Determinants of CPT-11 and SN-38 activities in human lung cancer cells
Irinotecan (CPT-11) is a semisynthetic camptothecin derivative with a broad spectrum of anti-tumour activity. Carboxylesterase (CE) catalyses the conversion of CPT-11 to SN-38 (7-ethyl-10-hydroxycamptothecin), the active form of CPT-11. The antiproliferative effects of CPT-11 and SN-38, CE-activity...
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description | Irinotecan (CPT-11) is a semisynthetic camptothecin derivative with a broad spectrum of anti-tumour activity. Carboxylesterase (CE) catalyses the conversion of CPT-11 to SN-38 (7-ethyl-10-hydroxycamptothecin), the active form of CPT-11. The antiproliferative effects of CPT-11 and SN-38, CE-activity and topoisomerase I protein expression were investigated in five human small-cell lung cancer (SCLC) cell lines and four human non-small-cell lung cancer (NSCLC) cell lines. Antiproliferative activity, expressed as IC50 values, was determined using the MTT assay. CPT-11 was significantly more active in SCLC than in NSCLC cell lines (P = 0.0036), whereas no significant difference between histological types was observed with SN-38. A significant correlation (r2 = 0.52, P = 0.028) was observed between CE activity and chemosensitivity to CPT-11 but not to SN-38, and significantly higher CE activity was observed in SCLC compared with NSCLC cell lines (P = 0.025). Western blotting experiments showed topoisomerase I protein expressions within a factor of 2, and a granular nuclear staining was detectable in all cell lines by immunocytochemistry of cytospins. No correlation was observed between protein expression and sensitivity to CPT-11 or SN-38. Cellular and medium concentrations of CPT-11 and SN-38 were measured by high-performance liquid chromatography (HPLC) in one SCLC cell line with high CE activity and high sensitivity to CPT-11, and one NSCLC cell line with low sensitivity to CPT-11 and CE activity. Intracellular concentrations of CPT-11 and SN-38 were higher in the SCLC cell line, and this was associated with an increase in cellular uptake of CPT-11 compared with the medium, and an increased intracellular formation of SN-38. In conclusion, CE activity appears to be associated with higher sensitivity to CPT-11 in human lung cancer cell lines and may partly explain the difference in the in vitro sensitivity to CPT-11 between SCLC and NSCLC cells. The assessment of CE activity in clinical material of lung cancer patients undergoing treatment with CPT-11 may be warranted. However, other mechanisms may influence sensitivity to CPT-11, possibly including drug transport. |
doi_str_mv | 10.1038/bjc.1998.362 |
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Carboxylesterase (CE) catalyses the conversion of CPT-11 to SN-38 (7-ethyl-10-hydroxycamptothecin), the active form of CPT-11. The antiproliferative effects of CPT-11 and SN-38, CE-activity and topoisomerase I protein expression were investigated in five human small-cell lung cancer (SCLC) cell lines and four human non-small-cell lung cancer (NSCLC) cell lines. Antiproliferative activity, expressed as IC50 values, was determined using the MTT assay. CPT-11 was significantly more active in SCLC than in NSCLC cell lines (P = 0.0036), whereas no significant difference between histological types was observed with SN-38. A significant correlation (r2 = 0.52, P = 0.028) was observed between CE activity and chemosensitivity to CPT-11 but not to SN-38, and significantly higher CE activity was observed in SCLC compared with NSCLC cell lines (P = 0.025). Western blotting experiments showed topoisomerase I protein expressions within a factor of 2, and a granular nuclear staining was detectable in all cell lines by immunocytochemistry of cytospins. No correlation was observed between protein expression and sensitivity to CPT-11 or SN-38. Cellular and medium concentrations of CPT-11 and SN-38 were measured by high-performance liquid chromatography (HPLC) in one SCLC cell line with high CE activity and high sensitivity to CPT-11, and one NSCLC cell line with low sensitivity to CPT-11 and CE activity. Intracellular concentrations of CPT-11 and SN-38 were higher in the SCLC cell line, and this was associated with an increase in cellular uptake of CPT-11 compared with the medium, and an increased intracellular formation of SN-38. In conclusion, CE activity appears to be associated with higher sensitivity to CPT-11 in human lung cancer cell lines and may partly explain the difference in the in vitro sensitivity to CPT-11 between SCLC and NSCLC cells. The assessment of CE activity in clinical material of lung cancer patients undergoing treatment with CPT-11 may be warranted. However, other mechanisms may influence sensitivity to CPT-11, possibly including drug transport.