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Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma

BACKGROUND: Cholangiocarcinomas (CCAs) are rare and aggressive malignant tumors of the biliary tract. Serotonin (5HT) has tumor-promoting effects in CCA while inhibition of 5HT synthesis can decrease tumor growth. METHODS: In this retrospective study, we evaluated the expression of 5HT and tryptopha...

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Autores principales: Fountzilas, Christos, Velasco, Sylvia Alarcon, Bshara, Wiam, LeVea, Charles M., Gupta, Medhavi, Ji, Wenyan, George, Anthony, Attwood, Kristopher, Iyer, Renuka V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643599/
https://www.ncbi.nlm.nih.gov/pubmed/37969829
http://dx.doi.org/10.21037/jgo-23-115
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author Fountzilas, Christos
Velasco, Sylvia Alarcon
Bshara, Wiam
LeVea, Charles M.
Gupta, Medhavi
Ji, Wenyan
George, Anthony
Attwood, Kristopher
Iyer, Renuka V.
author_facet Fountzilas, Christos
Velasco, Sylvia Alarcon
Bshara, Wiam
LeVea, Charles M.
Gupta, Medhavi
Ji, Wenyan
George, Anthony
Attwood, Kristopher
Iyer, Renuka V.
author_sort Fountzilas, Christos
collection PubMed
description BACKGROUND: Cholangiocarcinomas (CCAs) are rare and aggressive malignant tumors of the biliary tract. Serotonin (5HT) has tumor-promoting effects in CCA while inhibition of 5HT synthesis can decrease tumor growth. METHODS: In this retrospective study, we evaluated the expression of 5HT and tryptophane hydroxylase-1 (TPH-1) in tumor specimens from patients treated with cisplatin plus gemcitabine (CisGem). We included consecutive patients ≥18 years, with locally advanced unresectable, recurrent, or metastatic CCA who were treated with CisGem and had available archival tumor tissue for immunohistochemistry. Formalin-fixed paraffin (FFPE) sections were stained for 5HT and TPH-1. Specimens were evaluated for neuroendocrine features and tumor-infiltrating lymphocytes (TILs). Serum 5HT was measured. RESULTS: We identified 23 patients fulfilling the inclusion criteria. 5HT expression was absent in almost all tumors examined. TPH-1 expression was neither associated with stage or primary tumor location nor predictive of response to CisGem. There was a trend for improved overall survival (OS) in patients whose tumors had high TPH-1 expression. The examined tumor specimens had no neuroendocrine features. Most sections had no TILs. There was a trend for worse OS in patients with high serum 5HT concentration. CONCLUSIONS: Tumor TPH-1 expression was not predictive of response to treatment. There was a trend for improved long-term outcomes in patients with high tumor TPH expression and lower serum 5HT concentration.
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spelling pubmed-106435992023-11-15 Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma Fountzilas, Christos Velasco, Sylvia Alarcon Bshara, Wiam LeVea, Charles M. Gupta, Medhavi Ji, Wenyan George, Anthony Attwood, Kristopher Iyer, Renuka V. J Gastrointest Oncol Original Article BACKGROUND: Cholangiocarcinomas (CCAs) are rare and aggressive malignant tumors of the biliary tract. Serotonin (5HT) has tumor-promoting effects in CCA while inhibition of 5HT synthesis can decrease tumor growth. METHODS: In this retrospective study, we evaluated the expression of 5HT and tryptophane hydroxylase-1 (TPH-1) in tumor specimens from patients treated with cisplatin plus gemcitabine (CisGem). We included consecutive patients ≥18 years, with locally advanced unresectable, recurrent, or metastatic CCA who were treated with CisGem and had available archival tumor tissue for immunohistochemistry. Formalin-fixed paraffin (FFPE) sections were stained for 5HT and TPH-1. Specimens were evaluated for neuroendocrine features and tumor-infiltrating lymphocytes (TILs). Serum 5HT was measured. RESULTS: We identified 23 patients fulfilling the inclusion criteria. 5HT expression was absent in almost all tumors examined. TPH-1 expression was neither associated with stage or primary tumor location nor predictive of response to CisGem. There was a trend for improved overall survival (OS) in patients whose tumors had high TPH-1 expression. The examined tumor specimens had no neuroendocrine features. Most sections had no TILs. There was a trend for worse OS in patients with high serum 5HT concentration. CONCLUSIONS: Tumor TPH-1 expression was not predictive of response to treatment. There was a trend for improved long-term outcomes in patients with high tumor TPH expression and lower serum 5HT concentration. AME Publishing Company 2023-09-15 2023-10-31 /pmc/articles/PMC10643599/ /pubmed/37969829 http://dx.doi.org/10.21037/jgo-23-115 Text en 2023 Journal of Gastrointestinal Oncology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Fountzilas, Christos
Velasco, Sylvia Alarcon
Bshara, Wiam
LeVea, Charles M.
Gupta, Medhavi
Ji, Wenyan
George, Anthony
Attwood, Kristopher
Iyer, Renuka V.
Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title_full Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title_fullStr Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title_full_unstemmed Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title_short Evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
title_sort evaluation of the serotonin pathway as a biomarker in cholangiocarcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643599/
https://www.ncbi.nlm.nih.gov/pubmed/37969829
http://dx.doi.org/10.21037/jgo-23-115
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