Changes in calcitonin gene RNA processing during growth of a human medullary thyroid carcinoma cell line
The ratios of calcitonin (CT) to calcitonin gene-related peptide (CGRP) mRNA, both generated by alternative RNA processing from the same primary RNA transcript, are shown by Northern blotting of cytoplasmic RNA to vary as a function of growth in a human medullary thyroid carcinoma cell line (TT). Up...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1989-12, Vol.49 (24), p.6949-6952 |
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description | The ratios of calcitonin (CT) to calcitonin gene-related peptide (CGRP) mRNA, both generated by alternative RNA processing from the same primary RNA transcript, are shown by Northern blotting of cytoplasmic RNA to vary as a function of growth in a human medullary thyroid carcinoma cell line (TT). Upon initial seeding, CT mRNA levels are relatively high, and CGRP mRNA levels are relatively low. During the early logarithmic growth phase, CGRP mRNA levels rise severalfold, while CT mRNA levels change only slightly. As the cells approach confluence, both CT and CGRP mRNA levels rise. Subsequently, CGRP mRNA levels fall substantially in postconfluent cells, while CT mRNA levels remain high. By actinomycin D blocking of nascent transcription, we have shown that these growth-related, reversible changes in the ratio of CT to CGRP mRNA are not due to changes in mRNA stability. Our data rather suggest that TT cells reversibly alter alternative RNA-processing patterns dependent upon growth conditions in vitro, such that CT mRNA is lowest and CGRP mRNA is highest during rapid growth. The mechanisms underlying this RNA-processing alteration may play a role in certain patients with aggressive forms of medullary thyroid carcinoma, in whom a decrease or loss of CT levels heralds a poor prognosis. |
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D ; CHEN, K. Y ; DE BUSTROS, A ; ROOS, B. A ; BAYLIN, S. B</creator><creatorcontrib>NELKIN, B. D ; CHEN, K. Y ; DE BUSTROS, A ; ROOS, B. A ; BAYLIN, S. B</creatorcontrib><description>The ratios of calcitonin (CT) to calcitonin gene-related peptide (CGRP) mRNA, both generated by alternative RNA processing from the same primary RNA transcript, are shown by Northern blotting of cytoplasmic RNA to vary as a function of growth in a human medullary thyroid carcinoma cell line (TT). Upon initial seeding, CT mRNA levels are relatively high, and CGRP mRNA levels are relatively low. During the early logarithmic growth phase, CGRP mRNA levels rise severalfold, while CT mRNA levels change only slightly. As the cells approach confluence, both CT and CGRP mRNA levels rise. Subsequently, CGRP mRNA levels fall substantially in postconfluent cells, while CT mRNA levels remain high. By actinomycin D blocking of nascent transcription, we have shown that these growth-related, reversible changes in the ratio of CT to CGRP mRNA are not due to changes in mRNA stability. Our data rather suggest that TT cells reversibly alter alternative RNA-processing patterns dependent upon growth conditions in vitro, such that CT mRNA is lowest and CGRP mRNA is highest during rapid growth. The mechanisms underlying this RNA-processing alteration may play a role in certain patients with aggressive forms of medullary thyroid carcinoma, in whom a decrease or loss of CT levels heralds a poor prognosis.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 2582437</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Biological and medical sciences ; Blotting, Northern ; Calcitonin - genetics ; calcitonin gene-related peptide ; Calcitonin Gene-Related Peptide - genetics ; carcinoma ; Carcinoma - genetics ; Carcinoma - pathology ; Endocrinopathies ; Gene Expression ; genes ; Half-Life ; Humans ; Malignant tumors ; Medical sciences ; mRNA ; Nucleic Acid Hybridization ; RNA Processing, Post-Transcriptional ; RNA, Messenger - genetics ; thyroid ; Thyroid Neoplasms - genetics ; Thyroid Neoplasms - pathology ; Thyroid. Thyroid axis (diseases) ; Tumor Cells, Cultured</subject><ispartof>Cancer research (Chicago, Ill.), 1989-12, Vol.49 (24), p.6949-6952</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6716533$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2582437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NELKIN, B. D</creatorcontrib><creatorcontrib>CHEN, K. Y</creatorcontrib><creatorcontrib>DE BUSTROS, A</creatorcontrib><creatorcontrib>ROOS, B. A</creatorcontrib><creatorcontrib>BAYLIN, S. B</creatorcontrib><title>Changes in calcitonin gene RNA processing during growth of a human medullary thyroid carcinoma cell line</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>The ratios of calcitonin (CT) to calcitonin gene-related peptide (CGRP) mRNA, both generated by alternative RNA processing from the same primary RNA transcript, are shown by Northern blotting of cytoplasmic RNA to vary as a function of growth in a human medullary thyroid carcinoma cell line (TT). Upon initial seeding, CT mRNA levels are relatively high, and CGRP mRNA levels are relatively low. During the early logarithmic growth phase, CGRP mRNA levels rise severalfold, while CT mRNA levels change only slightly. As the cells approach confluence, both CT and CGRP mRNA levels rise. Subsequently, CGRP mRNA levels fall substantially in postconfluent cells, while CT mRNA levels remain high. By actinomycin D blocking of nascent transcription, we have shown that these growth-related, reversible changes in the ratio of CT to CGRP mRNA are not due to changes in mRNA stability. Our data rather suggest that TT cells reversibly alter alternative RNA-processing patterns dependent upon growth conditions in vitro, such that CT mRNA is lowest and CGRP mRNA is highest during rapid growth. The mechanisms underlying this RNA-processing alteration may play a role in certain patients with aggressive forms of medullary thyroid carcinoma, in whom a decrease or loss of CT levels heralds a poor prognosis.