dc.contributor.author | Lundberg, A | |
dc.contributor.author | Yi, JJJ | |
dc.contributor.author | Lindström, LS | |
dc.contributor.author | Tobin, NP | |
dc.coverage.spatial | England | |
dc.date.accessioned | 2024-01-12T13:56:27Z | |
dc.date.available | 2024-01-12T13:56:27Z | |
dc.date.issued | 2022-08-20 | |
dc.identifier | ARTN 59 | |
dc.identifier | 10.1038/s41698-022-00302-7 | |
dc.identifier.citation | npj Precision Oncology, 2022, 6 (1), pp. 59 - | en_US |
dc.identifier.issn | 2397-768X | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/6102 | |
dc.identifier.eissn | 2397-768X | |
dc.identifier.eissn | 2397-768X | |
dc.identifier.doi | 10.1038/s41698-022-00302-7 | |
dc.identifier.doi | 10.1038/s41698-022-00302-7 | |
dc.description.abstract | Genomic alterations resulting in loss of control over the cell cycle is a fundamental hallmark of human malignancies. Whilst pan-cancer studies have broadly assessed tumour genomics and their impact on oncogenic pathways, analyses taking the baseline signalling levels in normal tissue into account are lacking. To this end, we aimed to reclassify the cell cycle activity of tumours in terms of their tissue of origin and determine if any common DNA mutations, chromosome arm-level changes or signalling pathways contribute to an increase in baseline corrected cell cycle activity. Combining normal tissue and pan-cancer data from over 13,000 samples we demonstrate that tumours of gynaecological origin show the highest levels of corrected cell cycle activity, partially owing to hormonal signalling and gene expression changes. We also show that normal and tumour tissues can be separated into groups (quadrants) of low/high cell cycle activity and propose the hypothesis of an upper limit on these activity levels in tumours. | |
dc.format | Electronic | |
dc.format.extent | 59 - | |
dc.language | eng | |
dc.language.iso | eng | en_US |
dc.publisher | NATURE PORTFOLIO | en_US |
dc.relation.ispartof | npj Precision Oncology | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
dc.subject | Science & Technology | |
dc.subject | Life Sciences & Biomedicine | |
dc.subject | Oncology | |
dc.subject | CANCER | |
dc.subject | GENE | |
dc.subject | METASTASES | |
dc.subject | PLASTICITY | |
dc.title | Reclassifying tumour cell cycle activity in terms of its tissue of origin. | en_US |
dc.type | Journal Article | |
dcterms.dateAccepted | 2022-07-13 | |
dc.date.updated | 2024-01-11T12:07:09Z | |
rioxxterms.version | VoR | en_US |
rioxxterms.versionofrecord | 10.1038/s41698-022-00302-7 | en_US |
rioxxterms.licenseref.startdate | 2022-08-20 | |
rioxxterms.type | Journal Article/Review | en_US |
pubs.author-url | https://www.ncbi.nlm.nih.gov/pubmed/35987928 | |
pubs.issue | 1 | |
pubs.organisational-group | ICR | |
pubs.organisational-group | ICR/Primary Group | |
pubs.organisational-group | ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | ICR/Primary Group/ICR Divisions/Cancer Therapeutics | |
pubs.organisational-group | ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Cancer Biomarkers | |
pubs.organisational-group | ICR/Primary Group/ICR Divisions/Clinical Studies | |
pubs.organisational-group | ICR/Primary Group/ICR Divisions/Clinical Studies/Cancer Biomarkers | |
pubs.publication-status | Published online | |
pubs.publisher-url | http://dx.doi.org/10.1038/s41698-022-00302-7 | |
pubs.volume | 6 | |
icr.researchteam | Cancer Biomarkers | en_US |
dc.contributor.icrauthor | Lundberg, Arian | |
icr.provenance | Deposited by Dr Arian Lundberg on 2024-01-11. Deposit type is initial. No. of files: 1. Files: Reclassifying tumour cell cycle activity in terms of its tissue of origin.pdf | |