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针对结直肠癌细胞(CRC)转移、免疫反应和耐药性的特定小干扰 RNA(siRNA)。

Specific small interfering RNAs (siRNAs) for targeting the metastasis, immune responses, and drug resistance of colorectal cancer cells (CRC).

机构信息

Manipur International University, Imphal, Manipur, India.

Thunderbird School of Global Management, Arizona State University Tempe Campus, Phoenix, Arizona 85004, USA.

出版信息

Int Immunopharmacol. 2024 Oct 25;140:112730. doi: 10.1016/j.intimp.2024.112730. Epub 2024 Jul 30.

Abstract

Colorectal cancer (CRC) involves various genetic alterations, with liver metastasis posing a significant clinical challenge. Furthermore, CRC cells mostly show an increase in resistance to traditional treatments like chemotherapy. It is essential to investigate more advanced and effective therapies to prevent medication resistance and metastases and extend patient life. As a result, it is anticipated that small interfering RNAs (siRNAs) would be exceptional instruments that can control gene expression by RNA interference (RNAi). In eukaryotes, RNAi is a biological mechanism that destroys specific messenger RNA (mRNA) molecules, thereby inhibiting gene expression. In the management of CRC, this method of treatment represents a potential therapeutic agent. However, it is important to acknowledge that siRNA therapies have significant issues, such as low serum stability and nonspecific absorption into biological systems. Delivery mechanisms are thus being created to address these issues. In the current work, we address the potential benefits of siRNA therapy and outline the difficulties in treating CRCby focusing on the primary signaling pathways linked to metastasis as well as genes implicated in the multi-drug resistance (MDR) process.

摘要

结直肠癌(CRC)涉及多种遗传改变,肝转移是一个重大的临床挑战。此外,CRC 细胞对化疗等传统治疗方法的耐药性大多增加。有必要研究更先进和有效的治疗方法,以防止耐药性和转移,延长患者生命。因此,人们预计小干扰 RNA(siRNA)将是一种特殊的工具,可以通过 RNA 干扰(RNAi)控制基因表达。在真核生物中,RNAi 是一种破坏特定信使 RNA(mRNA)分子的生物机制,从而抑制基因表达。在 CRC 的治疗中,这种治疗方法代表了一种潜在的治疗剂。然而,需要认识到,siRNA 治疗存在一些重大问题,如血清稳定性低和非特异性吸收到生物系统中。因此,正在创建传递机制来解决这些问题。在当前的工作中,我们关注与转移相关的主要信号通路以及多药耐药(MDR)过程中涉及的基因,探讨了 siRNA 治疗的潜在益处,并概述了治疗 CRC 所面临的困难。

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