Presence of a carcinoma-associated antigen(s) in the spent chemically defined medium of a human colon carcinoma cell line
The human colon carcinoma cell line HT‐29 was adapted to grow in chemically defined medium (CDM). The spent CDM (S‐CDM) was concentrated by Amicon filtration and the crude HT‐29 S‐CDM purified by 40% saturated(NH4)2 SO4 precipitation. The purified antigen was tested by a micro‐complement fixation (M...
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Veröffentlicht in: | Journal of surgical oncology 1980-01, Vol.13 (1), p.45-51 |
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creator | Chee, Darwin O. Gupta, Rishab K. Morton, Donald L. |
description | The human colon carcinoma cell line HT‐29 was adapted to grow in chemically defined medium (CDM). The spent CDM (S‐CDM) was concentrated by Amicon filtration and the crude HT‐29 S‐CDM purified by 40% saturated(NH4)2 SO4 precipitation. The purified antigen was tested by a micro‐complement fixation (MCF) assay against the sera of cancer patients of various histologic types and against the sera of normal donors. Fifteen of 20 (75%) colon cancer, 16/20 (80%) breast cancer sera, 14/19 (74%) lung cancer sera, and 13/20 (65%) miscellaneous carcinoma sera were positive in the MCF. By contrast, 2/21 (10%) melanoma sera, 7/20 (35%) sarcoma sera, and 2/19 (11 %) normal sera were positive. These data suggest the presence of a carcinoma‐associated antigen in the spent CDM of the HT‐29 colon carcinoma cell line adapted to grow in CDM. |
doi_str_mv | 10.1002/jso.2930130108 |
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The spent CDM (S‐CDM) was concentrated by Amicon filtration and the crude HT‐29 S‐CDM purified by 40% saturated(NH4)2 SO4 precipitation. The purified antigen was tested by a micro‐complement fixation (MCF) assay against the sera of cancer patients of various histologic types and against the sera of normal donors. Fifteen of 20 (75%) colon cancer, 16/20 (80%) breast cancer sera, 14/19 (74%) lung cancer sera, and 13/20 (65%) miscellaneous carcinoma sera were positive in the MCF. By contrast, 2/21 (10%) melanoma sera, 7/20 (35%) sarcoma sera, and 2/19 (11 %) normal sera were positive. These data suggest the presence of a carcinoma‐associated antigen in the spent CDM of the HT‐29 colon carcinoma cell line adapted to grow in CDM.</description><identifier>ISSN: 0022-4790</identifier><identifier>EISSN: 1096-9098</identifier><identifier>DOI: 10.1002/jso.2930130108</identifier><identifier>PMID: 6153228</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Antibodies, Neoplasm ; antigen (s) ; Antigens, Neoplasm ; Breast Neoplasms - immunology ; Cell Line ; Colonic Neoplasms - immunology ; Cross Reactions ; Culture Media ; Epitopes ; Female ; HT-29 cell line ; Humans ; Melanoma - immunology ; Sarcoma - immunology ; spent medium</subject><ispartof>Journal of surgical oncology, 1980-01, Vol.13 (1), p.45-51</ispartof><rights>Copyright © 1980 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3788-3d49b5a52b8a487d04bc1f1fa9d905b3fbd5fc67c021d35be4645183c8de9ee43</citedby><cites>FETCH-LOGICAL-c3788-3d49b5a52b8a487d04bc1f1fa9d905b3fbd5fc67c021d35be4645183c8de9ee43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjso.2930130108$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjso.2930130108$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4009,27902,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6153228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chee, Darwin O.</creatorcontrib><creatorcontrib>Gupta, Rishab K.</creatorcontrib><creatorcontrib>Morton, Donald L.</creatorcontrib><title>Presence of a carcinoma-associated antigen(s) in the spent chemically defined medium of a human colon carcinoma cell line</title><title>Journal of surgical oncology</title><addtitle>J. Surg. Oncol</addtitle><description>The human colon carcinoma cell line HT‐29 was adapted to grow in chemically defined medium (CDM). The spent CDM (S‐CDM) was concentrated by Amicon filtration and the crude HT‐29 S‐CDM purified by 40% saturated(NH4)2 SO4 precipitation. The purified antigen was tested by a micro‐complement fixation (MCF) assay against the sera of cancer patients of various histologic types and against the sera of normal donors. Fifteen of 20 (75%) colon cancer, 16/20 (80%) breast cancer sera, 14/19 (74%) lung cancer sera, and 13/20 (65%) miscellaneous carcinoma sera were positive in the MCF. By contrast, 2/21 (10%) melanoma sera, 7/20 (35%) sarcoma sera, and 2/19 (11 %) normal sera were positive. These data suggest the presence of a carcinoma‐associated antigen in the spent CDM of the HT‐29 colon carcinoma cell line adapted to grow in CDM.