Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line
Bussink, J., Kaanders, J. H. A. M., Rijken, P. F. J. W., Raleigh, J. A. and Van der Kogel, A. J. Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line. The effect of irradiation depends on the oxygenation status of the tissue, while irradiat...
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Veröffentlicht in: | Radiation research 2000-04, Vol.153 (4), p.398-404 |
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description | Bussink, J., Kaanders, J. H. A. M., Rijken, P. F. J. W., Raleigh, J. A. and Van der Kogel, A. J. Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line. The effect of irradiation depends on the oxygenation status of the tissue, while irradiation itself also changes the oxygenation and perfusion status of tissues. A better understanding of the changes in tumor oxygenation and perfusion over time after irradiation will allow a better planning of fractionated radiotherapy in combination with modifiers of blood flow and oxygenation. Vascular architecture (endothelial marker), perfusion (Hoechst 33342) and oxygenation (pimonidazole) were studied in a human laryngeal squamous cell carcinoma tumor line grown as xenografts in nude mice. The effect of a single dose of 10 Gy X rays on these parameters was evaluated from 2 h to 11 days after irradiation. Shortly after irradiation, there was an 8% increase in perfused blood vessels (from 57% to 65%) followed by a significant decrease, with a minimum value of 42% at 26 h after irradiation, and a subsequent increase to control levels at 7 to 11 days after irradiation. The hypoxic fraction showed a decrease at 7 h after treatment from 13% to 5% with an increase to 19% at 11 days after irradiation. These experiments show that irradiation causes rapid changes in oxygenation and perfusion which may have consequences for the optimal timing of radiotherapy schedules employing multiple fractions per day and the introduction of oxygenation- and perfusion-modifying drugs. |
doi_str_mv | 10.1667/0033-7587(2000)153[0398:CIBPAH]2.0.CO;2 |
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H A. M. ; Rijken, P. F J. W. ; Raleigh, J. A. ; Van der Kogel, A. J.</creator><creatorcontrib>Bussink, J. ; Kaanders, J. H A. M. ; Rijken, P. F J. W. ; Raleigh, J. A. ; Van der Kogel, A. J.</creatorcontrib><description>Bussink, J., Kaanders, J. H. A. M., Rijken, P. F. J. W., Raleigh, J. A. and Van der Kogel, A. J. Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line. The effect of irradiation depends on the oxygenation status of the tissue, while irradiation itself also changes the oxygenation and perfusion status of tissues. A better understanding of the changes in tumor oxygenation and perfusion over time after irradiation will allow a better planning of fractionated radiotherapy in combination with modifiers of blood flow and oxygenation. Vascular architecture (endothelial marker), perfusion (Hoechst 33342) and oxygenation (pimonidazole) were studied in a human laryngeal squamous cell carcinoma tumor line grown as xenografts in nude mice. The effect of a single dose of 10 Gy X rays on these parameters was evaluated from 2 h to 11 days after irradiation. Shortly after irradiation, there was an 8% increase in perfused blood vessels (from 57% to 65%) followed by a significant decrease, with a minimum value of 42% at 26 h after irradiation, and a subsequent increase to control levels at 7 to 11 days after irradiation. The hypoxic fraction showed a decrease at 7 h after treatment from 13% to 5% with an increase to 19% at 11 days after irradiation. These experiments show that irradiation causes rapid changes in oxygenation and perfusion which may have consequences for the optimal timing of radiotherapy schedules employing multiple fractions per day and the introduction of oxygenation- and perfusion-modifying drugs.