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1998.362</identifier><identifier>PMID: 9649129</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Antineoplastic Agents, Phytogenic - pharmacokinetics ; Antineoplastic Agents, Phytogenic - pharmacology ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Camptothecin - analogs & derivatives ; Camptothecin - pharmacokinetics ; Camptothecin - pharmacology ; Cancer Research ; Carboxylic Ester Hydrolases - metabolism ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Small Cell - drug therapy ; Carcinoma, Small Cell - metabolism ; Carcinoma, Small Cell - pathology ; Cell Division - drug effects ; DNA Topoisomerases, Type I - biosynthesis ; DNA Topoisomerases, Type I - metabolism ; Drug Resistance ; Drug Screening Assays, Antitumor ; Enzyme Inhibitors - pharmacokinetics ; Enzyme Inhibitors - pharmacology ; Epidemiology ; experimental-oncology ; Humans ; Irinotecan ; Lung Neoplasms - drug therapy ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Medical sciences ; Molecular Medicine ; Oncology ; Pneumology ; Topoisomerase I Inhibitors ; Tumor Cells, Cultured ; Tumors of the respiratory system and mediastinum</subject><ispartof>British journal of cancer, 1998-06, Vol.77 (12), p.2171-2176</ispartof><rights>Cancer Research Campaign 1998</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-65b911d4cd6dc87b6151da36c6ac000445280e4944afa793b8de0a7ed09ce5c43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150393/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150393/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2276162$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9649129$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van Ark-Otte, J</creatorcontrib><creatorcontrib>Kedde, MA</creatorcontrib><creatorcontrib>van der Vijgh, WJF</creatorcontrib><creatorcontrib>Dingemans, A-MC</creatorcontrib><creatorcontrib>Jansen, WJM</creatorcontrib><creatorcontrib>Pinedo, HM</creatorcontrib><creatorcontrib>Boven, E</creatorcontrib><creatorcontrib>Giaccone, G</creatorcontrib><title>Determinants of CPT-11 and SN-38 activities in human lung cancer cells</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>Irinotecan (CPT-11) is a semisynthetic camptothecin derivative with a broad spectrum of anti-tumour activity. Carboxylesterase (CE) catalyses the conversion of CPT-11 to SN-38 (7-ethyl-10-hydroxycamptothecin), the active form of CPT-11. The antiproliferative effects of CPT-11 and SN-38, CE-activity and topoisomerase I protein expression were investigated in five human small-cell lung cancer (SCLC) cell lines and four human non-small-cell lung cancer (NSCLC) cell lines. Antiproliferative activity, expressed as IC50 values, was determined using the MTT assay. CPT-11 was significantly more active in SCLC than in NSCLC cell lines (P = 0.0036), whereas no significant difference between histological types was observed with SN-38. A significant correlation (r2 = 0.52, P = 0.028) was observed between CE activity and chemosensitivity to CPT-11 but not to SN-38, and significantly higher CE activity was observed in SCLC compared with NSCLC cell lines (P = 0.025). Western blotting experiments showed topoisomerase I protein expressions within a factor of 2, and a granular nuclear staining was detectable in all cell lines by immunocytochemistry of cytospins. No correlation was observed between protein expression and sensitivity to CPT-11 or SN-38. Cellular and medium concentrations of CPT-11 and SN-38 were measured by high-performance liquid chromatography (HPLC) in one SCLC cell line with high CE activity and high sensitivity to CPT-11, and one NSCLC cell line with low sensitivity to CPT-11 and CE activity. Intracellular