Evaluation of the change in sphingolipids in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 treated with arsenic trioxide
•An HPLC-ESI–MS/MS method was applied to investigate the changes in sphingolipids.•Arsenic trioxide (As2O3) was used to treat human U266 and MGC-803 cells.•The distributions of sphingolipids are different in the human U266 and MGC-803 cells.•The levels of Hex2Cer in human U266 cells decreased when t...
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creator | Zou, Jianhua Ma, Xiaoqiong Zhang, Guangji Shen, Li Zhou, Liting Yu, Yu Zhu, Fanfan Chen, Zhe |
description | •An HPLC-ESI–MS/MS method was applied to investigate the changes in sphingolipids.•Arsenic trioxide (As2O3) was used to treat human U266 and MGC-803 cells.•The distributions of sphingolipids are different in the human U266 and MGC-803 cells.•The levels of Hex2Cer in human U266 cells decreased when treated with As2O3.•The levels of S1P and dhS1P in human MGC-803 cells decreased when treated with As2O3.
Arsenic trioxide (As2O3) has been found to display anticancer activity against many types of tumors and has been developed into an anticancer drug in clinical treatments. Sphingolipids are membrane lipids that participate in many signal transduction pathways. In this paper, the changes in sphingolipids of the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803 treated with arsenic trioxide were investigated using an HPLC-ESI–MS/MS method. Analytes were separated by an XBridge BEH C8 column used for Cer, HexCer, LacCer and SM chromatographic separation, and a Capcell PAK MG II C18 column was used for Sph, dhSph, S1P and dhS1P chromatographic separation and gradient elution with acetonitrile–water containing 0.1% formic acid as a mobile phase. A tandem mass spectrometer QTrap in SRM mode was employed in combination with RPLC as a detector for quantitative analysis. The ceramide/sphingolipid internal standard (IS) mixture was used to quantify the levels of sphingolipids. The distributions of sphingolipids were found to be different in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803. Ceramide (Cer), hexosylceramide (HexCer) and dihexosylceramide (Hex2Cer) levels in U266 cell line are higher than those in MGC-803 cell line. Additionally, sphingomyelin (SM), sphingosine-1-phosphate (S1P) and sphinganine-1-phosphate (dhS1P) levels in the MGC-803 cell line are higher than those in the U266 cell line. When treated with arsenic trioxide (1–5μM iAsIII(AsIII ions)), the levels of Hex2Cer in the human multiple myeloma cell line U266 decreased, and the levels of S1P and dhS1P in the human gastric cancer cell line MGC-803 decreased. The decrease of Hex2Cer, S1P and dhS1P in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 were observed when the concentration of iAsIII is 1.0μM. Therefore, arsenic trioxide exhibits anti-cancer activity by altering the sphingolipid pathway in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803. |
doi_str_mv | 10.1016/j.jchromb.2015.09.015 |
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Arsenic trioxide (As2O3) has been found to display anticancer activity against many types of tumors and has been developed into an anticancer drug in clinical treatments. Sphingolipids are membrane lipids that participate in many signal transduction pathways. In this paper, the changes in sphingolipids of the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803 treated with arsenic trioxide were investigated using an HPLC-ESI–MS/MS method. Analytes were separated by an XBridge BEH C8 column used for Cer, HexCer, LacCer