Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines

Kim, K-U., Xiao, J., Ni, H-T., Cho, K. H., Spellman, S. R., Low, W. C. and Hall, W. A. Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines. Radiat. Res. 160, 224–231 (2003). Various imm...

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Veröffentlicht in:Radiation research 2003-08, Vol.160 (2), p.224-231
Hauptverfasser: Kim, Ki-Uk, Xiao, Jing, Ni, Hsiao-Tzu, Cho, Kwan H., Spellman, Stephen R., Low, Walter C., Hall, Walter A.
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container_end_page 231
container_issue 2
container_start_page 224
container_title Radiation research
container_volume 160
creator Kim, Ki-Uk
Xiao, Jing
Ni, Hsiao-Tzu
Cho, Kwan H.
Spellman, Stephen R.
Low, Walter C.
Hall, Walter A.
description Kim, K-U., Xiao, J., Ni, H-T., Cho, K. H., Spellman, S. R., Low, W. C. and Hall, W. A. Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines. Radiat. Res. 160, 224–231 (2003). Various immunotoxins have been developed for the treatment of cancer. The toxin is internalized by target cells through cell-surface receptors, and it is essential for these receptors to be expressed for the immunotoxin to have specific anti-tumor activity. Radiation therapy is one of the main treatment modalities for primary malignant brain tumors. The purpose of this study was to determine whether radiation influences the expression of cell-surface receptors. Cells of one human medulloblastoma (Daoy) and two glioblastoma (U373-MG and T98-G) cell lines were tested by exposing the cells to a single dose of 5 Gy γ rays. Expression of transferrin receptors, type-1 insulin-like growth factor receptors (IGF1R), and interleukin 4 receptors (IL4R) was measured by flow cytometry analysis on unirradiated cells and on cells 3 to 120 h after irradiation. In Daoy cells, the absolute expression index of transferrin receptors increased during the 24 h after irradiation with the greatest change of 26% above control at 9 h. The absolute expression index of IGF1R increased 26.5% above control at 12 h. The absolute expression index of IL4R decreased 9 h after irradiation. In U373-MG cells the absolute expression index of transferrin receptors increased during the 24 h after irradiation, and the greatest increase was 45% above control at 9 h. The absolute expression index of IGF1R increased during the 12 h after irradiation with a maximum increase of 33% above control at 6 h. The absolute expression index of IL4R decreased with time after irradiation. In T98-G cells, the absolute expression index of both transferrin receptors and IL4R decreased after irradiation. The results suggest that the expression of growth factor receptors on brain tumor cells may be influenced by radiation. The effect of ionizing radiation on receptor expression should be considered when administration of targeted toxin is combined with radiation. Similar studies with other growth factor receptors used in targeted toxin therapy are recommended.
doi_str_mv 10.1667/RR3040
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H., Spellman, S. R., Low, W. C. and Hall, W. A. Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines. Radiat. Res. 160, 224–231 (2003). Various immunotoxins have been developed for the treatment of cancer. The toxin is internalized by target cells through cell-surface receptors, and it is essential for these receptors to be expressed for the immunotoxin to have specific anti-tumor activity. Radiation therapy is one of the main treatment modalities for primary malignant brain tumors. The purpose of this study was to determine whether radiation influences the expression of cell-surface receptors. Cells of one human medulloblastoma (Daoy) and two glioblastoma (U373-MG and T98-G) cell lines were tested by exposing the cells to a single dose of 5 Gy γ rays. Expression of transferrin receptors, type-1 insulin-like growth factor receptors (IGF1R), and interleukin 4 receptors (IL4R) was measured by flow cytometry analysis on unirradiated cells and on cells 3 to 120 h after irradiation. In Daoy cells, the absolute expression index of transferrin receptors increased during the 24 h after irradiation with the greatest change of 26% above control at 9 h. The absolute expression index of IGF1R increased 26.5% above control at 12 h. The absolute expression index of IL4R decreased 9 h after irradiation. In U373-MG cells the absolute expression index of transferrin receptors increased during the 24 h after irradiation, and the greatest