concentrations of CPT-11 and SN-38 were higher in the SCLC cell line, and this was associated with an increase in cellular uptake of CPT-11 compared with the medium, and an increased intracellular formation of SN-38. In conclusion, CE activity appears to be associated with higher sensitivity to CPT-11 in human lung cancer cell lines and may partly explain the difference in the in vitro sensitivity to CPT-11 between SCLC and NSCLC cells. The assessment of CE activity in clinical material of lung cancer patients undergoing treatment with CPT-11 may be warranted. However, other mechanisms may influence sensitivity to CPT-11, possibly including drug transport.</description><subject>Antineoplastic Agents, Phytogenic - pharmacokinetics</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Camptothecin - analogs & derivatives</subject><subject>Camptothecin - pharmacokinetics</subject><subject>Camptothecin - pharmacology</subject><subject>Cancer Research</subject><subject>Carboxylic Ester Hydrolases - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Small Cell - drug therapy</subject><subject>Carcinoma, Small Cell - metabolism</subject><subject>Carcinoma, Small Cell - pathology</subject><subject>Cell Division - drug effects</subject><subject>DNA Topoisomerases, Type I - biosynthesis</subject><subject>DNA Topoisomerases, Type I - metabolism</subject><subject>Drug Resistance</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Enzyme Inhibitors - pharmacokinetics</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Epidemiology</subject><subject>experimental-oncology</subject><subject>Humans</subject><subject>Irinotecan</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>Molecular Medicine</subject><subject>Oncology</subject><subject>Pneumology</subject><subject>Topoisomerase I Inhibitors</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkMFrFDEUh4Moda3evAo5iCdnm5dkJslFkNWqUKxgPYc3mcw2y0ymJjOF_vdm3WVR6CmE38fvvfcR8hrYGpjQF-3OrcEYvRYNf0JWUAtegebqKVkxxlTFDGfPyYucd-VrmFZn5Mw00gA3K3L5yc8-jSFinDOderr5cVMBUIwd_fm9Epqim8N9mIPPNER6u4wY6bDELXUYnU_U-WHIL8mzHofsXx3fc_Lr8vPN5mt1df3l2-bjVeVq4HPV1K0B6KTrms5p1TZQQ4eicQ26spyUNdfMSyMl9qiMaHXnGSrfMeN87aQ4Jx8OvXdLO_rO-TgnHOxdCiOmBzthsP8nMdza7XRvOdRMGFEK3h0L0vR78Xm2Y8j7EzD6aclWGaNkraGA7w-gS1POyfenIcDs3rst3u3euy3eC_7m38VO8FF0yd8ec8wOhz4VeSGfMM5VA39rqgOWSxK3PtndtKRYlD4-9g-tEpkg</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>van Ark-Otte, J</creator><creator>Kedde, MA</creator><creator>van der Vijgh, WJF</creator><creator>Dingemans, A-MC</creator><creator>Jansen, WJM</creator><creator>Pinedo, HM</creator><creator>Boven, E</creator><creator>Giaccone, G</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980601</creationdate><title>Determinants of CPT-11 and SN-38 activities in human lung cancer cells</title><author>van Ark-Otte, J ; Kedde, MA ; van der Vijgh, WJF ; Dingemans, A-MC ; Jansen, WJM ; Pinedo, HM ; Boven, E ; Giaccone, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-65b911d4cd6dc87b6151da36c6ac000445280e4944afa793b8de0a7ed09ce5c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Antineoplastic Agents, Phytogenic - pharmacokinetics</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Camptothecin - analogs & derivatives</topic><topic>Camptothecin - pharmacokinetics</topic><topic>Camptothecin - pharmacology</topic><topic>Cancer Research</topic><topic>Carboxylic Ester Hydrolases - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Small Cell - drug therapy</topic><topic>Carcinoma, Small Cell - metabolism</topic><topic>Carcinoma, Small Cell - pathology</topic><topic>Cell Division - drug effects</topic><topic>DNA Topoisomerases, Type I - biosynthesis</topic><topic>DNA Topoisomerases, Type I - metabolism</topic><topic>Drug Resistance</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Enzyme Inhibitors - pharmacokinetics</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Epidemiology</topic><topic>experimental-oncology</topic><topic>Humans</topic><topic>Irinotecan</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>Molecular Medicine</topic><topic>Oncology</topic><topic>Pneumology</topic><topic>Topoisomerase I Inhibitors</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Ark-Otte, J</creatorcontrib><creatorcontrib>Kedde, MA</creatorcontrib><creatorcontrib>van