Expression of multidrug resistance protein gene in patients with glioma after chemotherapy
Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated wi...
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Veröffentlicht in: | Journal of neuro-oncology 1998-10, Vol.40 (1), p.11-18 |
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creator | ABE, T MORI, T WAKABAYASHI, Y NAKAGAWA, M COLE, S. P. C KOIKE, K KUWANO, M HORI, S |
description | Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated with anticancer agents. In this study, we asked whether MRP was overexpressed in human gliomas after cancer chemotherapy. We investigated expression of MRP and P-gp before and after chemotherapy in tumor samples from patients with glioma. MRP expression was observed in 16 (70%) of 23 untreated patients, and the proportion of MRP-positive cells in the whole cell population ranged from 3 to 32% in the 16 MRP-positive patients. P-gp-positive tumors were observed in 4 (18%) of 23 patients, and the proportional rates of P-gp-positive cells in the whole cell population ranged from 4 to 23%. The proportional rate of MRP-positive or P-gp-positive glioma cells increased after chemotherapy when compared with that before chemotherapy in all patients examined. We could observe no statistically significant correlation between expression of MRP or P-gp and tumor grade. These results suggest that MRP as well as P-gp may be involved in acquired or intrinsic drug resistance in human glioma. |
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P. C ; KOIKE, K ; KUWANO, M ; HORI, S</creator><creatorcontrib>ABE, T ; MORI, T ; WAKABAYASHI, Y ; NAKAGAWA, M ; COLE, S. P. C ; KOIKE, K ; KUWANO, M ; HORI, S</creatorcontrib><description>Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated with anticancer agents. In this study, we asked whether MRP was overexpressed in human gliomas after cancer chemotherapy. We investigated expression of MRP and P-gp before and after chemotherapy in tumor samples from patients with glioma. MRP expression was observed in 16 (70%) of 23 untreated patients, and the proportion of MRP-positive cells in the whole cell population ranged from 3 to 32% in the 16 MRP-positive patients. P-gp-positive tumors were observed in 4 (18%) of 23 patients, and the proportional rates of P-gp-positive cells in the whole cell population ranged from 4 to 23%. The proportional rate of MRP-positive or P-gp-positive glioma cells increased after chemotherapy when compared with that before chemotherapy in all patients examined. We could observe no statistically significant correlation between expression of MRP or P-gp and tumor grade. These results suggest that MRP as well as P-gp may be involved in acquired or intrinsic drug resistance in human glioma.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1023/A:1005954406809</identifier><identifier>PMID: 9874181</identifier><identifier>CODEN: JNODD2</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject><![CDATA[Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents, Phytogenic - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics ; Biological and medical sciences ; Blotting, Northern ; Child ; Doxorubicin - administration & dosage ; Etoposide - administration & dosage ; Female ; Gene Expression Regulation, Neoplastic - drug effects ; Genes, MDR - genetics ; Glioblastoma - drug therapy ; Glioblastoma - genetics ; Humans ; Male ; Medical sciences ; Middle Aged ; Neurology ; Nimustine - administration & dosage ; RNA, Messenger - analysis ; RNA, Neoplasm - analysis ; Tumors of the nervous system. Phacomatoses ; Vincristine - administration & dosage]]></subject><ispartof>Journal of neuro-oncology, 1998-10, Vol.40 (1), p.11-18</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-fdc836f78685192c1ae30107b7fc9d4672ca60dc465c0b1f1689b9759c6efac83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1637795$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9874181$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ABE, T</creatorcontrib><creatorcontrib>MORI, T</creatorcontrib><creatorcontrib>WAKABAYASHI, Y</creatorcontrib><creatorcontrib>NAKAGAWA, M</creatorcontrib><creatorcontrib>COLE, S. P. C</creatorcontrib><creatorcontrib>KOIKE, K</creatorcontrib><creatorcontrib>KUWANO, M</creatorcontrib><creatorcontrib>HORI, S</creatorcontrib><title>Expression of multidrug resistance protein gene in patients with glioma after chemotherapy</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><description>Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated with anticancer agents. In this study, we asked whether MRP was overexpressed in human gliomas after cancer chemotherapy. We investigated expression of MRP and P-gp before and after chemotherapy in tumor samples from patients with glioma. MRP expression was observed in 16 (70%) of 23 untreated patients, and the proportion of MRP-positive cells in the whole cell population ranged from 3 to 32% in the 16 MRP-positive patients. P-gp-positive tumors were observed in 4 (18%) of 23 patients, and the proportional rates of P-gp-positive cells in the whole cell population ranged from 4 to 23%. The proportional rate of MRP-positive or P-gp-positive glioma cells increased after chemotherapy when compared with that before chemotherapy in all patients examined. We could observe no statistically significant correlation between expression of MRP or P-gp and tumor grade. These results suggest that MRP as well as P-gp may be involved in acquired or intrinsic drug resistance in human glioma.