Esterase Activity, Exclusion of Propidium Iodide, and Proliferation in Tumor Cells Exposed to Anticancer Agents: Phenomena Relevant to Chemosensitivity Determinations
Abstract Cellular esterase activity and the ability to exclude propidium iodide were examined after exposing tumor cells to anticancer agents. In general, esterase activity and the ability to exclude propidium iodide continued when cells proliferated and disappeared when proliferation was inhibited....
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Veröffentlicht in: | Cancer investigation 1985, Vol.3 (5), p.413-426 |
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container_title | Cancer investigation |
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creator | Pavlik, Edward J. Flanigan, Robert C. Van Nagell, John R. Hanson, Michael B. Donaldson, Elvis S. Keaton, Kathryn Doss, Beverly Bartmas, Jon Kenady, Daniel E. |
description | Abstract
Cellular esterase activity and the ability to exclude propidium iodide were examined after exposing tumor cells to anticancer agents. In general, esterase activity and the ability to exclude propidium iodide continued when cells proliferated and disappeared when proliferation was inhibited. However, with a number of preparations, drug exposure inhibited proliferation while esterase activity and propidium iodide exclusion persisted. These indications of persisting cell function or viability after drug exposure may be relevant to a potential for tumor cell recovery. When the viability of established cell lines progressively declined on days 4 and 7 following drug exposure, recovery did not occur. When proliferative recoveries occurred, viabilities remained elevated. Estimates of in vitro sensitivity by proliferation-related criteria were contrasted by persistent high viability estimates in 22% of the determinations performed with primary tumor cell preparations. The potential for recovery may explain the disappointing ability of proliferative chemosensitivity assays to predict clinical sensitivity. |
doi_str_mv | 10.3109/07357908509039802 |
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Cellular esterase activity and the ability to exclude propidium iodide were examined after exposing tumor cells to anticancer agents. In general, esterase activity and the ability to exclude propidium iodide continued when cells proliferated and disappeared when proliferation was inhibited. However, with a number of preparations, drug exposure inhibited proliferation while esterase activity and propidium iodide exclusion persisted. These indications of persisting cell function or viability after drug exposure may be relevant to a potential for tumor cell recovery. When the viability of established cell lines progressively declined on days 4 and 7 following drug exposure, recovery did not occur. When proliferative recoveries occurred, viabilities remained elevated. Estimates of in vitro sensitivity by proliferation-related criteria were contrasted by persistent high viability estimates in 22% of the determinations performed with primary tumor cell preparations. The potential for recovery may explain the disappointing ability of proliferative chemosensitivity assays to predict clinical sensitivity.</description><identifier>ISSN: 0735-7907</identifier><identifier>EISSN: 1532-4192</identifier><identifier>DOI: 10.3109/07357908509039802</identifier><identifier>PMID: 4052831</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Antineoplastic Agents - pharmacology ; Cell Division - drug effects ; Cell Line ; Cell Survival ; Colony-Forming Units Assay ; Esterases - analysis ; Flow Cytometry - methods ; Humans ; Microscopy, Fluorescence ; Neoplasms ; Phenanthridines ; Propidium ; Tumor Stem Cell Assay</subject><ispartof>Cancer investigation, 1985, Vol.3 (5), p.413-426</ispartof><rights>1985 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1985</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-89fbd622c5ca7e9f1dad61e68be4add6b0dc42a47e5a04231cd81ebab206ed613</citedby><cites>FETCH-LOGICAL-c401t-89fbd622c5ca7e9f1dad61e68be4add6b0dc42a47e5a04231cd81ebab206ed613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/07357908509039802$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/07357908509039802$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,776,780,4010,27900,27901,27902,59620,59726,60409,60515,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4052831$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pavlik, Edward J.