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The role of insulin-related substance in Hodgkin's disease
An insulin-related growth-promoting substance was detected in the serum of a patient with Hodgkin's disease who suffered from severe hypoglycaemia, as well as in the supernatant of homogenized spleen tissue of the same patient. Low concentrations of this substance enhanced DNA synthesis of shor...
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Published in: | Journal of cancer research and clinical oncology 1991-01, Vol.117 (6), p.615-619 |
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container_issue | 6 |
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container_title | Journal of cancer research and clinical oncology |
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creator | CABRIJAN, T LEVANAT, S GRAZLO, S PAVELIC, K PEKIC, B PAVELIC, J SPAVENTI, R FRAHM, H ZJACIC-ROTKVIC, V GOLDONI, V VRBANEC, D MISJAK, M |
description | An insulin-related growth-promoting substance was detected in the serum of a patient with Hodgkin's disease who suffered from severe hypoglycaemia, as well as in the supernatant of homogenized spleen tissue of the same patient. Low concentrations of this substance enhanced DNA synthesis of short-term-cultured spleen tumour cells obtained from the same patient, while the addition of anti-insulin antiserum interfered with that effect. Moreover, the preincubation of this insulin-related substance with the anti-insulin antiserum abrogated its stimulatory effect on tumour cell proliferation. Both insulin and the insulin-related substance bound to patients splenocytes to a similar extent. The data suggest that the insulin-related substance, found in this particular case of Hodgkin's disease, plays a role in tumour progression by an autocrine mechanism. |
doi_str_mv | 10.1007/BF01613298 |
format | article |
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Low concentrations of this substance enhanced DNA synthesis of short-term-cultured spleen tumour cells obtained from the same patient, while the addition of anti-insulin antiserum interfered with that effect. Moreover, the preincubation of this insulin-related substance with the anti-insulin antiserum abrogated its stimulatory effect on tumour cell proliferation. Both insulin and the insulin-related substance bound to patients splenocytes to a similar extent. The data suggest that the insulin-related substance, found in this particular case of Hodgkin's disease, plays a role in tumour progression by an autocrine mechanism.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/BF01613298</identifier><identifier>PMID: 1744168</identifier><identifier>CODEN: JCROD7</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; Blood Glucose ; Cell Division - physiology ; Chromatography, Ion Exchange ; DNA - biosynthesis ; Endothelial Growth Factors - physiology ; Epidermal Growth Factor - physiology ; Fibroblast Growth Factors - physiology ; Hematologic and hematopoietic diseases ; Hodgkin Disease - metabolism ; Humans ; Insulin - metabolism ; Insulin-Like Growth Factor I - physiology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Platelet-Derived Growth Factor - physiology ; Somatomedins - biosynthesis ; Somatomedins - isolation & purification ; Tumor Cells, Cultured</subject><ispartof>Journal of cancer research and clinical oncology, 1991-01, Vol.117 (6), p.615-619</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-b8397651d621fe170e008670a89a8111220b4fa4ecce733c7f74b135195a804a3</citedby><cites>FETCH-LOGICAL-c311t-b8397651d621fe170e008670a89a8111220b4fa4ecce733c7f74b135195a804a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5091198$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1744168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CABRIJAN, T</creatorcontrib><creatorcontrib>LEVANAT, S</creatorcontrib><creatorcontrib>GRAZLO, S</creatorcontrib><creatorcontrib>PAVELIC, K</creatorcontrib><creatorcontrib>PEKIC, B</creatorcontrib><creatorcontrib>PAVELIC, J</creatorcontrib><creatorcontrib>SPAVENTI, R</creatorcontrib><creatorcontrib>FRAHM, H</creatorcontrib><creatorcontrib>ZJACIC-ROTKVIC, V</creatorcontrib><creatorcontrib>GOLDONI, V</creatorcontrib><creatorcontrib>VRBANEC, D</creatorcontrib><creatorcontrib>MISJAK, M</creatorcontrib><title>The role of insulin-related substance in Hodgkin's disease</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><description>An insulin-related growth-promoting substance was detected in the serum of a patient with Hodgkin's disease who suffered from severe hypoglycaemia, as well as in the supernatant of homogenized spleen tissue of the same patient. Low concentrations of this substance enhanced DNA synthesis of short-term-cultured spleen tumour cells obtained from the same patient, while the addition of anti-insulin antiserum interfered with that effect. Moreover, the preincubation of this insulin-related substance with the anti-insulin antiserum abrogated its stimulatory effect on tumour cell proliferation. Both insulin and the insulin-related substance bound to patients splenocytes to a similar extent. The data suggest that the insulin-related substance, found in this particular case of Hodgkin's disease, plays a role in tumour progression by an autocrine mechanism.