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LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles

Advancements in omics‐based technologies over the past few years have led to the discovery of numerous biologically relevant peptides encoded by small open reading frames (smORFs) embedded in long noncoding RNA (lncRNA) transcripts (referred to as microproteins here) in a variety of species. However...

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Autores principales: Cai, Tanxi, Zhang, Qing, Wu, Bowen, Wang, Jifeng, Li, Na, Zhang, Tingting, Wang, Zhipeng, Luo, Jianjun, Guo, Xiaojing, Ding, Xiang, Xie, Zhensheng, Niu, Lili, Ning, Weihai, Fan, Zhen, Chen, Xiaowei, Guo, Xiangqian, Chen, Runsheng, Zhang, Hongwei, Yang, Fuquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275822/
https://www.ncbi.nlm.nih.gov/pubmed/34276900
http://dx.doi.org/10.1002/jev2.12123
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author Cai, Tanxi
Zhang, Qing
Wu, Bowen
Wang, Jifeng
Li, Na
Zhang, Tingting
Wang, Zhipeng
Luo, Jianjun
Guo, Xiaojing
Ding, Xiang
Xie, Zhensheng
Niu, Lili
Ning, Weihai
Fan, Zhen
Chen, Xiaowei
Guo, Xiangqian
Chen, Runsheng
Zhang, Hongwei
Yang, Fuquan
author_facet Cai, Tanxi
Zhang, Qing
Wu, Bowen
Wang, Jifeng
Li, Na
Zhang, Tingting
Wang, Zhipeng
Luo, Jianjun
Guo, Xiaojing
Ding, Xiang
Xie, Zhensheng
Niu, Lili
Ning, Weihai
Fan, Zhen
Chen, Xiaowei
Guo, Xiangqian
Chen, Runsheng
Zhang, Hongwei
Yang, Fuquan
author_sort Cai, Tanxi
collection PubMed
description Advancements in omics‐based technologies over the past few years have led to the discovery of numerous biologically relevant peptides encoded by small open reading frames (smORFs) embedded in long noncoding RNA (lncRNA) transcripts (referred to as microproteins here) in a variety of species. However, the mechanisms and modes of action that underlie the roles of microproteins have yet to be fully characterized. Herein, we provide the first experimental evidence of abundant microproteins in extracellular vesicles (EVs) derived from glioma cancer cells, indicating that the EV‐mediated transfer of microproteins may represent a novel mechanism for intercellular communication. Intriguingly, when examining human plasma, 48, 11 and 3 microproteins were identified from purified EVs, whole plasma and EV‐free plasma, respectively, suggesting that circulating microproteins are primarily enriched in EVs. Most importantly, the preliminary data showed that the expression profile of EV microproteins in glioma patient diverged from the health donors, suggesting that the circulating microproteins in EVs might have potential diagnostic application in identifying patients with glioma.
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spelling pubmed-82758222021-07-15 LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles Cai, Tanxi Zhang, Qing Wu, Bowen Wang, Jifeng Li, Na Zhang, Tingting Wang, Zhipeng Luo, Jianjun Guo, Xiaojing Ding, Xiang Xie, Zhensheng Niu, Lili Ning, Weihai Fan, Zhen Chen, Xiaowei Guo, Xiangqian Chen, Runsheng Zhang, Hongwei Yang, Fuquan J Extracell Vesicles Research Articles Advancements in omics‐based technologies over the past few years have led to the discovery of numerous biologically relevant peptides encoded by small open reading frames (smORFs) embedded in long noncoding RNA (lncRNA) transcripts (referred to as microproteins here) in a variety of species. However, the mechanisms and modes of action that underlie the roles of microproteins have yet to be fully characterized. Herein, we provide the first experimental evidence of abundant microproteins in extracellular vesicles (EVs) derived from glioma cancer cells, indicating that the EV‐mediated transfer of microproteins may represent a novel mechanism for intercellular communication. Intriguingly, when examining human plasma, 48, 11 and 3 microproteins were identified from purified EVs, whole plasma and EV‐free plasma, respectively, suggesting that circulating microproteins are primarily enriched in EVs. Most importantly, the preliminary data showed that the expression profile of EV microproteins in glioma patient diverged from the health donors, suggesting that the circulating microproteins in EVs might have potential diagnostic application in identifying patients with glioma. John Wiley and Sons Inc. 2021-07-12 2021-07 /pmc/articles/PMC8275822/ /pubmed/34276900 http://dx.doi.org/10.1002/jev2.12123 Text en © 2021 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Cai, Tanxi
Zhang, Qing
Wu, Bowen
Wang, Jifeng
Li, Na
Zhang, Tingting
Wang, Zhipeng
Luo, Jianjun
Guo, Xiaojing
Ding, Xiang
Xie, Zhensheng
Niu, Lili
Ning, Weihai
Fan, Zhen
Chen, Xiaowei
Guo, Xiangqian
Chen, Runsheng
Zhang, Hongwei
Yang, Fuquan
LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title_full LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title_fullStr LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title_full_unstemmed LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title_short LncRNA‐encoded microproteins: A new form of cargo in cell culture‐derived and circulating extracellular vesicles
title_sort lncrna‐encoded microproteins: a new form of cargo in cell culture‐derived and circulating extracellular vesicles
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275822/
https://www.ncbi.nlm.nih.gov/pubmed/34276900
http://dx.doi.org/10.1002/jev2.12123
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