</creatorcontrib><creatorcontrib>Flanigan, Robert C.</creatorcontrib><creatorcontrib>Van Nagell, John R.</creatorcontrib><creatorcontrib>Hanson, Michael B.</creatorcontrib><creatorcontrib>Donaldson, Elvis S.</creatorcontrib><creatorcontrib>Keaton, Kathryn</creatorcontrib><creatorcontrib>Doss, Beverly</creatorcontrib><creatorcontrib>Bartmas, Jon</creatorcontrib><creatorcontrib>Kenady, Daniel E.</creatorcontrib><title>Esterase Activity, Exclusion of Propidium Iodide, and Proliferation in Tumor Cells Exposed to Anticancer Agents: Phenomena Relevant to Chemosensitivity Determinations</title><title>Cancer investigation</title><addtitle>Cancer Invest</addtitle><description>Abstract
Cellular esterase activity and the ability to exclude propidium iodide were examined after exposing tumor cells to anticancer agents. In general, esterase activity and the ability to exclude propidium iodide continued when cells proliferated and disappeared when proliferation was inhibited. However, with a number of preparations, drug exposure inhibited proliferation while esterase activity and propidium iodide exclusion persisted. These indications of persisting cell function or viability after drug exposure may be relevant to a potential for tumor cell recovery. When the viability of established cell lines progressively declined on days 4 and 7 following drug exposure, recovery did not occur. When proliferative recoveries occurred, viabilities remained elevated. Estimates of in vitro sensitivity by proliferation-related criteria were contrasted by persistent high viability estimates in 22% of the determinations performed with primary tumor cell preparations. The potential for recovery may explain the disappointing ability of proliferative chemosensitivity assays to predict clinical sensitivity.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Cell Division - drug effects</subject><subject>Cell Line</subject><subject>Cell Survival</subject><subject>Colony-Forming Units Assay</subject><subject>Esterases - analysis</subject><subject>Flow Cytometry - methods</subject><subject>Humans</subject><subject>Microscopy, Fluorescence</subject><subject>Neoplasms</subject><subject>Phenanthridines</subject><subject>Propidium</subject><subject>Tumor Stem Cell Assay</subject><issn>0735-7907</issn><issn>1532-4192</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2KFDEUhYMoYzv6AC6ErFxNaZKq1I-6adpWBwYcZFwXt5JbdoZU0iap0X4hn9OU3QgiugrkfOfk5F5CnnL2ouSse8maUjYdayXrWNm1TNwjKy5LUVS8E_fJatGLDDQPyaMYbxnjrWjkGTmrmBRtyVfkxzYmDBCRrlUydyYdLuj2u7JzNN5RP9Lr4PdGm3mil14bjRcUnF5urRmzMS2YcfRmnnygG7Q2Zv_eR9Q0ebp2yShwCgNdf0GX4it6vUPnJ3RAP6HFO3BpATc7nLLJRXNsQd9i7jUZ9-uF-Jg8GMFGfHI6z8nnd9ubzYfi6uP7y836qlAV46lou3HQtRBKKmiwG7kGXXOs2wEr0LoemFaVgKpBCawSJVe65TjAIFiNmSzPyfNj7j74rzPG1E8mqvwrcOjn2Dd1JSSXbQb5EVTBxxhw7PfBTBAOPWf9spv-r91kz7NT-DxMqH87TsvI-pujbtzowwTffLC6T3CwPowhT9HEJfrf8a__sO8QbNopCNjf-jm4PLf_lPsJ2gazmA</recordid><startdate>1985</startdate><enddate>1985</enddate><creator>Pavlik, Edward J.</creator><creator>Flanigan, Robert C.</creator><creator>Van Nagell, John R.</creator><creator>Hanson, Michael B.</creator><creator>Donaldson, Elvis S.</creator><creator>Keaton, Kathryn</creator><creator>Doss, Beverly</creator><creator>Bartmas, Jon</creator><creator>Kenady, Daniel E.