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A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells
BACKGROUND: Biomarkers allowing the characterization of malignancy and therapy response of oral squamous cell carcinomas (OSCC) or other types of carcinomas are still outstanding. The biochemical suicide molecule endonuclease DNaseX (DNaseI-like 1) has been used to identify the Apo10 protein epitope...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235042/ https://www.ncbi.nlm.nih.gov/pubmed/24304513 http://dx.doi.org/10.1186/1471-2407-13-569 |
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author | Grimm, Martin Schmitt, Steffen Teriete, Peter Biegner, Thorsten Stenzl, Arnulf Hennenlotter, Jörg Muhs, Hans-Joachim Munz, Adelheid Nadtotschi, Tatjana König, Klemens Sänger, Jörg Feyen, Oliver Hofmann, Heiko Reinert, Siegmar Coy, Johannes F |
author_facet | Grimm, Martin Schmitt, Steffen Teriete, Peter Biegner, Thorsten Stenzl, Arnulf Hennenlotter, Jörg Muhs, Hans-Joachim Munz, Adelheid Nadtotschi, Tatjana König, Klemens Sänger, Jörg Feyen, Oliver Hofmann, Heiko Reinert, Siegmar Coy, Johannes F |
author_sort | Grimm, Martin |
collection | PubMed |
description | BACKGROUND: Biomarkers allowing the characterization of malignancy and therapy response of oral squamous cell carcinomas (OSCC) or other types of carcinomas are still outstanding. The biochemical suicide molecule endonuclease DNaseX (DNaseI-like 1) has been used to identify the Apo10 protein epitope that marks tumor cells with abnormal apoptosis and proliferation. The transketolase-like protein 1 (TKTL1) represents the enzymatic basis for an anaerobic glucose metabolism even in the presence of oxygen (aerobic glycolysis/Warburg effect), which is concomitant with a more malignant phenotype due to invasive growth/metastasis and resistance to radical and apoptosis inducing therapies. METHODS: Expression of Apo10 and TKTL1 was analysed retrospectively in OSCC specimen (n = 161) by immunohistochemistry. Both markers represent independent markers for poor survival. Furthermore Apo10 and TKTL1 have been used prospectively for epitope detection in monocytes (EDIM)-blood test in patients with OSCC (n = 50), breast cancer (n = 48), prostate cancer (n = 115), and blood donors/controls (n = 74). RESULTS: Positive Apo10 and TKTL1 expression were associated with recurrence of the tumor. Multivariate analysis demonstrated Apo10 and TKTL1 expression as an independent prognostic factor for reduced tumor-specific survival. Apo10+/TKTL1+ subgroup showed the worst disease-free survival rate in OSCC. EDIM-Apo10 and EDIM-TKTL1 blood tests allowed a sensitive and specific detection of patients with OSCC, breast cancer and prostate cancer before surgery and in after care. A combined score of Apo10+/TKTL1+ led to a sensitivity of 95.8% and a specificity of 97.3% for the detection of carcinomas independent of the tumor entity. CONCLUSIONS: The combined detection of two independent fundamental biophysical processes by the two biomarkers Apo10 and TKTL1 allows a sensitive and specific detection of neoplasia in a noninvasive and cost-effective way. Further prospective trials are warranted to validate this new concept for the diagnosis of neoplasia and tumor recurrence. |
format | Online Article Text |
id | pubmed-4235042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42350422014-11-19 A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells Grimm, Martin Schmitt, Steffen Teriete, Peter Biegner, Thorsten Stenzl, Arnulf Hennenlotter, Jörg Muhs, Hans-Joachim Munz, Adelheid Nadtotschi, Tatjana König, Klemens Sänger, Jörg Feyen, Oliver Hofmann, Heiko Reinert, Siegmar Coy, Johannes F BMC Cancer Research Article BACKGROUND: Biomarkers allowing the characterization of malignancy and therapy response of oral squamous cell carcinomas (OSCC) or other types of carcinomas are still outstanding. The biochemical suicide molecule endonuclease DNaseX (DNaseI-like 1) has been used to identify the Apo10 protein epitope that marks tumor cells with abnormal apoptosis and proliferation. The transketolase-like protein 1 (TKTL1) represents the enzymatic basis for an anaerobic glucose metabolism even in the presence of oxygen (aerobic glycolysis/Warburg effect), which is concomitant with a more malignant phenotype due to invasive growth/metastasis and resistance to radical and apoptosis inducing therapies. METHODS: Expression of Apo10 and TKTL1 was analysed retrospectively in OSCC specimen (n = 161) by immunohistochemistry. Both markers represent independent markers for poor survival. Furthermore Apo10 and TKTL1 have been used prospectively for epitope detection in monocytes (EDIM)-blood test in patients with OSCC (n = 50), breast cancer (n = 48), prostate cancer (n = 115), and blood donors/controls (n = 74). RESULTS: Positive Apo10 and TKTL1 expression were associated with recurrence of the tumor. Multivariate analysis demonstrated Apo10 and TKTL1 expression as an independent prognostic factor for reduced tumor-specific survival. Apo10+/TKTL1+ subgroup showed the worst disease-free survival rate in OSCC. EDIM-Apo10 and EDIM-TKTL1 blood tests allowed a sensitive and specific detection of patients with OSCC, breast cancer and prostate cancer before surgery and in after care. A combined score of Apo10+/TKTL1+ led to a sensitivity of 95.8% and a specificity of 97.3% for the detection of carcinomas independent of the tumor entity. CONCLUSIONS: The combined detection of two independent fundamental biophysical processes by the two biomarkers Apo10 and TKTL1 allows a sensitive and specific detection of neoplasia in a noninvasive and cost-effective way. Further prospective trials are warranted to validate this new concept for the diagnosis of neoplasia and tumor recurrence. BioMed Central 2013-12-04 /pmc/articles/PMC4235042/ /pubmed/24304513 http://dx.doi.org/10.1186/1471-2407-13-569 Text en Copyright © 2013 Grimm et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Grimm, Martin Schmitt, Steffen Teriete, Peter Biegner, Thorsten Stenzl, Arnulf Hennenlotter, Jörg Muhs, Hans-Joachim Munz, Adelheid Nadtotschi, Tatjana König, Klemens Sänger, Jörg Feyen, Oliver Hofmann, Heiko Reinert, Siegmar Coy, Johannes F A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title | A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title_full | A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title_fullStr | A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title_full_unstemmed | A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title_short | A biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
title_sort | biomarker based detection and characterization of carcinomas exploiting two fundamental biophysical mechanisms in mammalian cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235042/ https://www.ncbi.nlm.nih.gov/pubmed/24304513 http://dx.doi.org/10.1186/1471-2407-13-569 |
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