</description><identifier>ISSN: 0033-7587</identifier><identifier>EISSN: 1938-5404</identifier><identifier>DOI: 10.1667/0033-7587(2000)153[0398:CIBPAH]2.0.CO;2</identifier><identifier>PMID: 10760999</identifier><identifier>CODEN: RAREAE</identifier><language>eng</language><publisher>Oak Brook, Il: Radiation Research Society</publisher><subject>Biological and medical sciences ; Blood ; Cancer ; Carcinogenesis, carcinogens and anticarcinogens ; Carcinoma, Squamous Cell - blood ; Carcinoma, Squamous Cell - pathology ; Cell Hypoxia - radiation effects ; Heterologous transplantation ; Humans ; Hypoxia ; Image Processing, Computer-Assisted ; Immunohistochemistry ; Irradiation ; Laryngeal Neoplasms - blood ; Laryngeal Neoplasms - pathology ; Medical sciences ; Perfusion ; Physical agents ; Radiotherapy ; REGULAR ARTICLES ; Space life sciences ; Squamous cell carcinoma ; Tissue oxygenation ; Tumor Cells, Cultured ; Tumors</subject><ispartof>Radiation research, 2000-04, Vol.153 (4), p.398-404</ispartof><rights>Radiation Research Society</rights><rights>Copyright 2000 The Radiation Research Society</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b519t-205cd0cd2841872771e3cfef322083a2ed0a37cdc954574856ca6061f8986043</citedby><cites>FETCH-LOGICAL-b519t-205cd0cd2841872771e3cfef322083a2ed0a37cdc954574856ca6061f8986043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bioone.org/doi/pdf/10.1667/0033-7587(2000)153[0398:CIBPAH]2.0.CO;2$$EPDF$$P50$$Gbioone$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3580237$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,26978,27924,27925,52363,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1327290$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10760999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bussink, J.</creatorcontrib><creatorcontrib>Kaanders, J. H A. M.</creatorcontrib><creatorcontrib>Rijken, P. F J. W.</creatorcontrib><creatorcontrib>Raleigh, J. A.</creatorcontrib><creatorcontrib>Van der Kogel, A. J.</creatorcontrib><title>Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line</title><title>Radiation research</title><addtitle>Radiat Res</addtitle><description>Bussink, J., Kaanders, J. H. A. M., Rijken, P. F. J. W., Raleigh, J. A. and Van der Kogel, A. J. Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line. The effect of irradiation depends on the oxygenation status of the tissue, while irradiation itself also changes the oxygenation and perfusion status of tissues. A better understanding of the changes in tumor oxygenation and perfusion over time after irradiation will allow a better planning of fractionated radiotherapy in combination with modifiers of blood flow and oxygenation. Vascular architecture (endothelial marker), perfusion (Hoechst 33342) and oxygenation (pimonidazole) were studied in a human laryngeal squamous cell carcinoma tumor line grown as xenografts in nude mice. The effect of a single dose of 10 Gy X rays on these parameters was evaluated from 2 h to 11 days after irradiation. Shortly after irradiation, there was an 8% increase in perfused blood vessels (from 57% to 65%) followed by a significant decrease, with a minimum value of 42% at 26 h after irradiation, and a subsequent increase to control levels at 7 to 11 days after irradiation. The hypoxic fraction showed a decrease at 7 h after treatment from 13% to 5% with an increase to 19% at 11 days after irradiation. These experiments show that irradiation causes rapid changes in oxygenation and perfusion which may have consequences for the optimal timing of radiotherapy schedules employing multiple fractions per day and the introduction of oxygenation- and perfusion-modifying drugs.</description><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Cancer</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Carcinoma, Squamous Cell - blood</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Hypoxia - radiation effects</subject><subject>Heterologous transplantation</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Image Processing, Computer-Assisted</subject><subject>Immunohistochemistry</subject><subject>Irradiation</subject><subject>Laryngeal Neoplasms - blood</subject><subject>Laryngeal Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>Perfusion</subject><subject>Physical agents</subject><subject>Radiotherapy</subject><subject>REGULAR ARTICLES</subject><subject>Space life sciences</subject><subject>Squamous cell carcinoma</subject><subject>Tissue oxygenation</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0033-7587</issn><issn>1938-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqdkEFr2zAYhsXYWNNs_2AMHcboDk4_SbYlbafWdE0gkMJyGIwhFFnuVGwplWxY__1sHLqdd9Lhfd5XHw9ClwRWpCz5JQBjGS8Ev6AA8IkU7AcwKT5Xm-u7q_VPuoJVtftCX6AFkUxkRQ75S7R4bp2h85QexiYjpXyNzgjwEqSUC3Ssfml_bxN2Hl-3IdT4zsZmSC54rH2N10_H8NtprJveRryJUddO91MaGqzxeui0x98eB92FIeHKti2udDTOh07j79aH-zhW8X7oQsRb5-0b9KrRbbJvT-8S7b_e7Kt1tt3dbqqrbXYoiOwzCoWpwdRU5ERwyjmxzDS2YZSCYJraGjTjpjayyAuei6I0uoSSNEKKEnK2RB_n2WMMj4NNvepcMuN52tvxUsUJFKUYZS3R7QyaGFKKtlHH6DodnxQBNblXk0U1WVSTezW6V5N7NbtXVIGqdoqOS-9PXw6Hztb_7MyyR-DDCdDJ6LaJ2huX_nKMciphxN7N2EPqQ3yOWSGAMj7GN3N8cCF4-9_n_gF61KzH</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>Bussink, J.</creator><creator>Kaanders, J. H A. M.