Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 남진우 | - |
dc.date.accessioned | 2019-03-15T02:12:42Z | - |
dc.date.available | 2019-03-15T02:12:42Z | - |
dc.date.issued | 2016-11 | - |
dc.identifier.citation | SCIENTIFIC REPORTS, v. 6, Article number 37767 | en_US |
dc.identifier.issn | 2045-2322 | - |
dc.identifier.uri | https://www.nature.com/articles/srep37767 | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/100836 | - |
dc.description.abstract | Intratumor heterogeneity (ITH) is observed at different stages of tumor progression, metastasis and reouccurence, which can be important for clinical applications. We used RNA-sequencing data from tumor samples, and measured the level of ITH in terms of biological network states. To model complex relationships among genes, we used a protein interaction network to consider gene-gene dependency. ITH was measured by using an entropy-based distance metric between two networks, nJSD, with Jensen-Shannon Divergence (JSD). With nJSD, we defined transcriptome-based ITH (tITH). The effectiveness of tITH was extensively tested for the issues related with ITH using real biological data sets. Human cancer cell line data and single-cell sequencing data were investigated to verify our approach. Then, we analyzed TCGA pan-cancer 6,320 patients. Our result was in agreement with widely used genome-based ITH inference methods, while showed better performance at survival analysis. Analysis of mouse clonal evolution data further confirmed that our transcriptome-based ITH was consistent with genetic heterogeneity at different clonal evolution stages. Additionally, we found that cell cycle related pathways have significant contribution to increasing heterogeneity on the network during clonal evolution. We believe that the proposed transcriptome-based ITH is useful to characterize heterogeneity of a tumor sample at RNA level. | en_US |
dc.description.sponsorship | This research was supported by Collaborative Genome Program for Fostering New Post-Genome industry through the National Research Foundation of Korea funded by the Ministry of Science ICT and Future Planning (NRF-2014M3C9A3063541), the Bio & Medical Technology Development Program of the National Research Foundation funded by the Ministry of Science, ICT & Future Planning (NRF-2012M3A9D1054622) and Next-Generation Information Computing Development Program through the National Research Foundation of Korea funded by the Ministry of Science, ICT & Future Planning (NRF-2012M3C4A7033341). | en_US |
dc.language.iso | en | en_US |
dc.publisher | NATURE PUBLISHING GROUP | en_US |
dc.subject | CANCER EVOLUTION | en_US |
dc.subject | TUMOR-GROWTH | en_US |
dc.subject | GENETIC-HETEROGENEITY | en_US |
dc.subject | COLORECTAL-CANCER | en_US |
dc.subject | CLONAL EVOLUTION | en_US |
dc.subject | CELL-POPULATIONS | en_US |
dc.subject | INFERENCE | en_US |
dc.subject | DISEASE | en_US |
dc.subject | TUMORIGENESIS | en_US |
dc.subject | CHEMOTHERAPY | en_US |
dc.title | Measuring intratumor heterogeneity by network entropy using RNA-seq data | en_US |
dc.type | Article | en_US |
dc.relation.volume | 6 | - |
dc.identifier.doi | 10.1038/srep37767 | - |
dc.relation.page | 1-10 | - |
dc.relation.journal | SCIENTIFIC REPORTS | - |
dc.contributor.googleauthor | Park, Youngjune | - |
dc.contributor.googleauthor | Lim, Sangsoo | - |
dc.contributor.googleauthor | Nam, JIn-Wu | - |
dc.contributor.googleauthor | Kim, Sun | - |
dc.relation.code | 2016012537 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF NATURAL SCIENCES[S] | - |
dc.sector.department | DEPARTMENT OF LIFE SCIENCE | - |
dc.identifier.pid | jwnam | - |
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