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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
Main Authors: Gainetdinov, Ildar V, Skvortsova, Yulia V, Stukacheva, Elena A, Bychenko, Oksana S, Kondratieva, Sofia A, Zinovieva, Marina V, Azhikina, Tatyana L
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cited_by cdi_FETCH-LOGICAL-c692t-bf0167fa6251034a35fc44600863eb14f351c8cfb3209b8941d6020f865bc9763
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creator Gainetdinov, Ildar V
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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.
doi_str_mv 10.1371/journal.pone.0112528
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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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