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Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers

BACKGROUND: The transmembrane receptor guanylate cyclase-C (GCC) has been found to be expressed in colorectal cancers. However, limited data are available on GCC protein expression in non-colorectal gastrointestinal tumors and few studies have reported whether GCC protein expression was consistently...

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Autores principales: Danaee, Hadi, Kalebic, Thea, Wyant, Timothy, Fassan, Matteo, Mescoli, Claudia, Gao, Feng, Trepicchio, William L., Rugge, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736218/
https://www.ncbi.nlm.nih.gov/pubmed/29261789
http://dx.doi.org/10.1371/journal.pone.0189953
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author Danaee, Hadi
Kalebic, Thea
Wyant, Timothy
Fassan, Matteo
Mescoli, Claudia
Gao, Feng
Trepicchio, William L.
Rugge, Massimo
author_facet Danaee, Hadi
Kalebic, Thea
Wyant, Timothy
Fassan, Matteo
Mescoli, Claudia
Gao, Feng
Trepicchio, William L.
Rugge, Massimo
author_sort Danaee, Hadi
collection PubMed
description BACKGROUND: The transmembrane receptor guanylate cyclase-C (GCC) has been found to be expressed in colorectal cancers. However, limited data are available on GCC protein expression in non-colorectal gastrointestinal tumors and few studies have reported whether GCC protein expression was consistently preserved in synchronous primary and metastatic cancer tissues. METHODS: GCC protein status was assessed by immunohistochemistry in tumor specimens from individuals (n = 627) with gastrointestinal tumors, including esophageal (n = 130), gastric (n = 276), pancreatic (n = 136), and colorectal (n = 85) primary and metastatic tumors. Tissue specimens consisted of tissue microarrays containing esophageal, gastric, pancreatic tumors, and whole-slide tissue sections from colorectal cancer patients with matching primary and metastatic tumors RESULT: Among the evaluated esophageal, gastric, and pancreatic tumors, the frequency of GCC positivity at the protein level ranged from 59% to 68%. GCC was consistently expressed in primary and matched/synchronous metastatic lesions of colorectal cancer tissues derived from the same patients. CONCLUSION: This observational study demonstrated the protein expression of GCC across various gastrointestinal malignancies. In all cancer histotypes, GCC protein localization was observed predominantly in the cytoplasm compared to the membrane region of tumor cells. Consistent immunohistochemistry detection of GCC protein expression in primary colorectal cancers and in their matched liver metastases suggests that the expression of GCC is maintained throughout the process of tumor progression and formation of metastatic disease.
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spelling pubmed-57362182017-12-22 Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers Danaee, Hadi Kalebic, Thea Wyant, Timothy Fassan, Matteo Mescoli, Claudia Gao, Feng Trepicchio, William L. Rugge, Massimo PLoS One Research Article BACKGROUND: The transmembrane receptor guanylate cyclase-C (GCC) has been found to be expressed in colorectal cancers. However, limited data are available on GCC protein expression in non-colorectal gastrointestinal tumors and few studies have reported whether GCC protein expression was consistently preserved in synchronous primary and metastatic cancer tissues. METHODS: GCC protein status was assessed by immunohistochemistry in tumor specimens from individuals (n = 627) with gastrointestinal tumors, including esophageal (n = 130), gastric (n = 276), pancreatic (n = 136), and colorectal (n = 85) primary and metastatic tumors. Tissue specimens consisted of tissue microarrays containing esophageal, gastric, pancreatic tumors, and whole-slide tissue sections from colorectal cancer patients with matching primary and metastatic tumors RESULT: Among the evaluated esophageal, gastric, and pancreatic tumors, the frequency of GCC positivity at the protein level ranged from 59% to 68%. GCC was consistently expressed in primary and matched/synchronous metastatic lesions of colorectal cancer tissues derived from the same patients. CONCLUSION: This observational study demonstrated the protein expression of GCC across various gastrointestinal malignancies. In all cancer histotypes, GCC protein localization was observed predominantly in the cytoplasm compared to the membrane region of tumor cells. Consistent immunohistochemistry detection of GCC protein expression in primary colorectal cancers and in their matched liver metastases suggests that the expression of GCC is maintained throughout the process of tumor progression and formation of metastatic disease. Public Library of Science 2017-12-19 /pmc/articles/PMC5736218/ /pubmed/29261789 http://dx.doi.org/10.1371/journal.pone.0189953 Text en © 2017 Danaee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Danaee, Hadi
Kalebic, Thea
Wyant, Timothy
Fassan, Matteo
Mescoli, Claudia
Gao, Feng
Trepicchio, William L.
Rugge, Massimo
Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title_full Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title_fullStr Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title_full_unstemmed Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title_short Consistent expression of guanylyl cyclase-C in primary and metastatic gastrointestinal cancers
title_sort consistent expression of guanylyl cyclase-c in primary and metastatic gastrointestinal cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736218/
https://www.ncbi.nlm.nih.gov/pubmed/29261789
http://dx.doi.org/10.1371/journal.pone.0189953
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