author_facet Sun, Longci
Xue, Hanbing
Jiang, Chunhui
Zhou, Hong
Gu, Lei
Liu, Ye
Xu, Chunjie
Xu, Qing
Sun, Longci
Xue, Hanbing
Jiang, Chunhui
Zhou, Hong
Gu, Lei
Liu, Ye
Xu, Chunjie
Xu, Qing
author Sun, Longci
Xue, Hanbing
Jiang, Chunhui
Zhou, Hong
Gu, Lei
Liu, Ye
Xu, Chunjie
Xu, Qing
spellingShingle Sun, Longci
Xue, Hanbing
Jiang, Chunhui
Zhou, Hong
Gu, Lei
Liu, Ye
Xu, Chunjie
Xu, Qing
Bioscience Reports
LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
Cell Biology
Molecular Biology
Biochemistry
Biophysics
author_sort sun, longci
spelling Sun, Longci Xue, Hanbing Jiang, Chunhui Zhou, Hong Gu, Lei Liu, Ye Xu, Chunjie Xu, Qing 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20160048 <jats:p>Accumulating evidence demonstrates that long non-coding RNAs (LncRNAs) play important roles in regulating gene expression and are involved in various cancers, including colorectal cancer (CRC). However, LncRNA profiles in CRC remain largely unknown. The present study aims to find the key LncRNA associated with CRC and to study its biological functions in CRC progression. We focused on LncRNA DQ786243, one of LncRNAs which promoted development of CRC from the Gene Expression Omnibus (GEO) and validated using quantitative real-time PCR among about 20 paired CRC tissues. The effects of LncRNA DQ786243 were assessed by silencing the LncRNA in vitro and in vivo. Results showed that the expression level LncRNA DQ786243 was significantly higher in CRC tissues and cell lines. We also found LncRNA DQ786243 knockdown by RNA interference with siRNA significantly arrested the cell cycle in the G2/M-phase, promoted apoptosis and weaken the abilities of cell proliferation and invasion in vitro. Further investigation into the mechanisms responsible for the growth inhibitory effects by DQ786243 silencing revealed that its knockdown resulted in the induction of cell cycle arrest and apoptosis through certain cell cycle-related and apoptosis-related proteins. Finally, xenograft experiments confirmed that the growth of xenograft tumours formed by CRC cells was suppressed after silencing LncRNA DQ786243 expression. In conclusion, the present study suggests that LncRNA DQ786243 is an oncogene that promotes tumour progression and leads us to propose that LncRNAs may serve as key regulatory hubs in CRC progression.</jats:p> LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both <i>in vitro</i> and <i>in vivo</i> Bioscience Reports
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title LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_unstemmed LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_full LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_fullStr LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_full_unstemmed LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_short LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_sort lncrna dq786243 contributes to proliferation and metastasis of colorectal cancer both <i>in vitro</i> and <i>in vivo</i>
topic Cell Biology
Molecular Biology
Biochemistry
Biophysics
url http://dx.doi.org/10.1042/bsr20160048
publishDate 2016
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description <jats:p>Accumulating evidence demonstrates that long non-coding RNAs (LncRNAs) play important roles in regulating gene expression and are involved in various cancers, including colorectal cancer (CRC). However, LncRNA profiles in CRC remain largely unknown. The present study aims to find the key LncRNA associated with CRC and to study its biological functions in CRC progression. We focused on LncRNA DQ786243, one of LncRNAs which promoted development of CRC from the Gene Expression Omnibus (GEO) and validated using quantitative real-time PCR among about 20 paired CRC tissues. The effects of LncRNA DQ786243 were assessed by silencing the LncRNA in vitro and in vivo. Results showed that the expression level LncRNA DQ786243 was significantly higher in CRC tissues and cell lines. We also found LncRNA DQ786243 knockdown by RNA interference with siRNA significantly arrested the cell cycle in the G2/M-phase, promoted apoptosis and weaken the abilities of cell proliferation and invasion in vitro. Further investigation into the mechanisms responsible for the growth inhibitory effects by DQ786243 silencing revealed that its knockdown resulted in the induction of cell cycle arrest and apoptosis through certain cell cycle-related and apoptosis-related proteins. Finally, xenograft experiments confirmed that the growth of xenograft tumours formed by CRC cells was suppressed after silencing LncRNA DQ786243 expression. In conclusion, the present study suggests that LncRNA DQ786243 is an oncogene that promotes tumour progression and leads us to propose that LncRNAs may serve as key regulatory hubs in CRC progression.</jats:p>
