lunes, 16 de octubre de 2017

Clinical Proteomics for Precision Medicine: The Bladder Cancer Case. - PubMed - NCBI

Clinical Proteomics for Precision Medicine: The Bladder Cancer Case. - PubMed - NCBI



 2017 Oct 5. doi: 10.1002/prca.201700074. [Epub ahead of print]

Clinical Proteomics for Precision Medicine: The Bladder Cancer Case.

Abstract

Precision medicine can improve patient management by guiding therapeutic decision based on molecular characteristics. The concept has been extensively addressed through the application of -omics based approaches. Proteomics attract high interest, as proteins reflect a "real-time" dynamic molecular phenotype. Focusing on proteomics applications for personalized medicine, a literature search was conducted to cover: a) disease prevention, b) monitoring/ prediction of treatment response, c) stratification to guide intervention and d) identification of drug targets. The review indicates the potential of proteomics for personalized medicine by also highlighting multiple challenges to be addressed prior to actual implementation. In oncology, particularly bladder cancer, application of precision medicine appears especially promising. The high heterogeneity and recurrence rates together with the limited treatment options, suggests that earlier and more efficient intervention, continuous monitoring and the development of alternative therapies could be accomplished by applying proteomics-guided personalized approaches. This notion is backed by studies presenting biomarkers that are of value in patient stratification and prognosis, and by recent studies demonstrating the identification of promising therapeutic targets. Herein, we aim to present an approach whereby combining the knowledge on biomarkers and therapeutic targets in bladder cancer could serve as basis towards proteomics- guided personalized patient management. This article is protected by copyright. All rights reserved.

KEYWORDS:

Biomarkers; Mass Spectrometry; Personalized Medicine; Proteomics; Urine

PMID:
 
28980455
 
DOI:
 
10.1002/prca.201700074

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