</description><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Calcitonin - genetics</subject><subject>calcitonin gene-related peptide</subject><subject>Calcitonin Gene-Related Peptide - genetics</subject><subject>carcinoma</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - pathology</subject><subject>Endocrinopathies</subject><subject>Gene Expression</subject><subject>genes</subject><subject>Half-Life</subject><subject>Humans</subject><subject>Malignant tumors</subject><subject>Medical sciences</subject><subject>mRNA</subject><subject>Nucleic Acid Hybridization</subject><subject>RNA Processing, Post-Transcriptional</subject><subject>RNA, Messenger - genetics</subject><subject>thyroid</subject><subject>Thyroid Neoplasms - genetics</subject><subject>Thyroid Neoplasms - pathology</subject><subject>Thyroid. Thyroid axis (diseases)</subject><subject>Tumor Cells, Cultured</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUE1LxDAUDKKs6-pPEHIQb4W0SZr2uCx-waIgei6vSdpG0mRNWsR_bxaLV0_zHjMMM3OC1jmnVSYY46doTQipMs5EcY4uYvxIL88JX6FVwauCUbFGw24A1-uIjcMSrDSTd-nstdP49XmLD8FLHaNxPVZzOEIf_Nc0YN9hwMM8gsOjVrO1EL7xNHwHb1RyCtI4PwKW2lpsjdOX6KwDG_XVghv0fn_3tnvM9i8PT7vtPhsoEVNWVq1SoiQ0JScKWlanOgUoLlrQjHDohCg7JSkDwjQAdJwDrQXJi66lnNMNuv31Tck_Zx2nZjTxmAKc9nNsRE0pq9j_wpwzwqqaJOH1IpzbVLU5BDOmss2yYeJvFh5imrAL4KSJf7JS5CWnlP4AEjx7hA</recordid><startdate>19891215</startdate><enddate>19891215</enddate><creator>NELKIN, B. D</creator><creator>CHEN, K. Y</creator><creator>DE BUSTROS, A</creator><creator>ROOS, B. A</creator><creator>BAYLIN, S. B</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>7T3</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19891215</creationdate><title>Changes in calcitonin gene RNA processing during growth of a human medullary thyroid carcinoma cell line</title><author>NELKIN, B. D ; CHEN, K. Y ; DE BUSTROS, A ; ROOS, B. A ; BAYLIN, S. B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h307t-68bdd76030080dab495382ad57bae405af776fdc34a04eaaaf55a397012fb3553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Calcitonin - genetics</topic><topic>calcitonin gene-related peptide</topic><topic>Calcitonin Gene-Related Peptide - genetics</topic><topic>carcinoma</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - pathology</topic><topic>Endocrinopathies</topic><topic>Gene Expression</topic><topic>genes</topic><topic>Half-Life</topic><topic>Humans</topic><topic>Malignant tumors</topic><topic>Medical sciences</topic><topic>mRNA</topic><topic>Nucleic Acid Hybridization</topic><topic>RNA Processing, Post-Transcriptional</topic><topic>RNA, Messenger - genetics</topic><topic>thyroid</topic><topic>Thyroid Neoplasms - genetics</topic><topic>Thyroid Neoplasms - pathology</topic><topic>Thyroid. Thyroid axis (diseases)</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NELKIN, B. D</creatorcontrib><creatorcontrib>CHEN, K. Y</creatorcontrib><creatorcontrib>DE BUSTROS, A</creatorcontrib><creatorcontrib>ROOS, B. A</creatorcontrib><creatorcontrib>BAYLIN, S. 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B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in calcitonin gene RNA processing during growth of a human medullary thyroid carcinoma cell line</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1989-12-15</date><risdate>1989</risdate><volume>49</volume><issue>24</issue><spage>6949</spage><epage>6952</epage><pages>6949-6952</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>The ratios of calcitonin (CT) to calcitonin gene-related peptide (CGRP) mRNA, both generated by alternative RNA processing from the same primary RNA transcript, are shown by Northern blotting of cytoplasmic RNA to vary as a function of growth in a human medullary thyroid carcinoma cell line (TT). Upon initial seeding, CT mRNA levels are relatively high, and CGRP mRNA levels are relatively low. During the early logarithmic growth phase, CGRP mRNA levels rise severalfold, while CT mRNA levels change only slightly. As the cells approach confluence, both CT and CGRP mRNA levels rise. Subsequently, CGRP mRNA levels fall substantially in postconfluent cells, while CT mRNA levels remain high. By actinomycin D blocking of nascent transcription, we have shown that these growth-related, reversible changes in the ratio of CT to CGRP mRNA are not due to changes in mRNA stability. Our data rather suggest that TT cells reversibly alter alternative RNA-processing patterns dependent upon growth conditions in vitro, such that CT mRNA is lowest and CGRP mRNA is highest during rapid growth. The mechanisms underlying this RNA-processing alteration may play a role in certain patients with aggressive forms of medullary thyroid carcinoma, in whom a decrease or loss of CT levels heralds a poor prognosis.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>2582437</pmid><tpages>4</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Northern Calcitonin - genetics calcitonin gene-related peptide Calcitonin Gene-Related Peptide - genetics carcinoma Carcinoma - genetics Carcinoma - pathology Endocrinopathies Gene Expression genes Half-Life Humans Malignant tumors Medical sciences mRNA Nucleic Acid Hybridization RNA Processing, Post-Transcriptional RNA, Messenger - genetics thyroid Thyroid Neoplasms - genetics Thyroid Neoplasms - pathology Thyroid. Thyroid axis (diseases) Tumor Cells, Cultured |
title | Changes in calcitonin gene RNA processing during growth of a human medullary thyroid carcinoma cell line |
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