C77G in PTPRC
The pan lymphocyte marker CD45 exists in various isoforms arising from alternative splicing of the exons 4, 5 and 6. While naïve T cells express CD45RA translated from an mRNA containing exon 4, exons 4-6 are spliced out to encode the shorter CD45R0 in antigen-experienced effector/memory T cells. Th...
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Veröffentlicht in: | PloS one 2017-07, Vol.12 (7), p.e0182030 |
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creator | Landskron, Johannes Kraggerud, Sigrid M Wik, Elisabeth Dørum, Anne Bjørnslett, Merete Melum, Espen Helland, Øystein Bjørge, Line Lothe, Ragnhild A Salvesen, Helga B Taskén, Kjetil |
description | The pan lymphocyte marker CD45 exists in various isoforms arising from alternative splicing of the exons 4, 5 and 6. While naïve T cells express CD45RA translated from an mRNA containing exon 4, exons 4-6 are spliced out to encode the shorter CD45R0 in antigen-experienced effector/memory T cells. The SNP C77G (rs17612648) is located in exon 4 and blocks the exon's differential splicing from the pre-mRNA, enforcing expression of CD45RA. Several studies have linked C77G to autoimmune diseases but lack of validation in other cohorts has left its role elusive. An incidental finding in an ovarian cancer patient cohort from West Norway (Bergen region, n = 312), suggested that the frequency of C77G was higher among ovarian cancer patients than in healthy Norwegians (n = 1,357) (3.0% vs. 1.8% allele frequency). However, this finding could not be validated in a larger patient cohort from South-East Norway (Oslo region, n = 1,198) with 1.2% allele frequency. Hence, C77G is not associated with ovarian cancer in the Norwegian population. However, its frequency was increased in patients with FIGO stage II, endometrioid histology or an age at diagnosis of 60 years or older indicating a possible association with a less aggressive cancer type. |
doi_str_mv | 10.1371/journal.pone.0182030 |
format | Article |
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While naïve T cells express CD45RA translated from an mRNA containing exon 4, exons 4-6 are spliced out to encode the shorter CD45R0 in antigen-experienced effector/memory T cells. The SNP C77G (rs17612648) is located in exon 4 and blocks the exon's differential splicing from the pre-mRNA, enforcing expression of CD45RA. Several studies have linked C77G to autoimmune diseases but lack of validation in other cohorts has left its role elusive. An incidental finding in an ovarian cancer patient cohort from West Norway (Bergen region, n = 312), suggested that the frequency of C77G was higher among ovarian cancer patients than in healthy Norwegians (n = 1,357) (3.0% vs. 1.8% allele frequency). However, this finding could not be validated in a larger patient cohort from South-East Norway (Oslo region, n = 1,198) with 1.2% allele frequency. Hence, C77G is not associated with ovarian cancer in the Norwegian population. However, its frequency was increased in patients with FIGO stage II, endometrioid histology or an age at diagnosis of 60 years or older indicating a possible association with a less aggressive cancer type.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0182030</identifier><language>eng</language><publisher>Public Library of Science</publisher><subject>Diagnosis ; Ligands (Biochemistry) ; Ovarian cancer</subject><ispartof>PloS one, 2017-07, Vol.12 (7), p.e0182030</ispartof><rights>COPYRIGHT 2017 Public Library of Science</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>314,777,781,861,27905,27906</link.rule.ids></links><search><creatorcontrib>Landskron, Johannes</creatorcontrib><creatorcontrib>Kraggerud, Sigrid M</creatorcontrib><creatorcontrib>Wik, Elisabeth</creatorcontrib><creatorcontrib>Dørum, Anne</creatorcontrib><creatorcontrib>Bjørnslett, Merete</creatorcontrib><creatorcontrib>Melum, Espen</creatorcontrib><creatorcontrib>Helland, Øystein</creatorcontrib><creatorcontrib>Bjørge, Line</creatorcontrib><creatorcontrib>Lothe, Ragnhild A</creatorcontrib><creatorcontrib>Salvesen, Helga B</creatorcontrib><creatorcontrib>Taskén, Kjetil</creatorcontrib><title>C77G in PTPRC</title><title>PloS one</title><description>The pan lymphocyte marker CD45 exists in various isoforms arising from alternative splicing of the exons 4, 5 and 6. While naïve T cells express CD45RA translated from an mRNA containing exon 4, exons 4-6 are spliced out to encode the shorter CD45R0 in antigen-experienced effector/memory T cells. The SNP C77G (rs17612648) is located in exon 4 and blocks the exon's differential splicing from the pre-mRNA, enforcing expression of CD45RA. Several studies have linked C77G to autoimmune diseases but lack of validation in other cohorts has left its role elusive. An incidental finding in an ovarian cancer patient cohort from West Norway (Bergen region, n = 312), suggested that the frequency of C77G was higher among ovarian cancer patients than in healthy Norwegians (n = 1,357) (3.0% vs. 1.8% allele frequency). However, this finding could not be validated in a larger patient cohort from South-East Norway (Oslo region, n = 1,198) with 1.2% allele frequency. Hence, C77G is not associated with ovarian cancer in the Norwegian population. However, its frequency was increased in patients with FIGO stage II, endometrioid histology or an age at diagnosis of 60 years or older indicating a possible association with a less aggressive cancer type.