lack of reciprocity in drug and light dose dependence of photodynamic therapy of pancreatic adenocarcinoma in vitro
Two human pancreatic cell lines, MIA PaCa 2 and Capan 2, were treated by photodynamic therapy in vitro with Photophrin (0.01-25 micrograms/ml; 24 h) and then light (1-50 J/cm2; lambda = 630 nm). The following model was fit to 6 datasets with weighted nonlinear regression: [sequence: see text] The sy...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1995-07, Vol.55 (14), p.3078-3084 |
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description | Two human pancreatic cell lines, MIA PaCa 2 and Capan 2, were treated by photodynamic therapy in vitro with Photophrin (0.01-25 micrograms/ml; 24 h) and then light (1-50 J/cm2; lambda = 630 nm). The following model was fit to 6 datasets with weighted nonlinear regression: [sequence: see text] The symbols are: E, cell growth; Econ, control growth in the absence of the combination; B, background signal; m, slope parameter; gamma, interaction parameter; D, concentration of Photofrin; L, light dose; F, fraction of Photofrin not photobleached by the light dose; k, k1, k2, bleaching parameters; A, distribution parameter for biexponential bleaching equation. Simple reciprocity of photosensitizer concentration and light dose was not found; compensation for photobleaching was critical. MIA PaCa2 required the monoexponential bleaching factor, whereas Capan 2 required the biexponential bleaching factor. The greater photosensitivity of MIA PaCa2 over Capan 2 can be best explained not by differences in the interaction parameter but rather by differences in the photobleaching pattern and rate. It may be possible to further enhance the selectivity of photodynamic therapy if differences in photobleaching between different cell types can be exploited by adequate dosimetry. |
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T ; GRECO, W. R ; NURSE-FINLAY, S. O ; PARSONS, J. C ; MANG, T. S</creator><creatorcontrib>MOESTA, K. T ; GRECO, W. R ; NURSE-FINLAY, S. O ; PARSONS, J. C ; MANG, T. S</creatorcontrib><description>Two human pancreatic cell lines, MIA PaCa 2 and Capan 2, were treated by photodynamic therapy in vitro with Photophrin (0.01-25 micrograms/ml; 24 h) and then light (1-50 J/cm2; lambda = 630 nm). The following model was fit to 6 datasets with weighted nonlinear regression: [sequence: see text] The symbols are: E, cell growth; Econ, control growth in the absence of the combination; B, background signal; m, slope parameter; gamma, interaction parameter; D, concentration of Photofrin; L, light dose; F, fraction of Photofrin not photobleached by the light dose; k, k1, k2, bleaching parameters; A, distribution parameter for biexponential bleaching equation. Simple reciprocity of photosensitizer concentration and light dose was not found; compensation for photobleaching was critical. MIA PaCa2 required the monoexponential bleaching factor, whereas Capan 2 required the biexponential bleaching factor. The greater photosensitivity of MIA PaCa2 over Capan 2 can be best explained not by differences in the interaction parameter but rather by differences in the photobleaching pattern and rate. It may be possible to further enhance the selectivity of photodynamic therapy if differences in photobleaching between different cell types can be exploited by adequate dosimetry.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 7606730</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - metabolism ; Biological and medical sciences ; Computer Simulation ; Dose-Response Relationship, Drug ; Hematoporphyrin Derivative - pharmacokinetics ; Hematoporphyrin Derivative - pharmacology ; Humans ; Medical sciences ; Models, Biological ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - metabolism ; Photochemotherapy - methods ; Photoradiation therapy and photosensitizing agent ; Thymidine - metabolism ; Treatment with physical agents ; Treatment. General aspects ; Tritium ; Tumor Cells, Cultured - drug effects ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 1995-07, Vol.55 (14), p.3078-3084</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3618222$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7606730$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MOESTA, K. T</creatorcontrib><creatorcontrib>GRECO, W. R</creatorcontrib><creatorcontrib>NURSE-FINLAY, S. O</creatorcontrib><creatorcontrib>PARSONS, J. C</creatorcontrib><creatorcontrib>MANG, T. S</creatorcontrib><title>lack of reciprocity in drug and light dose dependence of photodynamic therapy of pancreatic adenocarcinoma in vitro</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Two human pancreatic cell lines, MIA PaCa 2 and Capan 2, were treated by photodynamic therapy in vitro with Photophrin (0.01-25 micrograms/ml; 24 h) and then light (1-50 J/cm2; lambda = 630 nm). The following model was fit to 6 datasets with weighted nonlinear regression: [sequence: see text] The symbols are: E, cell growth; Econ, control growth in the absence of the combination; B, background signal; m, slope parameter; gamma, interaction parameter; D, concentration of Photofrin; L, light dose; F, fraction of Photofrin not photobleached by the light dose; k, k1, k2, bleaching parameters; A, distribution parameter for biexponential bleaching equation. Simple reciprocity of photosensitizer concentration and light dose was not found; compensation for photobleaching was critical. MIA PaCa2 required the monoexponential bleaching factor, whereas Capan 2 required the biexponential bleaching factor. The greater photosensitivity of MIA PaCa2 over Capan 2 can be best explained not by differences in the interaction parameter but rather by differences in the photobleaching pattern and rate. It may be possible to further enhance the selectivity of photodynamic therapy if differences in photobleaching between different cell types can be exploited by adequate dosimetry.