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合成生物标志物:二十一世纪早期癌症检测的新途径。

Synthetic biomarkers: a twenty-first century path to early cancer detection.

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory School of Medicine, Atlanta, GA, USA.

Parker H. Petit Institute of Bioengineering and Bioscience, Atlanta, GA, USA.

出版信息

Nat Rev Cancer. 2021 Oct;21(10):655-668. doi: 10.1038/s41568-021-00389-3. Epub 2021 Sep 6.

Abstract

Detection of cancer at an early stage when it is still localized improves patient response to medical interventions for most cancer types. The success of screening tools such as cervical cytology to reduce mortality has spurred significant interest in new methods for early detection (for example, using non-invasive blood-based or biofluid-based biomarkers). Yet biomarkers shed from early lesions are limited by fundamental biological and mass transport barriers - such as short circulation times and blood dilution - that limit early detection. To address this issue, synthetic biomarkers are being developed. These represent an emerging class of diagnostics that deploy bioengineered sensors inside the body to query early-stage tumours and amplify disease signals to levels that could potentially exceed those of shed biomarkers. These strategies leverage design principles and advances from chemistry, synthetic biology and cell engineering. In this Review, we discuss the rationale for development of biofluid-based synthetic biomarkers. We examine how these strategies harness dysregulated features of tumours to amplify detection signals, use tumour-selective activation to increase specificity and leverage natural processing of bodily fluids (for example, blood, urine and proximal fluids) for easy detection. Finally, we highlight the challenges that exist for preclinical development and clinical translation of synthetic biomarker diagnostics.

摘要

早期发现局部癌症可以提高患者对大多数癌症类型的医疗干预的反应。宫颈细胞学等筛查工具在降低死亡率方面的成功,激发了人们对新的早期检测方法(例如,使用非侵入性基于血液或生物流体的生物标志物)的极大兴趣。然而,早期病变释放的生物标志物受到基本的生物学和质量传输障碍的限制,例如循环时间短和血液稀释,这限制了早期检测。为了解决这个问题,正在开发合成生物标志物。这些标志物代表了一类新兴的诊断方法,它们在体内部署生物工程传感器来询问早期肿瘤,并放大疾病信号,使其潜在水平超过释放的生物标志物。这些策略利用了化学、合成生物学和细胞工程的设计原则和进展。在这篇综述中,我们讨论了开发基于生物流体的合成生物标志物的基本原理。我们研究了这些策略如何利用肿瘤失调的特征来放大检测信号,利用肿瘤选择性激活来提高特异性,并利用身体流体(例如血液、尿液和近端流体)的自然处理来进行轻松检测。最后,我们强调了合成生物标志物诊断在临床前开发和临床转化方面存在的挑战。

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