Transactivation of the PTHrP gene in squamous carcinomas predicts the occurrence of hypercalcemia in athymic mice
Humoral hypercalcemia of malignancy (HHM) is caused by the secretion of parathyroid hormone-related protein (PTHrP) by tumor cells, and tumors of squamous histology are the ones most commonly complicated by HHM. To determine why some squamous tumors cause HHM and others do not, we quantitated the le...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1996-03, Vol.56 (5), p.1043-1049 |
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creator | WYSOLMERSKI, J. J RUPANGI VASAVADA FOLEY, J WEIR, E. C BURTIS, W. J KUKREJA, S. C GUISE, T. A BROADUS, A. E PHILBRICK, W. M |
description | Humoral hypercalcemia of malignancy (HHM) is caused by the secretion of parathyroid hormone-related protein (PTHrP) by tumor cells, and tumors of squamous histology are the ones most commonly complicated by HHM. To determine why some squamous tumors cause HHM and others do not, we quantitated the levels of PTHrP mRNA expression and PTHrP secretion in a series of eight squamous tumor lines. As anticipated, we found that the level of PTHrP mRNA expression in individual lines correlated with their PTHrP secretion rates. However, PTHrP mRNA levels varied widely in individual lines, and only those tumor lines with the highest levels of PTHrP gene expression were able to cause hypercalcemia in athymic mice. We found that a specific segment of the PTHrP promoter could reproduce the relative pattern of PTHrP gene expression when cloned in front of a chloramphenicol acetyltransferase reporter gene and transiently transfected into these squamous lines. Deletional analysis confirmed that specific sequences within the PTHrP gene promoter appeared to be involved in the transactivation of the gene in tumor lines expressing high levels of PTHrP mRNA. These data suggest that the ability of a given squamous tumor to cause HHM is ultimately a function of its level of PTHrP gene expression, which in turn appears to be a function of the ability of specific transcription factors to transactivate PTHrP gene expression. |
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J ; RUPANGI VASAVADA ; FOLEY, J ; WEIR, E. C ; BURTIS, W. J ; KUKREJA, S. C ; GUISE, T. A ; BROADUS, A. E ; PHILBRICK, W. M</creator><creatorcontrib>WYSOLMERSKI, J. J ; RUPANGI VASAVADA ; FOLEY, J ; WEIR, E. C ; BURTIS, W. J ; KUKREJA, S. C ; GUISE, T. A ; BROADUS, A. E ; PHILBRICK, W. M</creatorcontrib><description>Humoral hypercalcemia of malignancy (HHM) is caused by the secretion of parathyroid hormone-related protein (PTHrP) by tumor cells, and tumors of squamous histology are the ones most commonly complicated by HHM. To determine why some squamous tumors cause HHM and others do not, we quantitated the levels of PTHrP mRNA expression and PTHrP secretion in a series of eight squamous tumor lines. As anticipated, we found that the level of PTHrP mRNA expression in individual lines correlated with their PTHrP secretion rates. However, PTHrP mRNA levels varied widely in individual lines, and only those tumor lines with the highest levels of PTHrP gene expression were able to cause hypercalcemia in athymic mice. We found that a specific segment of the PTHrP promoter could reproduce the relative pattern of PTHrP gene expression when cloned in front of a chloramphenicol acetyltransferase reporter gene and transiently transfected into these squamous lines. Deletional analysis confirmed that specific sequences within the PTHrP gene promoter appeared to be involved in the transactivation of the gene in tumor lines expressing high levels of PTHrP mRNA. These data suggest that the ability of a given squamous tumor to cause HHM is ultimately a function of its level of PTHrP gene expression, which in turn appears to be a function of the ability of specific transcription factors to transactivate PTHrP gene expression.