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Lnc00892 competes with c-Jun to block NCL transcription, reducing the stability of RhoA/RhoC mRNA and impairing bladder cancer invasion
by
Sun, Ning
, Zhang, Yuanmei
, Huang, Haishan
, Lin, Zhenni
, Chang, Yixin
, Xu, Jiheng
, Ren, Shuwei
, Jin, Honglei
, Shen, Liping
, Lu, Yongyong
, Zhang, Ning
in
13/1
/ 13/109
/ 38/70
/ 38/90
/ 631/67/589
/ 64/60
/ 692/53/2422
/ 82
/ 82/80
/ Analysis
/ Animals
/ Apoptosis
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Bladder cancer
/ c-Jun protein
/ Cancer
/ Care and treatment
/ Cell Biology
/ Cell Proliferation
/ Diagnosis
/ Female
/ Gene Expression Regulation, Neoplastic
/ Genetic transcription
/ Health aspects
/ Human Genetics
/ Humans
/ Internal Medicine
/ Invasiveness
/ Medicine
/ Medicine & Public Health
/ Messenger RNA
/ Metastases
/ Metastasis
/ Mice
/ Mice, Nude
/ mRNA stability
/ Neoplasm Invasiveness
/ Neoplasm Metastasis
/ Nucleolin
/ Observations
/ Oncology
/ Patients
/ Phosphoproteins - genetics
/ Phosphoproteins - metabolism
/ Proto-Oncogene Proteins c-jun - genetics
/ Proto-Oncogene Proteins c-jun - metabolism
/ rhoA GTP-Binding Protein - genetics
/ rhoA GTP-Binding Protein - metabolism
/ RhoA protein
/ rhoC GTP-Binding Protein - genetics
/ rhoC GTP-Binding Protein - metabolism
/ Risk factors
/ RNA, Long Noncoding - genetics
/ RNA, Long Noncoding - metabolism
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Transcription factors
/ Tumor Cells, Cultured
/ Urinary Bladder Neoplasms - genetics
/ Urinary Bladder Neoplasms - metabolism
/ Urinary Bladder Neoplasms - pathology
/ Xenograft Model Antitumor Assays
2021
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Lnc00892 competes with c-Jun to block NCL transcription, reducing the stability of RhoA/RhoC mRNA and impairing bladder cancer invasion
by
Sun, Ning
, Zhang, Yuanmei
, Huang, Haishan
, Lin, Zhenni
, Chang, Yixin
, Xu, Jiheng
, Ren, Shuwei
, Jin, Honglei
, Shen, Liping
, Lu, Yongyong
, Zhang, Ning
in
13/1
/ 13/109
/ 38/70
/ 38/90
/ 631/67/589
/ 64/60
/ 692/53/2422
/ 82
/ 82/80
/ Analysis
/ Animals
/ Apoptosis
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Bladder cancer
/ c-Jun protein
/ Cancer
/ Care and treatment
/ Cell Biology
/ Cell Proliferation
/ Diagnosis
/ Female
/ Gene Expression Regulation, Neoplastic
/ Genetic transcription
/ Health aspects
/ Human Genetics
/ Humans
/ Internal Medicine
/ Invasiveness
/ Medicine
/ Medicine & Public Health
/ Messenger RNA
/ Metastases
/ Metastasis
/ Mice
/ Mice, Nude
/ mRNA stability
/ Neoplasm Invasiveness
/ Neoplasm Metastasis
/ Nucleolin
/ Observations
/ Oncology
/ Patients
/ Phosphoproteins - genetics
/ Phosphoproteins - metabolism
/ Proto-Oncogene Proteins c-jun - genetics
/ Proto-Oncogene Proteins c-jun - metabolism
/ rhoA GTP-Binding Protein - genetics
/ rhoA GTP-Binding Protein - metabolism
/ RhoA protein
/ rhoC GTP-Binding Protein - genetics
/ rhoC GTP-Binding Protein - metabolism
/ Risk factors
/ RNA, Long Noncoding - genetics
/ RNA, Long Noncoding - metabolism
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Transcription factors
/ Tumor Cells, Cultured
/ Urinary Bladder Neoplasms - genetics
/ Urinary Bladder Neoplasms - metabolism
/ Urinary Bladder Neoplasms - pathology
/ Xenograft Model Antitumor Assays
2021
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Lnc00892 competes with c-Jun to block NCL transcription, reducing the stability of RhoA/RhoC mRNA and impairing bladder cancer invasion
by
Sun, Ning
, Zhang, Yuanmei
, Huang, Haishan
, Lin, Zhenni
, Chang, Yixin
, Xu, Jiheng
, Ren, Shuwei
