The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma

Tumor angiogenesis has been related to the initiation as well as progression toward more aggressive behavior of human tumors. We will discuss genetic events underlying the initiation and progression of colorectal and pancreatic adenocarcinoma with a particular focus on the modulation of angiogenesis...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Seminars in oncology 2006-12, Vol.33 (6), p.50-56
Hauptverfasser: Tassi, Elena, Wellstein, Anton
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 56
container_issue 6
container_start_page 50
container_title Seminars in oncology
container_volume 33
creator Tassi, Elena
Wellstein, Anton
description Tumor angiogenesis has been related to the initiation as well as progression toward more aggressive behavior of human tumors. We will discuss genetic events underlying the initiation and progression of colorectal and pancreatic adenocarcinoma with a particular focus on the modulation of angiogenesis. A secreted fibroblast growth factor (FGF) binding protein (FGF-BP), which is an extracellular chaperone molecule for FGFs, has been shown to enhance FGF-mediated biochemical and biologic events and to be a crucial rate-limiting factor for tumor-dependent angiogenesis. Histochemical and in situ hybridization studies with archival samples show that FGF-BP is induced early during the initiation of colorectal and pancreatic adenocarcinoma. We will discuss the potential of this secreted protein as a serum marker to identify at-risk subjects.
doi_str_mv 10.1053/j.seminoncol.2006.10.014
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1781498</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0093775406003915</els_id><sourcerecordid>68258064</sourcerecordid><originalsourceid>FETCH-LOGICAL-c573t-c3bcfca5797eccf7d737643166bb2257f2ed214234d4695e76b2f8f1216b5eb43</originalsourceid><addsrcrecordid>eNqFUU1vEzEQXSEQDYW_gHyBUzfY3g87F6Q0atpKRVRKOVve2dmNI69d7E1R_wC_G68SNXDiZHnmvTcz72UZYXTOaFV82c0jDsZ5B97OOaV1Ks8pK19lM1YVPJeCytfZjNJFkQtRlWfZuxh3lHImOH-bnTHBhORSzrLfD1skS9cb36MzQDa_zAhb8s1bhL3FC7JBCDhiS9bX6_zSuNa4ntwHP6JxF0Q7cptKoEcfiO_IlQ72mWxG3WOc_vfaJboek7J2LVl56wPCqC1Ztug86ADpjEG_z9502kb8cHzPsx_rq4fVTX73_fp2tbzLoRLFmEPRQAe6EguBAJ1oRSHqsmB13TScV6Lj2HJW8qJsy3pRoagb3smOcVY3FTZlcZ59Peg-7psBW0A3Bm3VYzCDDs_Ka6P-7TizVb1_UskvVi5kEvh8FAj-5x7jqAYTAa3VDv0-qlryStJ6miQPQAg-xoDdyxBG1RSi2qlTiGoKceqkEBP1499LnojH1BLg0xGgI2jbheSyiSecLMuqYBPu8oDDZOmTwaAiGHSArZlSUK03_9_mDwc0woA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68258064</pqid></control><display><type>article</type><title>The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Tassi, Elena ; Wellstein, Anton</creator><creatorcontrib>Tassi, Elena ; Wellstein, Anton</creatorcontrib><description>Tumor angiogenesis has been related to the initiation as well as progression toward more aggressive behavior of human tumors. We will discuss genetic events underlying the initiation and progression of colorectal and pancreatic adenocarcinoma with a particular focus on the modulation of angiogenesis. A secreted fibroblast growth factor (FGF) binding protein (FGF-BP), which is an extracellular chaperone molecule for FGFs, has been shown to enhance FGF-mediated biochemical and biologic events and to be a crucial rate-limiting factor for tumor-dependent angiogenesis. Histochemical and in situ hybridization studies with archival samples show that FGF-BP is induced early during the initiation of colorectal and pancreatic adenocarcinoma. We will discuss the potential of this secreted protein as a serum marker to identify at-risk subjects.</description><identifier>ISSN: 0093-7754</identifier><identifier>EISSN: 1532-8708</identifier><identifier>DOI: 10.1053/j.seminoncol.2006.10.014</identifier><identifier>PMID: 17178288</identifier><identifier>CODEN: SOLGAV</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Adenocarcinoma - blood supply ; Biological and medical sciences ; Biomarkers, Tumor - blood ; Carrier Proteins - blood ; Colorectal Neoplasms - blood supply ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Intercellular Signaling Peptides and Proteins ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Neovascularization, Pathologic - blood ; Pancreatic Neoplasms - blood supply ; Tumors</subject><ispartof>Seminars in oncology, 2006-12, Vol.33 (6), p.50-56</ispartof><rights>2006 Elsevier Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-c3bcfca5797eccf7d737643166bb2257f2ed214234d4695e76b2f8f1216b5eb43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0093775406003915$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,309,310,314,776,780,785,786,881,3537,23909,23910,25118,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18445318$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17178288$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tassi, Elena</creatorcontrib><creatorcontrib>Wellstein, Anton</creatorcontrib><title>The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma</title><title>Seminars in oncology</title><addtitle>Semin Oncol</addtitle><description>Tumor angiogenesis has been related to the initiation as well as progression toward more aggressive behavior of human tumors. We will discuss genetic events underlying the initiation and progression of colorectal and pancreatic adenocarcinoma with a particular focus on the modulation of angiogenesis. A secreted fibroblast growth factor (FGF) binding protein (FGF-BP), which is an extracellular chaperone molecule for FGFs, has been shown to enhance FGF-mediated biochemical and biologic events and to be a crucial rate-limiting factor for tumor-dependent angiogenesis. Histochemical and in situ hybridization studies with archival samples show that FGF-BP is induced early during the initiation of colorectal and pancreatic adenocarcinoma. We will discuss the potential of this secreted protein as a serum marker to identify at-risk subjects.