Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China
Abstract Elevated systemic levels of soluble cluster of differentiation 14 (sCD14) have been associated with gallbladder cancer (GBC), but the association with sCD14 levels within the gallbladder has not been investigated. Here, we evaluated sCD14 in the bile of 41 GBC cases and 117 gallstone contro...
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2021
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oai:doaj.org-article:518b12a2fc3d48b9938a3aa25bdab4082021-12-02T16:31:50ZSoluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China10.1038/s41598-021-92728-52045-2322https://doaj.org/article/518b12a2fc3d48b9938a3aa25bdab4082021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-92728-5https://doaj.org/toc/2045-2322Abstract Elevated systemic levels of soluble cluster of differentiation 14 (sCD14) have been associated with gallbladder cancer (GBC), but the association with sCD14 levels within the gallbladder has not been investigated. Here, we evaluated sCD14 in the bile of 41 GBC cases and 117 gallstone controls with data on 65 bile inflammation markers. We examined the relationship between bile sCD14 levels and GBC using logistic regression and stratified the analysis by stage. We included GBC-associated inflammatory biomarkers in the model to evaluate the influence of local inflammation. Bile sCD14 levels (third versus first tertile) were associated with GBC (adjusted odds ratio [OR]: 3.0, 95% confidence interval [CI]: 1.2–8.0). The association was equally strong for stage I/II (OR: 3.3, 95% CI: 0.9–15.6) and stage III/IV (OR: 3.2, 95% CI: 1.0–12.4) cancers. Including the GBC-associated inflammatory markers in the model removed the association between bile sCD14 and GBC (OR: 1.0, 95% CI: 0.3–3.5). The findings suggest that immune activation within the gallbladder may be related to GBC development, and the effect of sCD14 is influenced by inflammation. Similar associations across tumor stages suggest that elevated bile sCD14 levels may reflect changes early in GBC pathogenesis. Associations between GBC and sCD14 levels in both bile and plasma suggest sCD14 could be a potential biomarker for GBC.Victoria L. BrunAmanda F. CorbelAnn W. HsingTroy J. KempAlison L. Van DykeAllan HildesheimBin ZhuYu-Tang GaoLigia A. PintoJill KoshiolNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021) |
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Medicine R Science Q Victoria L. Brun Amanda F. Corbel Ann W. Hsing Troy J. Kemp Alison L. Van Dyke Allan Hildesheim Bin Zhu Yu-Tang Gao Ligia A. Pinto Jill Koshiol Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
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Abstract Elevated systemic levels of soluble cluster of differentiation 14 (sCD14) have been associated with gallbladder cancer (GBC), but the association with sCD14 levels within the gallbladder has not been investigated. Here, we evaluated sCD14 in the bile of 41 GBC cases and 117 gallstone controls with data on 65 bile inflammation markers. We examined the relationship between bile sCD14 levels and GBC using logistic regression and stratified the analysis by stage. We included GBC-associated inflammatory biomarkers in the model to evaluate the influence of local inflammation. Bile sCD14 levels (third versus first tertile) were associated with GBC (adjusted odds ratio [OR]: 3.0, 95% confidence interval [CI]: 1.2–8.0). The association was equally strong for stage I/II (OR: 3.3, 95% CI: 0.9–15.6) and stage III/IV (OR: 3.2, 95% CI: 1.0–12.4) cancers. Including the GBC-associated inflammatory markers in the model removed the association between bile sCD14 and GBC (OR: 1.0, 95% CI: 0.3–3.5). The findings suggest that immune activation within the gallbladder may be related to GBC development, and the effect of sCD14 is influenced by inflammation. Similar associations across tumor stages suggest that elevated bile sCD14 levels may reflect changes early in GBC pathogenesis. Associations between GBC and sCD14 levels in both bile and plasma suggest sCD14 could be a potential biomarker for GBC. |
format |
article |
author |
Victoria L. Brun Amanda F. Corbel Ann W. Hsing Troy J. Kemp Alison L. Van Dyke Allan Hildesheim Bin Zhu Yu-Tang Gao Ligia A. Pinto Jill Koshiol |
author_facet |
Victoria L. Brun Amanda F. Corbel Ann W. Hsing Troy J. Kemp Alison L. Van Dyke Allan Hildesheim Bin Zhu Yu-Tang Gao Ligia A. Pinto Jill Koshiol |
author_sort |
Victoria L. Brun |
title |
Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
title_short |
Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
title_full |
Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
title_fullStr |
Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
title_full_unstemmed |
Soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from Shanghai, China |
title_sort |
soluble cluster of differentiation 14 levels elevated in bile from gallbladder cancer cases from shanghai, china |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/518b12a2fc3d48b9938a3aa25bdab408 |
work_keys_str_mv |
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