Significance of M2-Polarized Tumor-Associated Macrophage in Pancreatic Cancer
Background The roles of infiltrating macrophages within the tumor microenvironment are complex because of their functional variety. The aim of this study is to examine the role and prognostic significance of tumor-associated macrophages (TAMs) that have an M2 polarized function in pancreatic cancer....
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creator | Kurahara, Hiroshi, M.D Shinchi, Hiroyuki, M.D Mataki, Yuko, M.D Maemura, Kousei, M.D Noma, Hidetoshi, M.D Kubo, Fumitake, M.D Sakoda, Masahiko, M.D Ueno, Shinichi, M.D Natsugoe, Shoji, M.D Takao, Sonshin, M.D |
description | Background The roles of infiltrating macrophages within the tumor microenvironment are complex because of their functional variety. The aim of this study is to examine the role and prognostic significance of tumor-associated macrophages (TAMs) that have an M2 polarized function in pancreatic cancer. Materials and Methods Formalin-fixed, paraffin-embedded blocks were obtained from 76 patients with pancreatic head cancer. All patients underwent macroscopic curative resection. We assessed the number of infiltrating macrophages within the tumor invasive front by not only CD68 but also by CD163 and CD204, which are specific receptors on M2-polarized macrophages. Furthermore, to evaluate lymphangiogenesis, we measured the density of lymphatic vessels in the tumor invasive front by using D2-40. Results High incidence of lymph node metastasis was shown in cases with a high number of CD163- or CD204-positive macrophages. Significantly increased lymphatic vessel density (LVD) was shown in cases with lymph node metastasis compared with cases without lymph node metastasis ( P = 0.0094). Significantly increased LVD ( P = 0.0175) and a poor prognosis ( P = 0.0171) were shown in cases with a high number of macrophages that express CD163 or CD204, however, there was no significant difference according to the number of CD68-positive macrophages. Conclusions M2-polarized TAMs in the invasive front of pancreatic cancer are associated with a poor prognosis due to accelerated lymphatic metastasis, and inhibition of the functional interaction between M2-polarized TAMs and tumor cells may improve the prognosis. |
doi_str_mv | 10.1016/j.jss.2009.05.026 |
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The aim of this study is to examine the role and prognostic significance of tumor-associated macrophages (TAMs) that have an M2 polarized function in pancreatic cancer. Materials and Methods Formalin-fixed, paraffin-embedded blocks were obtained from 76 patients with pancreatic head cancer. All patients underwent macroscopic curative resection. We assessed the number of infiltrating macrophages within the tumor invasive front by not only CD68 but also by CD163 and CD204, which are specific receptors on M2-polarized macrophages. Furthermore, to evaluate lymphangiogenesis, we measured the density of lymphatic vessels in the tumor invasive front by using D2-40. Results High incidence of lymph node metastasis was shown in cases with a high number of CD163- or CD204-positive macrophages. Significantly increased lymphatic vessel density (LVD) was shown in cases with lymph node metastasis compared with cases without lymph node metastasis ( P = 0.0094). Significantly increased LVD ( P = 0.0175) and a poor prognosis ( P = 0.0171) were shown in cases with a high number of macrophages that express CD163 or CD204, however, there was no significant difference according to the number of CD68-positive macrophages. Conclusions M2-polarized TAMs in the invasive front of pancreatic cancer are associated with a poor prognosis due to accelerated lymphatic metastasis, and inhibition of the functional interaction between M2-polarized TAMs and tumor cells may improve the prognosis.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2009.05.026</identifier><identifier>PMID: 19765725</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenocarcinoma - diagnosis ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adult ; Aged ; Aged, 80 and over ; Antigens, CD - metabolism ; Antigens, Differentiation, Myelomonocytic - metabolism ; Female ; Humans ; Kaplan-Meier Estimate ; Lymphangiogenesis ; Lymphatic Metastasis ; Macrophages - metabolism ; Macrophages - pathology ; Male ; Middle Aged ; pancreatic cancer ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - mortality ; Pancreatic Neoplasms - pathology ; Prognosis ; Receptors, Cell Surface - metabolism ; Retrospective Studies ; Scavenger Receptors, Class A - metabolism ; Surgery ; tumor microenvironment ; tumor-associated macrophage</subject><ispartof>The Journal