increase was 45% above control at 9 h. The absolute expression index of IGF1R increased during the 12 h after irradiation with a maximum increase of 33% above control at 6 h. The absolute expression index of IL4R decreased with time after irradiation. In T98-G cells, the absolute expression index of both transferrin receptors and IL4R decreased after irradiation. The results suggest that the expression of growth factor receptors on brain tumor cells may be influenced by radiation. The effect of ionizing radiation on receptor expression should be considered when administration of targeted toxin is combined with radiation. Similar studies with other growth factor receptors used in targeted toxin therapy are recommended.</description><identifier>ISSN: 0033-7587</identifier><identifier>EISSN: 1938-5404</identifier><identifier>DOI: 10.1667/RR3040</identifier><identifier>PMID: 12859234</identifier><identifier>CODEN: RAREAE</identifier><language>eng</language><publisher>Oak Brook, Il: Radiation Research Society</publisher><subject>Biological and medical sciences ; Brain neoplasms ; Brain Neoplasms - metabolism ; Brain Neoplasms - pathology ; Cell lines ; Flow Cytometry - methods ; Gene Expression Regulation, Neoplastic - radiation effects ; Glioblastoma - metabolism ; Glioblastoma - pathology ; Immunotoxins ; Irradiation ; Medical sciences ; Medulloblastoma - metabolism ; Medulloblastoma - pathology ; Neurons ; Receptor, IGF Type 1 - genetics ; Receptor, IGF Type 1 - metabolism ; Receptors ; Receptors, Cell Surface - genetics ; Receptors, Cell Surface - metabolism ; Receptors, Interleukin-4 - genetics ; Receptors, Interleukin-4 - metabolism ; Receptors, Transferrin - genetics ; Receptors, Transferrin - metabolism ; REGULAR PAPERS ; Somatomedins ; Transferrin ; Transferrin receptors ; Tumor cell line ; Tumor Cells, Cultured - metabolism ; Tumor Cells, Cultured - radiation effects ; Tumors</subject><ispartof>Radiation research, 2003-08, Vol.160 (2), p.224-231</ispartof><rights>Radiation Research Society</rights><rights>Copyright 2003 The Radiation Research Society</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b355t-67952cfd9e1217fa3b435d0d1b25aff2e74fe3cc834ea0cb7b9cfdd908a64e463</citedby><cites>FETCH-LOGICAL-b355t-67952cfd9e1217fa3b435d0d1b25aff2e74fe3cc834ea0cb7b9cfdd908a64e463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://bioone.org/doi/pdf/10.1667/RR3040$$EPDF$$P50$$Gbioone$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3581171$$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&amp;idt=15020552$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12859234$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ki-Uk</creatorcontrib><creatorcontrib>Xiao, Jing</creatorcontrib><creatorcontrib>Ni, Hsiao-Tzu</creatorcontrib><creatorcontrib>Cho, Kwan H.</creatorcontrib><creatorcontrib>Spellman, Stephen R.</creatorcontrib><creatorcontrib>Low, Walter C.</creatorcontrib><creatorcontrib>Hall, Walter A.</creatorcontrib><title>Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines</title><title>Radiation research</title><addtitle>Radiat Res</addtitle><description>Kim, K-U., Xiao, J., Ni, H-T., Cho, K. H., Spellman, S. R., Low, W. C. and Hall, W. A. Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines. Radiat. Res. 160, 224–231 (2003). Various immunotoxins have been developed for the treatment of cancer. The toxin is internalized by target cells through cell-surface receptors, and it is essential for these receptors to be expressed for the immunotoxin to have specific anti-tumor activity. Radiation therapy is one of the main treatment modalities for primary malignant brain tumors. The purpose of this study was to determine whether radiation influences the expression of cell-surface receptors. Cells of one human medulloblastoma (Daoy) and two glioblastoma (U373-MG and T98-G) cell lines were tested by exposing the cells to a single dose of 5 Gy γ rays. Expression of transferrin receptors, type-1 insulin-like growth factor receptors (IGF1R), and interleukin 4 receptors (IL4R) was measured by flow cytometry analysis on unirradiated cells and on cells 3 to 120 h after irradiation. In Daoy cells, the absolute expression index of transferrin receptors increased during the 24 h after irradiation with the greatest change of 26% above control at 9 h. The absolute expression index of IGF1R increased 26.5% above control at 12 h. The absolute expression index of IL4R decreased 9 h after irradiation. In U373-MG cells the absolute expression index of