Bcl-2, bax and bcl-xL expression in human sensitive and resistant leukemia cell lines
With the growing understanding of cytostatic drug-induced programmed cell death new drug-resistance mechanisms based on the altered ability of cells to die by apoptosis have been defined. At first, the sensitive and P-glycoprotein (P-gp)-related resistant cell lines were tested to induce apoptosis b...
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description | With the growing understanding of cytostatic drug-induced programmed cell death new drug-resistance mechanisms based on the altered ability of cells to die by apoptosis have been defined. At first, the sensitive and P-glycoprotein (P-gp)-related resistant cell lines were tested to induce apoptosis by a non-P-gp transported drug, such as cytosine arabinoside (ara-C). It was demonstrated that ara-C induces apoptosis in sensitive as well as in P-gp-related resistant cell lines, as expected. Furthermore, the role of bcl-2 and bcl-xL apoptosis inhibitors as well as bax expression (apoptosis inducer) in human sensitive leukemic cell lines (CCRF-CEM and HL-60) as compared to their resistant variants such as CCRF-CEM/ACT400, CCRF-CEM/VCR1000, HL-60/IDA40, HL-60/DNR250 was evaluated. In addition to the P-gp-related resistance, a possible multidrug resistance-associated protein (MRP) and the lung resistance protein (LRP)-related resistance were assessed by flow cytometry using the monoclonal antibodies 4E3.16, MRPr1 and LRP56. Furthermore, the function of P-gp was determined with the rhodamine-123 (R-123) accumulation test. Bcl-2 and bax were analyzed by both flow cytometry and ECL Western blot, bcl-xL by ECL-Western blot alone. Comparison of the two sensitive cell lines demonstrated different bcl-2, bax and bcl-xL patterns. The common characteristic was the increased expression of one of the apoptosis inhibitor proteins, such as bcl-2 or bcl-xL. The sensitive CCRF-CEM showed a high bax level, where a decrease of about 75% in resistant variants was measured. Compared to their sensitive counterpart HL-60, a low bax expression was analyzed, which increased in the resistant variant. The common characteristic of all resistant cell lines was the decreased expression of bax compared to bcl-2 or bcl-xL. In the P-gp-related resistant HL-60/DNR250 only an increase in bcl-xL was seen, whereas in the LRP-expressing as well as P-gp and MRP negative resistant HL-60/IDA40 both apoptotic inhibitor proteins bcl-2 and bcL-xL showed maximum increase, compared to the other resistant cell lines. The P-gp-related resistant cell lines CCRF-CEM/ACT400 and CCRF-CEM/VCR1000 also showed an increased expression of both bcl-2 and bcl-xL. Summarizing these results, it was shown that the examined sensitive human leukemic cell lines and their resistant variants demonstrated a different pattern of markers for preventing and promoting apoptosis. An association between P-gp and possible LRP-expressi |
doi_str_mv | 10.1038/sj.leu.2401571 |
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At first, the sensitive and P-glycoprotein (P-gp)-related resistant cell lines were tested to induce apoptosis by a non-P-gp transported drug, such as cytosine arabinoside (ara-C). It was demonstrated that ara-C induces apoptosis in sensitive as well as in P-gp-related resistant cell lines, as expected. Furthermore, the role of bcl-2 and bcl-xL apoptosis inhibitors as well as bax expression (apoptosis inducer) in human sensitive leukemic cell lines (CCRF-CEM and HL-60) as compared to their resistant variants such as CCRF-CEM/ACT400, CCRF-CEM/VCR1000, HL-60/IDA40, HL-60/DNR250 was evaluated. In addition to the P-gp-related resistance, a possible multidrug resistance-associated protein (MRP) and the lung resistance protein (LRP)-related resistance were assessed by flow cytometry using the monoclonal antibodies 4E3.16, MRPr1 and LRP56. Furthermore, the function of P-gp was determined with the rhodamine-123 (R-123) accumulation test. Bcl-2 and bax were analyzed by both flow cytometry and ECL Western blot, bcl-xL by ECL-Western blot alone. Comparison of the two sensitive cell lines demonstrated