Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma

Aim: The presence of cells within meningioma (MG) that express embryonic stem cell (ESC) markers has been previously reported. However, the precise location of these cells has yet to be determined.Methods: 3,3-Diaminobenzidine (DAB) immunohistochemical (IHC) staining was performed on 11 WHO grade I...

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Main Authors: Ganeshwaran Shivapathasundram, Agadha C. Wickremesekera, Helen D. Brasch, Reginald Marsh, Swee T. Tan, Tinte Itinteang
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Surgery
Subjects:
KLF
Online Access:https://www.frontiersin.org/article/10.3389/fsurg.2018.00065/full
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spelling doaj-b644b55b0fa54e9c89bbc90ef966ee152020-11-24T22:17:11ZengFrontiers Media S.A.Frontiers in Surgery2296-875X2018-10-01510.3389/fsurg.2018.00065408885Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I MeningiomaGaneshwaran Shivapathasundram0Ganeshwaran Shivapathasundram1Agadha C. Wickremesekera2Agadha C. Wickremesekera3Helen D. Brasch4Reginald Marsh5Reginald Marsh6Swee T. Tan7Swee T. Tan8Tinte Itinteang9Gillies McIndoe Research Institute, Wellington, New ZealandDepartment of Neurosurgery, Wellington Regional Hospital, Wellington, New ZealandGillies McIndoe Research Institute, Wellington, New ZealandDepartment of Neurosurgery, Wellington Regional Hospital, Wellington, New ZealandGillies McIndoe Research Institute, Wellington, New ZealandGillies McIndoe Research Institute, Wellington, New ZealandDepartment of Psychological Medicine, Auckland University, Auckland, New ZealandGillies McIndoe Research Institute, Wellington, New ZealandWellington Regional Plastic, Maxillofacial and Burns Unit, Hutt Hospital, Wellington, New ZealandGillies McIndoe Research Institute, Wellington, New ZealandAim: The presence of cells within meningioma (MG) that express embryonic stem cell (ESC) markers has been previously reported. However, the precise location of these cells has yet to be determined.Methods: 3,3-Diaminobenzidine (DAB) immunohistochemical (IHC) staining was performed on 11 WHO grade I MG tissue samples for the expression of the ESC markers OCT4, NANOG, SOX2, KLF4 and c-MYC. Immunofluorescence (IF) IHC staining was performed to investigate the localization of each of these ESC markers. NanoString and colorimetric in situ hybridization (CISH) mRNA expression analyses were performed on six snap-frozen MG tissue samples to confirm transcriptional activation of these proteins, respectively.Results: DAB IHC staining demonstrated expression of OCT4, NANOG, SOX2, KLF4, and c-MYC within all 11 MG tissue samples. IF IHC staining demonstrated the expression of the ESC markers OCT4, NANOG, SOX2, KLF4, and c-MYC on both the endothelial and pericyte layers of the microvessels. NanoString and CISH mRNA analyses confirmed transcription activation of these ESC markers.Conclusion: This novel finding of the expression of all aforementioned ESC markers in WHO grade I MG infers the presence of a putative stem cells population which may give rise to MG.https://www.frontiersin.org/article/10.3389/fsurg.2018.00065/fullmeningiomaOCT4NANOGSOX2KLFc-MYC
collection DOAJ
language English
format Article
sources DOAJ
author Ganeshwaran Shivapathasundram
Ganeshwaran Shivapathasundram
Agadha C. Wickremesekera
Agadha C. Wickremesekera
Helen D. Brasch
Reginald Marsh
Reginald Marsh
Swee T. Tan
Swee T. Tan
Tinte Itinteang
spellingShingle Ganeshwaran Shivapathasundram
Ganeshwaran Shivapathasundram
Agadha C. Wickremesekera
Agadha C. Wickremesekera
Helen D. Brasch
Reginald Marsh
Reginald Marsh
Swee T. Tan
Swee T. Tan
Tinte Itinteang
Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
Frontiers in Surgery
meningioma
OCT4
NANOG
SOX2
KLF
c-MYC
author_facet Ganeshwaran Shivapathasundram
Ganeshwaran Shivapathasundram
Agadha C. Wickremesekera
Agadha C. Wickremesekera
Helen D. Brasch
Reginald Marsh
Reginald Marsh
Swee T. Tan
Swee T. Tan
Tinte Itinteang
author_sort Ganeshwaran Shivapathasundram
title Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
title_short Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
title_full Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
title_fullStr Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
title_full_unstemmed Expression of Embryonic Stem Cell Markers on the Microvessels of WHO Grade I Meningioma
title_sort expression of embryonic stem cell markers on the microvessels of who grade i meningioma
publisher Frontiers Media S.A.
series Frontiers in Surgery
issn 2296-875X
publishDate 2018-10-01
description Aim: The presence of cells within meningioma (MG) that express embryonic stem cell (ESC) markers has been previously reported. However, the precise location of these cells has yet to be determined.Methods: 3,3-Diaminobenzidine (DAB) immunohistochemical (IHC) staining was performed on 11 WHO grade I MG tissue samples for the expression of the ESC markers OCT4, NANOG, SOX2, KLF4 and c-MYC. Immunofluorescence (IF) IHC staining was performed to investigate the localization of each of these ESC markers. NanoString and colorimetric in situ hybridization (CISH) mRNA expression analyses were performed on six snap-frozen MG tissue samples to confirm transcriptional activation of these proteins, respectively.Results: DAB IHC staining demonstrated expression of OCT4, NANOG, SOX2, KLF4, and c-MYC within all 11 MG tissue samples. IF IHC staining demonstrated the expression of the ESC markers OCT4, NANOG, SOX2, KLF4, and c-MYC on both the endothelial and pericyte layers of the microvessels. NanoString and CISH mRNA analyses confirmed transcription activation of these ESC markers.Conclusion: This novel finding of the expression of all aforementioned ESC markers in WHO grade I MG infers the presence of a putative stem cells population which may give rise to MG.
topic meningioma
OCT4
NANOG
SOX2
KLF
c-MYC
url https://www.frontiersin.org/article/10.3389/fsurg.2018.00065/full
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