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Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer

Background/Aims. Pancreatic ductal adenocarcinoma (PDA) has etiological association with chronic inflammation. Elevated circulating levels of inflammatory mediators, such as monocyte chemoattractant protein-1 (MCP-1), are found in obese individuals. We hypothesized that serum MCP-1 levels are elevat...

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Autores principales: Sullivan, Jennifer, Gong, Qiaoke, Hyslop, Terry, Lavu, Harish, Chipitsyna, Galina, Yeo, Charles J., Arafat, Hwyda A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184439/
https://www.ncbi.nlm.nih.gov/pubmed/21977031
http://dx.doi.org/10.1155/2011/518394
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author Sullivan, Jennifer
Gong, Qiaoke
Hyslop, Terry
Lavu, Harish
Chipitsyna, Galina
Yeo, Charles J.
Arafat, Hwyda A.
author_facet Sullivan, Jennifer
Gong, Qiaoke
Hyslop, Terry
Lavu, Harish
Chipitsyna, Galina
Yeo, Charles J.
Arafat, Hwyda A.
author_sort Sullivan, Jennifer
collection PubMed
description Background/Aims. Pancreatic ductal adenocarcinoma (PDA) has etiological association with chronic inflammation. Elevated circulating levels of inflammatory mediators, such as monocyte chemoattractant protein-1 (MCP-1), are found in obese individuals. We hypothesized that serum MCP-1 levels are elevated in obese PDA patients. Methods. ELISA was used to analyze MCP-1 serum levels in PDA (n = 62) and intraductal papillary mucinous neoplasms (IPMN) (n = 27). Recursive partitioning statistical analysis investigated the relationship between log MCP-1 and clinicopathological parameters. Results. Log MCP-1 values were significantly (P < 0.05) elevated in patients with BMI ≥ 37.5. In patients with BMI < 37.5, average log MCP-1 values were significantly elevated in PDA patients when compared to IPMN patients. Within the IPMN group, higher log MCP-1 levels correlated with increased age. Recursive partitioning analysis of IPMN versus PDA revealed a strategy of predicting characteristics of patients who are more likely to have cancer. This strategy utilizes log MCP-1 as the primary factor and also utilizes smoking status, gender, and age. Conclusion. MCP-1 is a promising biomarker in pancreatic cancer. The potential of using MCP-1 to distinguish PDA from IPMN patients must be studied in larger populations to validate and demonstrate its eventual clinical utility.
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spelling pubmed-31844392011-10-04 Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer Sullivan, Jennifer Gong, Qiaoke Hyslop, Terry Lavu, Harish Chipitsyna, Galina Yeo, Charles J. Arafat, Hwyda A. J Oncol Research Article Background/Aims. Pancreatic ductal adenocarcinoma (PDA) has etiological association with chronic inflammation. Elevated circulating levels of inflammatory mediators, such as monocyte chemoattractant protein-1 (MCP-1), are found in obese individuals. We hypothesized that serum MCP-1 levels are elevated in obese PDA patients. Methods. ELISA was used to analyze MCP-1 serum levels in PDA (n = 62) and intraductal papillary mucinous neoplasms (IPMN) (n = 27). Recursive partitioning statistical analysis investigated the relationship between log MCP-1 and clinicopathological parameters. Results. Log MCP-1 values were significantly (P < 0.05) elevated in patients with BMI ≥ 37.5. In patients with BMI < 37.5, average log MCP-1 values were significantly elevated in PDA patients when compared to IPMN patients. Within the IPMN group, higher log MCP-1 levels correlated with increased age. Recursive partitioning analysis of IPMN versus PDA revealed a strategy of predicting characteristics of patients who are more likely to have cancer. This strategy utilizes log MCP-1 as the primary factor and also utilizes smoking status, gender, and age. Conclusion. MCP-1 is a promising biomarker in pancreatic cancer. The potential of using MCP-1 to distinguish PDA from IPMN patients must be studied in larger populations to validate and demonstrate its eventual clinical utility. Hindawi Publishing Corporation 2011 2011-10-01 /pmc/articles/PMC3184439/ /pubmed/21977031 http://dx.doi.org/10.1155/2011/518394 Text en Copyright © 2011 Jennifer Sullivan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sullivan, Jennifer
Gong, Qiaoke
Hyslop, Terry
Lavu, Harish
Chipitsyna, Galina
Yeo, Charles J.
Arafat, Hwyda A.
Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title_full Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title_fullStr Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title_full_unstemmed Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title_short Serum Monocyte Chemoattractant Protein-1 in Pancreatic Cancer
title_sort serum monocyte chemoattractant protein-1 in pancreatic cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184439/
https://www.ncbi.nlm.nih.gov/pubmed/21977031
http://dx.doi.org/10.1155/2011/518394
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