Nucleic acid-based tissue biomarkers of urologic malignancies

生物 膀胱癌 生物标志物 表观遗传学 癌变 前列腺癌 癌症生物标志物 表观遗传学 生物标志物发现 DNA甲基化 疾病 生物信息学 癌症 计算生物学 医学 遗传学 病理 基因表达 基因 蛋白质组学
作者
Dimo Dietrich,Sebastian Meller,Barbara Uhl,Bernhard Ralla,Carsten Stephan,Klaus Jung,Jörg Ellinger,Glen Kristiansen
出处
期刊:Critical Reviews in Clinical Laboratory Sciences [Taylor & Francis]
卷期号:51 (4): 173-199 被引量:41
标识
DOI:10.3109/10408363.2014.906130
摘要

Molecular biomarkers play an important role in the clinical management of cancer patients. Biomarkers allow estimation of the risk of developing cancer; help to diagnose a tumor, ideally at an early stage when cure is still possible; and aid in monitoring disease progression. Furthermore, they hold the potential to predict the outcome of the disease (prognostic biomarkers) and the response to therapy (predictive biomarkers). Altogether, biomarkers will help to avoid tumor-related deaths and reduce overtreatment, and will contribute to increased survival and quality of life in cancer patients due to personalized treatments. It is well established that the process of carcinogenesis is a complex interplay between genomic predisposition, acquired somatic mutations, epigenetic changes and genomic aberrations. Within this complex interplay, nucleic acids, i.e. RNA and DNA, play a fundamental role and therefore represent ideal candidates for biomarkers. They are particularly promising candidates because sequence-specific hybridization and amplification technologies allow highly accurate and sensitive assessment of these biomarker levels over a broad dynamic range. This article provides an overview of nucleic acid-based biomarkers in tissues for the management of urologic malignancies, i.e. tumors of the prostate, testis, kidney, penis, urinary bladder, renal pelvis, ureter and other urinary organs. Special emphasis is put on genomic, transcriptomic and epigenomic biomarkers (SNPs, mutations [genomic and mitochondrial], microsatellite instabilities, viral and bacterial DNA, DNA methylation and hydroxymethylation, mRNA expression, and non-coding RNAs [lncRNA, miRNA, siRNA, piRNA, snRNA, snoRNA]). Due to the multitude of published biomarker candidates, special focus is given to the general applicability of different molecular classes as biomarkers and some particularly promising nucleic acid biomarkers. Furthermore, specific challenges regarding the development and clinical implementation of nucleic acid-based biomarkers are discussed.
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