, Jin, Honglei
, Shen, Liping
, Lu, Yongyong
, Zhang, Ning
in
13/1
/ 13/109
/ 38/70
/ 38/90
/ 631/67/589
/ 64/60
/ 692/53/2422
/ 82
/ 82/80
/ Analysis
/ Animals
/ Apoptosis
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Bladder cancer
/ c-Jun protein
/ Cancer
/ Care and treatment
/ Cell Biology
/ Cell Proliferation
/ Diagnosis
/ Female
/ Gene Expression Regulation, Neoplastic
/ Genetic transcription
/ Health aspects
/ Human Genetics
/ Humans
/ Internal Medicine
/ Invasiveness
/ Medicine
/ Medicine & Public Health
/ Messenger RNA
/ Metastases
/ Metastasis
/ Mice
/ Mice, Nude
/ mRNA stability
/ Neoplasm Invasiveness
/ Neoplasm Metastasis
/ Nucleolin
/ Observations
/ Oncology
/ Patients
/ Phosphoproteins - genetics
/ Phosphoproteins - metabolism
/ Proto-Oncogene Proteins c-jun - genetics
/ Proto-Oncogene Proteins c-jun - metabolism
/ rhoA GTP-Binding Protein - genetics
/ rhoA GTP-Binding Protein - metabolism
/ RhoA protein
/ rhoC GTP-Binding Protein - genetics
/ rhoC GTP-Binding Protein - metabolism
/ Risk factors
/ RNA, Long Noncoding - genetics
/ RNA, Long Noncoding - metabolism
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Transcription factors
/ Tumor Cells, Cultured
/ Urinary Bladder Neoplasms - genetics
/ Urinary Bladder Neoplasms - metabolism
/ Urinary Bladder Neoplasms - pathology
/ Xenograft Model Antitumor Assays
2021
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Lnc00892 competes with c-Jun to block NCL transcription, reducing the stability of RhoA/RhoC mRNA and impairing bladder cancer invasion
Journal Article
Lnc00892 competes with c-Jun to block NCL transcription, reducing the stability of RhoA/RhoC mRNA and impairing bladder cancer invasion
2021
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Overview
Metastasis of bladder cancer is a complex process and has been associated with poor clinical outcomes. However, the mechanisms of bladder cancer metastasis remain largely unknown. The present study found that the long noncoding RNA lnc00892 was significantly downregulated in bladder cancer tissues, with low lnc00892 expression associated with poor prognosis of bladder cancer patients. Lnc00892 significantly inhibited the migration, invasion, and metastasis of bladder cancer cells in vitro and in vivo. In-depth analysis showed that RhoA/C acted downstream of lnc00892 to inhibit bladder cancer metastasis. Mechanistically, lnc00892 reduces nucleolin gene transcription by competitively binding the promoter of nucleolin with c-Jun, thereby inhibiting nucleolin-mediated stabilization of RhoA/RhoC mRNA. Taken together, these findings provide novel insights into understanding the mechanisms of bladder cancer metastasis and suggest that lnc00892 can serve as a potential therapeutic target in patients with invasive bladder cancer.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 13/109
/ 38/70
/ 38/90
/ 64/60
/ 82
/ 82/80
/ Analysis
/ Animals
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Cancer
/ Female
/ Gene Expression Regulation, Neoplastic
/ Humans
/ Medicine
/ Mice
/ Oncology
/ Patients
/ Phosphoproteins - metabolism
/ Proto-Oncogene Proteins c-jun - genetics
/ Proto-Oncogene Proteins c-jun - metabolism
/ rhoA GTP-Binding Protein - genetics
/ rhoA GTP-Binding Protein - metabolism
/ rhoC GTP-Binding Protein - genetics
/ rhoC GTP-Binding Protein - metabolism
/ RNA, Long Noncoding - genetics
/ RNA, Long Noncoding - metabolism
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Urinary Bladder Neoplasms - genetics
/ Urinary Bladder Neoplasms - metabolism
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