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Expression profiles of PIWIL2 short isoforms differ in testicular germ cell tumors of various differentiation subtypes
PIWI family proteins have recently emerged as essential contributors in numerous biological processes including germ cell development, stem cell maintenance and epigenetic reprogramming. Expression of some of the family members has been shown to be elevated in tumors. In particular, PIWIL2 has been...
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Published in: | PloS one 2014-11, Vol.9 (11), p.e112528-e112528 |
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creator | Gainetdinov, Ildar V Skvortsova, Yulia V Stukacheva, Elena A Bychenko, Oksana S Kondratieva, Sofia A Zinovieva, Marina V Azhikina, Tatyana L |
description | PIWI family proteins have recently emerged as essential contributors in numerous biological processes including germ cell development, stem cell maintenance and epigenetic reprogramming. Expression of some of the family members has been shown to be elevated in tumors. In particular, PIWIL2 has been probed as a potential neoplasia biomarker in many cancers in humans. Previously, PIWIL2 was shown to be expressed in most tumours as a set of its shorter isoforms. In this work, we demonstrated the presence of its 60 kDa (PL2L60A) and 80 kDa (PL2L80A) isoforms in testicular cancer cell lines. We also ascertained the transcriptional boundaries of mRNAs and alternative promoter regions for these PIWIL2 isoforms. Further, we probed a range of testicular germ cell tumor (TGCT) samples and found PIWIL2 to be predominantly expressed as PL2L60A in most of them. Importantly, the levels of both PL2L60A mRNA and protein products were found to vary depending on the differentiation subtype of TGCTs, i.e., PL2L60A expression is significantly higher in undifferentiated seminomas and appears to be substantially decreased in mixed and nonseminomatous TGCTs. The higher level of PL2L60A expression in undifferentiated TGCTs was further validated in the model system of retinoic acid induced differentiation in NT2/D1 cell line. Therefore, both PL2L60A mRNA and protein abundance could serve as an additional marker distinguishing between seminomas and nonseminomatous tumors with different prognosis and therapy approaches. |
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Expression of some of the family members has been shown to be elevated in tumors. In particular, PIWIL2 has been probed as a potential neoplasia biomarker in many cancers in humans. Previously, PIWIL2 was shown to be expressed in most tumours as a set of its shorter isoforms. In this work, we demonstrated the presence of its 60 kDa (PL2L60A) and 80 kDa (PL2L80A) isoforms in testicular cancer cell lines. We also ascertained the transcriptional boundaries of mRNAs and alternative promoter regions for these PIWIL2 isoforms. Further, we probed a range of testicular germ cell tumor (TGCT) samples and found PIWIL2 to be predominantly expressed as PL2L60A in most of them. Importantly, the levels of both PL2L60A mRNA and protein products were found to vary depending on the differentiation subtype of TGCTs, i.e., PL2L60A expression is significantly higher in undifferentiated seminomas and appears to be substantially decreased in mixed and nonseminomatous TGCTs. The higher level of PL2L60A expression in undifferentiated TGCTs was further validated in the model system of retinoic acid induced differentiation in NT2/D1 cell line. Therefore, both PL2L60A mRNA and protein abundance could serve as an additional marker distinguishing between seminomas and nonseminomatous tumors with different prognosis and therapy approaches.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0112528</identifier><identifier>PMID: 25384072</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Argonaute Proteins - genetics ; Argonaute Proteins - metabolism ; Biological activity ; Biology and Life Sciences ; Biomarkers ; Cancer ; Cell culture ; Cell differentiation ; Cell Differentiation - drug effects ; Cell Line, Tumor ; Differentiation ; DNA methylation ; Epigenetic inheritance ; Epigenetics ; Gene expression ; Humans ; Isoforms ; Leukemia ; Liver cancer ; Lymphoma ; Male ; Medical research ; Medicine and Health Sciences ; Neoplasms, Germ Cell and Embryonal - genetics ; Neoplasms, Germ Cell and Embryonal - metabolism ; Neoplasms, Germ Cell and Embryonal - pathology ; Neuroblastoma ; Neurotrophin 2 ; Polyadenylation ; Protein Isoforms - genetics ; Protein Isoforms - metabolism ; Proteins ; Retinoic acid ; RNA ; RNA Splice Sites ; RNA, Messenger - metabolism ; Rodents ; Seminoma ; Spermatozoa - cytology ; Spermatozoa - metabolism ; Spermatozoa - pathology ; Stem cells ; Testes ; Testicular cancer ; Testicular Neoplasms - genetics ; Testicular Neoplasms - metabolism ; Testicular Neoplasms - pathology ; Transcription ; Transcriptome ; Tretinoin - pharmacology ; Tumor cell lines ; Tumors</subject><ispartof>PloS one, 2014-11, Vol.9 (11), p.e112528-e112528</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Gainetdinov et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Gainetdinov et al 2014 Gainetdinov et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-bf0167fa6251034a35fc44600863eb14f351c8cfb3209b8941d6020f865bc9763</citedby><cites>FETCH-LOGICAL-c692t-bf0167fa6251034a35fc44600863eb14f351c8cfb3209b8941d6020f865bc9763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1622299785/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1622299785?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25384072$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gao, Jian-Xin</contributor><creatorcontrib>Gainetdinov, Ildar V</creatorcontrib><creatorcontrib>Skvortsova, Yulia V</creatorcontrib><creatorcontrib>Stukacheva, Elena A</creatorcontrib><creatorcontrib>Bychenko, Oksana S</creatorcontrib><creatorcontrib>Kondratieva, Sofia A</creatorcontrib><creatorcontrib>Zinovieva, Marina V</creatorcontrib><creatorcontrib>Azhikina, Tatyana L</creatorcontrib><title>Expression profiles of PIWIL2 short isoforms differ in testicular germ cell tumors of various differentiation subtypes</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>PIWI family proteins have recently emerged as essential contributors in numerous biological processes including germ cell development, stem cell maintenance and epigenetic reprogramming. 