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Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma

Background: CD133 has been identified as a cancer stem cell marker for pancreatic ductal adenocarcinoma. Although leucine-rich-repeat-containing G-protein-coupled receptor 5 (LGR5), a marker of intestinal stem cells, has been shown to be on a higher level of the stem cell hierarchy than CD133, the e...

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Autores principales: Mizuno, Nobumasa, Yatabe, Yasushi, Hara, Kazuo, Hijioka, Susumu, Imaoka, Hiroshi, Shimizu, Yasuhiro, Ko, Shigeru B. H., Yamao, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783903/
https://www.ncbi.nlm.nih.gov/pubmed/24133453
http://dx.doi.org/10.3389/fphys.2013.00269
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author Mizuno, Nobumasa
Yatabe, Yasushi
Hara, Kazuo
Hijioka, Susumu
Imaoka, Hiroshi
Shimizu, Yasuhiro
Ko, Shigeru B. H.
Yamao, Kenji
author_facet Mizuno, Nobumasa
Yatabe, Yasushi
Hara, Kazuo
Hijioka, Susumu
Imaoka, Hiroshi
Shimizu, Yasuhiro
Ko, Shigeru B. H.
Yamao, Kenji
author_sort Mizuno, Nobumasa
collection PubMed
description Background: CD133 has been identified as a cancer stem cell marker for pancreatic ductal adenocarcinoma. Although leucine-rich-repeat-containing G-protein-coupled receptor 5 (LGR5), a marker of intestinal stem cells, has been shown to be on a higher level of the stem cell hierarchy than CD133, the expression and function of LGR5 in pancreatic cancer tissue remains unclear. This study investigated tissue expression of LGR5 and CD133 in resected pancreatic cancer tissue. Methods: LGR5 and CD133 expression was immunohistochemically examined in 9 patients with pancreatic ductal adenocarcinoma who underwent resection. Results: LGR5 was expressed in the cytoplasm of pancreatic cancer cells in 4 of 9 cases. CD133 was not detected in cancerous tissue. In non-neoplastic tissue, LGR5 was expressed in the basolateral membrane of a subset of endocrine cells. Conversely, CD133 was expressed in the apical membrane of small duct cells. Co-localization of LGR5 and CD133 was not found in either neoplastic or non-neoplastic tissue. LGR5 expression in pancreatic cancer cells showed no statistically significant correlation with survival after surgery. Conclusion: We have demonstrated that LGR5 is expressed in the cytoplasm of pancreatic adenocarcinoma cells, and the basolateral membrane of a subset of endocrine cells of the human pancreas. Further investigation is required to clarify any prognostic significance of LGR5 expression.
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spelling pubmed-37839032013-10-16 Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma Mizuno, Nobumasa Yatabe, Yasushi Hara, Kazuo Hijioka, Susumu Imaoka, Hiroshi Shimizu, Yasuhiro Ko, Shigeru B. H. Yamao, Kenji Front Physiol Physiology Background: CD133 has been identified as a cancer stem cell marker for pancreatic ductal adenocarcinoma. Although leucine-rich-repeat-containing G-protein-coupled receptor 5 (LGR5), a marker of intestinal stem cells, has been shown to be on a higher level of the stem cell hierarchy than CD133, the expression and function of LGR5 in pancreatic cancer tissue remains unclear. This study investigated tissue expression of LGR5 and CD133 in resected pancreatic cancer tissue. Methods: LGR5 and CD133 expression was immunohistochemically examined in 9 patients with pancreatic ductal adenocarcinoma who underwent resection. Results: LGR5 was expressed in the cytoplasm of pancreatic cancer cells in 4 of 9 cases. CD133 was not detected in cancerous tissue. In non-neoplastic tissue, LGR5 was expressed in the basolateral membrane of a subset of endocrine cells. Conversely, CD133 was expressed in the apical membrane of small duct cells. Co-localization of LGR5 and CD133 was not found in either neoplastic or non-neoplastic tissue. LGR5 expression in pancreatic cancer cells showed no statistically significant correlation with survival after surgery. Conclusion: We have demonstrated that LGR5 is expressed in the cytoplasm of pancreatic adenocarcinoma cells, and the basolateral membrane of a subset of endocrine cells of the human pancreas. Further investigation is required to clarify any prognostic significance of LGR5 expression. Frontiers Media S.A. 2013-09-26 /pmc/articles/PMC3783903/ /pubmed/24133453 http://dx.doi.org/10.3389/fphys.2013.00269 Text en Copyright © 2013 Mizuno, Yatabe, Hara, Hijioka, Imaoka, Shimizu, Ko and Yamao. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Physiology
Mizuno, Nobumasa
Yatabe, Yasushi
Hara, Kazuo
Hijioka, Susumu
Imaoka, Hiroshi
Shimizu, Yasuhiro
Ko, Shigeru B. H.
Yamao, Kenji
Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title_full Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title_fullStr Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title_full_unstemmed Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title_short Cytoplasmic expression of LGR5 in pancreatic adenocarcinoma
title_sort cytoplasmic expression of lgr5 in pancreatic adenocarcinoma
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783903/
https://www.ncbi.nlm.nih.gov/pubmed/24133453
http://dx.doi.org/10.3389/fphys.2013.00269
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