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Systematic characterization of cancer transcriptome at transcript resolution
Transcribed RNAs undergo various regulation and modification to become functional transcripts. Notably, cancer transcriptome has not been fully characterized at transcript resolution. Herein, we carry out a reference-based transcript assembly across >1000 cancer cell lines. We identify 498,255 tr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649690/ https://www.ncbi.nlm.nih.gov/pubmed/36357395 http://dx.doi.org/10.1038/s41467-022-34568-z |
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author | Hu, Wei Wu, Yangjun Shi, Qili Wu, Jingni Kong, Deping Wu, Xiaohua He, Xianghuo Liu, Teng Li, Shengli |
author_facet | Hu, Wei Wu, Yangjun Shi, Qili Wu, Jingni Kong, Deping Wu, Xiaohua He, Xianghuo Liu, Teng Li, Shengli |
author_sort | Hu, Wei |
collection | PubMed |
description | Transcribed RNAs undergo various regulation and modification to become functional transcripts. Notably, cancer transcriptome has not been fully characterized at transcript resolution. Herein, we carry out a reference-based transcript assembly across >1000 cancer cell lines. We identify 498,255 transcripts, approximately half of which are unannotated. Unannotated transcripts are closely associated with cancer-related hallmarks and show clinical significance. We build a high-confidence RNA binding protein (RBP)-transcript regulatory network, wherein most RBPs tend to regulate transcripts involved in cell proliferation. We identify numerous transcripts that are highly associated with anti-cancer drug sensitivity. Furthermore, we establish RBP-transcript-drug axes, wherein PTBP1 is experimentally validated to affect the sensitivity to decitabine by regulating KIAA1522-a6 transcript. Finally, we establish a user-friendly data portal to serve as a valuable resource for understanding cancer transcriptome diversity and its potential clinical utility at transcript level. Our study substantially extends cancer RNA repository and will facilitate anti-cancer drug discovery. |
format | Online Article Text |
id | pubmed-9649690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96496902022-11-15 Systematic characterization of cancer transcriptome at transcript resolution Hu, Wei Wu, Yangjun Shi, Qili Wu, Jingni Kong, Deping Wu, Xiaohua He, Xianghuo Liu, Teng Li, Shengli Nat Commun Article Transcribed RNAs undergo various regulation and modification to become functional transcripts. Notably, cancer transcriptome has not been fully characterized at transcript resolution. Herein, we carry out a reference-based transcript assembly across >1000 cancer cell lines. We identify 498,255 transcripts, approximately half of which are unannotated. Unannotated transcripts are closely associated with cancer-related hallmarks and show clinical significance. We build a high-confidence RNA binding protein (RBP)-transcript regulatory network, wherein most RBPs tend to regulate transcripts involved in cell proliferation. We identify numerous transcripts that are highly associated with anti-cancer drug sensitivity. Furthermore, we establish RBP-transcript-drug axes, wherein PTBP1 is experimentally validated to affect the sensitivity to decitabine by regulating KIAA1522-a6 transcript. Finally, we establish a user-friendly data portal to serve as a valuable resource for understanding cancer transcriptome diversity and its potential clinical utility at transcript level. Our study substantially extends cancer RNA repository and will facilitate anti-cancer drug discovery. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9649690/ /pubmed/36357395 http://dx.doi.org/10.1038/s41467-022-34568-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hu, Wei Wu, Yangjun Shi, Qili Wu, Jingni Kong, Deping Wu, Xiaohua He, Xianghuo Liu, Teng Li, Shengli Systematic characterization of cancer transcriptome at transcript resolution |
title | Systematic characterization of cancer transcriptome at transcript resolution |
title_full | Systematic characterization of cancer transcriptome at transcript resolution |
title_fullStr | Systematic characterization of cancer transcriptome at transcript resolution |
title_full_unstemmed | Systematic characterization of cancer transcriptome at transcript resolution |
title_short | Systematic characterization of cancer transcriptome at transcript resolution |
title_sort | systematic characterization of cancer transcriptome at transcript resolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649690/ https://www.ncbi.nlm.nih.gov/pubmed/36357395 http://dx.doi.org/10.1038/s41467-022-34568-z |
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