Apoptosis of Kasumi-1 cells induced by puerariae radix flavones and its molecular mechanism
To explore the effects and the molecular mechanism of puerariae radix flavones (PRF) on acute myeloid leukemia cell line Kasumi-1 cells in vitro. Kasumi-1 cells treated by PRF for 48 hours were observed with Wright's and Hoechst 33258 dying. The apoptotic cells were analyzed by flow cytometry w...
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Veröffentlicht in: | Zhōnghuá xuèyèxué zázhì 2012-01, Vol.33 (1), p.43-46 |
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creator | Shao, Hua-min Tang, Yu-hong Shen, Qun Zhu, Hong-qing Ji, Ou Zhang, Ya-cheng Ji, Jian-min Jiang, Peng-jun Si, Ye-jun Li, Zhao-rong |
description | To explore the effects and the molecular mechanism of puerariae radix flavones (PRF) on acute myeloid leukemia cell line Kasumi-1 cells in vitro.
Kasumi-1 cells treated by PRF for 48 hours were observed with Wright's and Hoechst 33258 dying. The apoptotic cells were analyzed by flow cytometry with AnnexinV/PI staining. The expression levels of bcl-2, Bim and Caspase-3/-8/-9 protein were assayed by Western blot and the AML1-ETO fusion gene was detected by real-time polymerase chain reaction.
PRF could induce Kasumi-1 cells to apoptosis effectively. The proportion of apoptotic cells in 50, 200 and 500 µg/ml PRF treatment groups were (14.1 ± 0.8)%, (17.7 ± 1.3)% and (32.4 ± 1.4)%, respectively, and significantly higher than that of control \[(7.8 ± 0.7)%\]. The relative expression levels of the anti-apoptotic Bcl-2 protein were 0.85 ± 0.05, 0.62 ± 0.07 and 0.43 ± 0.05; the apoptotic Bim protein were 0.21 ± 0.06, 0.39 ± 0.04 and 0.75 ± 0.05; the caspase-3 and caspase-9 were 0.92 ± 0.04, 1.21 ± 0.07, 1.33 ± 0.04 a |
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Kasumi-1 cells treated by PRF for 48 hours were observed with Wright's and Hoechst 33258 dying. The apoptotic cells were analyzed by flow cytometry with AnnexinV/PI staining. The expression levels of bcl-2, Bim and Caspase-3/-8/-9 protein were assayed by Western blot and the AML1-ETO fusion gene was detected by real-time polymerase chain reaction.
PRF could induce Kasumi-1 cells to apoptosis effectively. The proportion of apoptotic cells in 50, 200 and 500 µg/ml PRF treatment groups were (14.1 ± 0.8)%, (17.7 ± 1.3)% and (32.4 ± 1.4)%, respectively, and significantly higher than that of control \[(7.8 ± 0.7)%\]. The relative expression levels of the anti-apoptotic Bcl-2 protein were 0.85 ± 0.05, 0.62 ± 0.07 and 0.43 ± 0.05; the apoptotic Bim protein were 0.21 ± 0.06, 0.39 ± 0.04 and 0.75 ± 0.05; the caspase-3 and caspase-9 were 0.92 ± 0.04, 1.21 ± 0.07, 1.33 ± 0.04 a</description><identifier>ISSN: 0253-2727</identifier><identifier>PMID: 22575192</identifier><language>chi</language><publisher>China</publisher><subject>Apoptosis - drug effects ; Caspase 3 - metabolism ; Caspase 8 - metabolism ; Cell Line, Tumor ; Core Binding Factor Alpha 2 Subunit - genetics ; Core Binding Factor Alpha 2 Subunit - metabolism ; Flavones - pharmacology ; Humans ; Oncogene Proteins, Fusion - genetics ; Oncogene Proteins, Fusion - metabolism ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; Pueraria ; RUNX1 Translocation Partner 1 Protein</subject><ispartof>Zhōnghuá xuèyèxué zázhì, 2012-01, Vol.33 (1), p.43-46</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22575192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shao, Hua-min</creatorcontrib><creatorcontrib>Tang, Yu-hong</creatorcontrib><creatorcontrib>Shen, Qun</creatorcontrib><creatorcontrib>Zhu, Hong-qing</creatorcontrib><creatorcontrib>Ji, Ou</creatorcontrib><creatorcontrib>Zhang, Ya-cheng</creatorcontrib><creatorcontrib>Ji, Jian-min</creatorcontrib><creatorcontrib>Jiang, Peng-jun</creatorcontrib><creatorcontrib>Si, Ye-jun</creatorcontrib><creatorcontrib>Li, Zhao-rong</creatorcontrib><title>Apoptosis of Kasumi-1 cells induced by puerariae radix flavones and its molecular mechanism</title><title>Zhōnghuá xuèyèxué zázhì</title><addtitle>Zhonghua Xue Ye Xue Za Zhi</addtitle><description>To explore the effects and the molecular mechanism of puerariae radix flavones (PRF) on acute myeloid leukemia cell line Kasumi-1 cells in vitro.
