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Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty
Cancer ranks as one of the deadliest diseases worldwide. The high mortality rate associated with cancer is partially due to the lack of reliable early detection methods and/or inaccurate diagnostic tools such as certain protein biomarkers. Cell-free nucleic acids (cfNA) such as circulating long nonc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213432/ https://www.ncbi.nlm.nih.gov/pubmed/35729321 http://dx.doi.org/10.1038/s41698-022-00283-7 |
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author | Badowski, Cedric He, Bing Garmire, Lana X. |
author_facet | Badowski, Cedric He, Bing Garmire, Lana X. |
author_sort | Badowski, Cedric |
collection | PubMed |
description | Cancer ranks as one of the deadliest diseases worldwide. The high mortality rate associated with cancer is partially due to the lack of reliable early detection methods and/or inaccurate diagnostic tools such as certain protein biomarkers. Cell-free nucleic acids (cfNA) such as circulating long noncoding RNAs (lncRNAs) have been proposed as a new class of potential biomarkers for cancer diagnosis. The reported correlation between the presence of tumors and abnormal levels of lncRNAs in the blood of cancer patients has notably triggered a worldwide interest among clinicians and oncologists who have been actively investigating their potentials as reliable cancer biomarkers. In this report, we review the progress achieved (“the Good”) and challenges encountered (“the Bad”) in the development of circulating lncRNAs as potential biomarkers for early cancer diagnosis. We report and discuss the diagnostic performance of more than 50 different circulating lncRNAs and emphasize their numerous potential clinical applications (“the Beauty”) including therapeutic targets and agents, on top of diagnostic and prognostic capabilities. This review also summarizes the best methods of investigation and provides useful guidelines for clinicians and scientists who desire conducting their own clinical studies on circulating lncRNAs in cancer patients via RT-qPCR or Next Generation Sequencing (NGS). |
format | Online Article Text |
id | pubmed-9213432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92134322022-06-23 Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty Badowski, Cedric He, Bing Garmire, Lana X. NPJ Precis Oncol Review Article Cancer ranks as one of the deadliest diseases worldwide. The high mortality rate associated with cancer is partially due to the lack of reliable early detection methods and/or inaccurate diagnostic tools such as certain protein biomarkers. Cell-free nucleic acids (cfNA) such as circulating long noncoding RNAs (lncRNAs) have been proposed as a new class of potential biomarkers for cancer diagnosis. The reported correlation between the presence of tumors and abnormal levels of lncRNAs in the blood of cancer patients has notably triggered a worldwide interest among clinicians and oncologists who have been actively investigating their potentials as reliable cancer biomarkers. In this report, we review the progress achieved (“the Good”) and challenges encountered (“the Bad”) in the development of circulating lncRNAs as potential biomarkers for early cancer diagnosis. We report and discuss the diagnostic performance of more than 50 different circulating lncRNAs and emphasize their numerous potential clinical applications (“the Beauty”) including therapeutic targets and agents, on top of diagnostic and prognostic capabilities. This review also summarizes the best methods of investigation and provides useful guidelines for clinicians and scientists who desire conducting their own clinical studies on circulating lncRNAs in cancer patients via RT-qPCR or Next Generation Sequencing (NGS). Nature Publishing Group UK 2022-06-21 /pmc/articles/PMC9213432/ /pubmed/35729321 http://dx.doi.org/10.1038/s41698-022-00283-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Badowski, Cedric He, Bing Garmire, Lana X. Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title | Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title_full | Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title_fullStr | Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title_full_unstemmed | Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title_short | Blood-derived lncRNAs as biomarkers for cancer diagnosis: the Good, the Bad and the Beauty |
title_sort | blood-derived lncrnas as biomarkers for cancer diagnosis: the good, the bad and the beauty |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213432/ https://www.ncbi.nlm.nih.gov/pubmed/35729321 http://dx.doi.org/10.1038/s41698-022-00283-7 |
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