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Glioma in Schizophrenia: Is the Risk Higher or Lower?
Whether persons with schizophrenia have a higher or lower incidence of cancer has been discussed for a long time. Due to the complex mechanisms and characteristics of different types of cancer, it is difficult to evaluate the exact relationship between cancers and schizophrenia without considering t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129591/ https://www.ncbi.nlm.nih.gov/pubmed/30233327 http://dx.doi.org/10.3389/fncel.2018.00289 |
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author | Gao, Xingchun Mi, Yajing Guo, Na Xu, Hao Jiang, Pengtao Zhang, Ruisan Xu, Lixian Gou, Xingchun |
author_facet | Gao, Xingchun Mi, Yajing Guo, Na Xu, Hao Jiang, Pengtao Zhang, Ruisan Xu, Lixian Gou, Xingchun |
author_sort | Gao, Xingchun |
collection | PubMed |
description | Whether persons with schizophrenia have a higher or lower incidence of cancer has been discussed for a long time. Due to the complex mechanisms and characteristics of different types of cancer, it is difficult to evaluate the exact relationship between cancers and schizophrenia without considering the type of tumor. Schizophrenia, a disabling mental illness that is now recognized as a neurodevelopmental disorder, is more correlated with brain tumors, such as glioma, than other types of tumors. Thus, we mainly focused on the relationship between schizophrenia and glioma morbidity. Glioma tumorigenesis and schizophrenia may share similar mechanisms; gene/pathway disruption would affect neurodevelopment and reduce the risk of glioma. The molecular defects of disrupted-in-schizophrenia-1 (DISC1), P53, brain-derived neurotrophic factor (BDNF) and C-X-C chemokine receptors type 4 (CXCR4) involved in schizophrenia pathogenesis might play opposite roles in glioma development. Many microRNAs (miRNAs) such as miR-183, miR-9, miR-137 and miR-126 expression change may be involved in the cross talk between glioma prevalence and schizophrenia. Finally, antipsychotic drugs may have antitumor effects. All these factors show that persons with schizophrenia have a decreased incidence of glioma; therefore, epidemiological investigation and studies comparing genetic and epigenetic aberrations involved in both of these complex diseases should be performed. These studies can provide more insightful knowledge about glioma and schizophrenia pathophysiology and help to determine the target/strategies for the prevention and treatment of the two diseases. |
format | Online Article Text |
id | pubmed-6129591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61295912018-09-19 Glioma in Schizophrenia: Is the Risk Higher or Lower? Gao, Xingchun Mi, Yajing Guo, Na Xu, Hao Jiang, Pengtao Zhang, Ruisan Xu, Lixian Gou, Xingchun Front Cell Neurosci Neuroscience Whether persons with schizophrenia have a higher or lower incidence of cancer has been discussed for a long time. Due to the complex mechanisms and characteristics of different types of cancer, it is difficult to evaluate the exact relationship between cancers and schizophrenia without considering the type of tumor. Schizophrenia, a disabling mental illness that is now recognized as a neurodevelopmental disorder, is more correlated with brain tumors, such as glioma, than other types of tumors. Thus, we mainly focused on the relationship between schizophrenia and glioma morbidity. Glioma tumorigenesis and schizophrenia may share similar mechanisms; gene/pathway disruption would affect neurodevelopment and reduce the risk of glioma. The molecular defects of disrupted-in-schizophrenia-1 (DISC1), P53, brain-derived neurotrophic factor (BDNF) and C-X-C chemokine receptors type 4 (CXCR4) involved in schizophrenia pathogenesis might play opposite roles in glioma development. Many microRNAs (miRNAs) such as miR-183, miR-9, miR-137 and miR-126 expression change may be involved in the cross talk between glioma prevalence and schizophrenia. Finally, antipsychotic drugs may have antitumor effects. All these factors show that persons with schizophrenia have a decreased incidence of glioma; therefore, epidemiological investigation and studies comparing genetic and epigenetic aberrations involved in both of these complex diseases should be performed. These studies can provide more insightful knowledge about glioma and schizophrenia pathophysiology and help to determine the target/strategies for the prevention and treatment of the two diseases. Frontiers Media S.A. 2018-09-03 /pmc/articles/PMC6129591/ /pubmed/30233327 http://dx.doi.org/10.3389/fncel.2018.00289 Text en Copyright © 2018 Gao, Mi, Guo, Xu, Jiang, Zhang, Xu and Gou. 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 | Neuroscience Gao, Xingchun Mi, Yajing Guo, Na Xu, Hao Jiang, Pengtao Zhang, Ruisan Xu, Lixian Gou, Xingchun Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title | Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title_full | Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title_fullStr | Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title_full_unstemmed | Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title_short | Glioma in Schizophrenia: Is the Risk Higher or Lower? |
title_sort | glioma in schizophrenia: is the risk higher or lower? |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129591/ https://www.ncbi.nlm.nih.gov/pubmed/30233327 http://dx.doi.org/10.3389/fncel.2018.00289 |
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