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Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer

The high expression of metabolic enzymes, including glutaminase (GA) and lactate dehydrogenase A (LDHA), which contribute to bioenergetics and biosynthesis of mammalian cells, has been identified in a variety of cancer types. The current study indicated intratumoral heterogeneity with respect to pro...

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Autores principales: Mizuno, Yuta, Hattori, Kimiaki, Taniguchi, Kohei, Tanaka, Keitaro, Uchiyama, Kazuhisa, Hirose, Yoshinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068422/
https://www.ncbi.nlm.nih.gov/pubmed/32218849
http://dx.doi.org/10.3892/ol.2020.11390
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author Mizuno, Yuta
Hattori, Kimiaki
Taniguchi, Kohei
Tanaka, Keitaro
Uchiyama, Kazuhisa
Hirose, Yoshinobu
author_facet Mizuno, Yuta
Hattori, Kimiaki
Taniguchi, Kohei
Tanaka, Keitaro
Uchiyama, Kazuhisa
Hirose, Yoshinobu
author_sort Mizuno, Yuta
collection PubMed
description The high expression of metabolic enzymes, including glutaminase (GA) and lactate dehydrogenase A (LDHA), which contribute to bioenergetics and biosynthesis of mammalian cells, has been identified in a variety of cancer types. The current study indicated intratumoral heterogeneity with respect to protein expression of the metabolic enzymes in colorectal cancer (CRC). GA protein expression was determined using immunohistochemistry in 98 cases of surgically resected T3 CRC. A total of 75 cases (74%) exhibited moderate to strong immunopositivity of GA based on whole-section examination. A significant correlation was demonstrated between GA expression and clinicopathological features, including histological type and tumor budding in a patient population. Detailed histological analysis revealed the upregulation of GA protein expression at the invasive margin, including tumor budding of CRC tissues. Semi-quantitative examination revealed a significant difference in immunoexpression level of GA between the invasive margin and central CRC. However, LDHA expression exhibited an opposite pattern, with expression elevated at the center and significantly decreased at the tumors invasive margin. Immunohistochemical expression of another glycolytic enzyme hexokinase II was equivalent in both regions. Furthermore, gene silencing of GLS1, which encodes GA protein, and GA inhibitor treatment significantly inhibited cell growth of CRC cell lines. Therefore, the results of the present study demonstrated that the alteration in GA and LDHA expression is more prominent at the invasive margin, which involves tumor budding in CRC.
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spelling pubmed-70684222020-03-26 Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer Mizuno, Yuta Hattori, Kimiaki Taniguchi, Kohei Tanaka, Keitaro Uchiyama, Kazuhisa Hirose, Yoshinobu Oncol Lett Articles The high expression of metabolic enzymes, including glutaminase (GA) and lactate dehydrogenase A (LDHA), which contribute to bioenergetics and biosynthesis of mammalian cells, has been identified in a variety of cancer types. The current study indicated intratumoral heterogeneity with respect to protein expression of the metabolic enzymes in colorectal cancer (CRC). GA protein expression was determined using immunohistochemistry in 98 cases of surgically resected T3 CRC. A total of 75 cases (74%) exhibited moderate to strong immunopositivity of GA based on whole-section examination. A significant correlation was demonstrated between GA expression and clinicopathological features, including histological type and tumor budding in a patient population. Detailed histological analysis revealed the upregulation of GA protein expression at the invasive margin, including tumor budding of CRC tissues. Semi-quantitative examination revealed a significant difference in immunoexpression level of GA between the invasive margin and central CRC. However, LDHA expression exhibited an opposite pattern, with expression elevated at the center and significantly decreased at the tumors invasive margin. Immunohistochemical expression of another glycolytic enzyme hexokinase II was equivalent in both regions. Furthermore, gene silencing of GLS1, which encodes GA protein, and GA inhibitor treatment significantly inhibited cell growth of CRC cell lines. Therefore, the results of the present study demonstrated that the alteration in GA and LDHA expression is more prominent at the invasive margin, which involves tumor budding in CRC. D.A. Spandidos 2020-04 2020-02-13 /pmc/articles/PMC7068422/ /pubmed/32218849 http://dx.doi.org/10.3892/ol.2020.11390 Text en Copyright: © Mizuno et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Mizuno, Yuta
Hattori, Kimiaki
Taniguchi, Kohei
Tanaka, Keitaro
Uchiyama, Kazuhisa
Hirose, Yoshinobu
Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title_full Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title_fullStr Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title_full_unstemmed Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title_short Intratumoral heterogeneity of glutaminase and lactate dehydrogenase A protein expression in colorectal cancer
title_sort intratumoral heterogeneity of glutaminase and lactate dehydrogenase a protein expression in colorectal cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068422/
https://www.ncbi.nlm.nih.gov/pubmed/32218849
http://dx.doi.org/10.3892/ol.2020.11390
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