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - metabolism</subject><subject>Biological and medical sciences</subject><subject>Computer Simulation</subject><subject>Dose-Response Relationship, Drug</subject><subject>Hematoporphyrin Derivative - pharmacokinetics</subject><subject>Hematoporphyrin Derivative - pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Models, Biological</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Photochemotherapy - methods</subject><subject>Photoradiation therapy and photosensitizing agent</subject><subject>Thymidine - metabolism</subject><subject>Treatment with physical agents</subject><subject>Treatment. General aspects</subject><subject>Tritium</subject><subject>Tumor Cells, Cultured - drug effects</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLxDAUhYso4zj6E4QsxF0hTZqks5TBFwhudF1uHp2JtklNUqH_3owWV5d7zncPnHtSrCtGm1LUNTst1hjjpmS1IOfFRYwfeWUVZqtiJTjmguJ1EXtQn8h3KBhlx-CVTTOyDukw7RE4jXq7PySkfTRIm9E4bZwyx4Px4JPXs4PBKpQOJsA4_-rgVDCQsgoZ9gqCss4PcIz9tin4y-Ksgz6aq2VuiveH-7fdU_ny-vi8u3spD4RvUykFl5RKVlMthWw03jZSdrUQmgnDsYZKGOBaEUVxVWlNCSemY1gxTKpGbummuP3Lzb2-JhNTO9ioTN-DM36KrRC0IaRmGbxewEkORrdjsAOEuV2-lP2bxYeooO9CrmjjP0Z5lXMI_QF0q3Ln</recordid><startdate>19950715</startdate><enddate>19950715</enddate><creator>MOESTA, K. T</creator><creator>GRECO, W. R</creator><creator>NURSE-FINLAY, S. O</creator><creator>PARSONS, J. C</creator><creator>MANG, T. S</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19950715</creationdate><title>lack of reciprocity in drug and light dose dependence of photodynamic therapy of pancreatic adenocarcinoma in vitro</title><author>MOESTA, K. T ; GRECO, W. R ; NURSE-FINLAY, S. O ; PARSONS, J. C ; MANG, T. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h269t-b76b33b543db7b8d098bbf477d57e60da17ea6dc2c3011dd3262ef50c50218b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Adenocarcinoma - metabolism</topic><topic>Biological and medical sciences</topic><topic>Computer Simulation</topic><topic>Dose-Response Relationship, Drug</topic><topic>Hematoporphyrin Derivative - pharmacokinetics</topic><topic>Hematoporphyrin Derivative - pharmacology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Models, Biological</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Photochemotherapy - methods</topic><topic>Photoradiation therapy and photosensitizing agent</topic><topic>Thymidine - metabolism</topic><topic>Treatment with physical agents</topic><topic>Treatment. General aspects</topic><topic>Tritium</topic><topic>Tumor Cells, Cultured - drug effects</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MOESTA, K. T</creatorcontrib><creatorcontrib>GRECO, W. R</creatorcontrib><creatorcontrib>NURSE-FINLAY, S. O</creatorcontrib><creatorcontrib>PARSONS, J. C</creatorcontrib><creatorcontrib>MANG, T. 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>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MOESTA, K. T</au><au>GRECO, W. R</au><au>NURSE-FINLAY, S. O</au><au>PARSONS, J. C</au><au>MANG, T. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>lack of reciprocity in drug and light dose dependence of photodynamic therapy of pancreatic adenocarcinoma in vitro</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1995-07-15</date><risdate>1995</risdate><volume>55</volume><issue>14</issue><spage>3078</spage><epage>3084</epage><pages>3078-3084</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Two human pancreatic cell lines, MIA PaCa 2 and Capan 2, were treated by photodynamic therapy in vitro with Photophrin (0.01-25 micrograms/ml; 24 h) and then light (1-50 J/cm2; lambda = 630 nm). The following model was fit to 6 datasets with weighted nonlinear regression: [sequence: see text] The symbols are: E, cell growth; Econ, control growth in the absence of the combination; B, background signal; m, slope parameter; gamma, interaction parameter; D, concentration of Photofrin; L, light dose; F, fraction of Photofrin not photobleached by the light dose; k, k1, k2, bleaching parameters; A, distribution parameter for biexponential bleaching equation. Simple reciprocity of photosensitizer concentration and light dose was not found; compensation for photobleaching was critical. MIA PaCa2 required the monoexponential bleaching factor, whereas Capan 2 required the biexponential bleaching factor. The greater photosensitivity of MIA PaCa2 over Capan 2 can be best explained not by differences in the interaction parameter but rather by differences in the photobleaching pattern and rate. It may be possible to further enhance the selectivity of photodynamic therapy if differences in photobleaching between different cell types can be exploited by adequate dosimetry.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>7606730</pmid><tpages>7</tpages></addata></record> |
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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - metabolism Biological and medical sciences Computer Simulation Dose-Response Relationship, Drug Hematoporphyrin Derivative - pharmacokinetics Hematoporphyrin Derivative - pharmacology Humans Medical sciences Models, Biological Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - metabolism Photochemotherapy - methods Photoradiation therapy and photosensitizing agent Thymidine - metabolism Treatment with physical agents Treatment. General aspects Tritium Tumor Cells, Cultured - drug effects Tumors |
title | lack of reciprocity in drug and light dose dependence of photodynamic therapy of pancreatic adenocarcinoma in vitro |
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