der Vijgh, WJF</creatorcontrib><creatorcontrib>Dingemans, A-MC</creatorcontrib><creatorcontrib>Jansen, WJM</creatorcontrib><creatorcontrib>Pinedo, HM</creatorcontrib><creatorcontrib>Boven, E</creatorcontrib><creatorcontrib>Giaccone, G</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Ark-Otte, J</au><au>Kedde, MA</au><au>van der Vijgh, WJF</au><au>Dingemans, A-MC</au><au>Jansen, WJM</au><au>Pinedo, HM</au><au>Boven, E</au><au>Giaccone, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determinants of CPT-11 and SN-38 activities in human lung cancer cells</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>77</volume><issue>12</issue><spage>2171</spage><epage>2176</epage><pages>2171-2176</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Irinotecan (CPT-11) is a semisynthetic camptothecin derivative with a broad spectrum of anti-tumour activity. Carboxylesterase (CE) catalyses the conversion of CPT-11 to SN-38 (7-ethyl-10-hydroxycamptothecin), the active form of CPT-11. The antiproliferative effects of CPT-11 and SN-38, CE-activity and topoisomerase I protein expression were investigated in five human small-cell lung cancer (SCLC) cell lines and four human non-small-cell lung cancer (NSCLC) cell lines. Antiproliferative activity, expressed as IC50 values, was determined using the MTT assay. CPT-11 was significantly more active in SCLC than in NSCLC cell lines (P = 0.0036), whereas no significant difference between histological types was observed with SN-38. A significant correlation (r2 = 0.52, P = 0.028) was observed between CE activity and chemosensitivity to CPT-11 but not to SN-38, and significantly higher CE activity was observed in SCLC compared with NSCLC cell lines (P = 0.025). Western blotting experiments showed topoisomerase I protein expressions within a factor of 2, and a granular nuclear staining was detectable in all cell lines by immunocytochemistry of cytospins. No correlation was observed between protein expression and sensitivity to CPT-11 or SN-38. Cellular and medium concentrations of CPT-11 and SN-38 were measured by high-performance liquid chromatography (HPLC) in one SCLC cell line with high CE activity and high sensitivity to CPT-11, and one NSCLC cell line with low sensitivity to CPT-11 and CE activity. Intracellular concentrations of CPT-11 and SN-38 were higher in the SCLC cell line, and this was associated with an increase in cellular uptake of CPT-11 compared with the medium, and an increased intracellular formation of SN-38. In conclusion, CE activity appears to be associated with higher sensitivity to CPT-11 in human lung cancer cell lines and may partly explain the difference in the in vitro sensitivity to CPT-11 between SCLC and NSCLC cells. The assessment of CE activity in clinical material of lung cancer patients undergoing treatment with CPT-11 may be warranted. However, other mechanisms may influence sensitivity to CPT-11, possibly including drug transport.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>9649129</pmid><doi>10.1038/bjc.1998.362</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents, Phytogenic - pharmacokinetics Antineoplastic Agents, Phytogenic - pharmacology Biological and medical sciences Biomedical and Life Sciences Biomedicine Camptothecin - analogs & derivatives Camptothecin - pharmacokinetics Camptothecin - pharmacology Cancer Research Carboxylic Ester Hydrolases - metabolism Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - pathology Carcinoma, Small Cell - drug therapy Carcinoma, Small Cell - metabolism Carcinoma, Small Cell - pathology Cell Division - drug effects DNA Topoisomerases, Type I - biosynthesis DNA Topoisomerases, Type I - metabolism Drug Resistance Drug Screening Assays, Antitumor Enzyme Inhibitors - pharmacokinetics Enzyme Inhibitors - pharmacology Epidemiology experimental-oncology Humans Irinotecan Lung Neoplasms - drug therapy Lung Neoplasms - metabolism Lung Neoplasms - pathology Medical sciences Molecular Medicine Oncology Pneumology Topoisomerase I Inhibitors Tumor Cells, Cultured Tumors of the respiratory system and mediastinum |
title | Determinants of CPT-11 and SN-38 activities in human lung cancer cells |
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