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Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas

BACKGROUND: LAT1/4F2hc heterodimeric complex is a major route for the transport of large neutral essential amino acids through the plasma membrane. Although it has been shown that LAT1/4F2hc is highly expressed in a variety of human tumors including gliomas, and LAT1 over-expression is associated wi...

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Autores principales: Haining, Zhen, Kawai, Nobuyuki, Miyake, Keisuke, Okada, Masaki, Okubo, Shuichi, Zhang, Xiang, Fei, Zhou, Tamiya, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305678/
https://www.ncbi.nlm.nih.gov/pubmed/22373026
http://dx.doi.org/10.1186/1472-6890-12-4
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author Haining, Zhen
Kawai, Nobuyuki
Miyake, Keisuke
Okada, Masaki
Okubo, Shuichi
Zhang, Xiang
Fei, Zhou
Tamiya, Takashi
author_facet Haining, Zhen
Kawai, Nobuyuki
Miyake, Keisuke
Okada, Masaki
Okubo, Shuichi
Zhang, Xiang
Fei, Zhou
Tamiya, Takashi
author_sort Haining, Zhen
collection PubMed
description BACKGROUND: LAT1/4F2hc heterodimeric complex is a major route for the transport of large neutral essential amino acids through the plasma membrane. Although it has been shown that LAT1/4F2hc is highly expressed in a variety of human tumors including gliomas, and LAT1 over-expression is associated with glioma grade and poor prognosis of glioma patients, the precise tissue location of LAT1/4F2hc in gliomas and the precise role of LAT1/4F2hc in glioma biological features remain unclear. METHODS: In the current study, the expressions of LAT1, 4F2hc, CD34 and Ki-67 were investigated by immunohistochemistry in 62 cases of human brain glioma; LAT1/4F2hc expression level, Ki-67 labeling index (Ki-67 LI) and microvessel density (MVD) were measured semi-quantitatively; and the correlation of LAT1/4F2hc expression with histopathological features, Ki-67 LI and MVD in gliomas was further analyzed. RESULTS: The results showed that both LAT1 and 4F2hc were expressed in all examined specimens. LAT1 but 4F2hc expression levels significantly correlated with the pathological grade and both expression levels significantly correlated with Ki-67 LI of gliomas. We also demonstrated that both LAT1 and 4F2hc immunoreactivity were observed in tumor cells as well as vascular endothelia; furthermore, the LAT1 expression level was markedly associated with glioma MVD as well. CONCLUSION: LAT1/4F2hc over-expression is closely correlates with the malignant phenotype and proliferation of gliomas, and LAT1 was associates with glioma angiogenesis. LAT1/4F2hc, especially LAT1, may become a novel potential molecular target for glioma biological therapy.
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spelling pubmed-33056782012-03-16 Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas Haining, Zhen Kawai, Nobuyuki Miyake, Keisuke Okada, Masaki Okubo, Shuichi Zhang, Xiang Fei, Zhou Tamiya, Takashi BMC Clin Pathol Research Article BACKGROUND: LAT1/4F2hc heterodimeric complex is a major route for the transport of large neutral essential amino acids through the plasma membrane. Although it has been shown that LAT1/4F2hc is highly expressed in a variety of human tumors including gliomas, and LAT1 over-expression is associated with glioma grade and poor prognosis of glioma patients, the precise tissue location of LAT1/4F2hc in gliomas and the precise role of LAT1/4F2hc in glioma biological features remain unclear. METHODS: In the current study, the expressions of LAT1, 4F2hc, CD34 and Ki-67 were investigated by immunohistochemistry in 62 cases of human brain glioma; LAT1/4F2hc expression level, Ki-67 labeling index (Ki-67 LI) and microvessel density (MVD) were measured semi-quantitatively; and the correlation of LAT1/4F2hc expression with histopathological features, Ki-67 LI and MVD in gliomas was further analyzed. RESULTS: The results showed that both LAT1 and 4F2hc were expressed in all examined specimens. LAT1 but 4F2hc expression levels significantly correlated with the pathological grade and both expression levels significantly correlated with Ki-67 LI of gliomas. We also demonstrated that both LAT1 and 4F2hc immunoreactivity were observed in tumor cells as well as vascular endothelia; furthermore, the LAT1 expression level was markedly associated with glioma MVD as well. CONCLUSION: LAT1/4F2hc over-expression is closely correlates with the malignant phenotype and proliferation of gliomas, and LAT1 was associates with glioma angiogenesis. LAT1/4F2hc, especially LAT1, may become a novel potential molecular target for glioma biological therapy. BioMed Central 2012-02-28 /pmc/articles/PMC3305678/ /pubmed/22373026 http://dx.doi.org/10.1186/1472-6890-12-4 Text en Copyright ©2012 Haining et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Haining, Zhen
Kawai, Nobuyuki
Miyake, Keisuke
Okada, Masaki
Okubo, Shuichi
Zhang, Xiang
Fei, Zhou
Tamiya, Takashi
Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title_full Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title_fullStr Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title_full_unstemmed Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title_short Relation of LAT1/4F2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
title_sort relation of lat1/4f2hc expression with pathological grade, proliferation and angiogenesis in human gliomas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305678/
https://www.ncbi.nlm.nih.gov/pubmed/22373026
http://dx.doi.org/10.1186/1472-6890-12-4
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