of surgical research, 2011, Vol.167 (2), p.e211-e219</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c616t-8aa7da26a90f587d90e3d5908dba1358139caafa40b7d0fb80eb2d3f1aed25c53</citedby><cites>FETCH-LOGICAL-c616t-8aa7da26a90f587d90e3d5908dba1358139caafa40b7d0fb80eb2d3f1aed25c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022480409002844$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19765725$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kurahara, Hiroshi, M.D</creatorcontrib><creatorcontrib>Shinchi, Hiroyuki, M.D</creatorcontrib><creatorcontrib>Mataki, Yuko, M.D</creatorcontrib><creatorcontrib>Maemura, Kousei, M.D</creatorcontrib><creatorcontrib>Noma, Hidetoshi, M.D</creatorcontrib><creatorcontrib>Kubo, Fumitake, M.D</creatorcontrib><creatorcontrib>Sakoda, Masahiko, M.D</creatorcontrib><creatorcontrib>Ueno, Shinichi, M.D</creatorcontrib><creatorcontrib>Natsugoe, Shoji, M.D</creatorcontrib><creatorcontrib>Takao, Sonshin, M.D</creatorcontrib><title>Significance of M2-Polarized Tumor-Associated Macrophage in Pancreatic Cancer</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Background The roles of infiltrating macrophages within the tumor microenvironment are complex because of their functional variety. The aim of this study is to examine the role and prognostic significance of tumor-associated macrophages (TAMs) that have an M2 polarized function in pancreatic cancer. Materials and Methods Formalin-fixed, paraffin-embedded blocks were obtained from 76 patients with pancreatic head cancer. All patients underwent macroscopic curative resection. We assessed the number of infiltrating macrophages within the tumor invasive front by not only CD68 but also by CD163 and CD204, which are specific receptors on M2-polarized macrophages. Furthermore, to evaluate lymphangiogenesis, we measured the density of lymphatic vessels in the tumor invasive front by using D2-40. Results High incidence of lymph node metastasis was shown in cases with a high number of CD163- or CD204-positive macrophages. Significantly increased lymphatic vessel density (LVD) was shown in cases with lymph node metastasis compared with cases without lymph node metastasis ( P = 0.0094). Significantly increased LVD ( P = 0.0175) and a poor prognosis ( P = 0.0171) were shown in cases with a high number of macrophages that express CD163 or CD204, however, there was no significant difference according to the number of CD68-positive macrophages. Conclusions M2-polarized TAMs in the invasive front of pancreatic cancer are associated with a poor prognosis due to accelerated lymphatic metastasis, and inhibition of the functional interaction between M2-polarized TAMs and tumor cells may improve the prognosis.</description><subject>Adenocarcinoma - diagnosis</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, Myelomonocytic - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphangiogenesis</subject><subject>Lymphatic Metastasis</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>pancreatic cancer</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - mortality</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Prognosis</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Retrospective Studies</subject><subject>Scavenger Receptors, Class A - metabolism</subject><subject>Surgery</subject><subject>tumor microenvironment</subject><subject>tumor-associated macrophage</subject><issn>0022-4804</issn><issn>1095-8673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9r3DAQxUVpabZJP0Avxbee7I5ky5YoFMLSf5AlgaRnMZbGqVyvvZXsQPrpK7MLhRxy0mh47yH9HmPvOBQceP2xL_oYCwGgC5AFiPoF23DQMld1U75kGwAh8kpBdcbexNhDuuumfM3OuG5q2Qi5Ybtbfz_6zlscLWVTl-1EfjMNGPxfctndsp9CfhnjZD3OabFDG6bDL7ynzI_ZTTIFwtnbbLv6wwV71eEQ6e3pPGc_v365237Pr66__dheXuW25vWcK8TGoahRQydV4zRQ6aQG5VrkpVS81BaxwwraxkHXKqBWuLLjSE5IK8tz9uGYewjTn4XibPY-WhoGHGlaolG1EI3mHJKSH5Xp3TEG6swh-D2GR8PBrBBNbxJEs0I0IE2CmDzvT-lLuyf333GilgSfjgJKf3zwFEy0nhIA5wPZ2bjJPxv_-YnbDn5MDQy_6ZFiPy1hTPAMN1EYMLdri2uJoNOkqqr8B2z7lyw</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Kurahara, Hiroshi, M.D</creator><creator>Shinchi, Hiroyuki, M.D</creator><creator>Mataki, Yuko, M.D</creator><creator>Maemura, Kousei, M.D</creator><creator>Noma, Hidetoshi, M.D</creator><creator>Kubo, Fumitake, M.D</creator><creator>Sakoda, Masahiko, M.D</creator><creator>Ueno, Shinichi, M.D</creator><creator>Natsugoe, Shoji, M.D</creator><creator>Takao, Sonshin, M.D</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2011</creationdate><title>Significance of M2-Polarized Tumor-Associated Macrophage in Pancreatic Cancer</title><author>Kurahara, Hiroshi, M.D ; Shinchi, Hiroyuki, M.D ; Mataki, Yuko, M.D ; Maemura, Kousei, M.D ; Noma, Hidetoshi, M.D ; Kubo, Fumitake, M.D ; Sakoda, Masahiko, M.D ; Ueno, Shinichi, M.D ; Natsugoe, Shoji, M.D ; Takao, Sonshin, M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c616t-8aa7da26a90f587d90e3d5908dba1358139caafa40b7d0fb80eb2d3f1aed25c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adenocarcinoma - diagnosis</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, Myelomonocytic - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphangiogenesis</topic><topic>Lymphatic Metastasis</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>pancreatic cancer</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - mortality</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Prognosis</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Retrospective Studies</topic><topic>Scavenger Receptors, Class A - metabolism</topic><topic>Surgery</topic><topic>tumor microenvironment</topic><topic>tumor-associated macrophage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurahara, Hiroshi, M.D</creatorcontrib><creatorcontrib>Shinchi, Hiroyuki, M.D</creatorcontrib><creatorcontrib>Mataki, Yuko, M.D</creatorcontrib><creatorcontrib>Maemura, Kousei, M.D</creatorcontrib><creatorcontrib>Noma, Hidetoshi, M.D</creatorcontrib><creatorcontrib>Kubo, Fumitake, M.D</creatorcontrib><creatorcontrib>Sakoda, Masahiko, M.D</creatorcontrib><creatorcontrib>Ueno, Shinichi, M.D</creatorcontrib><creatorcontrib>Natsugoe, Shoji, M.D</creatorcontrib><creatorcontrib>Takao, Sonshin, M.D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kurahara, Hiroshi, M.D</au><au>Shinchi, Hiroyuki, M.D</au><au>Mataki, Yuko, M.D</au><au>Maemura, Kousei, M.D</au><au>Noma, Hidetoshi, M.D</au><au>Kubo, Fumitake, M.D</au><au>Sakoda, Masahiko, M.D</au><au>Ueno, Shinichi, M.D</au><au>Natsugoe, Shoji, M.D</au><au>Takao, Sonshin, M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Significance of M2-Polarized Tumor-Associated Macrophage in Pancreatic Cancer</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2011</date><risdate>2011</risdate><volume>167</volume><issue>2</issue><spage>e211</spage><epage>e219</epage><pages>e211-e219</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><abstract>Background The roles of infiltrating macrophages within the tumor microenvironment are complex because of their functional variety. The aim of this study is to examine the role and prognostic significance of tumor-associated macrophages (TAMs) that have an M2 polarized function in pancreatic cancer. Materials and Methods Formalin-fixed, paraffin-embedded blocks were obtained from 76 patients with pancreatic head cancer. All patients underwent macroscopic curative resection. We assessed the number of infiltrating macrophages within the tumor invasive front by not only CD68 but also by CD163 and CD204, which are specific receptors on M2-polarized macrophages. Furthermore, to evaluate lymphangiogenesis, we measured the density of lymphatic vessels in the tumor invasive front by using D2-40. Results High incidence of lymph node metastasis was shown in cases with a high number of CD163- or CD204-positive macrophages. Significantly increased lymphatic vessel density (LVD) was shown in cases with lymph node metastasis compared with cases without lymph node metastasis ( P = 0.0094). Significantly increased LVD ( P = 0.0175) and a poor prognosis ( P = 0.0171) were shown in cases with a high number of macrophages that express CD163 or CD204, however, there was no significant difference according to the number of CD68-positive macrophages. Conclusions M2-polarized TAMs in the invasive front of pancreatic cancer are associated with a poor prognosis due to accelerated lymphatic metastasis, and inhibition of the functional interaction between M2-polarized TAMs and tumor cells may improve the prognosis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19765725</pmid><doi>10.1016/j.jss.2009.05.026</doi></addata></record> |
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subjects | Adenocarcinoma - diagnosis Adenocarcinoma - mortality Adenocarcinoma - pathology Adult Aged Aged, 80 and over Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Female Humans Kaplan-Meier Estimate Lymphangiogenesis Lymphatic Metastasis Macrophages - metabolism Macrophages - pathology Male Middle Aged pancreatic cancer Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - mortality Pancreatic Neoplasms - pathology Prognosis Receptors, Cell Surface - metabolism Retrospective Studies Scavenger Receptors, Class A - metabolism Surgery tumor microenvironment tumor-associated macrophage |
title | Significance of M2-Polarized Tumor-Associated Macrophage in Pancreatic Cancer |
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