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SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer
BACKGROUND: Emerging evidence indicates that small nucleolar RNAs (snoRNAs) play a central role in oncogenesis. Herein, we systematically evaluated expression profiles of snoRNAs in colorectal cancer (CRC) and investigated their clinical and functional role in this malignancy. METHODS: We compared e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552212/ https://www.ncbi.nlm.nih.gov/pubmed/28734806 http://dx.doi.org/10.1016/j.ebiom.2017.07.009 |
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author | Yoshida, Kazuhiro Toden, Shusuke Weng, Wenhao Shigeyasu, Kunitoshi Miyoshi, Jinsei Turner, Jacob Nagasaka, Takeshi Ma, Yanlei Takayama, Tetsuji Fujiwara, Toshiyoshi Goel, Ajay |
author_facet | Yoshida, Kazuhiro Toden, Shusuke Weng, Wenhao Shigeyasu, Kunitoshi Miyoshi, Jinsei Turner, Jacob Nagasaka, Takeshi Ma, Yanlei Takayama, Tetsuji Fujiwara, Toshiyoshi Goel, Ajay |
author_sort | Yoshida, Kazuhiro |
collection | PubMed |
description | BACKGROUND: Emerging evidence indicates that small nucleolar RNAs (snoRNAs) play a central role in oncogenesis. Herein, we systematically evaluated expression profiles of snoRNAs in colorectal cancer (CRC) and investigated their clinical and functional role in this malignancy. METHODS: We compared expression levels of snoRNAs between cancer and normal tissues using publicly available datasets and identified the most differentially expressed and commonly upregulated snoRNAs in CRC. These results were examined in 489 colorectal tissues to assess their clinical significance, followed by a series of in vitro and in vivo experiments to evaluate the functional role of candidate snoRNAs. RESULTS: Using multiple RNA profiling datasets, we identified consistent overexpression of SNORA21 in CRC. In the clinical validation cohorts, the expression level of SNORA21 was upregulated in colorectal adenomas and cancers. Furthermore, elevated SNORA21 emerged as an independent factor for predicting poor survival. Both in vitro and in vivo experiments revealed that CRISPR/Cas9-mediated inhibition of SNORA21 expression resulted in decreased cell proliferation and invasion through modulation of multiple cancer related pathways. CONCLUSIONS: We systematically identified SNORA21 as a key oncogenic snoRNA in CRC, which plays an important role in cancer progression, and might serve as an important prognostic biomarker in CRC. |
format | Online Article Text |
id | pubmed-5552212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55522122017-08-22 SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer Yoshida, Kazuhiro Toden, Shusuke Weng, Wenhao Shigeyasu, Kunitoshi Miyoshi, Jinsei Turner, Jacob Nagasaka, Takeshi Ma, Yanlei Takayama, Tetsuji Fujiwara, Toshiyoshi Goel, Ajay EBioMedicine Research Paper BACKGROUND: Emerging evidence indicates that small nucleolar RNAs (snoRNAs) play a central role in oncogenesis. Herein, we systematically evaluated expression profiles of snoRNAs in colorectal cancer (CRC) and investigated their clinical and functional role in this malignancy. METHODS: We compared expression levels of snoRNAs between cancer and normal tissues using publicly available datasets and identified the most differentially expressed and commonly upregulated snoRNAs in CRC. These results were examined in 489 colorectal tissues to assess their clinical significance, followed by a series of in vitro and in vivo experiments to evaluate the functional role of candidate snoRNAs. RESULTS: Using multiple RNA profiling datasets, we identified consistent overexpression of SNORA21 in CRC. In the clinical validation cohorts, the expression level of SNORA21 was upregulated in colorectal adenomas and cancers. Furthermore, elevated SNORA21 emerged as an independent factor for predicting poor survival. Both in vitro and in vivo experiments revealed that CRISPR/Cas9-mediated inhibition of SNORA21 expression resulted in decreased cell proliferation and invasion through modulation of multiple cancer related pathways. CONCLUSIONS: We systematically identified SNORA21 as a key oncogenic snoRNA in CRC, which plays an important role in cancer progression, and might serve as an important prognostic biomarker in CRC. Elsevier 2017-07-12 /pmc/articles/PMC5552212/ /pubmed/28734806 http://dx.doi.org/10.1016/j.ebiom.2017.07.009 Text en © 2017 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Yoshida, Kazuhiro Toden, Shusuke Weng, Wenhao Shigeyasu, Kunitoshi Miyoshi, Jinsei Turner, Jacob Nagasaka, Takeshi Ma, Yanlei Takayama, Tetsuji Fujiwara, Toshiyoshi Goel, Ajay SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title | SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title_full | SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title_fullStr | SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title_full_unstemmed | SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title_short | SNORA21 – An Oncogenic Small Nucleolar RNA, with a Prognostic Biomarker Potential in Human Colorectal Cancer |
title_sort | snora21 – an oncogenic small nucleolar rna, with a prognostic biomarker potential in human colorectal cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552212/ https://www.ncbi.nlm.nih.gov/pubmed/28734806 http://dx.doi.org/10.1016/j.ebiom.2017.07.009 |
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