Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.

PIWIL2, a member of PIWI/AGO gene family, is expressed in the germline stem cells (GSCs) of testis for gametogenesis but not in adult somatic and stem cells. It has been implicated to play an important role in tumor development. We have previously reported that precancerous stem cells (pCSCs) consti...

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Autores principales: Yin Ye, De-Tao Yin, Li Chen, Quansheng Zhou, Rulong Shen, Gang He, Qingtao Yan, Zhenyu Tong, Andrew C Issekutz, Charles L Shapiro, Sanford H Barsky, Haifan Lin, Jian-Jian Li, Jian-Xin Gao
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Publicado: Public Library of Science (PLoS) 2010
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Acceso en línea:https://doaj.org/article/9a911db065244378b3e102cf91e5b5fd
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spelling oai:doaj.org-article:9a911db065244378b3e102cf91e5b5fd2021-11-18T07:03:06ZIdentification of Piwil2-like (PL2L) proteins that promote tumorigenesis.1932-620310.1371/journal.pone.0013406https://doaj.org/article/9a911db065244378b3e102cf91e5b5fd2010-10-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20975993/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203PIWIL2, a member of PIWI/AGO gene family, is expressed in the germline stem cells (GSCs) of testis for gametogenesis but not in adult somatic and stem cells. It has been implicated to play an important role in tumor development. We have previously reported that precancerous stem cells (pCSCs) constitutively express Piwil2 transcripts to promote their proliferation. Here we show that these transcripts de facto represent Piwil2-like (PL2L) proteins. We have identified several PL2L proteins including PL2L80, PL2L60, PL2L50 and PL2L40, using combined methods of Gene-Exon-Mapping Reverse Transcription Polymerase Chain Reaction (GEM RT-PCR), bioinformatics and a group of novel monoclonal antibodies. Among them, PL2L60 rather than Piwil2 and other PL2L proteins is predominantly expressed in various types of human and mouse tumor cells. It promotes tumor cell survival and proliferation in vitro through up-regulation of Stat3 and Bcl2 gene expressions, the cell cycle entry from G(0/1) into S-phase, and the nuclear expression of NF-κB, which contribute to the tumorigenicity of tumor cells in vivo. Consistently, PL2L proteins rather than Piwil2 are predominantly expressed in the cytoplasm or cytoplasm and nucleus of euchromatin-enriched tumor cells in human primary and metastatic cancers, such as breast and cervical cancers. Moreover, nuclear PL2L proteins are always co-expressed with nuclear NF-κB. These results reveal that PL2L60 can coordinate with NF-κB to promote tumorigenesis and might mediate a common pathway for tumor development without tissue restriction. The identification of PL2L proteins provides a novel insight into the mechanisms of cancer development as well as a novel bridge linking cancer diagnostics and anticancer drug development.Yin YeDe-Tao YinLi ChenQuansheng ZhouRulong ShenGang HeQingtao YanZhenyu TongAndrew C IssekutzCharles L ShapiroSanford H BarskyHaifan LinJian-Jian LiJian-Xin GaoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 10, p e13406 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yin Ye
De-Tao Yin
Li Chen
Quansheng Zhou
Rulong Shen
Gang He
Qingtao Yan
Zhenyu Tong
Andrew C Issekutz
Charles L Shapiro
Sanford H Barsky
Haifan Lin
Jian-Jian Li
Jian-Xin Gao
Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
description PIWIL2, a member of PIWI/AGO gene family, is expressed in the germline stem cells (GSCs) of testis for gametogenesis but not in adult somatic and stem cells. It has been implicated to play an important role in tumor development. We have previously reported that precancerous stem cells (pCSCs) constitutively express Piwil2 transcripts to promote their proliferation. Here we show that these transcripts de facto represent Piwil2-like (PL2L) proteins. We have identified several PL2L proteins including PL2L80, PL2L60, PL2L50 and PL2L40, using combined methods of Gene-Exon-Mapping Reverse Transcription Polymerase Chain Reaction (GEM RT-PCR), bioinformatics and a group of novel monoclonal antibodies. Among them, PL2L60 rather than Piwil2 and other PL2L proteins is predominantly expressed in various types of human and mouse tumor cells. It promotes tumor cell survival and proliferation in vitro through up-regulation of Stat3 and Bcl2 gene expressions, the cell cycle entry from G(0/1) into S-phase, and the nuclear expression of NF-κB, which contribute to the tumorigenicity of tumor cells in vivo. Consistently, PL2L proteins rather than Piwil2 are predominantly expressed in the cytoplasm or cytoplasm and nucleus of euchromatin-enriched tumor cells in human primary and metastatic cancers, such as breast and cervical cancers. Moreover, nuclear PL2L proteins are always co-expressed with nuclear NF-κB. These results reveal that PL2L60 can coordinate with NF-κB to promote tumorigenesis and might mediate a common pathway for tumor development without tissue restriction. The identification of PL2L proteins provides a novel insight into the mechanisms of cancer development as well as a novel bridge linking cancer diagnostics and anticancer drug development.
format article
author Yin Ye
De-Tao Yin
Li Chen
Quansheng Zhou
Rulong Shen
Gang He
Qingtao Yan
Zhenyu Tong
Andrew C Issekutz
Charles L Shapiro
Sanford H Barsky
Haifan Lin
Jian-Jian Li
Jian-Xin Gao
author_facet Yin Ye
De-Tao Yin
Li Chen
Quansheng Zhou
Rulong Shen
Gang He
Qingtao Yan
Zhenyu Tong
Andrew C Issekutz
Charles L Shapiro
Sanford H Barsky
Haifan Lin
Jian-Jian Li
Jian-Xin Gao
author_sort Yin Ye
title Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
title_short Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
title_full Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
title_fullStr Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
title_full_unstemmed Identification of Piwil2-like (PL2L) proteins that promote tumorigenesis.
title_sort identification of piwil2-like (pl2l) proteins that promote tumorigenesis.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/9a911db065244378b3e102cf91e5b5fd
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