Scintigraphic imaging of P-glycoprotein expression with a radiolabelled antibody
P-glycoprotein (P-gp) is a membrane efflux pump protein that is involved in multidrug resistance (MDR). Tumour cells with high P-gp expression show poor response to cancer treatment with several chemotherapeutics. In vivo targeting and visualisation of P-gp expression would allow MDR to be evaluated...
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creator | van Eerd, Julliëtte E M de Geus-Oei, Lioe-Fee Oyen, Wim J G Corstens, Frans H M Boerman, Otto C |
description | P-glycoprotein (P-gp) is a membrane efflux pump protein that is involved in multidrug resistance (MDR). Tumour cells with high P-gp expression show poor response to cancer treatment with several chemotherapeutics. In vivo targeting and visualisation of P-gp expression would allow MDR to be evaluated non-invasively prior to treatment. The aim of this study was to investigate the feasibility of visualising P-gp expression in tumours using a monoclonal anti-P-gp antibody, 15D3.
Nude BALB/c mice with subcutaneously growing human uterine sarcoma cell tumours with either high (MES-SA/Dx5 1977) or low (MES-SA 1976) P-gp expression were used. When tumours were 0.2-0.4 g, mice received (131)I-15D3 or (111)In-DTPA-15D3 monoclonal anti-P-gp antibody intravenously. Images were acquired up to 3 days p.i. and radioactivity concentration in various tissues was determined after euthanisation of the animals.
The images demonstrated that radioactivity accumulated to a higher concentration in high P-gp expressing tumours than in the low P-gp expressing MES-SA 1976 tumour. Furthermore, visualisation of the P-gp expressing tumours was superior with (111)In-DTPA-15D3 than with (131)I-15D3. After injection of (111)In-DTPA-15D3, the high P-gp expressing MES-SA/Dx5 1977 tumours were clearly visualised at 3 days p.i. The biodistribution data indicated that radioactivity concentration in the high P-gp expressing tumours was higher than in the tumours with low P-gp expression (20.78+/-1.42 %ID/g for MES-SA/Dx5 1977 tumours and 8.39+/-3.78 %ID/g for MES-SA 1976 tumours for (111)In-DTPA-15D3).
The (111)In-labelled monoclonal anti-P-gp antibody clearly visualised P-gp expression in a human uterine sarcoma tumour in nude mice. |
doi_str_mv | 10.1007/s00259-006-0152-0 |
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Nude BALB/c mice with subcutaneously growing human uterine sarcoma cell tumours with either high (MES-SA/Dx5 1977) or low (MES-SA 1976) P-gp expression were used. When tumours were 0.2-0.4 g, mice received (131)I-15D3 or (111)In-DTPA-15D3 monoclonal anti-P-gp antibody intravenously. Images were acquired up to 3 days p.i. and radioactivity concentration in various tissues was determined after euthanisation of the animals.
The images demonstrated that radioactivity accumulated to a higher concentration in high P-gp expressing tumours than in the low P-gp expressing MES-SA 1976 tumour. Furthermore, visualisation of the P-gp expressing tumours was superior with (111)In-DTPA-15D3 than with (131)I-15D3. After injection of (111)In-DTPA-15D3, the high P-gp expressing MES-SA/Dx5 1977 tumours were clearly visualised at 3 days p.i. The biodistribution data indicated that radioactivity concentration in the high P-gp expressing tumours was higher than in the tumours with low P-gp expression (20.78+/-1.42 %ID/g for MES-SA/Dx5 1977 tumours and 8.39+/-3.78 %ID/g for MES-SA 1976 tumours for (111)In-DTPA-15D3).
The (111)In-labelled monoclonal anti-P-gp antibody clearly visualised P-gp expression in a human uterine sarcoma tumour in nude mice.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-006-0152-0</identifier><identifier>PMID: 16832635</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Animals ; Antibodies, Monoclonal - pharmacokinetics ; ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism ; Drug resistance ; Feasibility Studies ; Female ; Gene expression ; Gene Expression Profiling - methods ; Glycoproteins ; Indium Radioisotopes - pharmacokinetics ; Medical imaging ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Monoclonal antibodies ; Nuclear medicine ; Radioactivity ; Radionuclide Imaging ; Reproducibility of Results ; Rodents ; Sensitivity and Specificity ; Tissue Distribution ; Uterine Neoplasms - diagnostic imaging ; Uterine Neoplasms - metabolism</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2006-11, Vol.33 (11), p.1266-1272</ispartof><rights>Springer-Verlag 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-b219c995e6ed0a901a10b0670bc2e0e8a2b4747eaa8364e7a74f2d297e5f28403</citedby><cites>FETCH-LOGICAL-c326t-b219c995e6ed0a901a10b0670bc2e0e8a2b4747eaa8364e7a74f2d297e5f28403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16832635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van Eerd, Julliëtte E M</creatorcontrib><creatorcontrib>de Geus-Oei, Lioe-Fee</creatorcontrib><creatorcontrib>Oyen, Wim J G</creatorcontrib><creatorcontrib>Corstens, Frans H M</creatorcontrib><creatorcontrib>Boerman, Otto C</creatorcontrib><title>Scintigraphic imaging of P-glycoprotein expression with a radiolabelled antibody</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>P-glycoprotein (P-gp) is a membrane efflux pump protein that is involved in multidrug resistance (MDR). Tumour cells with high P-gp expression show poor response to cancer treatment with several chemotherapeutics. In vivo targeting and visualisation of P-gp expression would allow MDR to be evaluated non-invasively prior to treatment. The aim of this study was to investigate the feasibility of visualising P-gp expression in tumours using a monoclonal anti-P-gp antibody, 15D3.