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author Sun, Longci, Xue, Hanbing, Jiang, Chunhui, Zhou, Hong, Gu, Lei, Liu, Ye, Xu, Chunjie, Xu, Qing
author_facet Sun, Longci, Xue, Hanbing, Jiang, Chunhui, Zhou, Hong, Gu, Lei, Liu, Ye, Xu, Chunjie, Xu, Qing, Sun, Longci, Xue, Hanbing, Jiang, Chunhui, Zhou, Hong, Gu, Lei, Liu, Ye, Xu, Chunjie, Xu, Qing
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description <jats:p>Accumulating evidence demonstrates that long non-coding RNAs (LncRNAs) play important roles in regulating gene expression and are involved in various cancers, including colorectal cancer (CRC). However, LncRNA profiles in CRC remain largely unknown. The present study aims to find the key LncRNA associated with CRC and to study its biological functions in CRC progression. We focused on LncRNA DQ786243, one of LncRNAs which promoted development of CRC from the Gene Expression Omnibus (GEO) and validated using quantitative real-time PCR among about 20 paired CRC tissues. The effects of LncRNA DQ786243 were assessed by silencing the LncRNA in vitro and in vivo. Results showed that the expression level LncRNA DQ786243 was significantly higher in CRC tissues and cell lines. We also found LncRNA DQ786243 knockdown by RNA interference with siRNA significantly arrested the cell cycle in the G2/M-phase, promoted apoptosis and weaken the abilities of cell proliferation and invasion in vitro. Further investigation into the mechanisms responsible for the growth inhibitory effects by DQ786243 silencing revealed that its knockdown resulted in the induction of cell cycle arrest and apoptosis through certain cell cycle-related and apoptosis-related proteins. Finally, xenograft experiments confirmed that the growth of xenograft tumours formed by CRC cells was suppressed after silencing LncRNA DQ786243 expression. In conclusion, the present study suggests that LncRNA DQ786243 is an oncogene that promotes tumour progression and leads us to propose that LncRNAs may serve as key regulatory hubs in CRC progression.</jats:p>
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spelling Sun, Longci Xue, Hanbing Jiang, Chunhui Zhou, Hong Gu, Lei Liu, Ye Xu, Chunjie Xu, Qing 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20160048 <jats:p>Accumulating evidence demonstrates that long non-coding RNAs (LncRNAs) play important roles in regulating gene expression and are involved in various cancers, including colorectal cancer (CRC). However, LncRNA profiles in CRC remain largely unknown. The present study aims to find the key LncRNA associated with CRC and to study its biological functions in CRC progression. We focused on LncRNA DQ786243, one of LncRNAs which promoted development of CRC from the Gene Expression Omnibus (GEO) and validated using quantitative real-time PCR among about 20 paired CRC tissues. The effects of LncRNA DQ786243 were assessed by silencing the LncRNA in vitro and in vivo. Results showed that the expression level LncRNA DQ786243 was significantly higher in CRC tissues and cell lines. We also found LncRNA DQ786243 knockdown by RNA interference with siRNA significantly arrested the cell cycle in the G2/M-phase, promoted apoptosis and weaken the abilities of cell proliferation and invasion in vitro. Further investigation into the mechanisms responsible for the growth inhibitory effects by DQ786243 silencing revealed that its knockdown resulted in the induction of cell cycle arrest and apoptosis through certain cell cycle-related and apoptosis-related proteins. Finally, xenograft experiments confirmed that the growth of xenograft tumours formed by CRC cells was suppressed after silencing LncRNA DQ786243 expression. In conclusion, the present study suggests that LncRNA DQ786243 is an oncogene that promotes tumour progression and leads us to propose that LncRNAs may serve as key regulatory hubs in CRC progression.</jats:p> LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both <i>in vitro</i> and <i>in vivo</i> Bioscience Reports
spellingShingle Sun, Longci, Xue, Hanbing, Jiang, Chunhui, Zhou, Hong, Gu, Lei, Liu, Ye, Xu, Chunjie, Xu, Qing, Bioscience Reports, LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo, Cell Biology, Molecular Biology, Biochemistry, Biophysics
title LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_full LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_fullStr LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_full_unstemmed LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_short LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
title_sort lncrna dq786243 contributes to proliferation and metastasis of colorectal cancer both <i>in vitro</i> and <i>in vivo</i>
title_unstemmed LncRNA DQ786243 contributes to proliferation and metastasis of colorectal cancer both in vitro and in vivo
topic Cell Biology, Molecular Biology, Biochemistry, Biophysics
url http://dx.doi.org/10.1042/bsr20160048