Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy

The macrophage is known to be a multifunctional antigen presenting cells and playing a central role in inflammation. Macrophages infiltrate into malignant tumor tissues in high numbers (the so-called tumor-associated macrophages [TAMs]) and many studies over the past decade have demonstrated that ma...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Advanced drug delivery reviews 2016-04, Vol.99 (Pt B), p.180-185
Hauptverfasser: Komohara, Yoshihiro, Fujiwara, Yukio, Ohnishi, Koji, Takeya, Motohiro
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 185
container_issue Pt B
container_start_page 180
container_title Advanced drug delivery reviews
container_volume 99
creator Komohara, Yoshihiro
Fujiwara, Yukio
Ohnishi, Koji
Takeya, Motohiro
description The macrophage is known to be a multifunctional antigen presenting cells and playing a central role in inflammation. Macrophages infiltrate into malignant tumor tissues in high numbers (the so-called tumor-associated macrophages [TAMs]) and many studies over the past decade have demonstrated that macrophages have protumor functions and are closely related to tumor progression. It has been shown that protumor macrophages that have differentiated through interaction with tumor cells are involved in stem cell niches, immunosuppression, invasion, and metastasis. Consistent with these functions, studies using human tumor samples have demonstrated that a higher density of macrophages, especially macrophages with the M2 phenotype, is closely associated with worse clinical prognosis in many kinds of malignant tumors. Infiltrating TAMs themselves or polarization pathway of TAMs are considered as new therapeutic targets for the therapy of malignant tumors. TAM, tumor associated macrophage; Treg, regulatory T cell; VEGF, vascular endothelial growth factor; Stat3, signal transducer and activator of transcription 3; EGF, epidermal growth factor; M-CSF, macrophage colony stimulating factor. [Display omitted]
doi_str_mv 10.1016/j.addr.2015.11.009
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1776630135</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0169409X15002732</els_id><sourcerecordid>1776630135</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-64c1d0a06a428d8305d19c8c228ce12c86288e5a7a339e36795e5da908891a3e3</originalsourceid><addsrcrecordid>eNp9kE1L9DAUhYMoOn78ARfS5btpzU3bNBE3In6BoKCCu3BN7miG6XRMUsF_b4YZ36Wru7jPOXAexo6BV8BBns4qdC5UgkNbAVSc6y02AdWJUgndbLNJhnTZcP26x_ZjnHEOopN8l-0JKQWAlhP29Dz2QygxxsF6TOSKHm0Ylh_4TvGseBwSLZLHeZE-KOCSxuRtkTC8U4rFdAgF5ndpcWEpbJjvQ7YzxXmko809YC_XV8-Xt-X9w83d5cV9aRshUikbC44jl9gI5VTNWwfaKiuEsgTCKimUohY7rGtNtex0S61DzZXSgDXVB-zfuncZhs-RYjK9j5bmc1zQMEYDXSdlzaFuMyrWaN4WY6CpWQbfY_g2wM1KppmZlUyzkmkATJaZQyeb_vGtJ_c_8msvA-drgPLKL0_BROspq3A-kE3GDf6v_h_eUYXR</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1776630135</pqid></control><display><type>article</type><title>Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Komohara, Yoshihiro ; Fujiwara, Yukio ; Ohnishi, Koji ; Takeya, Motohiro</creator><creatorcontrib>Komohara, Yoshihiro ; Fujiwara, Yukio ; Ohnishi, Koji ; Takeya, Motohiro</creatorcontrib><description>The macrophage is known to be a multifunctional antigen presenting cells and playing a central role in inflammation. Macrophages infiltrate into malignant tumor tissues in high numbers (the so-called tumor-associated macrophages [TAMs]) and many studies over the past decade have demonstrated that macrophages have protumor functions and are closely related to tumor progression. It has been shown that protumor macrophages that have differentiated through interaction with tumor cells are involved in stem cell niches, immunosuppression, invasion, and metastasis. Consistent with these functions, studies using human tumor samples have demonstrated that a higher density of macrophages, especially macrophages with the M2 phenotype, is closely associated with worse clinical prognosis in many kinds of malignant tumors. Infiltrating TAMs themselves or