</description><subject>Antibodies, Neoplasm</subject><subject>antigen (s)</subject><subject>Antigens, Neoplasm</subject><subject>Breast Neoplasms - immunology</subject><subject>Cell Line</subject><subject>Colonic Neoplasms - immunology</subject><subject>Cross Reactions</subject><subject>Culture Media</subject><subject>Epitopes</subject><subject>Female</subject><subject>HT-29 cell line</subject><subject>Humans</subject><subject>Melanoma - immunology</subject><subject>Sarcoma - immunology</subject><subject>spent medium</subject><issn>0022-4790</issn><issn>1096-9098</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtr3DAURkVoSSdpttkVtCrNwlPJelhalqF5tKEJfZClkKXrjlJbmlg26fz7ePCQ0FXhghb3fIerD6FTSpaUkPLjfU7LUjNCpyHqAC0o0bLQRKtXaDEBZcErTd6go5zvCSFaS36IDiUVrCzVAm1ve8gQHeDUYIud7V2IqbOFzTm5YAfw2MYh_Ib4IZ_hEPGwBpw3EAfs1tAFZ9t2iz00IU5oBz6M3exaj52N2KU2xRcvdtC2uJ3gt-h1Y9sMJ_v3GP06__xzdVlc31xcrT5dF45VShXMc10LK8paWa4qT3jtaEMbq70momZN7UXjZOVIST0TNXDJBVXMKQ8agLNj9H72bvr0MEIeTBfy7gobIY3ZVFzLSrIduJxB16ece2jMpg-d7beGErPr2kxdm5eup8C7vXmsp48_4_typ72e94-hhe1_bObLj5t_3MWcDXmAv89Z2_8xsmKVMHffLgz7_vVcrOStoewJAq6bLw</recordid><startdate>198001</startdate><enddate>198001</enddate><creator>Chee, Darwin O.</creator><creator>Gupta, Rishab K.</creator><creator>Morton, Donald L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>198001</creationdate><title>Presence of a carcinoma-associated antigen(s) in the spent chemically defined medium of a human colon carcinoma cell line</title><author>Chee, Darwin O. ; Gupta, Rishab K. ; Morton, Donald L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3788-3d49b5a52b8a487d04bc1f1fa9d905b3fbd5fc67c021d35be4645183c8de9ee43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Antibodies, Neoplasm</topic><topic>antigen (s)</topic><topic>Antigens, Neoplasm</topic><topic>Breast Neoplasms - immunology</topic><topic>Cell Line</topic><topic>Colonic Neoplasms - immunology</topic><topic>Cross Reactions</topic><topic>Culture Media</topic><topic>Epitopes</topic><topic>Female</topic><topic>HT-29 cell line</topic><topic>Humans</topic><topic>Melanoma - immunology</topic><topic>Sarcoma - immunology</topic><topic>spent medium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chee, Darwin O.</creatorcontrib><creatorcontrib>Gupta, Rishab K.</creatorcontrib><creatorcontrib>Morton, Donald L.</creatorcontrib><collection>Istex</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>Journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chee, Darwin O.</au><au>Gupta, Rishab K.</au><au>Morton, Donald L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presence of a carcinoma-associated antigen(s) in the spent chemically defined medium of a human colon carcinoma cell line</atitle><jtitle>Journal of surgical oncology</jtitle><addtitle>J. Surg. Oncol</addtitle><date>1980-01</date><risdate>1980</risdate><volume>13</volume><issue>1</issue><spage>45</spage><epage>51</epage><pages>45-51</pages><issn>0022-4790</issn><eissn>1096-9098</eissn><abstract>The human colon carcinoma cell line HT‐29 was adapted to grow in chemically defined medium (CDM). The spent CDM (S‐CDM) was concentrated by Amicon filtration and the crude HT‐29 S‐CDM purified by 40% saturated(NH4)2 SO4 precipitation. The purified antigen was tested by a micro‐complement fixation (MCF) assay against the sera of cancer patients of various histologic types and against the sera of normal donors. Fifteen of 20 (75%) colon cancer, 16/20 (80%) breast cancer sera, 14/19 (74%) lung cancer sera, and 13/20 (65%) miscellaneous carcinoma sera were positive in the MCF. By contrast, 2/21 (10%) melanoma sera, 7/20 (35%) sarcoma sera, and 2/19 (11 %) normal sera were positive. These data suggest the presence of a carcinoma‐associated antigen in the spent CDM of the HT‐29 colon carcinoma cell line adapted to grow in CDM.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>6153228</pmid><doi>10.1002/jso.2930130108</doi><tpages>7</tpages></addata></record> |
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subjects | Antibodies, Neoplasm antigen (s) Antigens, Neoplasm Breast Neoplasms - immunology Cell Line Colonic Neoplasms - immunology Cross Reactions Culture Media Epitopes Female HT-29 cell line Humans Melanoma - immunology Sarcoma - immunology spent medium |
title | Presence of a carcinoma-associated antigen(s) in the spent chemically defined medium of a human colon carcinoma cell line |
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