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小细胞外囊泡在癌症中不断演变的转化潜力。

The evolving translational potential of small extracellular vesicles in cancer.

机构信息

Tumour Microenvironment Laboratory, QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.

Centre for Personalized Nanomedicine, Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, Australia.

出版信息

Nat Rev Cancer. 2020 Dec;20(12):697-709. doi: 10.1038/s41568-020-00299-w. Epub 2020 Sep 21.

Abstract

Cancer-derived extracellular vesicles (EVs) are regarded as having promising potential to be used as therapeutics and disease biomarkers. Mechanistically, EVs have been shown to function in most, if not all, steps of cancer progression. Cancer EVs, including small EVs (sEVs), contain unique biomolecular cargo, consisting of protein, nucleic acid and lipids. Through progress in the identification of this specific cargo, cancer biomarkers have been identified and developed, opening up novel and interesting opportunities for cancer diagnosis and prognosis. Intriguingly, we still lack a comprehensive understanding of the cancer-specific pathways that govern EV biogenesis in cancer cells. Filling this knowledge gap will rapidly improve cancer EV biomarkers, as it will also allow discrimination of the procancer and anticancer actions of those EVs. Even more promising is uncovering therapeutically targetable, tumour-specific EV pathways and content, which will generate novel classes of cancer therapies. This Review highlights the progress the cancer sEV field has made in the areas of biomarker discovery and validation as well as sEV-based therapeutics, highlights the challenges we are facing and identifies gaps in our knowledge, which currently prevent us from developing the full potential of sEVs in cancer diagnostic and therapy.

摘要

癌症来源的细胞外囊泡 (EVs) 被认为具有很大的潜力,可作为治疗方法和疾病生物标志物。从机制上讲,EVs 已被证明在癌症进展的大多数(如果不是全部)步骤中发挥作用。癌症 EVs,包括小 EVs (sEVs),含有独特的生物分子货物,由蛋白质、核酸和脂质组成。通过对这种特定货物的鉴定取得进展,癌症生物标志物得以鉴定和开发,为癌症诊断和预后开辟了新的有趣机会。有趣的是,我们仍然缺乏对控制癌细胞中 EV 生物发生的癌症特异性途径的全面了解。填补这一知识空白将迅速提高癌症 EV 生物标志物的水平,因为它还将允许区分那些 EV 的致癌和抗癌作用。更有前途的是揭示治疗靶点的、肿瘤特异性的 EV 途径和内容,这将产生新的癌症治疗类别。这篇综述强调了癌症 sEV 领域在生物标志物发现和验证以及基于 sEV 的治疗方面取得的进展,强调了我们面临的挑战,并确定了我们知识中的差距,这些差距目前阻碍了我们充分发挥 sEV 在癌症诊断和治疗中的潜力。

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