Ganglioside GD3 shedding by human malignant melanoma cells
Gangliosides appear to be important target molecules for immunological effector mechanisms on neuro‐ectodermal tumors. Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the...
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Veröffentlicht in: | International journal of cancer 1989-07, Vol.44 (1), p.155-160 |
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creator | Bernhard, Helga Zum Büschenfelde, Karl‐Hermann Meyer Dippold, Wolfgang G. |
description | Gangliosides appear to be important target molecules for immunological effector mechanisms on neuro‐ectodermal tumors. Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the culture medium. Measurable quantities of gangliosides GM3 and in particular GD3 were shed by the melanoma cells we have tested as detected on thin‐layer chromatograms (TLC) stained with orcinol. Ganglioside GD3 was also evidenced by immunoassaying with anti‐GD3 MAb and by ELISA. The concentration of GD3 in the supernatant of human melanoma cells depended on the ganglioside pattern of the cell line. Cells containing high levels of GD3 shed large amounts, cells with low levels shed no detectable GD3. Ganglioside GD3 was detectable in sera, but no major quantitative differences were observed in sera of patients with GD3‐positive tumors and normal controls. This points to a local accumulation of ganglioside GD3 at the tumor site. |
doi_str_mv | 10.1002/ijc.2910440127 |
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Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the culture medium. Measurable quantities of gangliosides GM3 and in particular GD3 were shed by the melanoma cells we have tested as detected on thin‐layer chromatograms (TLC) stained with orcinol. Ganglioside GD3 was also evidenced by immunoassaying with anti‐GD3 MAb and by ELISA. The concentration of GD3 in the supernatant of human melanoma cells depended on the ganglioside pattern of the cell line. Cells containing high levels of GD3 shed large amounts, cells with low levels shed no detectable GD3. Ganglioside GD3 was detectable in sera, but no major quantitative differences were observed in sera of patients with GD3‐positive tumors and normal controls. This points to a local accumulation of ganglioside GD3 at the tumor site.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910440127</identifier><identifier>PMID: 2744885</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Dermatology ; G(M3) Ganglioside - analysis ; Gangliosides - analysis ; Humans ; Medical sciences ; Melanoma - analysis ; Tumor Cells, Cultured ; Tumors of the skin and soft tissue. 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Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the culture medium. Measurable quantities of gangliosides GM3 and in particular GD3 were shed by the melanoma cells we have tested as detected on thin‐layer chromatograms (TLC) stained with orcinol. Ganglioside GD3 was also evidenced by immunoassaying with anti‐GD3 MAb and by ELISA. The concentration of GD3 in the supernatant of human melanoma cells depended on the ganglioside pattern of the cell line. Cells containing high levels of GD3 shed large amounts, cells with low levels shed no detectable GD3. Ganglioside GD3 was detectable in sera, but no major quantitative differences were observed in sera of patients with GD3‐positive tumors and normal controls. This points to a local accumulation of ganglioside GD3 at the tumor site.</description><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>G(M3) Ganglioside - analysis</subject><subject>Gangliosides - analysis</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Melanoma - analysis</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQhi0EKqWwsiFlQGwpd_6IYzZUoBRVYoHZchKndZU4JW6E-u9J1aqwMd3wPvfe6SHkGmGMAPTerfIxVQicA1J5QoYISsZAUZySYQ9ALJEl5-QihBUAogA-IAMqOU9TMSQPU-MXlWuCK2w0fWJRWNqicH4RZdto2dXGR7Wp3MIbv4lqWxnf1CbKbVWFS3JWmirYq8Mckc-X54_Jazx_n84mj_M450zIWDGFSWoNKksxZ2mRpshkgoIWCBnlIslUkjNqoJSlsjLhIpM9rCRHKa1hI3K37123zVdnw0bXLuw-MN42XdBSgRKUQw-O92DeNiG0ttTr1tWm3WoEvZOle1n6V1a_cHNo7rLaFkf8YKfPbw-5Cbmpytb43IUjJqmSkNIeU3vs21V2-89RPXub_HnhB-Enf3c</recordid><startdate>19890715</startdate><enddate>19890715</enddate><creator>Bernhard, Helga</creator><creator>Zum Büschenfelde, Karl‐Hermann Meyer</creator><creator>Dippold, Wolfgang G.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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></search><sort><creationdate>19890715</creationdate><title>Ganglioside GD3 shedding by human malignant melanoma cells</title><author>Bernhard, Helga ; Zum Büschenfelde, Karl‐Hermann Meyer ; Dippold, Wolfgang G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4357-939168ea19e21c38d881376152d10b2456b96c32a0f7f9e7645b719e974177ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>G(M3) Ganglioside - analysis</topic><topic>Gangliosides - analysis</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Melanoma - analysis</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bernhard, Helga</creatorcontrib><creatorcontrib>Zum Büschenfelde, Karl‐Hermann Meyer</creatorcontrib><creatorcontrib>Dippold, Wolfgang 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><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bernhard, Helga</au><au>Zum Büschenfelde, Karl‐Hermann Meyer</au><au>Dippold, Wolfgang G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ganglioside GD3 shedding by human malignant melanoma cells</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1989-07-15</date><risdate>1989</risdate><volume>44</volume><issue>1</issue><spage>155</spage><epage>160</epage><pages>155-160</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Gangliosides appear to be important target molecules for immunological effector mechanisms on neuro‐ectodermal tumors. Therefore in vitro studies were performed to examine whether ganglioside GD3, which is highly expressed on the cell surface of cultured human melanoma cells, is being shed into the culture medium. Measurable quantities of gangliosides GM3 and in particular GD3 were shed by the melanoma cells we have tested as detected on thin‐layer chromatograms (TLC) stained with orcinol. Ganglioside GD3 was also evidenced by immunoassaying with anti‐GD3 MAb and by ELISA. The concentration of GD3 in the supernatant of human melanoma cells depended on the ganglioside pattern of the cell line. Cells containing high levels of GD3 shed large amounts, cells with low levels shed no detectable GD3. Ganglioside GD3 was detectable in sera, but no major quantitative differences were observed in sera of patients with GD3‐positive tumors and normal controls. This points to a local accumulation of ganglioside GD3 at the tumor site.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2744885</pmid><doi>10.1002/ijc.2910440127</doi><tpages>6</tpages></addata></record> |
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subjects | Biological and medical sciences Dermatology G(M3) Ganglioside - analysis Gangliosides - analysis Humans Medical sciences Melanoma - analysis Tumor Cells, Cultured Tumors of the skin and soft tissue. Premalignant lesions |
title | Ganglioside GD3 shedding by human malignant melanoma cells |
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