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LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations

Gene regulatory network perturbations contribute to the development and progression of cancer, however, molecular determinants that mediate transcriptional perturbations remain a fundamental challenge for cancer biology. We show that transcriptional perturbations are widely mediated by long noncodin...

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Autores principales: Li, Yongsheng, Li, Lili, Wang, Zishan, Pan, Tao, Sahni, Nidhi, Jin, Xiyun, Wang, Guangjuan, Li, Junyi, Zheng, Xiangyi, Zhang, Yunpeng, Xu, Juan, Yi, Song, Li, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815097/
https://www.ncbi.nlm.nih.gov/pubmed/29325141
http://dx.doi.org/10.1093/nar/gkx1311
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author Li, Yongsheng
Li, Lili
Wang, Zishan
Pan, Tao
Sahni, Nidhi
Jin, Xiyun
Wang, Guangjuan
Li, Junyi
Zheng, Xiangyi
Zhang, Yunpeng
Xu, Juan
Yi, Song
Li, Xia
author_facet Li, Yongsheng
Li, Lili
Wang, Zishan
Pan, Tao
Sahni, Nidhi
Jin, Xiyun
Wang, Guangjuan
Li, Junyi
Zheng, Xiangyi
Zhang, Yunpeng
Xu, Juan
Yi, Song
Li, Xia
author_sort Li, Yongsheng
collection PubMed
description Gene regulatory network perturbations contribute to the development and progression of cancer, however, molecular determinants that mediate transcriptional perturbations remain a fundamental challenge for cancer biology. We show that transcriptional perturbations are widely mediated by long noncoding RNAs (lncRNAs) via integration of genome-wide transcriptional regulation with paired lncRNA and gene expression profiles. Systematic construction of an LncRNA Modulator Atlas in Pan-cancer (LncMAP) reveals distinct types of lncRNA regulatory molecules, which are expressed in multiple tissues, exhibit higher conservation. Strikingly, cancers with similar tissue origin share lncRNA modulators which perturb the regulation of cell cycle and immune response-related functions. Furthermore, we identified a large number of pan-cancer lncRNA modulators with potential clinical significance, which are differentially expressed in cancer or are strongly correlated with drug sensitivity across cell lines. Further stratification of cancer patients based on lncRNA-mediated transcriptional perturbations identifies subtypes with distinct survival rates. Finally, we made a user-friendly web interface available for exploring lncRNA-mediated transcriptional perturbations across cancer types. Our study provides a systems-level dissection of lncRNA-mediated regulatory perturbations in cancer, and also presents a valuable tool and resource for investigating the function of lncRNAs in cancer.
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spelling pubmed-58150972018-02-23 LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations Li, Yongsheng Li, Lili Wang, Zishan Pan, Tao Sahni, Nidhi Jin, Xiyun Wang, Guangjuan Li, Junyi Zheng, Xiangyi Zhang, Yunpeng Xu, Juan Yi, Song Li, Xia Nucleic Acids Res Data Resources and Analyses Gene regulatory network perturbations contribute to the development and progression of cancer, however, molecular determinants that mediate transcriptional perturbations remain a fundamental challenge for cancer biology. We show that transcriptional perturbations are widely mediated by long noncoding RNAs (lncRNAs) via integration of genome-wide transcriptional regulation with paired lncRNA and gene expression profiles. Systematic construction of an LncRNA Modulator Atlas in Pan-cancer (LncMAP) reveals distinct types of lncRNA regulatory molecules, which are expressed in multiple tissues, exhibit higher conservation. Strikingly, cancers with similar tissue origin share lncRNA modulators which perturb the regulation of cell cycle and immune response-related functions. Furthermore, we identified a large number of pan-cancer lncRNA modulators with potential clinical significance, which are differentially expressed in cancer or are strongly correlated with drug sensitivity across cell lines. Further stratification of cancer patients based on lncRNA-mediated transcriptional perturbations identifies subtypes with distinct survival rates. Finally, we made a user-friendly web interface available for exploring lncRNA-mediated transcriptional perturbations across cancer types. Our study provides a systems-level dissection of lncRNA-mediated regulatory perturbations in cancer, and also presents a valuable tool and resource for investigating the function of lncRNAs in cancer. Oxford University Press 2018-02-16 2018-01-09 /pmc/articles/PMC5815097/ /pubmed/29325141 http://dx.doi.org/10.1093/nar/gkx1311 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Data Resources and Analyses
Li, Yongsheng
Li, Lili
Wang, Zishan
Pan, Tao
Sahni, Nidhi
Jin, Xiyun
Wang, Guangjuan
Li, Junyi
Zheng, Xiangyi
Zhang, Yunpeng
Xu, Juan
Yi, Song
Li, Xia
LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title_full LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title_fullStr LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title_full_unstemmed LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title_short LncMAP: Pan-cancer atlas of long noncoding RNA-mediated transcriptional network perturbations
title_sort lncmap: pan-cancer atlas of long noncoding rna-mediated transcriptional network perturbations
topic Data Resources and Analyses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815097/
https://www.ncbi.nlm.nih.gov/pubmed/29325141
http://dx.doi.org/10.1093/nar/gkx1311
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