different bcl-2, bax and bcl-xL patterns. The common characteristic was the increased expression of one of the apoptosis inhibitor proteins, such as bcl-2 or bcl-xL. The sensitive CCRF-CEM showed a high bax level, where a decrease of about 75% in resistant variants was measured. Compared to their sensitive counterpart HL-60, a low bax expression was analyzed, which increased in the resistant variant. The common characteristic of all resistant cell lines was the decreased expression of bax compared to bcl-2 or bcl-xL. In the P-gp-related resistant HL-60/DNR250 only an increase in bcl-xL was seen, whereas in the LRP-expressing as well as P-gp and MRP negative resistant HL-60/IDA40 both apoptotic inhibitor proteins bcl-2 and bcL-xL showed maximum increase, compared to the other resistant cell lines. The P-gp-related resistant cell lines CCRF-CEM/ACT400 and CCRF-CEM/VCR1000 also showed an increased expression of both bcl-2 and bcl-xL. Summarizing these results, it was shown that the examined sensitive human leukemic cell lines and their resistant variants demonstrated a different pattern of markers for preventing and promoting apoptosis. An association between P-gp and possible LRP-expressing leukemic cells as well as apoptosis-preventing markers (bcl-2, bcl-xL) seems to exist. The clinical relevance of the coexpression of various resistance mechanisms remains to be confirmed in large leukemia patient groups.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/sj.leu.2401571</identifier><identifier>PMID: 10557064</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Annexin A5 - analysis ; Antineoplastic Agents - pharmacology ; Apoptosis ; Apoptosis - drug effects ; ATP Binding Cassette Transporter, Sub-Family B - metabolism ; ATP-Binding Cassette Transporters - analysis ; BAX protein ; Bcl-2 protein ; bcl-2-Associated X Protein ; Bcl-x protein ; Blotting, Western ; Cell death ; Cytarabine ; Cytarabine - pharmacology ; Cytosine ; Drug Resistance, Neoplasm ; Drug Screening Assays, Antitumor ; Flow Cytometry ; Gene Expression ; glycoprotein P ; Glycoproteins ; HL-60 Cells ; Humans ; Inhibitors ; Inhibitory Concentration 50 ; Leukemia ; Leukemia - metabolism ; Leukemia - pathology ; Markers ; Material requirements planning ; Microscopy, Fluorescence ; Monoclonal antibodies ; Multidrug resistance ; Multidrug Resistance-Associated Proteins ; Multidrug resistant organisms ; Neoplasm Proteins ; P-Glycoprotein ; Proteins ; Proto-Oncogene Proteins - biosynthesis ; Proto-Oncogene Proteins c-bcl-2 - biosynthesis ; Rhodamine ; Tumor cell lines ; Tumor Cells, Cultured ; Vault Ribonucleoprotein Particles</subject><ispartof>Leukemia, 1999-11, Vol.13 (11), p.1864-1872</ispartof><rights>Macmillan Publishers Limited 1999.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10557064$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nuessler, V</creatorcontrib><creatorcontrib>Stötzer, O</creatorcontrib><creatorcontrib>Gullis, E</creatorcontrib><creatorcontrib>Pelka-Fleischer, R</creatorcontrib><creatorcontrib>Pogrebniak, A</creatorcontrib><creatorcontrib>Gieseler, F</creatorcontrib><creatorcontrib>Wilmanns, W</creatorcontrib><title>Bcl-2, bax and bcl-xL expression in human sensitive and resistant leukemia cell lines</title><title>Leukemia</title><addtitle>Leukemia</addtitle><description>With the growing understanding of cytostatic drug-induced programmed cell death new drug-resistance mechanisms based on the altered ability of cells to die by apoptosis have been defined. At first, the sensitive and P-glycoprotein (P-gp)-related resistant cell lines were tested to induce apoptosis by a non-P-gp transported drug, such as cytosine arabinoside (ara-C). It was demonstrated that ara-C induces apoptosis in sensitive as well as in P-gp-related resistant cell lines, as expected. Furthermore, the role of bcl-2 and bcl-xL apoptosis inhibitors as well as bax expression (apoptosis inducer) in human sensitive leukemic cell lines (CCRF-CEM and HL-60) as compared to their resistant variants such as CCRF-CEM/ACT400, CCRF-CEM/VCR1000, HL-60/IDA40, HL-60/DNR250 was evaluated. In addition to the P-gp-related resistance, a possible