transferrin receptors increased during the 24 h after irradiation, and the greatest increase was 45% above control at 9 h. The absolute expression index of IGF1R increased during the 12 h after irradiation with a maximum increase of 33% above control at 6 h. The absolute expression index of IL4R decreased with time after irradiation. In T98-G cells, the absolute expression index of both transferrin receptors and IL4R decreased after irradiation. The results suggest that the expression of growth factor receptors on brain tumor cells may be influenced by radiation. The effect of ionizing radiation on receptor expression should be considered when administration of targeted toxin is combined with radiation. Similar studies with other growth factor receptors used in targeted toxin therapy are recommended.</description><subject>Biological and medical sciences</subject><subject>Brain neoplasms</subject><subject>Brain Neoplasms - metabolism</subject><subject>Brain Neoplasms - pathology</subject><subject>Cell lines</subject><subject>Flow Cytometry - methods</subject><subject>Gene Expression Regulation, Neoplastic - radiation effects</subject><subject>Glioblastoma - metabolism</subject><subject>Glioblastoma - pathology</subject><subject>Immunotoxins</subject><subject>Irradiation</subject><subject>Medical sciences</subject><subject>Medulloblastoma - metabolism</subject><subject>Medulloblastoma - pathology</subject><subject>Neurons</subject><subject>Receptor, IGF Type 1 - genetics</subject><subject>Receptor, IGF Type 1 - metabolism</subject><subject>Receptors</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Interleukin-4 - genetics</subject><subject>Receptors, Interleukin-4 - metabolism</subject><subject>Receptors, Transferrin - genetics</subject><subject>Receptors, Transferrin - metabolism</subject><subject>REGULAR PAPERS</subject><subject>Somatomedins</subject><subject>Transferrin</subject><subject>Transferrin receptors</subject><subject>Tumor cell line</subject><subject>Tumor Cells, Cultured - metabolism</subject><subject>Tumor Cells, Cultured - radiation effects</subject><subject>Tumors</subject><issn>0033-7587</issn><issn>1938-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtKAzEUhoMoWm9PIJKFunI0mSRzWWrxUqgopa7LmcyJRqeZkkxRX8jnNGWKrlydnPwfH4efkEPOLniW5ZeTiWCSbZABL0WRKMnkJhkwJkSSqyLfIbshvLG486zcJjs8LVSZCjkg38NXcC8YqHX05nPhMQTbOtoaOvXggkHvrTunIxeWjXVJY9-R3vn2o3ult6C71lN-TsHVkejQN7h8jyJJJ6hxEdNAwcR_OvIeagvd2j3Epgmrx5O3c_Bf9AEa--LAdfTaQzRMl_OoXmF0bB2GfbJloAl4sJ575Pn2Zjq8T8aPd6Ph1TiphFJdkuWlSrWpS-Qpzw2ISgpVs5pXqQJjUsylQaF1ISQC01VelZGuS1ZAJlFmYo-c9V7t2xA8mtmiv3DG2WxV9KwvOoLHPbhYVnOs_7B1sxE4XQMQNDQmtqlt-OMUS5lSaeSOeu4txL5-c6EKznMe45M-rmzbOvzvnB8iAZxR</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Kim, Ki-Uk</creator><creator>Xiao, Jing</creator><creator>Ni, Hsiao-Tzu</creator><creator>Cho, Kwan H.</creator><creator>Spellman, Stephen R.</creator><creator>Low, Walter C.</creator><creator>Hall, Walter A.</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></search><sort><creationdate>20030801</creationdate><title>Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines</title><author>Kim, Ki-Uk ; Xiao, Jing ; Ni, Hsiao-Tzu ; Cho, Kwan H. ; Spellman, Stephen R. ; Low, Walter C. ; Hall, Walter A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b355t-67952cfd9e1217fa3b435d0d1b25aff2e74fe3cc834ea0cb7b9cfdd908a64e463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Biological and medical sciences</topic><topic>Brain neoplasms</topic><topic>Brain Neoplasms - metabolism</topic><topic>Brain Neoplasms - pathology</topic><topic>Cell lines</topic><topic>Flow Cytometry - methods</topic><topic>Gene Expression Regulation, Neoplastic - radiation effects</topic><topic>Glioblastoma - metabolism</topic><topic>Glioblastoma - pathology</topic><topic>Immunotoxins</topic><topic>Irradiation</topic><topic>Medical sciences</topic><topic>Medulloblastoma - metabolism</topic><topic>Medulloblastoma - pathology</topic><topic>Neurons</topic><topic>Receptor, IGF Type 1 - genetics</topic><topic>Receptor, IGF Type 1 - metabolism</topic><topic>Receptors</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Receptors, Interleukin-4 - genetics</topic><topic>Receptors, Interleukin-4 - metabolism</topic><topic>Receptors, Transferrin - genetics</topic><topic>Receptors, Transferrin - metabolism</topic><topic>REGULAR PAPERS</topic><topic>Somatomedins</topic><topic>Transferrin</topic><topic>Transferrin receptors</topic><topic>Tumor cell line</topic><topic>Tumor Cells, Cultured - metabolism</topic><topic>Tumor Cells, Cultured - radiation effects</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ki-Uk</creatorcontrib><creatorcontrib>Xiao, Jing</creatorcontrib><creatorcontrib>Ni, Hsiao-Tzu</creatorcontrib><creatorcontrib>Cho, Kwan H.