polarization pathway of TAMs are considered as new therapeutic targets for the therapy of malignant tumors. TAM, tumor associated macrophage; Treg, regulatory T cell; VEGF, vascular endothelial growth factor; Stat3, signal transducer and activator of transcription 3; EGF, epidermal growth factor; M-CSF, macrophage colony stimulating factor. [Display omitted]</description><identifier>ISSN: 0169-409X</identifier><identifier>EISSN: 1872-8294</identifier><identifier>DOI: 10.1016/j.addr.2015.11.009</identifier><identifier>PMID: 26621196</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Disease Progression ; Heterogeneity ; Humans ; Inflammation - pathology ; Macrophages - drug effects ; Macrophages - pathology ; Neoplasm Invasiveness - pathology ; Neoplasm Metastasis - pathology ; Neoplasms - drug therapy ; Neoplasms - pathology ; Polarization ; Protumor macrophage</subject><ispartof>Advanced drug delivery reviews, 2016-04, Vol.99 (Pt B), p.180-185</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-64c1d0a06a428d8305d19c8c228ce12c86288e5a7a339e36795e5da908891a3e3</citedby><cites>FETCH-LOGICAL-c422t-64c1d0a06a428d8305d19c8c228ce12c86288e5a7a339e36795e5da908891a3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.addr.2015.11.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26621196$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Fujiwara, Yukio</creatorcontrib><creatorcontrib>Ohnishi, Koji</creatorcontrib><creatorcontrib>Takeya, Motohiro</creatorcontrib><title>Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy</title><title>Advanced drug delivery reviews</title><addtitle>Adv Drug Deliv Rev</addtitle><description>The macrophage is known to be a multifunctional antigen presenting cells and playing a central role in inflammation. Macrophages infiltrate into malignant tumor tissues in high numbers (the so-called tumor-associated macrophages [TAMs]) and many studies over the past decade have demonstrated that macrophages have protumor functions and are closely related to tumor progression. It has been shown that protumor macrophages that have differentiated through interaction with tumor cells are involved in stem cell niches, immunosuppression, invasion, and metastasis. Consistent with these functions, studies using human tumor samples have demonstrated that a higher density of macrophages, especially macrophages with the M2 phenotype, is closely associated with worse clinical prognosis in many kinds of malignant tumors. Infiltrating TAMs themselves or polarization pathway of TAMs are considered as new therapeutic targets for the therapy of malignant tumors. TAM, tumor associated macrophage; Treg, regulatory T cell; VEGF, vascular endothelial growth factor; Stat3, signal transducer and activator of transcription 3; EGF, epidermal growth factor; M-CSF, macrophage colony stimulating factor. [Display omitted]</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Disease Progression</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Inflammation - pathology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - pathology</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Metastasis - pathology</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Polarization</subject><subject>Protumor macrophage</subject><issn>0169-409X</issn><issn>1872-8294</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1L9DAUhYMoOn78ARfS5btpzU3bNBE3In6BoKCCu3BN7miG6XRMUsF_b4YZ36Wru7jPOXAexo6BV8BBns4qdC5UgkNbAVSc6y02AdWJUgndbLNJhnTZcP26x_ZjnHEOopN8l-0JKQWAlhP29Dz2QygxxsF6TOSKHm0Ylh_4TvGseBwSLZLHeZE-KOCSxuRtkTC8U4rFdAgF5ndpcWEpbJjvQ7YzxXmko809YC_XV8-Xt-X9w83d5cV9aRshUikbC44jl9gI5VTNWwfaKiuEsgTCKimUohY7rGtNtex0S61DzZXSgDXVB-zfuncZhs-RYjK9j5bmc1zQMEYDXSdlzaFuMyrWaN4WY6CpWQbfY_g2wM1KppmZlUyzkmkATJaZQyeb_vGtJ_c_8msvA-drgPLKL0_BROspq3A-kE3GDf6v_h_eUYXR</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Komohara, Yoshihiro</creator><creator>Fujiwara, Yukio</creator><creator>Ohnishi, Koji</creator><creator>Takeya, Motohiro</creator><general>Elsevier