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 8640759</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Animals ; Biological and medical sciences ; Carcinoma, Squamous Cell - complications ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - metabolism ; Gene Expression Regulation, Neoplastic ; Hypercalcemia - etiology ; Hypercalcemia - genetics ; Hypercalcemia - metabolism ; Medical sciences ; Mice ; Mice, Nude ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Neoplasm Transplantation ; Neoplasms, Experimental - complications ; Neoplasms, Experimental - genetics ; Neoplasms, Experimental - metabolism ; Parathyroid Hormone-Related Protein ; Protein Biosynthesis ; Proteins - genetics ; Transcriptional Activation ; Tumor Cells, Cultured ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 1996-03, Vol.56 (5), p.1043-1049</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3008097$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8640759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WYSOLMERSKI, J. J</creatorcontrib><creatorcontrib>RUPANGI VASAVADA</creatorcontrib><creatorcontrib>FOLEY, J</creatorcontrib><creatorcontrib>WEIR, E. C</creatorcontrib><creatorcontrib>BURTIS, W. J</creatorcontrib><creatorcontrib>KUKREJA, S. C</creatorcontrib><creatorcontrib>GUISE, T. A</creatorcontrib><creatorcontrib>BROADUS, A. E</creatorcontrib><creatorcontrib>PHILBRICK, W. M</creatorcontrib><title>Transactivation of the PTHrP gene in squamous carcinomas predicts the occurrence of hypercalcemia in athymic mice</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Humoral hypercalcemia of malignancy (HHM) is caused by the secretion of parathyroid hormone-related protein (PTHrP) by tumor cells, and tumors of squamous histology are the ones most commonly complicated by HHM. To determine why some squamous tumors cause HHM and others do not, we quantitated the levels of PTHrP mRNA expression and PTHrP secretion in a series of eight squamous tumor lines. As anticipated, we found that the level of PTHrP mRNA expression in individual lines correlated with their PTHrP secretion rates. However, PTHrP mRNA levels varied widely in individual lines, and only those tumor lines with the highest levels of PTHrP gene expression were able to cause hypercalcemia in athymic mice. We found that a specific segment of the PTHrP promoter could reproduce the relative pattern of PTHrP gene expression when cloned in front of a chloramphenicol acetyltransferase reporter gene and transiently transfected into these squamous lines. Deletional analysis confirmed that specific sequences within the PTHrP gene promoter appeared to be involved in the transactivation of the gene in tumor lines expressing high levels of PTHrP mRNA. These data suggest that the ability of a given squamous tumor to cause HHM is ultimately a function of its level of PTHrP gene expression, which in turn appears to be a function of the ability of specific transcription factors to transactivate PTHrP gene expression.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - complications</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hypercalcemia - etiology</subject><subject>Hypercalcemia - genetics</subject><subject>Hypercalcemia - metabolism</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Neoplasm Transplantation</subject><subject>Neoplasms, Experimental - complications</subject><subject>Neoplasms, Experimental - genetics</subject><subject>Neoplasms, Experimental - metabolism</subject><subject>Parathyroid Hormone-Related Protein</subject><subject>Protein Biosynthesis</subject><subject>Proteins - genetics</subject><subject>Transcriptional Activation</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9LxDAQxYMo67r6EYQcxFshaZqmOcqiriC4h_VcpunERvpvk1bYb29WF68ehmF4v3kwb87IkktRJCrL5DlZMsaKRGYqvSRXIXzGUXImF2RR5BlTUi_JfuehD2Am9wWTG3o6WDo1SLe7jd_SD-yRup6G_QzdMAdqwBvXDx0EOnqsnZnCDz4YM3uPvcGjQXMY0RtoDXYOjvswNYfOGRoLr8mFhTbgzamvyPvT4269SV7fnl_WD69Jk2o9JVUGsqoMVlzlmGuueAZWIc8F1ykoWQEzRSq0qK20khtmwaZpVgAoMLbWYkXuf31HP-xnDFPZuWCwbaHHeEqpCpZrLf8HuWIyLUQewdsTOFcd1uXoXQf-UJ7CjPrdSYcQr7cxWePCHybiM5hW4htDxoAG</recordid><startdate>19960301</startdate><enddate>19960301</enddate><creator>WYSOLMERSKI, J. J</creator><creator>RUPANGI VASAVADA</creator><creator>FOLEY, J</creator><creator>WEIR, E. C</creator><creator>BURTIS, W. J</creator><creator>KUKREJA, S. C</creator><creator>GUISE, T. A</creator><creator>BROADUS, A. E</creator><creator>PHILBRICK, W. M</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>19960301</creationdate><title>Transactivation of the PTHrP gene in squamous carcinomas predicts the occurrence of hypercalcemia in athymic mice</title><author>WYSOLMERSKI, J. J ; RUPANGI VASAVADA ; FOLEY, J ; WEIR, E. C ; BURTIS, W. J ; KUKREJA, S. C ; GUISE, T. A ; BROADUS, A. E ; PHILBRICK, W. