Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid

[...]targeting stromal signalling pathways such as sonic hedgehog signalling has also shown promising preclinical effects, and the results of ongoing clinical trials are eagerly awaited. [...]other cellular and acellular stromal components should be explored as further potential targets, among them...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gut 2012-10, Vol.61 (10), p.1377-1379
Hauptverfasser: Michl, Patrick, Gress, Thomas M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1379
container_issue 10
container_start_page 1377
container_title Gut
container_volume 61
creator Michl, Patrick
Gress, Thomas M
description [...]targeting stromal signalling pathways such as sonic hedgehog signalling has also shown promising preclinical effects, and the results of ongoing clinical trials are eagerly awaited. [...]other cellular and acellular stromal components should be explored as further potential targets, among them pancreatic stellate cells and activated stromal fibroblasts as major sources of the pancreatic stroma, as well as inflammatory cells, such as tumour-associated macrophages and other immune cells, 11 12 that are also involved in modulating tumour vasculature and matrix deposition. 13 Furthermore, stroma-related signalling pathways active in these cell types, such as the transforming growth factor β pathway, are promising candidates.
doi_str_mv 10.1136/gutjnl-2012-302604
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1753477532</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1039039142</sourcerecordid><originalsourceid>FETCH-LOGICAL-b506t-ddd3199d67484252063bb59639943e90676e54b4e89d9413424d5b60e8e883263</originalsourceid><addsrcrecordid>eNqNkUuLFDEUhYMoTs_oH3AhBW7clOb9cCc9jg4M42aUwU1IKre7q61Hm6QG-9-bosYR3CiEm1zudw65HIReEPyGECbfbqe8H7qaYkJrhqnE_BFaES51zajWj9EKY6Jqobg5Qacp7THGWhvyFJ1QKiXhRq5Qe9kf4njXDtsqxKkU6No7iMcqj9XBDU0El9umasoT4rvKl77ZzXTeQZVyHHvXVZsx5ggpVb7oXNxCnond0XVTHIcid00bnqEnG9cleH5_n6EvFx9u1p_qq88fL9fvr2ovsMx1CIERY4JUXHMqKJbMe2EkM4YzMFgqCYJ7DtoEwwnjlAfhJQYNWjMq2Rl6vfiWvX5MkLLt29RA17kBxilZogTjqhT6bxQzUw7hM_rqL3Q_TnEoixRDZTiVQvNC0YVq4phShI09xLZ38Vis7JyZXTKzc2Z2yayIXt5bT76H8CD5HVIB6gVoU4afD3MXv1upmBL2-uvafrs919fnt9Le_OF9v_-fD_wCcxqwDA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1779426584</pqid></control><display><type>article</type><title>Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid</title><source>MEDLINE</source><source>BMJ Journals - NESLi2</source><source>PubMed Central</source><creator>Michl, Patrick ; Gress, Thomas M</creator><creatorcontrib>Michl, Patrick ; Gress, Thomas M</creatorcontrib><description>[...]targeting stromal signalling pathways such as sonic hedgehog signalling has also shown promising preclinical effects, and the results of ongoing clinical trials are eagerly awaited. [...]other cellular and acellular stromal components should be explored as further potential targets, among them pancreatic stellate cells and activated stromal fibroblasts as major sources of the pancreatic stroma, as well as inflammatory cells, such as tumour-associated macrophages and other immune cells, 11 12 that are also involved in modulating tumour vasculature and matrix deposition. 13 Furthermore, stroma-related signalling pathways active in these cell types, such as the transforming growth factor β pathway, are promising candidates.</description><identifier>ISSN: 0017-5749</identifier><identifier>EISSN: 1468-3288</identifier><identifier>DOI: 10.1136/gutjnl-2012-302604</identifier><identifier>PMID: 22661496</identifier><identifier>CODEN: GUTTAK</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and British Society of Gastroenterology</publisher><subject><![CDATA[Animals ; Antimetabolites, Antineoplastic - administration & dosage ; Antimetabolites, Antineoplastic - therapeutic use ; Biomarkers, Tumor - metabolism ; Cancer ; carcinogenesis ; Cell Adhesion Molecules - administration & dosage ; Cell Adhesion Molecules - pharmacology ; cell migration ; Clinical trials ; Cytotoxicity ; Deoxycytidine - administration & dosage ; Deoxycytidine - analogs & derivatives ; Deoxycytidine - therapeutic use ; Drug Delivery Systems ; Drug dosages ; Drug resistance ; Drug Resistance, Neoplasm - drug effects ; Drug Resistance, Neoplasm - physiology ; endoscopy ; Extracellular matrix ; Fibroblasts ; gastrointestinal cancer ; gene expression ; Humans ; Hyaluronic Acid - metabolism ; Hyaluronoglucosaminidase - administration & dosage ; Hyaluronoglucosaminidase - pharmacology ; Medical prognosis ; Metastasis ; Mice ; Mortality ; Pancreatic cancer ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - metabolism ; pancreatic tumours ; pancreatitis ; Permeability ; Pharmaceutical industry ; Recombinant Proteins - administration & dosage ; Recombinant Proteins - pharmacology ; Studies ; Tumors ; Vascular endothelial growth factor]]></subject><ispartof>Gut, 2012-10, Vol.61 (10), p.1377-1379</ispartof><rights>2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>Copyright: 2012 (c) 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b506t-ddd3199d67484252063bb59639943e90676e54b4e89d9413424d5b60e8e883263</citedby><cites>FETCH-LOGICAL-b506t-ddd3199d67484252063bb59639943e90676e54b4e89d9413424d5b60e8e883263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://gut.bmj.com/content/61/10/1377.