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The higher level of PL2L60A expression in undifferentiated TGCTs was further validated in the model system of retinoic acid induced differentiation in NT2/D1 cell line. Therefore, both PL2L60A mRNA and protein abundance could serve as an additional marker distinguishing between seminomas and nonseminomatous tumors with different prognosis and therapy approaches.</description><subject>Acids</subject><subject>Argonaute Proteins - genetics</subject><subject>Argonaute Proteins - metabolism</subject><subject>Biological activity</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Cell culture</subject><subject>Cell differentiation</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Differentiation</subject><subject>DNA methylation</subject><subject>Epigenetic inheritance</subject><subject>Epigenetics</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Isoforms</subject><subject>Leukemia</subject><subject>Liver cancer</subject><subject>Lymphoma</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Neoplasms, Germ Cell and Embryonal - genetics</subject><subject>Neoplasms, Germ Cell and Embryonal - metabolism</subject><subject>Neoplasms, Germ Cell and Embryonal - pathology</subject><subject>Neuroblastoma</subject><subject>Neurotrophin 2</subject><subject>Polyadenylation</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Isoforms - metabolism</subject><subject>Proteins</subject><subject>Retinoic acid</subject><subject>RNA</subject><subject>RNA Splice Sites</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Seminoma</subject><subject>Spermatozoa - cytology</subject><subject>Spermatozoa - metabolism</subject><subject>Spermatozoa - pathology</subject><subject>Stem cells</subject><subject>Testes</subject><subject>Testicular cancer</subject><subject>Testicular Neoplasms - genetics</subject><subject>Testicular Neoplasms - metabolism</subject><subject>Testicular Neoplasms - pathology</subject><subject>Transcription</subject><subject>Transcriptome</subject><subject>Tretinoin - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gainetdinov, Ildar V</au><au>Skvortsova, Yulia V</au><au>Stukacheva, Elena A</au><au>Bychenko, Oksana S</au><au>Kondratieva, Sofia A</au><au>Zinovieva, Marina V</au><au>Azhikina, Tatyana L</au><au>Gao, Jian-Xin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression profiles of PIWIL2 short isoforms differ in testicular germ cell tumors of various differentiation subtypes</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-11-10</date><risdate>2014</risdate><volume>9</volume><issue>11</issue><spage>e112528</spage><epage>e112528</epage><pages>e112528-e112528</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>PIWI family proteins have recently emerged as essential contributors in numerous biological processes including germ cell development, stem cell maintenance and epigenetic reprogramming. Expression of some of the family members has been shown to be elevated in tumors. In particular, PIWIL2 has been probed as a potential neoplasia biomarker in many cancers in humans. Previously, PIWIL2 was shown to be expressed in most tumours as a set of its shorter isoforms. In this work, we demonstrated the presence of its 60 kDa (PL2L60A) and 80 kDa (PL2L80A) isoforms in testicular cancer cell lines. We also ascertained the transcriptional boundaries of mRNAs and alternative promoter regions for these PIWIL2 isoforms. Further, we probed a range of testicular germ cell tumor (TGCT) samples and found PIWIL2 to be predominantly expressed as PL2L60A in most of them. Importantly, the levels of both PL2L60A mRNA and protein products were found to vary depending on the differentiation subtype of TGCTs, i.e., PL2L60A expression is significantly higher in undifferentiated seminomas and appears to be substantially decreased in mixed and nonseminomatous TGCTs. The higher level of PL2L60A expression in undifferentiated TGCTs was further validated in the model system of retinoic acid induced differentiation in NT2/D1 cell line. Therefore, both PL2L60A mRNA and protein abundance could serve as an additional marker distinguishing between seminomas and nonseminomatous tumors with different prognosis and therapy approaches.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25384072</pmid><doi>10.1371/journal.pone.0112528</doi><oa>free_for_read</oa></addata></record> |
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source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Acids Argonaute Proteins - genetics Argonaute Proteins - metabolism Biological activity Biology and Life Sciences Biomarkers Cancer Cell culture Cell differentiation Cell Differentiation - drug effects Cell Line, Tumor Differentiation DNA methylation Epigenetic inheritance Epigenetics Gene expression Humans Isoforms Leukemia Liver cancer Lymphoma Male Medical research Medicine and Health Sciences Neoplasms, Germ Cell and Embryonal - genetics Neoplasms, Germ Cell and Embryonal - metabolism Neoplasms, Germ Cell and Embryonal - pathology Neuroblastoma Neurotrophin 2 Polyadenylation Protein Isoforms - genetics Protein Isoforms - metabolism Proteins Retinoic acid RNA RNA Splice Sites RNA, Messenger - metabolism Rodents Seminoma Spermatozoa - cytology Spermatozoa - metabolism Spermatozoa - pathology Stem cells Testes Testicular cancer Testicular Neoplasms - genetics Testicular Neoplasms - metabolism Testicular Neoplasms - pathology Transcription Transcriptome Tretinoin - pharmacology Tumor cell lines Tumors |
title | Expression profiles of PIWIL2 short isoforms differ in testicular germ cell tumors of various differentiation subtypes |
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