Prominence of bioresponsive DNA nanococoons in tackling post-surgery cancer recurrence.

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Pharmaceutical patent analyst Pub Date : 2023-09-01 Epub Date: 2023-11-20 DOI:10.4155/ppa-2023-0013
Sravani Yerram, Ramesh Joga, Pooja Shende, Priya Varpe, Kiran Kumar Bellapu, Sandeep Kumar
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引用次数: 0

Abstract

Post-surgery cancer recurrence is one of the reasons for increased cancer cases. The effective usage of the enhanced permeability and retention effect of a nanocarrier infused with the bioresponsive release mechanism of checkpoint inhibitors (aPD1 and aCTLA4) can become a boon to mankind. DNA nanococoons (DNCs) comprising cytosine-phosphorothioate-guanine oligodeoxynucleotides (CpG-ODNs) with potent immunostimulatory effects can significantly enhance anti-cancer activity. Triglycerylmonostearate (TGMS) with enzymatic cleavage potential at the wound sites of tumor resection, upon caging with restriction enzyme (HhaI) followed by attaching to DNCs, makes the immunotherapy bioresponsive. Hhal-TGMS-DNCs-aPD1 triggered by the inflammation at the wound site undergoes enzymatic cleavage, releases the restriction enzyme, converts DNCs to CpG ODNs sequentially and with sustained aPD1 release exerts an appreciable anti-cancer effect.

生物反应性DNA纳米茧在治疗术后癌症复发中的突出作用。
术后癌症复发是癌症病例增加的原因之一。有效利用注入检查点抑制剂(aPD1和aCTLA4)生物反应性释放机制的纳米载体的增强渗透性和滞留效应,可以成为人类的福音。含有胞嘧啶-硫代磷酸酯-鸟嘌呤寡聚脱氧核苷酸(CpG-ODNs)的DNA纳米cocoons (dnc)具有较强的免疫刺激作用,可以显著增强抗癌活性。甘油三酯单硬脂酸酯(TGMS)在肿瘤切除的伤口部位具有酶切电位,在用限制性内切酶(HhaI)笼化后附着在dnc上,使免疫治疗具有生物反应性。伤口部位炎症触发的hhal - tgms - dnc -aPD1经过酶裂解,释放限制性内切酶,将dnc依次转化为CpG ODNs,并持续释放aPD1,具有明显的抗癌作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceutical patent analyst
Pharmaceutical patent analyst PHARMACOLOGY & PHARMACY-
CiteScore
1.80
自引率
0.00%
发文量
22
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