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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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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. |
format | Online Article Text |
id | pubmed-3184439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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