Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?

Abstract The promise of precision and personalized medicine is rooted in accurate, highly sensitive, and specific disease biomarkers. This is particularly true for cancer-a disease characterized by marked tumor heterogeneity and diverse molecular signatures. Although thousands of biomarkers have bee...

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Main Authors: Grannum R. Sant, Kevin B. Knopf, David M. Albala
Format: Article
Language:English
Published: Nature Publishing Group 2017-06-01
Series:npj Precision Oncology
Online Access:https://doi.org/10.1038/s41698-017-0025-y
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spelling doaj-adb7c741220b4a5fbd1231712d4b99002021-04-02T16:21:20ZengNature Publishing Groupnpj Precision Oncology2397-768X2017-06-01111710.1038/s41698-017-0025-yLive-single-cell phenotypic cancer biomarkers-future role in precision oncology?Grannum R. Sant0Kevin B. Knopf1David M. Albala2Department of Urology, Tufts University School of MedicineCancer Commons, 35050 El Camino RealDepartment of Urology, Crouse HospitalAbstract The promise of precision and personalized medicine is rooted in accurate, highly sensitive, and specific disease biomarkers. This is particularly true for cancer-a disease characterized by marked tumor heterogeneity and diverse molecular signatures. Although thousands of biomarkers have been described, only a very small number have been successfully translated into clinical use. Undoubtedly, there is need for rapid, quantitative, and more cost effective biomarkers for tumor diagnosis and prognosis, to allow for better risk stratification and aid clinicians in making personalized treatment decisions. This is particularly true for cancers where specific biomarkers are either not available (e.g., renal cell carcinoma) or where current biomarkers tend to classify individuals into broad risk categories unable to accurately assess individual tumor aggressiveness and adverse pathology potential (e.g., prostate cancer), thereby leading to problems of over-diagnosis and over-treatment of indolent cancer and under-treatment of aggressive cancer. This perspective highlights an emerging class of cancer biomarkers-live-single-cell phenotypic biomarkers, as compared to genomic biomarkers, and their potential application for cancer diagnosis, risk-stratification, and prognosis.https://doi.org/10.1038/s41698-017-0025-y
collection DOAJ
language English
format Article
sources DOAJ
author Grannum R. Sant
Kevin B. Knopf
David M. Albala
spellingShingle Grannum R. Sant
Kevin B. Knopf
David M. Albala
Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
npj Precision Oncology
author_facet Grannum R. Sant
Kevin B. Knopf
David M. Albala
author_sort Grannum R. Sant
title Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
title_short Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
title_full Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
title_fullStr Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
title_full_unstemmed Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
title_sort live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
publisher Nature Publishing Group
series npj Precision Oncology
issn 2397-768X
publishDate 2017-06-01
description Abstract The promise of precision and personalized medicine is rooted in accurate, highly sensitive, and specific disease biomarkers. This is particularly true for cancer-a disease characterized by marked tumor heterogeneity and diverse molecular signatures. Although thousands of biomarkers have been described, only a very small number have been successfully translated into clinical use. Undoubtedly, there is need for rapid, quantitative, and more cost effective biomarkers for tumor diagnosis and prognosis, to allow for better risk stratification and aid clinicians in making personalized treatment decisions. This is particularly true for cancers where specific biomarkers are either not available (e.g., renal cell carcinoma) or where current biomarkers tend to classify individuals into broad risk categories unable to accurately assess individual tumor aggressiveness and adverse pathology potential (e.g., prostate cancer), thereby leading to problems of over-diagnosis and over-treatment of indolent cancer and under-treatment of aggressive cancer. This perspective highlights an emerging class of cancer biomarkers-live-single-cell phenotypic biomarkers, as compared to genomic biomarkers, and their potential application for cancer diagnosis, risk-stratification, and prognosis.
url https://doi.org/10.1038/s41698-017-0025-y
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