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents, Phytogenic - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Child</subject><subject>Doxorubicin - administration & dosage</subject><subject>Etoposide - administration & dosage</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Genes, MDR - genetics</subject><subject>Glioblastoma - drug therapy</subject><subject>Glioblastoma - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Nimustine - administration & dosage</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Neoplasm - analysis</subject><subject>Tumors of the nervous system. 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C ; KOIKE, K ; KUWANO, M ; HORI, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-fdc836f78685192c1ae30107b7fc9d4672ca60dc465c0b1f1689b9759c6efac83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents, Phytogenic - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</topic><topic>ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Child</topic><topic>Doxorubicin - administration & dosage</topic><topic>Etoposide - administration & dosage</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Genes, MDR - genetics</topic><topic>Glioblastoma - drug therapy</topic><topic>Glioblastoma - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Nimustine - administration & dosage</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Neoplasm - analysis</topic><topic>Tumors of the nervous system. Phacomatoses</topic><topic>Vincristine - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ABE, T</creatorcontrib><creatorcontrib>MORI, T</creatorcontrib><creatorcontrib>WAKABAYASHI, Y</creatorcontrib><creatorcontrib>NAKAGAWA, M</creatorcontrib><creatorcontrib>COLE, S. P. C</creatorcontrib><creatorcontrib>KOIKE, K</creatorcontrib><creatorcontrib>KUWANO, M</creatorcontrib><creatorcontrib>HORI, S</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>MEDLINE - Academic</collection><jtitle>Journal of neuro-oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ABE, T</au><au>MORI, T</au><au>WAKABAYASHI, Y</au><au>NAKAGAWA, M</au><au>COLE, S. P. C</au><au>KOIKE, K</au><au>KUWANO, M</au><au>HORI, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of multidrug resistance protein gene in patients with glioma after chemotherapy</atitle><jtitle>Journal of neuro-oncology</jtitle><addtitle>J Neurooncol</addtitle><date>1998-10-01</date><risdate>1998</risdate><volume>40</volume><issue>1</issue><spage>11</spage><epage>18</epage><pages>11-18</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><coden>JNODD2</coden><abstract>Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated with anticancer agents. In this study, we asked whether MRP was overexpressed in human gliomas after cancer chemotherapy. We investigated expression of MRP and P-gp before and after chemotherapy in tumor samples from patients with glioma. MRP expression was observed in 16 (70%) of 23 untreated patients, and the proportion of MRP-positive cells in the whole cell population ranged from 3 to 32% in the 16 MRP-positive patients. P-gp-positive tumors were observed in 4 (18%) of 23 patients, and the proportional rates of P-gp-positive cells in the whole cell population ranged from 4 to 23%. The proportional rate of MRP-positive or P-gp-positive glioma cells increased after chemotherapy when compared with that before chemotherapy in all patients examined. We could observe no statistically significant correlation between expression of MRP or P-gp and tumor grade. These results suggest that MRP as well as P-gp may be involved in acquired or intrinsic drug resistance in human glioma.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>9874181</pmid><doi>10.1023/A:1005954406809</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antineoplastic Agents, Phytogenic - administration & dosage Antineoplastic Combined Chemotherapy Protocols - administration & dosage ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics Biological and medical sciences Blotting, Northern Child Doxorubicin - administration & dosage Etoposide - administration & dosage Female Gene Expression Regulation, Neoplastic - drug effects Genes, MDR - genetics Glioblastoma - drug therapy Glioblastoma - genetics Humans Male Medical sciences Middle Aged Neurology Nimustine - administration & dosage RNA, Messenger - analysis RNA, Neoplasm - analysis Tumors of the nervous system. Phacomatoses Vincristine - administration & dosage |
title | Expression of multidrug resistance protein gene in patients with glioma after chemotherapy |
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