and SM chromatographic separation, and a Capcell PAK MG II C18 column was used for Sph, dhSph, S1P and dhS1P chromatographic separation and gradient elution with acetonitrile–water containing 0.1% formic acid as a mobile phase. A tandem mass spectrometer QTrap in SRM mode was employed in combination with RPLC as a detector for quantitative analysis. The ceramide/sphingolipid internal standard (IS) mixture was used to quantify the levels of sphingolipids. The distributions of sphingolipids were found to be different in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803. Ceramide (Cer), hexosylceramide (HexCer) and dihexosylceramide (Hex2Cer) levels in U266 cell line are higher than those in MGC-803 cell line. Additionally, sphingomyelin (SM), sphingosine-1-phosphate (S1P) and sphinganine-1-phosphate (dhS1P) levels in the MGC-803 cell line are higher than those in the U266 cell line. When treated with arsenic trioxide (1–5μM iAsIII(AsIII ions)), the levels of Hex2Cer in the human multiple myeloma cell line U266 decreased, and the levels of S1P and dhS1P in the human gastric cancer cell line MGC-803 decreased. The decrease of Hex2Cer, S1P and dhS1P in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 were observed when the concentration of iAsIII is 1.0μM. Therefore, arsenic trioxide exhibits anti-cancer activity by altering the sphingolipid pathway in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803.</description><identifier>ISSN: 1570-0232</identifier><identifier>EISSN: 1873-376X</identifier><identifier>DOI: 10.1016/j.jchromb.2015.09.015</identifier><identifier>PMID: 26454796</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Arsenic trioxide ; Arsenicals - pharmacology ; Cell Line, Tumor ; Chromatography, High Pressure Liquid ; HPLC-ESI–MS/MS ; Human gastric cancer cell line MGC-803 ; Human multiple myeloma cell line U266 ; Humans ; Multiple Myeloma - metabolism ; Multiple Myeloma - pathology ; Oxides - pharmacology ; Spectrometry, Mass, Electrospray Ionization ; Sphingolipids ; Sphingolipids - metabolism ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - pathology ; Tandem Mass Spectrometry</subject><ispartof>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2015-11, Vol.1004, p.98-107</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-f24bdb1c3788d4541e8e709eea2d672cb7c38400173369868ab086c8a79772353</citedby><cites>FETCH-LOGICAL-c365t-f24bdb1c3788d4541e8e709eea2d672cb7c38400173369868ab086c8a79772353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jchromb.2015.09.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26454796$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zou, Jianhua</creatorcontrib><creatorcontrib>Ma, Xiaoqiong</creatorcontrib><creatorcontrib>Zhang, Guangji</creatorcontrib><creatorcontrib>Shen, Li</creatorcontrib><creatorcontrib>Zhou, Liting</creatorcontrib><creatorcontrib>Yu, Yu</creatorcontrib><creatorcontrib>Zhu, Fanfan</creatorcontrib><creatorcontrib>Chen, Zhe</creatorcontrib><title>Evaluation of the change in sphingolipids in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 treated with arsenic trioxide</title><title>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>•An HPLC-ESI–MS/MS method was applied to investigate the changes in sphingolipids.•Arsenic trioxide (As2O3) was used to treat human U266 and MGC-803 cells.•The distributions of sphingolipids are different in the human U266 and MGC-803 cells.•The levels of Hex2Cer in human U266 cells decreased when treated with As2O3.•The levels of S1P and dhS1P in human MGC-803 cells decreased when treated with As2O3.