multidrug resistance-associated protein (MRP) and the lung resistance protein (LRP)-related resistance were assessed by flow cytometry using the monoclonal antibodies 4E3.16, MRPr1 and LRP56. Furthermore, the function of P-gp was determined with the rhodamine-123 (R-123) accumulation test. Bcl-2 and bax were analyzed by both flow cytometry and ECL Western blot, bcl-xL by ECL-Western blot alone. Comparison of the two sensitive cell lines demonstrated different bcl-2, bax and bcl-xL patterns. The common characteristic was the increased expression of one of the apoptosis inhibitor proteins, such as bcl-2 or bcl-xL. The sensitive CCRF-CEM showed a high bax level, where a decrease of about 75% in resistant variants was measured. Compared to their sensitive counterpart HL-60, a low bax expression was analyzed, which increased in the resistant variant. The common characteristic of all resistant cell lines was the decreased expression of bax compared to bcl-2 or bcl-xL. In the P-gp-related resistant HL-60/DNR250 only an increase in bcl-xL was seen, whereas in the LRP-expressing as well as P-gp and MRP negative resistant HL-60/IDA40 both apoptotic inhibitor proteins bcl-2 and bcL-xL showed maximum increase, compared to the other resistant cell lines. The P-gp-related resistant cell lines CCRF-CEM/ACT400 and CCRF-CEM/VCR1000 also showed an increased expression of both bcl-2 and bcl-xL. Summarizing these results, it was shown that the examined sensitive human leukemic cell lines and their resistant variants demonstrated a different pattern of markers for preventing and promoting apoptosis. An association between P-gp and possible LRP-expressing leukemic cells as well as apoptosis-preventing markers (bcl-2, bcl-xL) seems to exist. The clinical relevance of the coexpression of various resistance mechanisms remains to be confirmed in large leukemia patient groups.</description><subject>Annexin A5 - analysis</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>ATP Binding Cassette Transporter, Sub-Family B - metabolism</subject><subject>ATP-Binding Cassette Transporters - analysis</subject><subject>BAX protein</subject><subject>Bcl-2 protein</subject><subject>bcl-2-Associated X Protein</subject><subject>Bcl-x protein</subject><subject>Blotting, Western</subject><subject>Cell death</subject><subject>Cytarabine</subject><subject>Cytarabine - pharmacology</subject><subject>Cytosine</subject><subject>Drug Resistance, Neoplasm</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Flow Cytometry</subject><subject>Gene Expression</subject><subject>glycoprotein P</subject><subject>Glycoproteins</subject><subject>HL-60 Cells</subject><subject>Humans</subject><subject>Inhibitors</subject><subject>Inhibitory Concentration 50</subject><subject>Leukemia</subject><subject>Leukemia - metabolism</subject><subject>Leukemia - pathology</subject><subject>Markers</subject><subject>Material requirements planning</subject><subject>Microscopy, Fluorescence</subject><subject>Monoclonal antibodies</subject><subject>Multidrug resistance</subject><subject>Multidrug Resistance-Associated Proteins</subject><subject>Multidrug resistant organisms</subject><subject>Neoplasm Proteins</subject><subject>P-Glycoprotein</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins - biosynthesis</subject><subject>Proto-Oncogene Proteins c-bcl-2 - biosynthesis</subject><subject>Rhodamine</subject><subject>Tumor cell lines</subject><subject>Tumor Cells, Cultured</subject><subject>Vault Ribonucleoprotein Particles</subject><issn>0887-6924</issn><issn>1476-5551</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEtPwzAQhC0EoqVw5YgsIXEixW87R6h4SZW40HNk1xvhkDglTlD596RQLpxWu_NpZrQInVMyp4Sbm1TNaxjmTBAqNT1AUyq0yqSU9BBNiTE6UzkTE3SSUkXITlTHaEKJlJooMUWru3WdsWvs7Bbb6LEb1-0Sw3bTQUqhjThE_DY0NuIEMYU-fMIPOMoh9Tb2eMx_hyZYvIa6xnWIkE7RUWnrBGf7OUOrh_vXxVO2fHl8Xtwus4pr1mdOlCCYdkw67XNBvCuFMvl4JsZTq7ViIB0rGVhmvQIKzlvKcyNUKQXzfIaufn03XfsxQOqLJqRdDRuhHVJBteDKCD2Cl__Aqh26OHYrmBJSGc0kH6mLPTW4Bnyx6UJju6_i7138G62VbBs</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Nuessler, V</creator><creator>Stötzer, O</creator><creator>Gullis, E</creator><creator>Pelka-Fleischer, R</creator><creator>Pogrebniak, A</creator><creator>Gieseler, F</creator><creator>Wilmanns, W</creator><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>19991101</creationdate><title>Bcl-2, bax