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蛋白质组学作为一种用于表征膀胱癌的补充技术。

Proteomics as a Complementary Technique to Characterize Bladder Cancer.

作者信息

López-Cortés Rubén, Vázquez-Estévez Sergio, Fernández Javier Álvarez, Núñez Cristina

机构信息

Research Unit, Hospital Universitario Lucus Augusti (HULA), Servizo Galego de Saúde (SERGAS), 27002 Lugo, Spain.

Oncology Division, Hospital Universitario Lucus Augusti (HULA), Servizo Galego de Saúde (SERGAS), 27002 Lugo, Spain.

出版信息

Cancers (Basel). 2021 Nov 4;13(21):5537. doi: 10.3390/cancers13215537.

DOI:10.3390/cancers13215537
PMID:34771699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8582709/
Abstract

Bladder cancer (BC) is the most common tumor of the urinary tract and is conventionally classified as either non-muscle invasive or muscle invasive. In addition, histological variants exist, as organized by the WHO-2016 classification. However, innovations in next-generation sequencing have led to molecular classifications of BC. These innovations have also allowed for the tracing of major tumorigenic pathways and, therefore, are positioned as strong supporters of precision medicine. In parallel, immunohistochemistry is still the clinical reference to discriminate histological layers and to stage BC. Key contributions have been made to enlarge the panel of protein immunomarkers. Moreover, the analysis of proteins in liquid biopsy has also provided potential markers. Notwithstanding, their clinical adoption is still low, with very few approved tests. In this context, mass spectrometry-based proteomics has remained a step behind; hence, we aimed to develop them in the community. Herein, the authors introduce the epidemiology and the conventional classifications to review the molecular classification of BC, highlighting the contributions of proteomics. Then, the advances in mass spectrometry techniques focusing on maintaining the integrity of the biological structures are presented, a milestone for the emergence of histoproteomics. Within this field, the review then discusses selected proteins for the comprehension of the pathophysiological mechanisms of BC. Finally, because there is still insufficient knowledge, this review considers proteomics as an important source for the development of BC therapies.

摘要

膀胱癌(BC)是泌尿系统最常见的肿瘤,传统上分为非肌层浸润性或肌层浸润性。此外,根据世界卫生组织2016年分类,还存在组织学变异。然而,下一代测序技术的创新导致了膀胱癌的分子分类。这些创新还使得追踪主要的致癌途径成为可能,因此,被视为精准医学的有力支持者。与此同时,免疫组织化学仍然是鉴别组织学层次和对膀胱癌进行分期的临床参考方法。在扩大蛋白质免疫标志物方面已经取得了关键进展。此外,液体活检中蛋白质的分析也提供了潜在的标志物。尽管如此,它们在临床上的应用仍然很低,获批的检测方法很少。在这种背景下,基于质谱的蛋白质组学一直落后一步;因此,我们旨在在该领域开展相关研究。在此,作者介绍了膀胱癌的流行病学和传统分类,以回顾其分子分类,突出蛋白质组学的贡献。然后,介绍了聚焦于维持生物结构完整性的质谱技术进展,这是组织蛋白质组学出现的一个里程碑。在这个领域内,该综述接着讨论了用于理解膀胱癌病理生理机制的特定蛋白质。最后,由于目前仍缺乏足够的知识,本综述将蛋白质组学视为膀胱癌治疗发展的重要来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/fc603da2eace/cancers-13-05537-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/6a3b89e620c2/cancers-13-05537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/3b7c74efa38e/cancers-13-05537-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/6818a5ad8e87/cancers-13-05537-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/c63a7bcbcb4b/cancers-13-05537-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/7a64374e6be1/cancers-13-05537-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/1803400e46fc/cancers-13-05537-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/ae50db6eb815/cancers-13-05537-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/e04b5cb7998f/cancers-13-05537-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/79d6108b8776/cancers-13-05537-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/fc603da2eace/cancers-13-05537-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/6a3b89e620c2/cancers-13-05537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/3b7c74efa38e/cancers-13-05537-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/6818a5ad8e87/cancers-13-05537-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/c63a7bcbcb4b/cancers-13-05537-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/7a64374e6be1/cancers-13-05537-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/1803400e46fc/cancers-13-05537-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/ae50db6eb815/cancers-13-05537-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/e04b5cb7998f/cancers-13-05537-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/79d6108b8776/cancers-13-05537-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8582709/fc603da2eace/cancers-13-05537-g010.jpg

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