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Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation

Glioblastoma multiforme (GBM), the most malignant of all gliomas is characterized by a high degree of heterogeneity and poor response to treatment. The sub-ventricular zone (SVZ) is the major site of neurogenesis in the brain and is rich in neural stem cells. Based on the proximity of the GBM tumors...

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Autores principales: Gollapalli, Kishore, Ghantasala, Saicharan, Kumar, Sachendra, Srivastava, Rajneesh, Rapole, Srikanth, Moiyadi, Aliasgar, Epari, Sridhar, Srivastava, Sanjeeva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431125/
https://www.ncbi.nlm.nih.gov/pubmed/28469129
http://dx.doi.org/10.1038/s41598-017-01202-8
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author Gollapalli, Kishore
Ghantasala, Saicharan
Kumar, Sachendra
Srivastava, Rajneesh
Rapole, Srikanth
Moiyadi, Aliasgar
Epari, Sridhar
Srivastava, Sanjeeva
author_facet Gollapalli, Kishore
Ghantasala, Saicharan
Kumar, Sachendra
Srivastava, Rajneesh
Rapole, Srikanth
Moiyadi, Aliasgar
Epari, Sridhar
Srivastava, Sanjeeva
author_sort Gollapalli, Kishore
collection PubMed
description Glioblastoma multiforme (GBM), the most malignant of all gliomas is characterized by a high degree of heterogeneity and poor response to treatment. The sub-ventricular zone (SVZ) is the major site of neurogenesis in the brain and is rich in neural stem cells. Based on the proximity of the GBM tumors to the SVZ, the tumors can be further classified into SVZ+ and SVZ−. The tumors located in close contact with the SVZ are classified as SVZ+, while the tumors located distantly from the SVZ are classified as SVZ−. To gain an insight into the increased aggressiveness of SVZ+ over SVZ− tumors, we have used proteomics techniques like 2D-DIGE and LC-MS/MS to investigate any possible proteomic differences between the two subtypes. Serum proteomic analysis revealed significant alterations of various acute phase proteins and lipid carrying proteins, while tissue proteomic analysis revealed significant alterations in cytoskeletal, lipid binding, chaperone and cell cycle regulating proteins, which are already known to be associated with disease pathobiology. These findings provide cues to molecular basis behind increased aggressiveness of SVZ+ GBM tumors over SVZ− GBM tumors and plausible therapeutic targets to improve treatment modalities for these highly invasive tumors.
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spelling pubmed-54311252017-05-16 Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation Gollapalli, Kishore Ghantasala, Saicharan Kumar, Sachendra Srivastava, Rajneesh Rapole, Srikanth Moiyadi, Aliasgar Epari, Sridhar Srivastava, Sanjeeva Sci Rep Article Glioblastoma multiforme (GBM), the most malignant of all gliomas is characterized by a high degree of heterogeneity and poor response to treatment. The sub-ventricular zone (SVZ) is the major site of neurogenesis in the brain and is rich in neural stem cells. Based on the proximity of the GBM tumors to the SVZ, the tumors can be further classified into SVZ+ and SVZ−. The tumors located in close contact with the SVZ are classified as SVZ+, while the tumors located distantly from the SVZ are classified as SVZ−. To gain an insight into the increased aggressiveness of SVZ+ over SVZ− tumors, we have used proteomics techniques like 2D-DIGE and LC-MS/MS to investigate any possible proteomic differences between the two subtypes. Serum proteomic analysis revealed significant alterations of various acute phase proteins and lipid carrying proteins, while tissue proteomic analysis revealed significant alterations in cytoskeletal, lipid binding, chaperone and cell cycle regulating proteins, which are already known to be associated with disease pathobiology. These findings provide cues to molecular basis behind increased aggressiveness of SVZ+ GBM tumors over SVZ− GBM tumors and plausible therapeutic targets to improve treatment modalities for these highly invasive tumors. Nature Publishing Group UK 2017-05-03 /pmc/articles/PMC5431125/ /pubmed/28469129 http://dx.doi.org/10.1038/s41598-017-01202-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gollapalli, Kishore
Ghantasala, Saicharan
Kumar, Sachendra
Srivastava, Rajneesh
Rapole, Srikanth
Moiyadi, Aliasgar
Epari, Sridhar
Srivastava, Sanjeeva
Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title_full Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title_fullStr Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title_full_unstemmed Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title_short Subventricular zone involvement in Glioblastoma – A proteomic evaluation and clinicoradiological correlation
title_sort subventricular zone involvement in glioblastoma – a proteomic evaluation and clinicoradiological correlation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431125/
https://www.ncbi.nlm.nih.gov/pubmed/28469129
http://dx.doi.org/10.1038/s41598-017-01202-8
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