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://gut.bmj.com/content/61/10/1377.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3182,23551,27903,27904,77347,77378</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22661496$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Michl, Patrick</creatorcontrib><creatorcontrib>Gress, Thomas M</creatorcontrib><title>Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid</title><title>Gut</title><addtitle>Gut</addtitle><description>[...]targeting stromal signalling pathways such as sonic hedgehog signalling has also shown promising preclinical effects, and the results of ongoing clinical trials are eagerly awaited. [...]other cellular and acellular stromal components should be explored as further potential targets, among them pancreatic stellate cells and activated stromal fibroblasts as major sources of the pancreatic stroma, as well as inflammatory cells, such as tumour-associated macrophages and other immune cells, 11 12 that are also involved in modulating tumour vasculature and matrix deposition. 13 Furthermore, stroma-related signalling pathways active in these cell types, such as the transforming growth factor β pathway, are promising candidates.</description><subject>Animals</subject><subject>Antimetabolites, Antineoplastic - administration &amp; dosage</subject><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>carcinogenesis</subject><subject>Cell Adhesion Molecules - administration &amp; dosage</subject><subject>Cell Adhesion Molecules - pharmacology</subject><subject>cell migration</subject><subject>Clinical trials</subject><subject>Cytotoxicity</subject><subject>Deoxycytidine - administration &amp; dosage</subject><subject>Deoxycytidine - analogs &amp; derivatives</subject><subject>Deoxycytidine - therapeutic use</subject><subject>Drug Delivery Systems</subject><subject>Drug dosages</subject><subject>Drug resistance</subject><subject>Drug Resistance, Neoplasm - drug effects</subject><subject>Drug Resistance, Neoplasm - physiology</subject><subject>endoscopy</subject><subject>Extracellular matrix</subject><subject>Fibroblasts</subject><subject>gastrointestinal cancer</subject><subject>gene expression</subject><subject>Humans</subject><subject>Hyaluronic Acid - metabolism</subject><subject>Hyaluronoglucosaminidase - administration &amp; dosage</subject><subject>Hyaluronoglucosaminidase - pharmacology</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Mice</subject><subject>Mortality</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>pancreatic tumours</subject><subject>pancreatitis</subject><subject>Permeability</subject><subject>Pharmaceutical industry</subject><subject>Recombinant Proteins - administration &amp; dosage</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Studies</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><issn>0017-5749</issn><issn>1468-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkUuLFDEUhYMoTs_oH3AhBW7clOb9cCc9jg4M42aUwU1IKre7q61Hm6QG-9-bosYR3CiEm1zudw65HIReEPyGECbfbqe8H7qaYkJrhqnE_BFaES51zajWj9EKY6Jqobg5Qacp7THGWhvyFJ1QKiXhRq5Qe9kf4njXDtsqxKkU6No7iMcqj9XBDU0El9umasoT4rvKl77ZzXTeQZVyHHvXVZsx5ggpVb7oXNxCnond0XVTHIcid00bnqEnG9cleH5_n6EvFx9u1p_qq88fL9fvr2ovsMx1CIERY4JUXHMqKJbMe2EkM4YzMFgqCYJ7DtoEwwnjlAfhJQYNWjMq2Rl6vfiWvX5MkLLt29RA17kBxilZogTjqhT6bxQzUw7hM_rqL3Q_TnEoixRDZTiVQvNC0YVq4phShI09xLZ38Vis7JyZXTKzc2Z2yayIXt5bT76H8CD5HVIB6gVoU4afD3MXv1upmBL2-uvafrs919fnt9Le_OF9v_-fD_wCcxqwDA</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Michl, Patrick</creator><creator>Gress, Thomas M</creator><general>BMJ Publishing Group Ltd and British Society of Gastroenterology</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20121001</creationdate><title>Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid</title><author>Michl, Patrick ; Gress, Thomas M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b506t-ddd3199d67484252063bb59639943e90676e54b4e89d9413424d5b60e8e883263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antimetabolites, Antineoplastic - administration &amp; dosage</topic><topic>Antimetabolites, Antineoplastic - therapeutic use</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer</topic><topic>carcinogenesis</topic><topic>Cell Adhesion Molecules - administration &amp; dosage</topic><topic>Cell Adhesion Molecules - pharmacology</topic><topic>cell migration</topic><topic>Clinical trials</topic><topic>Cytotoxicity</topic><topic>Deoxycytidine - administration &amp; dosage</topic><topic>Deoxycytidine - analogs &amp; derivatives</topic><topic>Deoxycytidine - therapeutic use</topic><topic>Drug Delivery Systems</topic><topic>Drug dosages</topic><topic>Drug resistance</topic><topic>Drug Resistance, Neoplasm - drug effects</topic><topic>Drug Resistance, Neoplasm - physiology</topic><topic>endoscopy</topic><topic>Extracellular matrix</topic><topic>Fibroblasts</topic><topic>gastrointestinal cancer</topic><topic>gene expression</topic><topic>Humans</topic><topic>Hyaluronic Acid - metabolism</topic><topic>Hyaluronoglucosaminidase - administration &amp; dosage</topic><topic>Hyaluronoglucosaminidase - pharmacology</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Mice</topic><topic>Mortality</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>pancreatic tumours</topic><topic>pancreatitis</topic><topic>Permeability</topic><topic>Pharmaceutical industry</topic><topic>Recombinant Proteins - administration &amp; dosage</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Studies</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Michl, Patrick</creatorcontrib><creatorcontrib>Gress, Thomas M</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Gut</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Michl, Patrick</au><au>Gress, Thomas M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid</atitle><jtitle>Gut</jtitle><addtitle>Gut</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>61</volume><issue>10</issue><spage>1377</spage><epage>1379</epage><pages>1377-1379</pages><issn>0017-5749</issn><eissn>1468-3288</eissn><coden>GUTTAK</coden><abstract>[...]targeting stromal signalling pathways such as sonic hedgehog signalling has also shown promising preclinical effects, and the results of ongoing clinical trials are eagerly awaited. [...]other cellular and acellular stromal components should be explored as further potential targets, among them pancreatic stellate cells and activated stromal fibroblasts as major sources of the pancreatic stroma, as well as inflammatory cells, such as tumour-associated macrophages and other immune cells, 11 12 that are also involved in modulating tumour vasculature and matrix deposition. 13 Furthermore, stroma-related signalling pathways active in these cell types, such as the transforming growth factor β pathway, are promising candidates.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and British Society of Gastroenterology</pub><pmid>22661496</pmid><doi>10.1136/gutjnl-2012-302604</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0017-5749
ispartof Gut, 2012-10, Vol.61 (10), p.1377-1379
issn 0017-5749
1468-3288
language eng
recordid cdi_proquest_miscellaneous_1753477532
source MEDLINE; BMJ Journals - NESLi2; PubMed Central
subjects Animals
Antimetabolites, Antineoplastic - administration & dosage
Antimetabolites, Antineoplastic - therapeutic use
Biomarkers, Tumor - metabolism
Cancer
carcinogenesis
Cell Adhesion Molecules - administration & dosage
Cell Adhesion Molecules - pharmacology
cell migration
Clinical trials
Cytotoxicity
Deoxycytidine - administration & dosage
Deoxycytidine - analogs & derivatives
Deoxycytidine - therapeutic use
Drug Delivery Systems
Drug dosages
Drug resistance
Drug Resistance, Neoplasm - drug effects
Drug Resistance, Neoplasm - physiology
endoscopy
Extracellular matrix
Fibroblasts
gastrointestinal cancer
gene expression
Humans
Hyaluronic Acid - metabolism
Hyaluronoglucosaminidase - administration & dosage
Hyaluronoglucosaminidase - pharmacology
Medical prognosis
Metastasis
Mice
Mortality
Pancreatic cancer
Pancreatic Neoplasms - drug therapy
Pancreatic Neoplasms - metabolism
pancreatic tumours
pancreatitis
Permeability
Pharmaceutical industry
Recombinant Proteins - administration & dosage
Recombinant Proteins - pharmacology
Studies
Tumors
Vascular endothelial growth factor
title Improving drug delivery to pancreatic cancer: breaching the stromal fortress by targeting hyaluronic acid
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T06%3A32%3A26IST&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=Improving%20drug%20delivery%20to%20pancreatic%20cancer:%20breaching%20the%20stromal%20fortress%20by%20targeting%20hyaluronic%20acid&rft.jtitle=Gut&rft.au=Michl,%20Patrick&rft.date=2012-10-01&rft.volume=61&rft.issue=10&rft.spage=1377&rft.epage=1379&rft.pages=1377-1379&rft.issn=0017-5749&rft.eissn=1468-3288&rft.coden=GUTTAK&rft_id=info:doi/10.1136/gutjnl-2012-302604&rft_dat=%3Cproquest_cross%3E1039039142%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=1779426584&rft_id=info:pmid/22661496&rfr_iscdi=true