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h299t-b4a5bbceb176e691714af7e163192a75ba0c82393df5f51c0faf2248aa7acfd93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - complications</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Hypercalcemia - etiology</topic><topic>Hypercalcemia - genetics</topic><topic>Hypercalcemia - metabolism</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Neoplasm Transplantation</topic><topic>Neoplasms, Experimental - complications</topic><topic>Neoplasms, Experimental - genetics</topic><topic>Neoplasms, Experimental - metabolism</topic><topic>Parathyroid Hormone-Related Protein</topic><topic>Protein Biosynthesis</topic><topic>Proteins - genetics</topic><topic>Transcriptional Activation</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WYSOLMERSKI, J. J</creatorcontrib><creatorcontrib>RUPANGI VASAVADA</creatorcontrib><creatorcontrib>FOLEY, J</creatorcontrib><creatorcontrib>WEIR, E. C</creatorcontrib><creatorcontrib>BURTIS, W. J</creatorcontrib><creatorcontrib>KUKREJA, S. C</creatorcontrib><creatorcontrib>GUISE, T. A</creatorcontrib><creatorcontrib>BROADUS, A. E</creatorcontrib><creatorcontrib>PHILBRICK, W. M</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>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WYSOLMERSKI, J. J</au><au>RUPANGI VASAVADA</au><au>FOLEY, J</au><au>WEIR, E. C</au><au>BURTIS, W. J</au><au>KUKREJA, S. C</au><au>GUISE, T. A</au><au>BROADUS, A. E</au><au>PHILBRICK, W. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transactivation of the PTHrP gene in squamous carcinomas predicts the occurrence of hypercalcemia in athymic mice</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1996-03-01</date><risdate>1996</risdate><volume>56</volume><issue>5</issue><spage>1043</spage><epage>1049</epage><pages>1043-1049</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Humoral hypercalcemia of malignancy (HHM) is caused by the secretion of parathyroid hormone-related protein (PTHrP) by tumor cells, and tumors of squamous histology are the ones most commonly complicated by HHM. To determine why some squamous tumors cause HHM and others do not, we quantitated the levels of PTHrP mRNA expression and PTHrP secretion in a series of eight squamous tumor lines. As anticipated, we found that the level of PTHrP mRNA expression in individual lines correlated with their PTHrP secretion rates. However, PTHrP mRNA levels varied widely in individual lines, and only those tumor lines with the highest levels of PTHrP gene expression were able to cause hypercalcemia in athymic mice. We found that a specific segment of the PTHrP promoter could reproduce the relative pattern of PTHrP gene expression when cloned in front of a chloramphenicol acetyltransferase reporter gene and transiently transfected into these squamous lines. Deletional analysis confirmed that specific sequences within the PTHrP gene promoter appeared to be involved in the transactivation of the gene in tumor lines expressing high levels of PTHrP mRNA. These data suggest that the ability of a given squamous tumor to cause HHM is ultimately a function of its level of PTHrP gene expression, which in turn appears to be a function of the ability of specific transcription factors to transactivate PTHrP gene expression.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>8640759</pmid><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Carcinoma, Squamous Cell - complications Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - metabolism Gene Expression Regulation, Neoplastic Hypercalcemia - etiology Hypercalcemia - genetics Hypercalcemia - metabolism Medical sciences Mice Mice, Nude Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Neoplasm Transplantation Neoplasms, Experimental - complications Neoplasms, Experimental - genetics Neoplasms, Experimental - metabolism Parathyroid Hormone-Related Protein Protein Biosynthesis Proteins - genetics Transcriptional Activation Tumor Cells, Cultured Tumors |
title | Transactivation of the PTHrP gene in squamous carcinomas predicts the occurrence of hypercalcemia in athymic mice |
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