Characterizing dedifferentiation of thyroid cancer by integrated analysis
Author
Luo, H.Xia, X.
Kim, G.D.
Liu, Y.
Xue, Z.
Zhang, L.
Shu, Y.
Yang, T.
Chen, Y.
Zhang, S.
Chen, H.
Zhang, W.
Li, R.
Tang, H.
Dong, B.
Fu, X.
Cheng, W.
Zhang, W.
Yang, L.
Peng, Y.
Dai, L.
Hu, H.
Jiang, Y.
Gong, C.
Hu, Y.
Zhu, J.
Li, Z.
Caulin, C.
Wei, T.
Park, J.
Xu, H.
Affiliation
Department of Otolaryngology—Head and Neck Surgery, University of Arizona Cancer Center, University of ArizonaIssue Date
2021
Metadata
Show full item recordCitation
Luo, H., Xia, X., Kim, G. D., Liu, Y., Xue, Z., Zhang, L., Shu, Y., Yang, T., Chen, Y., Zhang, S., Chen, H., Zhang, W., Li, R., Tang, H., Dong, B., Fu, X., Cheng, W., Zhang, W., Yang, L., … Xu, H. (2021). Characterizing dedifferentiation of thyroid cancer by integrated analysis. Science Advances, 7(31).Journal
Science AdvancesRights
Copyright © 2021 The Authors, some rights reserved. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Understanding of dedifferentiation, an indicator of poo prognosis for patients with thyroid cancer, has been hampered by imprecise and incomplete characterization of its heterogeneity and its attributes. Using single-cell RNA sequencing, we explored the landscape of thyroid cancer at single-cell resolution with 46,205 cells and delineated its dedifferentiation process and suppressive immune microenvironment. The developmental trajectory indicated that anaplastic thyroid cancer (ATC) cells were derived from a small subset of papillary thyroid cancer (PTC) cells. Moreover, a potential functional role of CREB3L1 on ATC development was revealed by integrated analyses of copy number alteration and transcriptional regulatory network. Multiple genes in differentiation-related pathways (e.g., EMT) were involved as the downstream targets of CREB3L1, increased expression of which can thus predict higher relapse risk of PTC. Collectively, our study provided insights into the heterogeneity and molecular evolution of thyroid cancer and highlighted the potential driver role of CREB3L1 in its dedifferentiation process. Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).Note
Open access journalISSN
2375-2548Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1126/sciadv.abf3657
Scopus Count
Collections
Except where otherwise noted, this item's license is described as Copyright © 2021 The Authors, some rights reserved. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).