</description><subject>Biological and medical sciences</subject><subject>Blood Glucose</subject><subject>Cell Division - physiology</subject><subject>Chromatography, Ion Exchange</subject><subject>DNA - biosynthesis</subject><subject>Endothelial Growth Factors - physiology</subject><subject>Epidermal Growth Factor - physiology</subject><subject>Fibroblast Growth Factors - physiology</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hodgkin Disease - metabolism</subject><subject>Humans</subject><subject>Insulin - metabolism</subject><subject>Insulin-Like Growth Factor I - physiology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Platelet-Derived Growth Factor - physiology</subject><subject>Somatomedins - biosynthesis</subject><subject>Somatomedins - isolation & purification</subject><subject>Tumor Cells, Cultured</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNpFkM1Lw0AQRxdRaq1evAs5iIIQndmPbOJNi7VCwUs9h81motE0qTvNwf_eSIs9DcPv8Q5PiHOEWwSwd48zwASVzNIDMUatZIxKmUMxBrQYG4nJsThh_oThN1aOxAit1pikY3G__KAodA1FXRXVLfdN3caBGrehMuK-4I1rPQ1LNO_K96-6veaorJkc06k4qlzDdLa7E_E2e1pO5_Hi9fll-rCIvULcxEWqMpsYLBOJFaEFAkgTCy7NXIqIUkKhK6fJe7JKeVtZXaAymBmXgnZqIq623nXovnviTb6q2VPTuJa6nnMrDUpQegBvtqAPHXOgKl-HeuXCT46Q_4XK96EG-GJn7YsVlXt0W2bYL3e7Y--aKgwdav7HDGSIg-YXnL9spg</recordid><startdate>19910101</startdate><enddate>19910101</enddate><creator>CABRIJAN, T</creator><creator>LEVANAT, S</creator><creator>GRAZLO, S</creator><creator>PAVELIC, K</creator><creator>PEKIC, B</creator><creator>PAVELIC, J</creator><creator>SPAVENTI, R</creator><creator>FRAHM, H</creator><creator>ZJACIC-ROTKVIC, V</creator><creator>GOLDONI, V</creator><creator>VRBANEC, D</creator><creator>MISJAK, M</creator><general>Springer</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>19910101</creationdate><title>The role of insulin-related substance in Hodgkin's disease</title><author>CABRIJAN, T ; LEVANAT, S ; GRAZLO, S ; PAVELIC, K ; PEKIC, B ; PAVELIC, J ; SPAVENTI, R ; FRAHM, H ; ZJACIC-ROTKVIC, V ; GOLDONI, V ; VRBANEC, D ; MISJAK, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-b8397651d621fe170e008670a89a8111220b4fa4ecce733c7f74b135195a804a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Biological and medical sciences</topic><topic>Blood Glucose</topic><topic>Cell Division - physiology</topic><topic>Chromatography, Ion Exchange</topic><topic>DNA - biosynthesis</topic><topic>Endothelial Growth Factors - physiology</topic><topic>Epidermal Growth Factor - physiology</topic><topic>Fibroblast Growth Factors - physiology</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hodgkin Disease - metabolism</topic><topic>Humans</topic><topic>Insulin - metabolism</topic><topic>Insulin-Like Growth Factor I - physiology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. 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Low concentrations of this substance enhanced DNA synthesis of short-term-cultured spleen tumour cells obtained from the same patient, while the addition of anti-insulin antiserum interfered with that effect. Moreover, the preincubation of this insulin-related substance with the anti-insulin antiserum abrogated its stimulatory effect on tumour cell proliferation. Both insulin and the insulin-related substance bound to patients splenocytes to a similar extent. The data suggest that the insulin-related substance, found in this particular case of Hodgkin's disease, plays a role in tumour progression by an autocrine mechanism.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>1744168</pmid><doi>10.1007/BF01613298</doi><tpages>5</tpages></addata></record> |
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subjects | Biological and medical sciences Blood Glucose Cell Division - physiology Chromatography, Ion Exchange DNA - biosynthesis Endothelial Growth Factors - physiology Epidermal Growth Factor - physiology Fibroblast Growth Factors - physiology Hematologic and hematopoietic diseases Hodgkin Disease - metabolism Humans Insulin - metabolism Insulin-Like Growth Factor I - physiology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged Platelet-Derived Growth Factor - physiology Somatomedins - biosynthesis Somatomedins - isolation & purification Tumor Cells, Cultured |
title | The role of insulin-related substance in Hodgkin's disease |
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