</description><subject>Diagnosis</subject><subject>Ligands (Biochemistry)</subject><subject>Ovarian cancer</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFjE9LwzAYh4MoOOe-gYedBA-tb_o2aXIcRedgsDGL15JkSddREjEt-PEtuEM9efn9gYeHkAcKKcWCPp_D8OVVl34Gb1OgIgOEKzKjErOEj-d6sm_JXYxnAIaC8xlZlEWxXrZ-ua_2h_Ke3DjVRbu49JxUry9V-ZZsd-tNudomjZSQaE2FY5mymhU4ehAMd1mhHRqGmjINSnKQArP8yHJOKRydc0ZYBkaPgXPy9KttVGfr1pvge_vdN2qIsd68H-pVLiVHTsV_7O7jL_s4YU9Wdf0phm7o2-DjFPwB7ZNVvA</recordid><startdate>20170731</startdate><enddate>20170731</enddate><creator>Landskron, Johannes</creator><creator>Kraggerud, Sigrid M</creator><creator>Wik, Elisabeth</creator><creator>Dørum, Anne</creator><creator>Bjørnslett, Merete</creator><creator>Melum, Espen</creator><creator>Helland, Øystein</creator><creator>Bjørge, Line</creator><creator>Lothe, Ragnhild A</creator><creator>Salvesen, Helga B</creator><creator>Taskén, Kjetil</creator><general>Public Library of Science</general><scope>IOV</scope><scope>ISR</scope></search><sort><creationdate>20170731</creationdate><title>C77G in PTPRC</title><author>Landskron, Johannes ; Kraggerud, Sigrid M ; Wik, Elisabeth ; Dørum, Anne ; Bjørnslett, Merete ; Melum, Espen ; Helland, Øystein ; Bjørge, Line ; Lothe, Ragnhild A ; Salvesen, Helga B ; Taskén, Kjetil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g990-bb18f52aeb57353830c6f27bf3c53b15b0a96098324d546110dfffc8e50cbe503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Diagnosis</topic><topic>Ligands (Biochemistry)</topic><topic>Ovarian cancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Landskron, Johannes</creatorcontrib><creatorcontrib>Kraggerud, Sigrid M</creatorcontrib><creatorcontrib>Wik, Elisabeth</creatorcontrib><creatorcontrib>Dørum, Anne</creatorcontrib><creatorcontrib>Bjørnslett, Merete</creatorcontrib><creatorcontrib>Melum, Espen</creatorcontrib><creatorcontrib>Helland, Øystein</creatorcontrib><creatorcontrib>Bjørge, Line</creatorcontrib><creatorcontrib>Lothe, Ragnhild A</creatorcontrib><creatorcontrib>Salvesen, Helga B</creatorcontrib><creatorcontrib>Taskén, Kjetil</creatorcontrib><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Landskron, Johannes</au><au>Kraggerud, Sigrid M</au><au>Wik, Elisabeth</au><au>Dørum, Anne</au><au>Bjørnslett, Merete</au><au>Melum, Espen</au><au>Helland, Øystein</au><au>Bjørge, Line</au><au>Lothe, Ragnhild A</au><au>Salvesen, Helga B</au><au>Taskén, Kjetil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>C77G in PTPRC</atitle><jtitle>PloS one</jtitle><date>2017-07-31</date><risdate>2017</risdate><volume>12</volume><issue>7</issue><spage>e0182030</spage><pages>e0182030-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The pan lymphocyte marker CD45 exists in various isoforms arising from alternative splicing of the exons 4, 5 and 6. While naïve T cells express CD45RA translated from an mRNA containing exon 4, exons 4-6 are spliced out to encode the shorter CD45R0 in antigen-experienced effector/memory T cells. The SNP C77G (rs17612648) is located in exon 4 and blocks the exon's differential splicing from the pre-mRNA, enforcing expression of CD45RA. Several studies have linked C77G to autoimmune diseases but lack of validation in other cohorts has left its role elusive. An incidental finding in an ovarian cancer patient cohort from West Norway (Bergen region, n = 312), suggested that the frequency of C77G was higher among ovarian cancer patients than in healthy Norwegians (n = 1,357) (3.0% vs. 1.8% allele frequency). However, this finding could not be validated in a larger patient cohort from South-East Norway (Oslo region, n = 1,198) with 1.2% allele frequency. Hence, C77G is not associated with ovarian cancer in the Norwegian population. However, its frequency was increased in patients with FIGO stage II, endometrioid histology or an age at diagnosis of 60 years or older indicating a possible association with a less aggressive cancer type.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0182030</doi><tpages>e0182030</tpages></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Diagnosis Ligands (Biochemistry) Ovarian cancer |
title | C77G in PTPRC |
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