and bcl-xL expression in human sensitive and resistant leukemia cell lines</title><author>Nuessler, V ; 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At first, the sensitive and P-glycoprotein (P-gp)-related resistant cell lines were tested to induce apoptosis by a non-P-gp transported drug, such as cytosine arabinoside (ara-C). It was demonstrated that ara-C induces apoptosis in sensitive as well as in P-gp-related resistant cell lines, as expected. Furthermore, the role of bcl-2 and bcl-xL apoptosis inhibitors as well as bax expression (apoptosis inducer) in human sensitive leukemic cell lines (CCRF-CEM and HL-60) as compared to their resistant variants such as CCRF-CEM/ACT400, CCRF-CEM/VCR1000, HL-60/IDA40, HL-60/DNR250 was evaluated. In addition to the P-gp-related resistance, a possible multidrug resistance-associated protein (MRP) and the lung resistance protein (LRP)-related resistance were assessed by flow cytometry using the monoclonal antibodies 4E3.16, MRPr1 and LRP56. Furthermore, the function of P-gp was determined with the rhodamine-123 (R-123) accumulation test. Bcl-2 and bax were analyzed by both flow cytometry and ECL Western blot, bcl-xL by ECL-Western blot alone. Comparison of the two sensitive cell lines demonstrated different bcl-2, bax and bcl-xL patterns. The common characteristic was the increased expression of one of the apoptosis inhibitor proteins, such as bcl-2 or bcl-xL. The sensitive CCRF-CEM showed a high bax level, where a decrease of about 75% in resistant variants was measured. Compared to their sensitive counterpart HL-60, a low bax expression was analyzed, which increased in the resistant variant. The common characteristic of all resistant cell lines was the decreased expression of bax compared to bcl-2 or bcl-xL. In the P-gp-related resistant HL-60/DNR250 only an increase in bcl-xL was seen, whereas in the LRP-expressing as well as P-gp and MRP negative resistant HL-60/IDA40 both apoptotic inhibitor proteins bcl-2 and bcL-xL showed maximum increase, compared to the other resistant cell lines. The P-gp-related resistant cell lines CCRF-CEM/ACT400 and CCRF-CEM/VCR1000 also showed an increased expression of both bcl-2 and bcl-xL. Summarizing these results, it was shown that the examined sensitive human leukemic cell lines and their resistant variants demonstrated a different pattern of markers for preventing and promoting apoptosis. An association between P-gp and possible LRP-expressing leukemic cells as well as apoptosis-preventing markers (bcl-2, bcl-xL) seems to exist. The clinical relevance of the coexpression of various resistance mechanisms remains to be confirmed in large leukemia patient groups.</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>10557064</pmid><doi>10.1038/sj.leu.2401571</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Annexin A5 - analysis Antineoplastic Agents - pharmacology Apoptosis Apoptosis - drug effects ATP Binding Cassette Transporter, Sub-Family B - metabolism ATP-Binding Cassette Transporters - analysis BAX protein Bcl-2 protein bcl-2-Associated X Protein Bcl-x protein Blotting, Western Cell death Cytarabine Cytarabine - pharmacology Cytosine Drug Resistance, Neoplasm Drug Screening Assays, Antitumor Flow Cytometry Gene Expression glycoprotein P Glycoproteins HL-60 Cells Humans Inhibitors Inhibitory Concentration 50 Leukemia Leukemia - metabolism Leukemia - pathology Markers Material requirements planning Microscopy, Fluorescence Monoclonal antibodies Multidrug resistance Multidrug Resistance-Associated Proteins Multidrug resistant organisms Neoplasm Proteins P-Glycoprotein Proteins Proto-Oncogene Proteins - biosynthesis Proto-Oncogene Proteins c-bcl-2 - biosynthesis Rhodamine Tumor cell lines Tumor Cells, Cultured Vault Ribonucleoprotein Particles |
title | Bcl-2, bax and bcl-xL expression in human sensitive and resistant leukemia cell lines |
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