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Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis

Classic tumor therapy, consisting of cytotoxic agents and/or targeted therapy, has not overcome therapeutic limitations like poor risk genetic parameters, genetic heterogeneity at different metastatic sites or the problem of undruggable targets. Here we summarize data and trials principally followin...

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Autores principales: Heudobler, Daniel, Rechenmacher, Michael, Lüke, Florian, Vogelhuber, Martin, Klobuch, Sebastian, Thomas, Simone, Pukrop, Tobias, Hackl, Christina, Herr, Wolfgang, Ghibelli, Lina, Gerner, Christopher, Reichle, Albrecht
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279883/
https://www.ncbi.nlm.nih.gov/pubmed/30546308
http://dx.doi.org/10.3389/fphar.2018.01357
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author Heudobler, Daniel
Rechenmacher, Michael
Lüke, Florian
Vogelhuber, Martin
Klobuch, Sebastian
Thomas, Simone
Pukrop, Tobias
Hackl, Christina
Herr, Wolfgang
Ghibelli, Lina
Gerner, Christopher
Reichle, Albrecht
author_facet Heudobler, Daniel
Rechenmacher, Michael
Lüke, Florian
Vogelhuber, Martin
Klobuch, Sebastian
Thomas, Simone
Pukrop, Tobias
Hackl, Christina
Herr, Wolfgang
Ghibelli, Lina
Gerner, Christopher
Reichle, Albrecht
author_sort Heudobler, Daniel
collection PubMed
description Classic tumor therapy, consisting of cytotoxic agents and/or targeted therapy, has not overcome therapeutic limitations like poor risk genetic parameters, genetic heterogeneity at different metastatic sites or the problem of undruggable targets. Here we summarize data and trials principally following a completely different treatment concept tackling systems biologic processes: the principle of communicative reprogramming of tumor tissues, i.e., anakoinosis (ancient greek for communication), aims at establishing novel communicative behavior of tumor tissue, the hosting organ and organism via re-modeling gene expression, thus recovering differentiation, and apoptosis competence leading to cancer control – in contrast to an immediate, “poisoning” with maximal tolerable doses of targeted or cytotoxic therapies. Therefore, we introduce the term “Master modulators” for drugs or drug combinations promoting evolutionary processes or regulating homeostatic pathways. These “master modulators” comprise a broad diversity of drugs, characterized by the capacity for reprogramming tumor tissues, i.e., transcriptional modulators, metronomic low-dose chemotherapy, epigenetically modifying agents, protein binding pro-anakoinotic drugs, such as COX-2 inhibitors, IMiDs etc., or for example differentiation inducing therapies. Data on 97 anakoinosis inducing schedules indicate a favorable toxicity profile: The combined administration of master modulators, frequently (with poor or no monoactivity) may even induce continuous complete remission in refractory metastatic neoplasia, irrespectively of the tumor type. That means recessive components of the tumor, successively developing during tumor ontogenesis, are accessible by regulatory active drug combinations in a therapeutically meaningful way. Drug selection is now dependent on situative systems characteristics, to less extent histology dependent. To sum up, anakoinosis represents a new substantive therapy principle besides novel targeted therapies.
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spelling pubmed-62798832018-12-13 Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis Heudobler, Daniel Rechenmacher, Michael Lüke, Florian Vogelhuber, Martin Klobuch, Sebastian Thomas, Simone Pukrop, Tobias Hackl, Christina Herr, Wolfgang Ghibelli, Lina Gerner, Christopher Reichle, Albrecht Front Pharmacol Pharmacology Classic tumor therapy, consisting of cytotoxic agents and/or targeted therapy, has not overcome therapeutic limitations like poor risk genetic parameters, genetic heterogeneity at different metastatic sites or the problem of undruggable targets. Here we summarize data and trials principally following a completely different treatment concept tackling systems biologic processes: the principle of communicative reprogramming of tumor tissues, i.e., anakoinosis (ancient greek for communication), aims at establishing novel communicative behavior of tumor tissue, the hosting organ and organism via re-modeling gene expression, thus recovering differentiation, and apoptosis competence leading to cancer control – in contrast to an immediate, “poisoning” with maximal tolerable doses of targeted or cytotoxic therapies. Therefore, we introduce the term “Master modulators” for drugs or drug combinations promoting evolutionary processes or regulating homeostatic pathways. These “master modulators” comprise a broad diversity of drugs, characterized by the capacity for reprogramming tumor tissues, i.e., transcriptional modulators, metronomic low-dose chemotherapy, epigenetically modifying agents, protein binding pro-anakoinotic drugs, such as COX-2 inhibitors, IMiDs etc., or for example differentiation inducing therapies. Data on 97 anakoinosis inducing schedules indicate a favorable toxicity profile: The combined administration of master modulators, frequently (with poor or no monoactivity) may even induce continuous complete remission in refractory metastatic neoplasia, irrespectively of the tumor type. That means recessive components of the tumor, successively developing during tumor ontogenesis, are accessible by regulatory active drug combinations in a therapeutically meaningful way. Drug selection is now dependent on situative systems characteristics, to less extent histology dependent. To sum up, anakoinosis represents a new substantive therapy principle besides novel targeted therapies. Frontiers Media S.A. 2018-11-28 /pmc/articles/PMC6279883/ /pubmed/30546308 http://dx.doi.org/10.3389/fphar.2018.01357 Text en Copyright © 2018 Heudobler, Rechenmacher, Lüke, Vogelhuber, Klobuch, Thomas, Pukrop, Hackl, Herr, Ghibelli, Gerner and Reichle. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Heudobler, Daniel
Rechenmacher, Michael
Lüke, Florian
Vogelhuber, Martin
Klobuch, Sebastian
Thomas, Simone
Pukrop, Tobias
Hackl, Christina
Herr, Wolfgang
Ghibelli, Lina
Gerner, Christopher
Reichle, Albrecht
Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title_full Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title_fullStr Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title_full_unstemmed Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title_short Clinical Efficacy of a Novel Therapeutic Principle, Anakoinosis
title_sort clinical efficacy of a novel therapeutic principle, anakoinosis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279883/
https://www.ncbi.nlm.nih.gov/pubmed/30546308
http://dx.doi.org/10.3389/fphar.2018.01357
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