from PS and paclitaxel, downregulated Ki-67 and inhibited angiogenesis leading to apoptosis by activating caspase-3 and downregulating Bcl-2, resulting in DNA fragmentation. The nanovesicles, while increasing the systemic circulation time of paclitaxel by 6.9-fold reduced systemic toxic effects of paclitaxel and were found to be nonimmunogenic.

CONCLUSION

These results suggest the therapeutic potential of PS-based proapoptotic nanovesicles encapsulating paclitaxel in chemoresistant human colon carcinoma.

摘要

未标记

受凋亡级联反应的启发,我们开发了基于磷脂酰丝氨酸(PS)的促凋亡脂质纳米囊泡,其能够绕过耐药性,并在耐化疗的人结肠腺癌(HCT-15)中与封装的紫杉醇表现出协同抗癌活性。

材料与方法

开发纳米囊泡并在体外和体内评估其促凋亡活性、与封装的紫杉醇的协同作用以及绕过耐药性的能力。

结果

发现尺寸为110±7nm的纳米囊泡具有促凋亡作用且与紫杉醇协同,并能绕过耐药性。该制剂在PS和紫杉醇的协同作用下,下调Ki-67并抑制血管生成,通过激活caspase-3和下调Bcl-2导致凋亡,从而引起DNA片段化。纳米囊泡在将紫杉醇的全身循环时间延长6.9倍的同时,降低了紫杉醇的全身毒性作用,且被发现无免疫原性。

结论

这些结果表明基于PS的封装紫杉醇的促凋亡纳米囊泡在耐化疗的人结肠癌中的治疗潜力。

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