SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop

Abstract Background Small nucleolar RNA host gene (SNHG) long noncoding RNAs (lncRNAs) are frequently dysregulated in human cancers and involved in tumorigenesis and progression. SNHG17 has been reported as a candidate oncogene in several cancer types, however, its regulatory role in colorectal canc...

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Autores principales: Zehua Bian, Mingyue Zhou, Kaisa Cui, Fan Yang, Yulin Cao, Shengbai Sun, Bingxin Liu, Liang Gong, Jiuming Li, Xue Wang, Chaoqun Li, Surui Yao, Yuan Yin, Shenglin Huang, Bojian Fei, Zhaohui Huang
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Publicado: BMC 2021
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CRC
Acceso en línea:https://doaj.org/article/1e6f84728b4e4065a415298aff24a600
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spelling oai:doaj.org-article:1e6f84728b4e4065a415298aff24a6002021-11-21T12:13:20ZSNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop10.1186/s13046-021-02162-81756-9966https://doaj.org/article/1e6f84728b4e4065a415298aff24a6002021-11-01T00:00:00Zhttps://doi.org/10.1186/s13046-021-02162-8https://doaj.org/toc/1756-9966Abstract Background Small nucleolar RNA host gene (SNHG) long noncoding RNAs (lncRNAs) are frequently dysregulated in human cancers and involved in tumorigenesis and progression. SNHG17 has been reported as a candidate oncogene in several cancer types, however, its regulatory role in colorectal cancer (CRC) is unclear. Methods SNHG17 expression in multiple CRC cohorts was assessed by RT-qPCR or bioinformatic analyses. Cell viability was evaluated using Cell Counting Kit-8 (CCK-8) and colony formation assays. Cell mobility and invasiveness were assessed by Transwell assays. Tumor xenograft and metastasis models were applied to confirm the effects of SNHG17 on CRC tumorigenesis and metastasis in vivo. Immunohistochemistry staining was used to measure protein expression in cancer tissues. RNA pull-down, RNA immunoprecipitation, chromatin immunoprecipitation, and dual luciferase assays were used to investigate the molecular mechanism of SNHG17 in CRC. Results Using multiple cohorts, we confirmed that SNHG17 is aberrantly upregulated in CRC and correlated with poor survival. In vitro and in vivo functional assays indicated that SNHG17 facilitates CRC proliferation and metastasis. SNHG17 impedes PES1 degradation by inhibiting Trim23-mediated ubiquitination of PES1. SNHG17 upregulates FOSL2 by sponging miR-339-5p, and FOSL2 transcription activates SNHG17 expression, uncovering a SNHG17-miR-339-5p-FOSL2-SNHG17 positive feedback loop. Conclusions We identified SNHG17 as an oncogenic lncRNA in CRC and identified abnormal upregulation of SNHG17 as a prognostic risk factor for CRC. Our mechanistic investigations demonstrated, for the first time, that SNHG17 promotes tumor growth and metastasis through two different regulatory mechanisms, SNHG17-Trim23-PES1 axis and SNHG17-miR-339-5p-FOSL2-SNHG17 positive feedback loop, which may be exploited for CRC therapy.Zehua BianMingyue ZhouKaisa CuiFan YangYulin CaoShengbai SunBingxin LiuLiang GongJiuming LiXue WangChaoqun LiSurui YaoYuan YinShenglin HuangBojian FeiZhaohui HuangBMCarticleCRClncRNASNHG17PES1FOSL2miR-339-5pNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENJournal of Experimental & Clinical Cancer Research, Vol 40, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic CRC
lncRNA
SNHG17
PES1
FOSL2
miR-339-5p
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle CRC
lncRNA
SNHG17
PES1
FOSL2
miR-339-5p
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Zehua Bian
Mingyue Zhou
Kaisa Cui
Fan Yang
Yulin Cao
Shengbai Sun
Bingxin Liu
Liang Gong
Jiuming Li
Xue Wang
Chaoqun Li
Surui Yao
Yuan Yin
Shenglin Huang
Bojian Fei
Zhaohui Huang
SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
description Abstract Background Small nucleolar RNA host gene (SNHG) long noncoding RNAs (lncRNAs) are frequently dysregulated in human cancers and involved in tumorigenesis and progression. SNHG17 has been reported as a candidate oncogene in several cancer types, however, its regulatory role in colorectal cancer (CRC) is unclear. Methods SNHG17 expression in multiple CRC cohorts was assessed by RT-qPCR or bioinformatic analyses. Cell viability was evaluated using Cell Counting Kit-8 (CCK-8) and colony formation assays. Cell mobility and invasiveness were assessed by Transwell assays. Tumor xenograft and metastasis models were applied to confirm the effects of SNHG17 on CRC tumorigenesis and metastasis in vivo. Immunohistochemistry staining was used to measure protein expression in cancer tissues. RNA pull-down, RNA immunoprecipitation, chromatin immunoprecipitation, and dual luciferase assays were used to investigate the molecular mechanism of SNHG17 in CRC. Results Using multiple cohorts, we confirmed that SNHG17 is aberrantly upregulated in CRC and correlated with poor survival. In vitro and in vivo functional assays indicated that SNHG17 facilitates CRC proliferation and metastasis. SNHG17 impedes PES1 degradation by inhibiting Trim23-mediated ubiquitination of PES1. SNHG17 upregulates FOSL2 by sponging miR-339-5p, and FOSL2 transcription activates SNHG17 expression, uncovering a SNHG17-miR-339-5p-FOSL2-SNHG17 positive feedback loop. Conclusions We identified SNHG17 as an oncogenic lncRNA in CRC and identified abnormal upregulation of SNHG17 as a prognostic risk factor for CRC. Our mechanistic investigations demonstrated, for the first time, that SNHG17 promotes tumor growth and metastasis through two different regulatory mechanisms, SNHG17-Trim23-PES1 axis and SNHG17-miR-339-5p-FOSL2-SNHG17 positive feedback loop, which may be exploited for CRC therapy.
format article
author Zehua Bian
Mingyue Zhou
Kaisa Cui
Fan Yang
Yulin Cao
Shengbai Sun
Bingxin Liu
Liang Gong
Jiuming Li
Xue Wang
Chaoqun Li
Surui Yao
Yuan Yin
Shenglin Huang
Bojian Fei
Zhaohui Huang
author_facet Zehua Bian
Mingyue Zhou
Kaisa Cui
Fan Yang
Yulin Cao
Shengbai Sun
Bingxin Liu
Liang Gong
Jiuming Li
Xue Wang
Chaoqun Li
Surui Yao
Yuan Yin
Shenglin Huang
Bojian Fei
Zhaohui Huang
author_sort Zehua Bian
title SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
title_short SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
title_full SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
title_fullStr SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
title_full_unstemmed SNHG17 promotes colorectal tumorigenesis and metastasis via regulating Trim23-PES1 axis and miR-339-5p-FOSL2-SNHG17 positive feedback loop
title_sort snhg17 promotes colorectal tumorigenesis and metastasis via regulating trim23-pes1 axis and mir-339-5p-fosl2-snhg17 positive feedback loop
publisher BMC
publishDate 2021
url https://doaj.org/article/1e6f84728b4e4065a415298aff24a600
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