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Bile acid distributions, sex-specificity, and prognosis in colorectal cancer

BACKGROUND: Bile acids are known to be genotoxic and contribute to colorectal cancer (CRC). However, the link between CRC tumor bile acids to tumor location, patient sex, microbiome, immune-regulatory cells, and prognosis is not clear. METHODS: We conducted bile acid analysis using targeted liquid c...

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Autores principales: Cai, Yuping, Shen, Xinyi, Lu, Lingeng, Yan, Hong, Huang, Huang, Gaule, Patricia, Muca, Engjel, Theriot, Casey M., Rattray, Zahra, Rattray, Nicholas J. W., Lu, Jun, Ahuja, Nita, Zhang, Yawei, Paty, Philip B., Khan, Sajid A., Johnson, Caroline H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590160/
https://www.ncbi.nlm.nih.gov/pubmed/36274154
http://dx.doi.org/10.1186/s13293-022-00473-9
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author Cai, Yuping
Shen, Xinyi
Lu, Lingeng
Yan, Hong
Huang, Huang
Gaule, Patricia
Muca, Engjel
Theriot, Casey M.
Rattray, Zahra
Rattray, Nicholas J. W.
Lu, Jun
Ahuja, Nita
Zhang, Yawei
Paty, Philip B.
Khan, Sajid A.
Johnson, Caroline H.
author_facet Cai, Yuping
Shen, Xinyi
Lu, Lingeng
Yan, Hong
Huang, Huang
Gaule, Patricia
Muca, Engjel
Theriot, Casey M.
Rattray, Zahra
Rattray, Nicholas J. W.
Lu, Jun
Ahuja, Nita
Zhang, Yawei
Paty, Philip B.
Khan, Sajid A.
Johnson, Caroline H.
author_sort Cai, Yuping
collection PubMed
description BACKGROUND: Bile acids are known to be genotoxic and contribute to colorectal cancer (CRC). However, the link between CRC tumor bile acids to tumor location, patient sex, microbiome, immune-regulatory cells, and prognosis is not clear. METHODS: We conducted bile acid analysis using targeted liquid chromatography–mass spectrometry (LC–MS) on tumor tissues from CRC patients (n = 228) with survival analysis. We performed quantitative immunofluorescence (QIF) on tumors to examine immune cells. RESULTS: Twelve of the bile acids were significantly higher in right-sided colon tumors compared to left-sided colon tumors. Furthermore, in male patients, right-sided colon tumors had elevated secondary bile acids (deoxycholic acid, lithocholic acid, ursodeoxycholic acid) compared to left-sided colon tumors, but this difference between tumors by location was not observed in females. A high ratio of glycoursodeoxycholic to ursodeoxycholic was associated with 5-year overall survival (HR = 3.76, 95% CI = 1.17 to 12.1, P = 0.026), and a high ratio of glycochenodeoxycholic acid to chenodeoxycholic acid was associated with 5-year recurrence-free survival (HR = 3.61, 95% CI = 1.10 to 11.84, P = 0.034). We also show correlation between these bile acids and FoxP3 + T regulatory cells. CONCLUSIONS: This study revealed that the distribution of bile acid abundances in colon cancer patients is tumor location-, age- and sex-specific, and are linked to patient prognosis. This study provides new implications for targeting bile acid metabolism, microbiome, and immune responses for colon cancer patients by taking into account primary tumor location and sex. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13293-022-00473-9.
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spelling pubmed-95901602022-10-25 Bile acid distributions, sex-specificity, and prognosis in colorectal cancer Cai, Yuping Shen, Xinyi Lu, Lingeng Yan, Hong Huang, Huang Gaule, Patricia Muca, Engjel Theriot, Casey M. Rattray, Zahra Rattray, Nicholas J. W. Lu, Jun Ahuja, Nita Zhang, Yawei Paty, Philip B. Khan, Sajid A. Johnson, Caroline H. Biol Sex Differ Research BACKGROUND: Bile acids are known to be genotoxic and contribute to colorectal cancer (CRC). However, the link between CRC tumor bile acids to tumor location, patient sex, microbiome, immune-regulatory cells, and prognosis is not clear. METHODS: We conducted bile acid analysis using targeted liquid chromatography–mass spectrometry (LC–MS) on tumor tissues from CRC patients (n = 228) with survival analysis. We performed quantitative immunofluorescence (QIF) on tumors to examine immune cells. RESULTS: Twelve of the bile acids were significantly higher in right-sided colon tumors compared to left-sided colon tumors. Furthermore, in male patients, right-sided colon tumors had elevated secondary bile acids (deoxycholic acid, lithocholic acid, ursodeoxycholic acid) compared to left-sided colon tumors, but this difference between tumors by location was not observed in females. A high ratio of glycoursodeoxycholic to ursodeoxycholic was associated with 5-year overall survival (HR = 3.76, 95% CI = 1.17 to 12.1, P = 0.026), and a high ratio of glycochenodeoxycholic acid to chenodeoxycholic acid was associated with 5-year recurrence-free survival (HR = 3.61, 95% CI = 1.10 to 11.84, P = 0.034). We also show correlation between these bile acids and FoxP3 + T regulatory cells. CONCLUSIONS: This study revealed that the distribution of bile acid abundances in colon cancer patients is tumor location-, age- and sex-specific, and are linked to patient prognosis. This study provides new implications for targeting bile acid metabolism, microbiome, and immune responses for colon cancer patients by taking into account primary tumor location and sex. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13293-022-00473-9. BioMed Central 2022-10-23 /pmc/articles/PMC9590160/ /pubmed/36274154 http://dx.doi.org/10.1186/s13293-022-00473-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cai, Yuping
Shen, Xinyi
Lu, Lingeng
Yan, Hong
Huang, Huang
Gaule, Patricia
Muca, Engjel
Theriot, Casey M.
Rattray, Zahra
Rattray, Nicholas J. W.
Lu, Jun
Ahuja, Nita
Zhang, Yawei
Paty, Philip B.
Khan, Sajid A.
Johnson, Caroline H.
Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title_full Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title_fullStr Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title_full_unstemmed Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title_short Bile acid distributions, sex-specificity, and prognosis in colorectal cancer
title_sort bile acid distributions, sex-specificity, and prognosis in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590160/
https://www.ncbi.nlm.nih.gov/pubmed/36274154
http://dx.doi.org/10.1186/s13293-022-00473-9
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