Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer

Abstract Background Long non-coding RNAs (lncRNAs) play a functional role in the progression of prostate cancer (PCa). However, the molecular mechanism, expression, or function of the lncRNA XIST in PCa is not well understood. Therefore, the major goal of this study was to investigate the involvemen...

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Published in:BMC Cancer
Main Authors: Jie Wang, Jie Huang, Yingxue Guo, Yuli Fu, Yifang Cao, Kang Zhou, Jianxiong Ma, Bodong Lv, Wenjie Huang
Format: Article
Language:English
Published: BMC 2022-08-01
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Online Access:https://doi.org/10.1186/s12885-022-10007-6
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author Jie Wang
Jie Huang
Yingxue Guo
Yuli Fu
Yifang Cao
Kang Zhou
Jianxiong Ma
Bodong Lv
Wenjie Huang
author_facet Jie Wang
Jie Huang
Yingxue Guo
Yuli Fu
Yifang Cao
Kang Zhou
Jianxiong Ma
Bodong Lv
Wenjie Huang
author_sort Jie Wang
collection DOAJ
container_title BMC Cancer
description Abstract Background Long non-coding RNAs (lncRNAs) play a functional role in the progression of prostate cancer (PCa). However, the molecular mechanism, expression, or function of the lncRNA XIST in PCa is not well understood. Therefore, the major goal of this study was to investigate the involvement of XIST in PCa. Methods We used the The Cancer Genome Atlas (TCGA) database to conduct a pan-cancer bioinformatics analysis of XIST and identified that it may play an important role in prostate cancer. This finding was verified using clinical samples and in vitro assays. Finally, we constructed an XIST ceRNA network for prostate cancer. Results Our in vitro and in vivo results showed that the XIST gene expression level was higher in PCa derived cells and tissues compared to that in normal cells and tissues. XIST gene expression level was positively correlated with the invasion and proliferation of tumour cells. Furthermore, the downregulation of XIST inhibited the growth of subcutaneous 22Rv1 xenografts in nude mice. In addition, we constructed a XIST ceRNA network. Consistent with previous studies, we found that the role of XIST is mediated through via sponges, such as miRNA -96-5p, miRNA -153-3p, and miRNA-182-5p. Conclusion High expression level of XIST can lead to enhanced carcinogenicity in PCa. Therefore, XIST has the potential to be used as a prognostic marker and may become a new research focus for the treatment of PCa.
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spelling doaj-art-e04c8145c97d431692cdb682d12acd972025-08-19T20:52:34ZengBMCBMC Cancer1471-24072022-08-0122111110.1186/s12885-022-10007-6Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancerJie Wang0Jie Huang1Yingxue Guo2Yuli Fu3Yifang Cao4Kang Zhou5Jianxiong Ma6Bodong Lv7Wenjie Huang8The Second Clinical Medical College, Zhejiang Chinese Medical UniversityThe Second Clinical Medical College, Zhejiang Chinese Medical UniversityCollege of Pharmaceutical Sciences, Zhejiang Chinese Medical UniversityThe Second Clinical Medical College, Zhejiang Chinese Medical UniversityUrology Department, Jiaxing First Hospital, Affiliated Hospital of Jiaxing UniversityThe Second Clinical Medical College, Zhejiang Chinese Medical UniversityThe Second Clinical Medical College, Zhejiang Chinese Medical UniversityDepartment of Urology, School of Medicine, The Second Affiliated Hospital, Zhejia-Ng UniversityDepartment of Urology, School of Medicine, The Second Affiliated Hospital, Zhejia-Ng UniversityAbstract Background Long non-coding RNAs (lncRNAs) play a functional role in the progression of prostate cancer (PCa). However, the molecular mechanism, expression, or function of the lncRNA XIST in PCa is not well understood. Therefore, the major goal of this study was to investigate the involvement of XIST in PCa. Methods We used the The Cancer Genome Atlas (TCGA) database to conduct a pan-cancer bioinformatics analysis of XIST and identified that it may play an important role in prostate cancer. This finding was verified using clinical samples and in vitro assays. Finally, we constructed an XIST ceRNA network for prostate cancer. Results Our in vitro and in vivo results showed that the XIST gene expression level was higher in PCa derived cells and tissues compared to that in normal cells and tissues. XIST gene expression level was positively correlated with the invasion and proliferation of tumour cells. Furthermore, the downregulation of XIST inhibited the growth of subcutaneous 22Rv1 xenografts in nude mice. In addition, we constructed a XIST ceRNA network. Consistent with previous studies, we found that the role of XIST is mediated through via sponges, such as miRNA -96-5p, miRNA -153-3p, and miRNA-182-5p. Conclusion High expression level of XIST can lead to enhanced carcinogenicity in PCa. Therefore, XIST has the potential to be used as a prognostic marker and may become a new research focus for the treatment of PCa.https://doi.org/10.1186/s12885-022-10007-6Prostate cancerLncRNA-XISTceRNA networkProliferationMigration
spellingShingle Jie Wang
Jie Huang
Yingxue Guo
Yuli Fu
Yifang Cao
Kang Zhou
Jianxiong Ma
Bodong Lv
Wenjie Huang
Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
Prostate cancer
LncRNA-XIST
ceRNA network
Proliferation
Migration
title Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
title_full Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
title_fullStr Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
title_full_unstemmed Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
title_short Identification and functional analysis of LncRNA-XIST ceRNA network in prostate cancer
title_sort identification and functional analysis of lncrna xist cerna network in prostate cancer
topic Prostate cancer
LncRNA-XIST
ceRNA network
Proliferation
Migration
url https://doi.org/10.1186/s12885-022-10007-6
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