</creator><creator>Rijken, P. F J. W.</creator><creator>Raleigh, J. A.</creator><creator>Van der Kogel, A. J.</creator><general>Radiation Research Society</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></search><sort><creationdate>20000401</creationdate><title>Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line</title><author>Bussink, J. ; Kaanders, J. H A. M. ; Rijken, P. F J. W. ; Raleigh, J. A. ; Van der Kogel, A. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b519t-205cd0cd2841872771e3cfef322083a2ed0a37cdc954574856ca6061f8986043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Cancer</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Carcinoma, Squamous Cell - blood</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Hypoxia - radiation effects</topic><topic>Heterologous transplantation</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Image Processing, Computer-Assisted</topic><topic>Immunohistochemistry</topic><topic>Irradiation</topic><topic>Laryngeal Neoplasms - blood</topic><topic>Laryngeal Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>Perfusion</topic><topic>Physical agents</topic><topic>Radiotherapy</topic><topic>REGULAR ARTICLES</topic><topic>Space life sciences</topic><topic>Squamous cell carcinoma</topic><topic>Tissue oxygenation</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bussink, J.</creatorcontrib><creatorcontrib>Kaanders, J. H A. M.</creatorcontrib><creatorcontrib>Rijken, P. F J. W.</creatorcontrib><creatorcontrib>Raleigh, J. A.</creatorcontrib><creatorcontrib>Van der Kogel, A. J.</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><jtitle>Radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bussink, J.</au><au>Kaanders, J. H A. M.</au><au>Rijken, P. F J. W.</au><au>Raleigh, J. A.</au><au>Van der Kogel, A. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line</atitle><jtitle>Radiation research</jtitle><addtitle>Radiat Res</addtitle><date>2000-04-01</date><risdate>2000</risdate><volume>153</volume><issue>4</issue><spage>398</spage><epage>404</epage><pages>398-404</pages><issn>0033-7587</issn><eissn>1938-5404</eissn><coden>RAREAE</coden><abstract>Bussink, J., Kaanders, J. H. A. M., Rijken, P. F. J. W., Raleigh, J. A. and Van der Kogel, A. J. Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line. The effect of irradiation depends on the oxygenation status of the tissue, while irradiation itself also changes the oxygenation and perfusion status of tissues. A better understanding of the changes in tumor oxygenation and perfusion over time after irradiation will allow a better planning of fractionated radiotherapy in combination with modifiers of blood flow and oxygenation. Vascular architecture (endothelial marker), perfusion (Hoechst 33342) and oxygenation (pimonidazole) were studied in a human laryngeal squamous cell carcinoma tumor line grown as xenografts in nude mice. The effect of a single dose of 10 Gy X rays on these parameters was evaluated from 2 h to 11 days after irradiation. Shortly after irradiation, there was an 8% increase in perfused blood vessels (from 57% to 65%) followed by a significant decrease, with a minimum value of 42% at 26 h after irradiation, and a subsequent increase to control levels at 7 to 11 days after irradiation. The hypoxic fraction showed a decrease at 7 h after treatment from 13% to 5% with an increase to 19% at 11 days after irradiation. These experiments show that irradiation causes rapid changes in oxygenation and perfusion which may have consequences for the optimal timing of radiotherapy schedules employing multiple fractions per day and the introduction of oxygenation- and perfusion-modifying drugs.</abstract><cop>Oak Brook, Il</cop><pub>Radiation Research Society</pub><pmid>10760999</pmid><doi>10.1667/0033-7587(2000)153[0398:CIBPAH]2.0.CO;2</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Blood Cancer Carcinogenesis, carcinogens and anticarcinogens Carcinoma, Squamous Cell - blood Carcinoma, Squamous Cell - pathology Cell Hypoxia - radiation effects Heterologous transplantation Humans Hypoxia Image Processing, Computer-Assisted Immunohistochemistry Irradiation Laryngeal Neoplasms - blood Laryngeal Neoplasms - pathology Medical sciences Perfusion Physical agents Radiotherapy REGULAR ARTICLES Space life sciences Squamous cell carcinoma Tissue oxygenation Tumor Cells, Cultured Tumors |
title | Changes in Blood Perfusion and Hypoxia after Irradiation of a Human Squamous Cell Carcinoma Xenograft Tumor Line |
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