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Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas
The classical somatic mutation theory (SMT) of carcinogenesis and metastasis postulates that malignant transformation occurs in cells that accumulate a sufficient amount of mutations in the appropriate oncogenes and/or tumor suppressor genes. These mutations result in cell-autonomous activation of t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355145/ https://www.ncbi.nlm.nih.gov/pubmed/22615799 http://dx.doi.org/10.1371/journal.pone.0036719 |
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author | Rückert, Felix Grützmann, Robert Pilarsky, Christian |
author_facet | Rückert, Felix Grützmann, Robert Pilarsky, Christian |
author_sort | Rückert, Felix |
collection | PubMed |
description | The classical somatic mutation theory (SMT) of carcinogenesis and metastasis postulates that malignant transformation occurs in cells that accumulate a sufficient amount of mutations in the appropriate oncogenes and/or tumor suppressor genes. These mutations result in cell-autonomous activation of the mutated cell and a growth advantage relative to neighboring cells. However, the SMT cannot completely explain many characteristics of carcinomas. Contrary to the cell-centered view of the SMT with respect to carcinogenesis, recent research has revealed evidence that the tumor microenvironment plays a role in carcinogenesis as well. In this review, we present a new model that accommodates the role of the tumor microenvironment in carcinogenesis and complements the classical SMT. Our “feedback” model emphasizes the role of an altered spatiotemporal communication between epithelial and stromal cells during carcinogenesis: a dysfunctional intracellular signaling in tumorigenic epithelial cells leads to inappropriate cellular responses to stimuli from associated stromal or inflammatory cells. Thus, a positive feedback loop of the information flow between parenchymal and stromal cells results. This constant communication between the stromal cells and the tumor cells causes a perpetually activated state of tumor cells analogous to resonance disaster. |
format | Online Article Text |
id | pubmed-3355145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33551452012-05-21 Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas Rückert, Felix Grützmann, Robert Pilarsky, Christian PLoS One Research Article The classical somatic mutation theory (SMT) of carcinogenesis and metastasis postulates that malignant transformation occurs in cells that accumulate a sufficient amount of mutations in the appropriate oncogenes and/or tumor suppressor genes. These mutations result in cell-autonomous activation of the mutated cell and a growth advantage relative to neighboring cells. However, the SMT cannot completely explain many characteristics of carcinomas. Contrary to the cell-centered view of the SMT with respect to carcinogenesis, recent research has revealed evidence that the tumor microenvironment plays a role in carcinogenesis as well. In this review, we present a new model that accommodates the role of the tumor microenvironment in carcinogenesis and complements the classical SMT. Our “feedback” model emphasizes the role of an altered spatiotemporal communication between epithelial and stromal cells during carcinogenesis: a dysfunctional intracellular signaling in tumorigenic epithelial cells leads to inappropriate cellular responses to stimuli from associated stromal or inflammatory cells. Thus, a positive feedback loop of the information flow between parenchymal and stromal cells results. This constant communication between the stromal cells and the tumor cells causes a perpetually activated state of tumor cells analogous to resonance disaster. Public Library of Science 2012-05-17 /pmc/articles/PMC3355145/ /pubmed/22615799 http://dx.doi.org/10.1371/journal.pone.0036719 Text en Rückert et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rückert, Felix Grützmann, Robert Pilarsky, Christian Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title | Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title_full | Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title_fullStr | Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title_full_unstemmed | Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title_short | Feedback within the Inter-Cellular Communication and Tumorigenesis in Carcinomas |
title_sort | feedback within the inter-cellular communication and tumorigenesis in carcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3355145/ https://www.ncbi.nlm.nih.gov/pubmed/22615799 http://dx.doi.org/10.1371/journal.pone.0036719 |
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