Kasumi-1 cells treated by PRF for 48 hours were observed with Wright's and Hoechst 33258 dying. The apoptotic cells were analyzed by flow cytometry with AnnexinV/PI staining. The expression levels of bcl-2, Bim and Caspase-3/-8/-9 protein were assayed by Western blot and the AML1-ETO fusion gene was detected by real-time polymerase chain reaction.
PRF could induce Kasumi-1 cells to apoptosis effectively. The proportion of apoptotic cells in 50, 200 and 500 µg/ml PRF treatment groups were (14.1 ± 0.8)%, (17.7 ± 1.3)% and (32.4 ± 1.4)%, respectively, and significantly higher than that of control \[(7.8 ± 0.7)%\]. The relative expression levels of the anti-apoptotic Bcl-2 protein were 0.85 ± 0.05, 0.62 ± 0.07 and 0.43 ± 0.05; the apoptotic Bim protein were 0.21 ± 0.06, 0.39 ± 0.04 and 0.75 ± 0.05; the caspase-3 and caspase-9 were 0.92 ± 0.04, 1.21 ± 0.07, 1.33 ± 0.04 a</description><subject>Apoptosis - drug effects</subject><subject>Caspase 3 - metabolism</subject><subject>Caspase 8 - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Core Binding Factor Alpha 2 Subunit - genetics</subject><subject>Core Binding Factor Alpha 2 Subunit - metabolism</subject><subject>Flavones - pharmacology</subject><subject>Humans</subject><subject>Oncogene Proteins, Fusion - genetics</subject><subject>Oncogene Proteins, Fusion - metabolism</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>Pueraria</subject><subject>RUNX1 Translocation Partner 1 Protein</subject><issn>0253-2727</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kL1OwzAYRT2AaFX6CsgjSyT_JLEzVhV_ohILTAzR5_izsBTHwY4RfXuoKNNdju7RvRdkzUQjK6GEWpFtzt6whstWS8muyEqIRjW8E2vyvpvjvMTsM42OPkMuwVecDjiOmfrJlgEtNUc6F0yQPCBNYP03dSN8xQkzhclSv2Qa4ohDGSHRgMMHTD6Ha3LpYMy4PeeGvN3fve4fq8PLw9N-d6hmLtqlUlrXmslOWzQ1q1szdEpDqzQznAEwpjlzTe1cw9GZGpV1hiPvWqctdJLJDbn9651T_CyYlz74fFoAE8aSe864UCdF_YvenNFiAtp-Tj5AOvb_h8gfo0Zcbw</recordid><startdate>201201</startdate><enddate>201201</enddate><creator>Shao, Hua-min</creator><creator>Tang, Yu-hong</creator><creator>Shen, Qun</creator><creator>Zhu, Hong-qing</creator><creator>Ji, Ou</creator><creator>Zhang, Ya-cheng</creator><creator>Ji, Jian-min</creator><creator>Jiang, Peng-jun</creator><creator>Si, Ye-jun</creator><creator>Li, Zhao-rong</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201201</creationdate><title>Apoptosis of Kasumi-1 cells induced by puerariae radix flavones and its molecular mechanism</title><author>Shao, Hua-min ; Tang, Yu-hong ; Shen, Qun ; Zhu, Hong-qing ; Ji, Ou ; Zhang, Ya-cheng ; Ji, Jian-min ; Jiang, Peng-jun ; Si, Ye-jun ; Li, Zhao-rong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-788480398deb4046bc978a6780b10aa00810f54ff51efb4e7dfb1e196f8da9303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2012</creationdate><topic>Apoptosis - drug effects</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase 8 - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Core Binding Factor Alpha 2 Subunit - genetics</topic><topic>Core Binding Factor Alpha 2 Subunit - metabolism</topic><topic>Flavones - pharmacology</topic><topic>Humans</topic><topic>Oncogene