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Thymidine kinase 1 through the ages: a comprehensive review
Proliferation markers, such as proliferating cell nuclear antigen (PCNA), Ki-67, and thymidine kinase 1 (TK1), have potential as diagnostic tools and as prognostic factors in assessing cancer treatment and disease progression. TK1 is involved in cellular proliferation through the recovery of the nuc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694900/ https://www.ncbi.nlm.nih.gov/pubmed/33292474 http://dx.doi.org/10.1186/s13578-020-00493-1 |
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author | Bitter, Eliza E. Townsend, Michelle H. Erickson, Rachel Allen, Carolyn O’Neill, Kim L. |
author_facet | Bitter, Eliza E. Townsend, Michelle H. Erickson, Rachel Allen, Carolyn O’Neill, Kim L. |
author_sort | Bitter, Eliza E. |
collection | PubMed |
description | Proliferation markers, such as proliferating cell nuclear antigen (PCNA), Ki-67, and thymidine kinase 1 (TK1), have potential as diagnostic tools and as prognostic factors in assessing cancer treatment and disease progression. TK1 is involved in cellular proliferation through the recovery of the nucleotide thymidine in the DNA salvage pathway. TK1 upregulation has been found to be an early event in cancer development. In addition, serum levels of TK1 have been shown to be tied to cancer stage, so that higher levels of TK1 indicate a more serious prognosis. As a result of these findings and others, TK1 is not only a potentially viable biomarker for cancer recurrence, treatment monitoring, and survival, but is potentially more advantageous than current biomarkers. Compared to other proliferation markers, TK1 levels during S phase more accurately determine the rate of DNA synthesis in actively dividing tumors. Several reviews of TK1 elaborate on various assays that have been developed to measure levels in the serum of cancer patients in clinical settings. In this review, we include a brief history of important TK1 discoveries and findings, a comprehensive overview of TK1 regulation at DNA to protein levels, and recent findings that indicate TK1’s potential role in cancer pathogenesis and its growing potential as a tumor biomarker and therapeutic target. |
format | Online Article Text |
id | pubmed-7694900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76949002020-11-30 Thymidine kinase 1 through the ages: a comprehensive review Bitter, Eliza E. Townsend, Michelle H. Erickson, Rachel Allen, Carolyn O’Neill, Kim L. Cell Biosci Review Proliferation markers, such as proliferating cell nuclear antigen (PCNA), Ki-67, and thymidine kinase 1 (TK1), have potential as diagnostic tools and as prognostic factors in assessing cancer treatment and disease progression. TK1 is involved in cellular proliferation through the recovery of the nucleotide thymidine in the DNA salvage pathway. TK1 upregulation has been found to be an early event in cancer development. In addition, serum levels of TK1 have been shown to be tied to cancer stage, so that higher levels of TK1 indicate a more serious prognosis. As a result of these findings and others, TK1 is not only a potentially viable biomarker for cancer recurrence, treatment monitoring, and survival, but is potentially more advantageous than current biomarkers. Compared to other proliferation markers, TK1 levels during S phase more accurately determine the rate of DNA synthesis in actively dividing tumors. Several reviews of TK1 elaborate on various assays that have been developed to measure levels in the serum of cancer patients in clinical settings. In this review, we include a brief history of important TK1 discoveries and findings, a comprehensive overview of TK1 regulation at DNA to protein levels, and recent findings that indicate TK1’s potential role in cancer pathogenesis and its growing potential as a tumor biomarker and therapeutic target. BioMed Central 2020-11-27 /pmc/articles/PMC7694900/ /pubmed/33292474 http://dx.doi.org/10.1186/s13578-020-00493-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Bitter, Eliza E. Townsend, Michelle H. Erickson, Rachel Allen, Carolyn O’Neill, Kim L. Thymidine kinase 1 through the ages: a comprehensive review |
title | Thymidine kinase 1 through the ages: a comprehensive review |
title_full | Thymidine kinase 1 through the ages: a comprehensive review |
title_fullStr | Thymidine kinase 1 through the ages: a comprehensive review |
title_full_unstemmed | Thymidine kinase 1 through the ages: a comprehensive review |
title_short | Thymidine kinase 1 through the ages: a comprehensive review |
title_sort | thymidine kinase 1 through the ages: a comprehensive review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694900/ https://www.ncbi.nlm.nih.gov/pubmed/33292474 http://dx.doi.org/10.1186/s13578-020-00493-1 |
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