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包含物理和生物屏障的体外肿瘤微环境模型,用于模拟多药耐药机制和多药传递策略。

In-vitro tumor microenvironment models containing physical and biological barriers for modelling multidrug resistance mechanisms and multidrug delivery strategies.

机构信息

Biomaterials and Tissue Engineering Department, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran 1517964311, Iran.

Genetics Department, Breast Cancer Research Center (BCRC), Motamed Cancer Institute, ACECR, Tehran 1517964311, Iran.

出版信息

J Control Release. 2021 Jun 10;334:164-177. doi: 10.1016/j.jconrel.2021.04.024. Epub 2021 Apr 22.

Abstract

The complexity and heterogeneity of the three-dimensional (3D) tumor microenvironment have brought challenges to tumor studies and cancer treatment. The complex functions and interactions of cells involved in tumor microenvironment have led to various multidrug resistance (MDR) and raised challenges for cancer treatment. Traditional tumor models are limited in their ability to simulate the resistance mechanisms and not conducive to the discovery of multidrug resistance and delivery processes. New technologies for making 3D tissue models have shown the potential to simulate the 3D tumor microenvironment and identify mechanisms underlying the MDR. This review overviews the main barriers against multidrug delivery in the tumor microenvironment and highlights the advances in microfluidic-based tumor models with the success in simulating several drug delivery barriers. It also presents the progress in modeling various genetic and epigenetic factors involved in regulating the tumor microenvironment as a noticeable insight in 3D microfluidic tumor models for recognizing multidrug resistance and delivery mechanisms. Further correlation between the results obtained from microfluidic drug resistance tumor models and the clinical MDR data would open up avenues to gain insight into the performance of different multidrug delivery treatment strategies.

摘要

三维(3D)肿瘤微环境的复杂性和异质性给肿瘤研究和癌症治疗带来了挑战。肿瘤微环境中涉及的细胞的复杂功能和相互作用导致了各种多药耐药(MDR),并对癌症治疗提出了挑战。传统的肿瘤模型在模拟耐药机制方面的能力有限,不利于发现多药耐药和传递过程。用于制作 3D 组织模型的新技术显示出模拟 3D 肿瘤微环境和识别 MDR 相关机制的潜力。本文综述了肿瘤微环境中多药传递的主要障碍,并重点介绍了基于微流控的肿瘤模型在模拟多种药物传递障碍方面的进展。还介绍了在建模参与调节肿瘤微环境的各种遗传和表观遗传因素方面的进展,这是在用于识别多药耐药和传递机制的 3D 微流控肿瘤模型中值得注意的见解。微流控耐药肿瘤模型中获得的结果与临床 MDR 数据之间的进一步相关性将为深入了解不同多药传递治疗策略的性能开辟途径。

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