Arsenic trioxide (As2O3) has been found to display anticancer activity against many types of tumors and has been developed into an anticancer drug in clinical treatments. Sphingolipids are membrane lipids that participate in many signal transduction pathways. In this paper, the changes in sphingolipids of the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803 treated with arsenic trioxide were investigated using an HPLC-ESI–MS/MS method. Analytes were separated by an XBridge BEH C8 column used for Cer, HexCer, LacCer and SM chromatographic separation, and a Capcell PAK MG II C18 column was used for Sph, dhSph, S1P and dhS1P chromatographic separation and gradient elution with acetonitrile–water containing 0.1% formic acid as a mobile phase. A tandem mass spectrometer QTrap in SRM mode was employed in combination with RPLC as a detector for quantitative analysis. The ceramide/sphingolipid internal standard (IS) mixture was used to quantify the levels of sphingolipids. The distributions of sphingolipids were found to be different in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803. Ceramide (Cer), hexosylceramide (HexCer) and dihexosylceramide (Hex2Cer) levels in U266 cell line are higher than those in MGC-803 cell line. Additionally, sphingomyelin (SM), sphingosine-1-phosphate (S1P) and sphinganine-1-phosphate (dhS1P) levels in the MGC-803 cell line are higher than those in the U266 cell line. When treated with arsenic trioxide (1–5μM iAsIII(AsIII ions)), the levels of Hex2Cer in the human multiple myeloma cell line U266 decreased, and the levels of S1P and dhS1P in the human gastric cancer cell line MGC-803 decreased. The decrease of Hex2Cer, S1P and dhS1P in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 were observed when the concentration of iAsIII is 1.0μM. Therefore, arsenic trioxide exhibits anti-cancer activity by altering the sphingolipid pathway in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803.</description><subject>Arsenic trioxide</subject><subject>Arsenicals - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Chromatography, High Pressure Liquid</subject><subject>HPLC-ESI–MS/MS</subject><subject>Human gastric cancer cell line MGC-803</subject><subject>Human multiple myeloma cell line U266</subject><subject>Humans</subject><subject>Multiple Myeloma - metabolism</subject><subject>Multiple Myeloma - pathology</subject><subject>Oxides - pharmacology</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Sphingolipids</subject><subject>Sphingolipids - metabolism</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - pathology</subject><subject>Tandem Mass Spectrometry</subject><issn>1570-0232</issn><issn>1873-376X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFvFCEcxSdGY2vrR9Bw9DIjDDvAnIzZ1GpS48UmvREG_rvDhoERmNZ-lH5bmexqvPX0CPwefx6vqt4R3BBM2MdDc9BjDNPQtJh0De6bIi-qcyI4rSlndy_LuuO4xi1tz6o3KR0wJhxz-ro6a9mm2_CenVdPV_fKLSrb4FHYoTwC0qPye0DWozSP1u-Ds7M1ad1Yj8dlUh5Ni8t2doCmR3BhUkiDc8hZD-i2ZQwpb9BepRytRlp5DfE_4vv1thaYohxBZTDoweYRqZjAF7pYwm9r4LJ6tVMuwduTXlS3X65-br_WNz-uv20_39Sasi7Xu3YzmIFoyoUwJRUBARz3AKo1jLd64JqKzRqdUtYLJtSABdNC8Z7zlnb0ovpwvHeO4dcCKcvJpvWtykNYkiSF4h3rCC5od0R1DClF2Mk52knFR0mwXFuRB3lqRa6tSNzLIsX3_jRiGSYw_1x_ayjApyMAJei9hSiTtlB-zdgIOksT7DMj_gA6Q6EP</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Zou, Jianhua</creator><creator>Ma, Xiaoqiong</creator><creator>Zhang, Guangji</creator><creator>Shen, Li</creator><creator>Zhou, Liting</creator><creator>Yu, Yu</creator><creator>Zhu, Fanfan</creator><creator>Chen, Zhe</creator><general>Elsevier B.V</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>20151101</creationdate><title>Evaluation of the change in sphingolipids in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 treated with arsenic trioxide</title><author>Zou, Jianhua ; Ma, Xiaoqiong ; Zhang, Guangji ; Shen, Li ; Zhou, Liting ; Yu, Yu ; Zhu, Fanfan ; Chen, Zhe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-f24bdb1c3788d4541e8e709eea2d672cb7c38400173369868ab086c8a79772353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Arsenic trioxide</topic><topic>Arsenicals - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Chromatography, High Pressure Liquid</topic><topic>HPLC-ESI–MS/MS</topic><topic>Human gastric cancer cell line MGC-803</topic><topic>Human multiple myeloma cell line U266</topic><topic>Humans</topic><topic>Multiple Myeloma - metabolism</topic><topic>Multiple Myeloma - pathology</topic><topic>Oxides - pharmacology</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Sphingolipids</topic><topic>Sphingolipids - metabolism</topic><topic>Stomach Neoplasms - metabolism</topic><topic>Stomach Neoplasms - pathology</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zou, Jianhua</creatorcontrib><creatorcontrib>Ma, Xiaoqiong</creatorcontrib><creatorcontrib>Zhang, Guangji</creatorcontrib><creatorcontrib>Shen, Li</creatorcontrib><creatorcontrib>Zhou, Liting</creatorcontrib><creatorcontrib>Yu, Yu</creatorcontrib><creatorcontrib>Zhu, Fanfan</creatorcontrib><creatorcontrib>Chen, Zhe</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>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zou, Jianhua</au><au>Ma, Xiaoqiong</au><au>Zhang, Guangji</au><au>Shen, Li</au><au>Zhou, Liting</au><au>Yu, Yu</au><au>Zhu, Fanfan</au><au>Chen, Zhe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the change in sphingolipids in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 treated with arsenic trioxide</atitle><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>1004</volume><spage>98</spage><epage>107</epage><pages>98-107</pages><issn>1570-0232</issn><eissn>1873-376X</eissn><abstract>•An HPLC-ESI–MS/MS method was applied to investigate the changes in sphingolipids.•Arsenic trioxide (As2O3) was used to treat human U266 and MGC-803 cells.•The distributions of sphingolipids are different in the human U266 and MGC-803 cells.•The levels of Hex2Cer in human U266 cells decreased when treated with As2O3.•The levels of S1P and dhS1P in human MGC-803 cells decreased when treated with As2O3.
Arsenic trioxide (As2O3) has been found to display anticancer activity against many types of tumors and has been developed into an anticancer drug in clinical treatments. Sphingolipids are membrane lipids that participate in many signal transduction pathways. In this paper, the changes in sphingolipids of the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803 treated with arsenic trioxide were investigated using an HPLC-ESI–MS/MS method. Analytes were separated by an XBridge BEH C8 column used for Cer, HexCer, LacCer and SM chromatographic separation, and a Capcell PAK MG II C18 column was used for Sph, dhSph, S1P and dhS1P chromatographic separation and gradient elution with acetonitrile–water containing 0.1% formic acid as a mobile phase. A tandem mass spectrometer QTrap in SRM mode was employed in combination with RPLC as a detector for quantitative analysis. The ceramide/sphingolipid internal standard (IS) mixture was used to quantify the levels of sphingolipids. The distributions of sphingolipids were found to be different in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803. Ceramide (Cer), hexosylceramide (HexCer) and dihexosylceramide (Hex2Cer) levels in U266 cell line are higher than those in MGC-803 cell line. Additionally, sphingomyelin (SM), sphingosine-1-phosphate (S1P) and sphinganine-1-phosphate (dhS1P) levels in the MGC-803 cell line are higher than those in the U266 cell line. When treated with arsenic trioxide (1–5μM iAsIII(AsIII ions)), the levels of Hex2Cer in the human multiple myeloma cell line U266 decreased, and the levels of S1P and dhS1P in the human gastric cancer cell line MGC-803 decreased. The decrease of Hex2Cer, S1P and dhS1P in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 were observed when the concentration of iAsIII is 1.0μM. Therefore, arsenic trioxide exhibits anti-cancer activity by altering the sphingolipid pathway in the human multiple myeloma cell line U266 and the gastric cancer cell line MGC-803.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26454796</pmid><doi>10.1016/j.jchromb.2015.09.015</doi><tpages>10</tpages></addata></record> |
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subjects | Arsenic trioxide Arsenicals - pharmacology Cell Line, Tumor Chromatography, High Pressure Liquid HPLC-ESI–MS/MS Human gastric cancer cell line MGC-803 Human multiple myeloma cell line U266 Humans Multiple Myeloma - metabolism Multiple Myeloma - pathology Oxides - pharmacology Spectrometry, Mass, Electrospray Ionization Sphingolipids Sphingolipids - metabolism Stomach Neoplasms - metabolism Stomach Neoplasms - pathology Tandem Mass Spectrometry |
title | Evaluation of the change in sphingolipids in the human multiple myeloma cell line U266 and gastric cancer cell line MGC-803 treated with arsenic trioxide |
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