揭开细胞外囊泡的秘密:在转移、抗药性和免疫逃避中协调肿瘤微环境动态

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.7150/jca.98426
Rashid Mir, Sadaf Khursheed Baba, Imadeldin Elfaki, Naseh Algehainy, Mohammad A Alanazi, Faisal H Altemani, Faris Jamal Tayeb, Jameel Barnawi, Eram Husain, Ruqaiah I Bedaiwi, Ibrahim Altedlawi Albalawi, Muhanad Alhujaily, Mohammad Muzaffar Mir, Reema Almotairi, Hanan E Alatwi, Aziz Dhaher Albalawi
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引用次数: 0

摘要

人们越来越认识到,细胞外载体(EVs)是肿瘤微环境(TME)错综复杂的重要组成部分。本手稿广泛探讨了EVs在塑造肿瘤微环境中发挥的多方面作用,特别强调了EVs在转移、耐药性和免疫逃避中的参与。转移是癌细胞向远处扩散的过程,它仍然是癌症治疗中的一个巨大挑战。EVs(包括外泌体和微囊泡)已成为这一系列事件的重要参与者。它们有助于上皮细胞向间质转化(EMT),促进转移前生态位的建立,并增强癌细胞的侵袭潜力。本手稿深入探讨了支撑这些过程的错综复杂的分子机制,强调了靶向EVs阻碍转移的治疗潜力。耐药性是成功治疗癌症的长期障碍。EVs在内在和获得性耐药性中起着重要作用,是细胞间通信的媒介。它们携带的分子,如 miRNA 和蛋白质,使传统化疗和靶向疗法产生耐药性。这篇手稿仔细研究了EV在传播耐药性方面所采用的各种策略,同时还考虑了以EV为基础的药物递送系统来对抗这一现象的创新方法。免疫逃避是癌症的一大特征,而EV是形成TME免疫抑制环境的核心。肿瘤衍生的EV通过各种机制挫败免疫反应,包括诱导T细胞功能紊乱、扩增调节性T细胞(Tregs)以及将巨噬细胞极化为免疫抑制表型。此外,手稿还探讨了EVs作为生物标记物的诊断潜力及其在免疫检查点阻断疗法中作为治疗剂的作用。本手稿全面概述了 EV 在介导 TME 内错综复杂的相互作用中的关键作用,最终影响癌症的进展和治疗效果。深刻理解EV介导的转移、耐药性和免疫逃避过程,为开发创新治疗策略和确定有价值的生物标记物开辟了一条大有可为的途径,从而不断与癌症作斗争。
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Unlocking the Secrets of Extracellular Vesicles: Orchestrating Tumor Microenvironment Dynamics in Metastasis, Drug Resistance, and Immune Evasion.

Extracellular vehicles (EVs) are gaining increasing recognition as central contributors to the intricate landscape of the tumor microenvironment (TME). This manuscript provides an extensive examination of the multifaceted roles played by EVs in shaping the TME, with a particular emphasis on their involvement in metastasis, drug resistance, and immune evasion. Metastasis, the process by which cancer cells disseminate to distant sites, remains a formidable challenge in cancer management. EVs, encompassing exosomes and microvesicles, have emerged as critical participants in this cascade of events. They facilitate the epithelial-to-mesenchymal transition (EMT), foster pre-metastatic niche establishment, and enhance the invasive potential of cancer cells. This manuscript delves into the intricate molecular mechanisms underpinning these processes, underscoring the therapeutic potential of targeting EVs to impede metastasis. Drug resistance represents a persistent impediment to successful cancer treatment. EVs are instrumental in intrinsic and acquired drug resistance, acting as mediators of intercellular communication. They ferry molecules like miRNAs and proteins, which confer resistance to conventional chemotherapy and targeted therapies. This manuscript scrutinizes the diverse strategies employed by EVs in propagating drug resistance while also considering innovative approaches involving EV-based drug delivery systems to counteract this phenomenon. Immune evasion is a hallmark of cancer, and EVs are central in sculpting the immunosuppressive milieu of the TME. Tumor-derived EVs thwart immune responses through various mechanisms, including T cell dysfunction induction, the expansion of regulatory T cells (Tregs), and polarization of macrophages towards an immunosuppressive phenotype. In addition, the manuscript explores the diagnostic potential of EVs as biomarkers and their role as therapeutic agents in immune checkpoint blockade therapies. This manuscript provides a comprehensive overview of EV's pivotal role in mediating intricate interactions within the TME, ultimately influencing cancer progression and therapeutic outcomes. A profound understanding of EV-mediated processes in metastasis, drug resistance, and immune evasion opens up promising avenues for developing innovative therapeutic strategies and identifying valuable biomarkers in the ongoing battle against cancer.

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