B.V</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>20160401</creationdate><title>Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy</title><author>Komohara, Yoshihiro ; Fujiwara, Yukio ; Ohnishi, Koji ; Takeya, Motohiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-64c1d0a06a428d8305d19c8c228ce12c86288e5a7a339e36795e5da908891a3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Disease Progression</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Inflammation - pathology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - pathology</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>Neoplasm Metastasis - pathology</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - pathology</topic><topic>Polarization</topic><topic>Protumor macrophage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Fujiwara, Yukio</creatorcontrib><creatorcontrib>Ohnishi, Koji</creatorcontrib><creatorcontrib>Takeya, Motohiro</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>Advanced drug delivery reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komohara, Yoshihiro</au><au>Fujiwara, Yukio</au><au>Ohnishi, Koji</au><au>Takeya, Motohiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy</atitle><jtitle>Advanced drug delivery reviews</jtitle><addtitle>Adv Drug Deliv Rev</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>99</volume><issue>Pt B</issue><spage>180</spage><epage>185</epage><pages>180-185</pages><issn>0169-409X</issn><eissn>1872-8294</eissn><abstract>The macrophage is known to be a multifunctional antigen presenting cells and playing a central role in inflammation. Macrophages infiltrate into malignant tumor tissues in high numbers (the so-called tumor-associated macrophages [TAMs]) and many studies over the past decade have demonstrated that macrophages have protumor functions and are closely related to tumor progression. It has been shown that protumor macrophages that have differentiated through interaction with tumor cells are involved in stem cell niches, immunosuppression, invasion, and metastasis. Consistent with these functions, studies using human tumor samples have demonstrated that a higher density of macrophages, especially macrophages with the M2 phenotype, is closely associated with worse clinical prognosis in many kinds of malignant tumors. Infiltrating TAMs themselves or polarization pathway of TAMs are considered as new therapeutic targets for the therapy of malignant tumors. TAM, tumor associated macrophage; Treg, regulatory T cell; VEGF, vascular endothelial growth factor; Stat3, signal transducer and activator of transcription 3; EGF, epidermal growth factor; M-CSF, macrophage colony stimulating factor. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26621196</pmid><doi>10.1016/j.addr.2015.11.009</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0169-409X
ispartof Advanced drug delivery reviews, 2016-04, Vol.99 (Pt B), p.180-185
issn 0169-409X
1872-8294
language eng
recordid cdi_proquest_miscellaneous_1776630135
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Animals
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Disease Progression
Heterogeneity
Humans
Inflammation - pathology
Macrophages - drug effects
Macrophages - pathology
Neoplasm Invasiveness - pathology
Neoplasm Metastasis - pathology
Neoplasms - drug therapy
Neoplasms - pathology
Polarization
Protumor macrophage
title Tumor-associated macrophages: Potential therapeutic targets for anti-cancer therapy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T02%3A15%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tumor-associated%20macrophages:%20Potential%20therapeutic%20targets%20for%20anti-cancer%20therapy&rft.jtitle=Advanced%20drug%20delivery%20reviews&rft.au=Komohara,%20Yoshihiro&rft.date=2016-04-01&rft.volume=99&rft.issue=Pt%20B&rft.spage=180&rft.epage=185&rft.pages=180-185&rft.issn=0169-409X&rft.eissn=1872-8294&rft_id=info:doi/10.1016/j.addr.2015.11.009&rft_dat=%3Cproquest_cross%3E1776630135%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1776630135&rft_id=info:pmid/26621196&rft_els_id=S0169409X15002732&rfr_iscdi=true