Genomic profiling in oncology clinical practice

被引:0
作者
N. Rodríguez
D. Viñal
J. Rodríguez-Cobos
J. De Castro
G. Domínguez
机构
[1] Catedra UAM-Medicina de Innovación,Department of Medical Oncology, Hospital Universitario La Paz
[2] Hospital Universitario La Paz,Department of Medical Oncology
[3] Instituto de Investigaciones Biomedicas “Alberto Sols”,Departamento de Bioquimica
[4] CSIC-UAM,undefined
来源
Clinical and Translational Oncology | 2020年 / 22卷
关键词
Genomic profiling; Next-generation sequencing; Sanger sequencing; Liquid biopsy; Hereditary cancer syndromes;
D O I
暂无
中图分类号
学科分类号
摘要
The development of high-throughput technologies such as next-generation sequencing for DNA sequencing together with the decrease in their cost has led to the progressive introduction of genomic profiling in our daily practice in oncology. Nowadays, genomic profiling is part of genetic counseling, cancer diagnosis, molecular characterization, and as a biomarker of prognosis and response to treatment. Furthermore, germline or somatic genomic characterization of the tumor may provide new treatment opportunities for patients with cancer. In this review, we will summarize the clinical applications and limitations of genomic profiling in oncology clinical practice, focusing on next-generation sequencing.
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页码:1430 / 1439
页数:9
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[1]  
Hartmaier RJ(2017)High-throughput genomic profiling of adult solid tumors reveals novel insights into cancer pathogenesis Cancer Res. 77 2464-2475
[2]  
Albacker LA(2017)Clinical applications of next-generation sequencing in cancer diagnosis Pathol Oncol Res. 23 225-234
[3]  
Chmielecki J(2012)Key principles and clinical applications of "next-generation" DNA sequencing Cancer Prev Res (Phila) 5 887-71035
[4]  
Sabour L(2019)Next generation sequencing and genetic alterations in squamous cell lung carcinoma: where are we today? Front Oncol. 9 166-4626
[5]  
Sabour M(2016)Cell-free DNA and next-generation sequencing in the service of personalized medicine for lung cancer Oncotarget. 7 71013-1291
[6]  
Ghorbian S(2008)Advantages and limitations of nextgeneration sequencing technologies: a comparison of electrophoresis and non-electrophoresis methods Electrophoresis 29 4618-3667
[7]  
Rizzo JM(2015)Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Nat Genet 47 717-366
[8]  
Buck MJ(2008)Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Hum Mutat. 29 1282-12633
[9]  
Friedlaender A(2011)Exome sequencing as a tool for Mendelian disease gene discovery Nat Rev Genet 12 745-39
[10]  
Banna G(2018)Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer Med Clin. 151 80-1487