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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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.
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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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