Nude BALB/c mice with subcutaneously growing human uterine sarcoma cell tumours with either high (MES-SA/Dx5 1977) or low (MES-SA 1976) P-gp expression were used. When tumours were 0.2-0.4 g, mice received (131)I-15D3 or (111)In-DTPA-15D3 monoclonal anti-P-gp antibody intravenously. Images were acquired up to 3 days p.i. and radioactivity concentration in various tissues was determined after euthanisation of the animals.
The images demonstrated that radioactivity accumulated to a higher concentration in high P-gp expressing tumours than in the low P-gp expressing MES-SA 1976 tumour. Furthermore, visualisation of the P-gp expressing tumours was superior with (111)In-DTPA-15D3 than with (131)I-15D3. After injection of (111)In-DTPA-15D3, the high P-gp expressing MES-SA/Dx5 1977 tumours were clearly visualised at 3 days p.i. The biodistribution data indicated that radioactivity concentration in the high P-gp expressing tumours was higher than in the tumours with low P-gp expression (20.78+/-1.42 %ID/g for MES-SA/Dx5 1977 tumours and 8.39+/-3.78 %ID/g for MES-SA 1976 tumours for (111)In-DTPA-15D3).
The (111)In-labelled monoclonal anti-P-gp antibody clearly visualised P-gp expression in a human uterine sarcoma tumour in nude mice.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - pharmacokinetics</subject><subject>ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism</subject><subject>Drug resistance</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Profiling - methods</subject><subject>Glycoproteins</subject><subject>Indium Radioisotopes - pharmacokinetics</subject><subject>Medical imaging</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Monoclonal antibodies</subject><subject>Nuclear medicine</subject><subject>Radioactivity</subject><subject>Radionuclide Imaging</subject><subject>Reproducibility of Results</subject><subject>Rodents</subject><subject>Sensitivity and Specificity</subject><subject>Tissue Distribution</subject><subject>Uterine Neoplasms - 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Academic</collection><jtitle>European journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Eerd, Julliëtte E M</au><au>de Geus-Oei, Lioe-Fee</au><au>Oyen, Wim J G</au><au>Corstens, Frans H M</au><au>Boerman, Otto C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Scintigraphic imaging of P-glycoprotein expression with a radiolabelled antibody</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><date>2006-11</date><risdate>2006</risdate><volume>33</volume><issue>11</issue><spage>1266</spage><epage>1272</epage><pages>1266-1272</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>P-glycoprotein (P-gp) is a membrane efflux pump protein that is involved in multidrug resistance (MDR). Tumour cells with high P-gp expression show poor response to cancer treatment with several chemotherapeutics. In vivo targeting and visualisation of P-gp expression would allow MDR to be evaluated non-invasively prior to treatment. The aim of this study was to investigate the feasibility of visualising P-gp expression in tumours using a monoclonal anti-P-gp antibody, 15D3.
Nude BALB/c mice with subcutaneously growing human uterine sarcoma cell tumours with either high (MES-SA/Dx5 1977) or low (MES-SA 1976) P-gp expression were used. When tumours were 0.2-0.4 g, mice received (131)I-15D3 or (111)In-DTPA-15D3 monoclonal anti-P-gp antibody intravenously. Images were acquired up to 3 days p.i. and radioactivity concentration in various tissues was determined after euthanisation of the animals.
The images demonstrated that radioactivity accumulated to a higher concentration in high P-gp expressing tumours than in the low P-gp expressing MES-SA 1976 tumour. Furthermore, visualisation of the P-gp expressing tumours was superior with (111)In-DTPA-15D3 than with (131)I-15D3. After injection of (111)In-DTPA-15D3, the high P-gp expressing MES-SA/Dx5 1977 tumours were clearly visualised at 3 days p.i. The biodistribution data indicated that radioactivity concentration in the high P-gp expressing tumours was higher than in the tumours with low P-gp expression (20.78+/-1.42 %ID/g for MES-SA/Dx5 1977 tumours and 8.39+/-3.78 %ID/g for MES-SA 1976 tumours for (111)In-DTPA-15D3).
The (111)In-labelled monoclonal anti-P-gp antibody clearly visualised P-gp expression in a human uterine sarcoma tumour in nude mice.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>16832635</pmid><doi>10.1007/s00259-006-0152-0</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Antibodies, Monoclonal - pharmacokinetics ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism Drug resistance Feasibility Studies Female Gene expression Gene Expression Profiling - methods Glycoproteins Indium Radioisotopes - pharmacokinetics Medical imaging Mice Mice, Inbred BALB C Mice, Nude Monoclonal antibodies Nuclear medicine Radioactivity Radionuclide Imaging Reproducibility of Results Rodents Sensitivity and Specificity Tissue Distribution Uterine Neoplasms - diagnostic imaging Uterine Neoplasms - metabolism |
title | Scintigraphic imaging of P-glycoprotein expression with a radiolabelled antibody |
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