</description><subject>Adenocarcinoma - blood supply</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Carrier Proteins - blood</subject><subject>Colorectal Neoplasms - blood supply</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>Neovascularization, Pathologic - blood</subject><subject>Pancreatic Neoplasms - blood supply</subject><subject>Tumors</subject><issn>0093-7754</issn><issn>1532-8708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1vEzEQXSEQDYW_gHyBUzfY3g87F6Q0atpKRVRKOVve2dmNI69d7E1R_wC_G68SNXDiZHnmvTcz72UZYXTOaFV82c0jDsZ5B97OOaV1Ks8pK19lM1YVPJeCytfZjNJFkQtRlWfZuxh3lHImOH-bnTHBhORSzrLfD1skS9cb36MzQDa_zAhb8s1bhL3FC7JBCDhiS9bX6_zSuNa4ntwHP6JxF0Q7cptKoEcfiO_IlQ72mWxG3WOc_vfaJboek7J2LVl56wPCqC1Ztug86ADpjEG_z9502kb8cHzPsx_rq4fVTX73_fp2tbzLoRLFmEPRQAe6EguBAJ1oRSHqsmB13TScV6Lj2HJW8qJsy3pRoagb3smOcVY3FTZlcZ59Peg-7psBW0A3Bm3VYzCDDs_Ka6P-7TizVb1_UskvVi5kEvh8FAj-5x7jqAYTAa3VDv0-qlryStJ6miQPQAg-xoDdyxBG1RSi2qlTiGoKceqkEBP1499LnojH1BLg0xGgI2jbheSyiSecLMuqYBPu8oDDZOmTwaAiGHSArZlSUK03_9_mDwc0woA</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Tassi, Elena</creator><creator>Wellstein, Anton</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20061201</creationdate><title>The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma</title><author>Tassi, Elena ; Wellstein, Anton</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-c3bcfca5797eccf7d737643166bb2257f2ed214234d4695e76b2f8f1216b5eb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adenocarcinoma - blood supply</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Carrier Proteins - blood</topic><topic>Colorectal Neoplasms - blood supply</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Neovascularization, Pathologic - blood</topic><topic>Pancreatic Neoplasms - blood supply</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tassi, Elena</creatorcontrib><creatorcontrib>Wellstein, Anton</creatorcontrib><collection>Pascal-Francis</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Seminars in oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tassi, Elena</au><au>Wellstein, Anton</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma</atitle><jtitle>Seminars in oncology</jtitle><addtitle>Semin Oncol</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>33</volume><issue>6</issue><spage>50</spage><epage>56</epage><pages>50-56</pages><issn>0093-7754</issn><eissn>1532-8708</eissn><coden>SOLGAV</coden><abstract>Tumor angiogenesis has been related to the initiation as well as progression toward more aggressive behavior of human tumors. We will discuss genetic events underlying the initiation and progression of colorectal and pancreatic adenocarcinoma with a particular focus on the modulation of angiogenesis. A secreted fibroblast growth factor (FGF) binding protein (FGF-BP), which is an extracellular chaperone molecule for FGFs, has been shown to enhance FGF-mediated biochemical and biologic events and to be a crucial rate-limiting factor for tumor-dependent angiogenesis. Histochemical and in situ hybridization studies with archival samples show that FGF-BP is induced early during the initiation of colorectal and pancreatic adenocarcinoma. We will discuss the potential of this secreted protein as a serum marker to identify at-risk subjects.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>17178288</pmid><doi>10.1053/j.seminoncol.2006.10.014</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0093-7754
ispartof Seminars in oncology, 2006-12, Vol.33 (6), p.50-56
issn 0093-7754
1532-8708
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1781498
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adenocarcinoma - blood supply
Biological and medical sciences
Biomarkers, Tumor - blood
Carrier Proteins - blood
Colorectal Neoplasms - blood supply
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Intercellular Signaling Peptides and Proteins
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Medical sciences
Neovascularization, Pathologic - blood
Pancreatic Neoplasms - blood supply
Tumors
title The Angiogenic Switch Molecule, Secreted FGF-Binding Protein, an Indicator of Early Stages of Pancreatic and Colorectal Adenocarcinoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T17%3A53%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Angiogenic%20Switch%20Molecule,%20Secreted%20FGF-Binding%20Protein,%20an%20Indicator%20of%20Early%20Stages%20of%20Pancreatic%20and%20Colorectal%20Adenocarcinoma&rft.jtitle=Seminars%20in%20oncology&rft.au=Tassi,%20Elena&rft.date=2006-12-01&rft.volume=33&rft.issue=6&rft.spage=50&rft.epage=56&rft.pages=50-56&rft.issn=0093-7754&rft.eissn=1532-8708&rft.coden=SOLGAV&rft_id=info:doi/10.1053/j.seminoncol.2006.10.014&rft_dat=%3Cproquest_pubme%3E68258064%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=68258064&rft_id=info:pmid/17178288&rft_els_id=S0093775406003915&rfr_iscdi=true