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High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis

BACKGROUND: Lymph node status is an important prognostic indicator and it significantly influences treatment decisions for colorectal cancer (CRC). The objective of this study was to evaluate the ability of serum monosaccharides in predicting lymph node metastasis (LNM) and prognosis. METHODS: High...

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Autores principales: Wang, Xueling, Li, Haoran, Chang, Xiaotian, Tian, Zibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479890/
https://www.ncbi.nlm.nih.gov/pubmed/37675224
http://dx.doi.org/10.3389/fonc.2023.1213952
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author Wang, Xueling
Li, Haoran
Chang, Xiaotian
Tian, Zibin
author_facet Wang, Xueling
Li, Haoran
Chang, Xiaotian
Tian, Zibin
author_sort Wang, Xueling
collection PubMed
description BACKGROUND: Lymph node status is an important prognostic indicator and it significantly influences treatment decisions for colorectal cancer (CRC). The objective of this study was to evaluate the ability of serum monosaccharides in predicting lymph node metastasis (LNM) and prognosis. METHODS: High performance anion exchange chromatography coupled with pulsed amperometric detector (HPAEC-PAD) was used to quantify serum monosaccharides from 252 CRC patients. Receiver operating characteristic (ROC) curves were used to evaluate predictive performance of parameters. Predictors of LNM were evaluated by univariate and multivariate analyses. The prognostic role of the factors was evaluated by survival analysis. RESULTS: The levels of serum mannose (Man) and galactose (Gal) were significantly increased in patients with LNM (p <0.0001, p =0.0017, respectively). The area under the curves (AUCs) of Man was 0.8140, which was higher than carcinoembryonic antigen (CEA) (AUC =0.6523). Univariate and multivariate analyses demonstrated histologic grade (G3) (odds ratio [OR] =2.60, p =0.043), histologic grade (mucin-producing subtype) (odds ratio [OR] =3.38, p =0.032), lymphovascular invasion (LVI) (OR =2.42, p <0.01), CEA (>5ng/ml) (OR =1.85, p =0.042) and high Man (OR =2.65, p =0.006) to be independent risk factors of LNM. The survival analysis showed that the high serum Man was independent risk factor for poor prognosis in CRC patients (HR=1.75, p =0.004). CONCLUSIONS: The Man is superior to CEA in prediction of LNM for CRC patients. Man is expected to be a predictor for LNM in CRC. High serum Man is associated with poor prognosis of CRC patients.
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spelling pubmed-104798902023-09-06 High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis Wang, Xueling Li, Haoran Chang, Xiaotian Tian, Zibin Front Oncol Oncology BACKGROUND: Lymph node status is an important prognostic indicator and it significantly influences treatment decisions for colorectal cancer (CRC). The objective of this study was to evaluate the ability of serum monosaccharides in predicting lymph node metastasis (LNM) and prognosis. METHODS: High performance anion exchange chromatography coupled with pulsed amperometric detector (HPAEC-PAD) was used to quantify serum monosaccharides from 252 CRC patients. Receiver operating characteristic (ROC) curves were used to evaluate predictive performance of parameters. Predictors of LNM were evaluated by univariate and multivariate analyses. The prognostic role of the factors was evaluated by survival analysis. RESULTS: The levels of serum mannose (Man) and galactose (Gal) were significantly increased in patients with LNM (p <0.0001, p =0.0017, respectively). The area under the curves (AUCs) of Man was 0.8140, which was higher than carcinoembryonic antigen (CEA) (AUC =0.6523). Univariate and multivariate analyses demonstrated histologic grade (G3) (odds ratio [OR] =2.60, p =0.043), histologic grade (mucin-producing subtype) (odds ratio [OR] =3.38, p =0.032), lymphovascular invasion (LVI) (OR =2.42, p <0.01), CEA (>5ng/ml) (OR =1.85, p =0.042) and high Man (OR =2.65, p =0.006) to be independent risk factors of LNM. The survival analysis showed that the high serum Man was independent risk factor for poor prognosis in CRC patients (HR=1.75, p =0.004). CONCLUSIONS: The Man is superior to CEA in prediction of LNM for CRC patients. Man is expected to be a predictor for LNM in CRC. High serum Man is associated with poor prognosis of CRC patients. Frontiers Media S.A. 2023-08-22 /pmc/articles/PMC10479890/ /pubmed/37675224 http://dx.doi.org/10.3389/fonc.2023.1213952 Text en Copyright © 2023 Wang, Li, Chang and Tian https://creativecommons.org/licenses/by/4.0/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) and the copyright owner(s) 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 Oncology
Wang, Xueling
Li, Haoran
Chang, Xiaotian
Tian, Zibin
High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title_full High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title_fullStr High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title_full_unstemmed High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title_short High serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
title_sort high serum mannose in colorectal cancer: a novel biomarker of lymph node metastasis and poor prognosis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10479890/
https://www.ncbi.nlm.nih.gov/pubmed/37675224
http://dx.doi.org/10.3389/fonc.2023.1213952
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