Proteins, Fusion - genetics</topic><topic>Oncogene Proteins, Fusion - metabolism</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><topic>Pueraria</topic><topic>RUNX1 Translocation Partner 1 Protein</topic><toplevel>online_resources</toplevel><creatorcontrib>Shao, Hua-min</creatorcontrib><creatorcontrib>Tang, Yu-hong</creatorcontrib><creatorcontrib>Shen, Qun</creatorcontrib><creatorcontrib>Zhu, Hong-qing</creatorcontrib><creatorcontrib>Ji, Ou</creatorcontrib><creatorcontrib>Zhang, Ya-cheng</creatorcontrib><creatorcontrib>Ji, Jian-min</creatorcontrib><creatorcontrib>Jiang, Peng-jun</creatorcontrib><creatorcontrib>Si, Ye-jun</creatorcontrib><creatorcontrib>Li, Zhao-rong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shao, Hua-min</au><au>Tang, Yu-hong</au><au>Shen, Qun</au><au>Zhu, Hong-qing</au><au>Ji, Ou</au><au>Zhang, Ya-cheng</au><au>Ji, Jian-min</au><au>Jiang, Peng-jun</au><au>Si, Ye-jun</au><au>Li, Zhao-rong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apoptosis of Kasumi-1 cells induced by puerariae radix flavones and its molecular mechanism</atitle><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle><addtitle>Zhonghua Xue Ye Xue Za Zhi</addtitle><date>2012-01</date><risdate>2012</risdate><volume>33</volume><issue>1</issue><spage>43</spage><epage>46</epage><pages>43-46</pages><issn>0253-2727</issn><abstract>To explore the effects and the molecular mechanism of puerariae radix flavones (PRF) on acute myeloid leukemia cell line Kasumi-1 cells in vitro.
Kasumi-1 cells treated by PRF for 48 hours were observed with Wright's and Hoechst 33258 dying. The apoptotic cells were analyzed by flow cytometry with AnnexinV/PI staining. The expression levels of bcl-2, Bim and Caspase-3/-8/-9 protein were assayed by Western blot and the AML1-ETO fusion gene was detected by real-time polymerase chain reaction.
PRF could induce Kasumi-1 cells to apoptosis effectively. The proportion of apoptotic cells in 50, 200 and 500 µg/ml PRF treatment groups were (14.1 ± 0.8)%, (17.7 ± 1.3)% and (32.4 ± 1.4)%, respectively, and significantly higher than that of control \[(7.8 ± 0.7)%\]. The relative expression levels of the anti-apoptotic Bcl-2 protein were 0.85 ± 0.05, 0.62 ± 0.07 and 0.43 ± 0.05; the apoptotic Bim protein were 0.21 ± 0.06, 0.39 ± 0.04 and 0.75 ± 0.05; the caspase-3 and caspase-9 were 0.92 ± 0.04, 1.21 ± 0.07, 1.33 ± 0.04 a</abstract><cop>China</cop><pmid>22575192</pmid><tpages>4</tpages></addata></record> |
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subjects | Apoptosis - drug effects Caspase 3 - metabolism Caspase 8 - metabolism Cell Line, Tumor Core Binding Factor Alpha 2 Subunit - genetics Core Binding Factor Alpha 2 Subunit - metabolism Flavones - pharmacology Humans Oncogene Proteins, Fusion - genetics Oncogene Proteins, Fusion - metabolism Proto-Oncogene Proteins c-bcl-2 - metabolism Pueraria RUNX1 Translocation Partner 1 Protein |
title | Apoptosis of Kasumi-1 cells induced by puerariae radix flavones and its molecular mechanism |
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