</creatorcontrib><creatorcontrib>Spellman, Stephen R.</creatorcontrib><creatorcontrib>Low, Walter C.</creatorcontrib><creatorcontrib>Hall, Walter A.</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><jtitle>Radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ki-Uk</au><au>Xiao, Jing</au><au>Ni, Hsiao-Tzu</au><au>Cho, Kwan H.</au><au>Spellman, Stephen R.</au><au>Low, Walter C.</au><au>Hall, Walter A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines</atitle><jtitle>Radiation research</jtitle><addtitle>Radiat Res</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>160</volume><issue>2</issue><spage>224</spage><epage>231</epage><pages>224-231</pages><issn>0033-7587</issn><eissn>1938-5404</eissn><coden>RAREAE</coden><abstract>Kim, K-U., Xiao, J., Ni, H-T., Cho, K. H., Spellman, S. R., Low, W. C. and Hall, W. A. Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines. Radiat. Res. 160, 224–231 (2003). Various immunotoxins have been developed for the treatment of cancer. The toxin is internalized by target cells through cell-surface receptors, and it is essential for these receptors to be expressed for the immunotoxin to have specific anti-tumor activity. Radiation therapy is one of the main treatment modalities for primary malignant brain tumors. The purpose of this study was to determine whether radiation influences the expression of cell-surface receptors. Cells of one human medulloblastoma (Daoy) and two glioblastoma (U373-MG and T98-G) cell lines were tested by exposing the cells to a single dose of 5 Gy γ rays. Expression of transferrin receptors, type-1 insulin-like growth factor receptors (IGF1R), and interleukin 4 receptors (IL4R) was measured by flow cytometry analysis on unirradiated cells and on cells 3 to 120 h after irradiation. In Daoy cells, the absolute expression index of transferrin receptors increased during the 24 h after irradiation with the greatest change of 26% above control at 9 h. The absolute expression index of IGF1R increased 26.5% above control at 12 h. The absolute expression index of IL4R decreased 9 h after irradiation. In U373-MG cells the absolute expression index of transferrin receptors increased during the 24 h after irradiation, and the greatest increase was 45% above control at 9 h. The absolute expression index of IGF1R increased during the 12 h after irradiation with a maximum increase of 33% above control at 6 h. The absolute expression index of IL4R decreased with time after irradiation. In T98-G cells, the absolute expression index of both transferrin receptors and IL4R decreased after irradiation. The results suggest that the expression of growth factor receptors on brain tumor cells may be influenced by radiation. The effect of ionizing radiation on receptor expression should be considered when administration of targeted toxin is combined with radiation. Similar studies with other growth factor receptors used in targeted toxin therapy are recommended.</abstract><cop>Oak Brook, Il</cop><pub>Radiation Research Society</pub><pmid>12859234</pmid><doi>10.1667/RR3040</doi><tpages>8</tpages></addata></record>
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source MEDLINE; BioOne Complete; JSTOR Archive Collection A-Z Listing
subjects Biological and medical sciences
Brain neoplasms
Brain Neoplasms - metabolism
Brain Neoplasms - pathology
Cell lines
Flow Cytometry - methods
Gene Expression Regulation, Neoplastic - radiation effects
Glioblastoma - metabolism
Glioblastoma - pathology
Immunotoxins
Irradiation
Medical sciences
Medulloblastoma - metabolism
Medulloblastoma - pathology
Neurons
Receptor, IGF Type 1 - genetics
Receptor, IGF Type 1 - metabolism
Receptors
Receptors, Cell Surface - genetics
Receptors, Cell Surface - metabolism
Receptors, Interleukin-4 - genetics
Receptors, Interleukin-4 - metabolism
Receptors, Transferrin - genetics
Receptors, Transferrin - metabolism
REGULAR PAPERS
Somatomedins
Transferrin
Transferrin receptors
Tumor cell line
Tumor Cells, Cultured - metabolism
Tumor Cells, Cultured - radiation effects
Tumors
title Changes in Expression of Transferrin, Insulin-like Growth Factor 1, and Interleukin 4 Receptors after Irradiation of Cells of Primary Malignant Brain Tumor Cell Lines
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