Multifunctional aptamer grafted targeted nano-drugs execute molecular cross-talks with cancer cells

Sounik Manna, Rumi Mahata, Surya K. Dey, Angsuman Das Chaudhuri, Sujata M. Choudhury
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引用次数: 0

Abstract

The biggest obstacles in treating cancer with traditional chemotherapy are unpleasant side effects and drug resistance. A growing amount of interest has been exhibited in using aptamers as target ligands for targeted cancer therapy and specific cancer cell identification due to their distinct benefits. Aptamer-conjugated nano-materials have recently provided new prospects in cancer treatment with their improved therapeutic efficacy and capability of reducing toxicity. Consequently, they are not perceived as alien substances our body, which allows their comfortable acceptance. Several tumor markers such as nucleolin, mucin, and the epidermal growth factor receptor can be effectively recognized by aptamers. In addition, glycoproteins on the surface of tumor cells can be recognized using aptamers. So surface modification of drug by aptamer are accomplished for enhanced tumor-specific recognition by which drug-specific accretion, internalization, and drug retention in tumors increased through specific ligand-mediated interactions and thus therapeutic index is increased. Here, we highlight some promising classes of aptamer-conjugated nanoparticles for the specific recognition of cancer cells and targeted drug delivery and the molecular mechanism and immunomodulatory regulation of these aptamer have been focused.

Abstract Image

多功能适配体接枝靶向纳米药物与癌细胞发生分子交叉作用
传统化疗治疗癌症的最大障碍是令人不快的副作用和耐药性。由于其独特的优势,越来越多的人开始关注使用适配体作为靶配体来进行癌症靶向治疗和特异性癌细胞识别。最近,适配体结合的纳米材料因其更好的疗效和减毒能力,为癌症治疗提供了新的前景。因此,它们不会被认为是人体内的外来物质,因而可以被人们轻松接受。一些肿瘤标志物,如核蛋白、粘蛋白和表皮生长因子受体,都能被适配体有效识别。此外,肿瘤细胞表面的糖蛋白也能被适配体识别。因此,通过适配体对药物进行表面修饰可增强对肿瘤的特异性识别,从而通过配体介导的特异性相互作用增加药物在肿瘤中的特异性吸附、内化和保留,从而提高治疗指数。本文受版权保护。本文受版权保护,未经许可不得转载。
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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