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><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>1985</creationdate><title>Esterase Activity, Exclusion of Propidium Iodide, and Proliferation in Tumor Cells Exposed to Anticancer Agents: Phenomena Relevant to Chemosensitivity Determinations</title><author>Pavlik, Edward J. ; Flanigan, Robert C. ; Van Nagell, John R. ; Hanson, Michael B. ; Donaldson, Elvis S. ; Keaton, Kathryn ; Doss, Beverly ; Bartmas, Jon ; Kenady, Daniel E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-89fbd622c5ca7e9f1dad61e68be4add6b0dc42a47e5a04231cd81ebab206ed613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Cell Division - drug effects</topic><topic>Cell Line</topic><topic>Cell Survival</topic><topic>Colony-Forming Units Assay</topic><topic>Esterases - analysis</topic><topic>Flow Cytometry - methods</topic><topic>Humans</topic><topic>Microscopy, Fluorescence</topic><topic>Neoplasms</topic><topic>Phenanthridines</topic><topic>Propidium</topic><topic>Tumor Stem Cell Assay</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pavlik, Edward J.</creatorcontrib><creatorcontrib>Flanigan, Robert C.</creatorcontrib><creatorcontrib>Van Nagell, John R.</creatorcontrib><creatorcontrib>Hanson, Michael B.</creatorcontrib><creatorcontrib>Donaldson, Elvis S.</creatorcontrib><creatorcontrib>Keaton, Kathryn</creatorcontrib><creatorcontrib>Doss, Beverly</creatorcontrib><creatorcontrib>Bartmas, Jon</creatorcontrib><creatorcontrib>Kenady, Daniel E.</creatorcontrib><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>Cancer investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pavlik, Edward J.</au><au>Flanigan, Robert C.</au><au>Van Nagell, John R.</au><au>Hanson, Michael B.</au><au>Donaldson, Elvis S.</au><au>Keaton, Kathryn</au><au>Doss, Beverly</au><au>Bartmas, Jon</au><au>Kenady, Daniel E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Esterase Activity, Exclusion of Propidium Iodide, and Proliferation in Tumor Cells Exposed to Anticancer Agents: Phenomena Relevant to Chemosensitivity Determinations</atitle><jtitle>Cancer investigation</jtitle><addtitle>Cancer Invest</addtitle><date>1985</date><risdate>1985</risdate><volume>3</volume><issue>5</issue><spage>413</spage><epage>426</epage><pages>413-426</pages><issn>0735-7907</issn><eissn>1532-4192</eissn><abstract>Abstract
Cellular esterase activity and the ability to exclude propidium iodide were examined after exposing tumor cells to anticancer agents. In general, esterase activity and the ability to exclude propidium iodide continued when cells proliferated and disappeared when proliferation was inhibited. However, with a number of preparations, drug exposure inhibited proliferation while esterase activity and propidium iodide exclusion persisted. These indications of persisting cell function or viability after drug exposure may be relevant to a potential for tumor cell recovery. When the viability of established cell lines progressively declined on days 4 and 7 following drug exposure, recovery did not occur. When proliferative recoveries occurred, viabilities remained elevated. Estimates of in vitro sensitivity by proliferation-related criteria were contrasted by persistent high viability estimates in 22% of the determinations performed with primary tumor cell preparations. The potential for recovery may explain the disappointing ability of proliferative chemosensitivity assays to predict clinical sensitivity.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>4052831</pmid><doi>10.3109/07357908509039802</doi><tpages>14</tpages></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Cell Division - drug effects Cell Line Cell Survival Colony-Forming Units Assay Esterases - analysis Flow Cytometry - methods Humans Microscopy, Fluorescence Neoplasms Phenanthridines Propidium Tumor Stem Cell Assay |
title | Esterase Activity, Exclusion of Propidium Iodide, and Proliferation in Tumor Cells Exposed to Anticancer Agents: Phenomena Relevant to Chemosensitivity Determinations |
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