Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma

American Association for the Advancement of Science (AAAS) - Tập 344 Số 6190 - Trang 1396-1401 - 2014
Anoop P. Patel1,2,3,4, Itay Tirosh1, John J. Trombetta1, Alex K. Shalek1, Shawn Gillespie1,3,4, Hiroaki Wakimoto2, Daniel P. Cahill2, Brian V. Nahed2, William T. Curry2, Robert L. Martuza2, David N. Louis3, Orit Rozenblatt‐Rosen1, Mario L. Suvà1,3, Aviv Regev1,5,4, B Bernstein1,3,4
1Broad Institute of Harvard and Massachusetts Institute of Techonology (MIT), Cambridge, MA 02142, USA.
2Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
3Department of Pathology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA
4Howard Hughes Medical Institute, Chevy Chase, MD 20815 USA
5Department of Biology, MIT, Cambridge, MA 02139, USA

Tóm tắt

Cancer at single-cell resolution Single-cell sequencing can illuminate the genetic properties of brain cancers and reveal heterogeneity within a tumor. Patel et al. examined the genome sequence of single cells isolated from brain glioblastomas. The findings revealed shared chromosomal changes but also extensive transcription variation, including genes related to signaling, which represent potential therapeutic targets. The authors suggest that the variation in tumor cells reflects neural development and that such variation among cancer cells may prove to have clinical significance. Science , this issue p. 1396

Từ khóa


Tài liệu tham khảo

10.1038/nature09515

10.1038/nm.2415

10.1126/science.1164382

10.1038/nature09807

10.1056/NEJMoa1113205

10.1038/nature11344

10.1126/science.1224676

10.1038/nature12627

10.1056/NEJMoa043330

10.1073/pnas.1219747110

10.1126/science.1142946

10.1126/science.1241328

10.1056/NEJMoa1308573

10.1038/nature12624

10.1038/nature03128

10.1038/nature11287

10.1016/j.ccr.2009.03.018

10.1038/nature05236

10.1016/j.ccr.2013.08.001

10.1016/j.cell.2013.09.034

10.1016/j.ccr.2009.12.020

10.1038/nbt.2282

10.1038/nature12172

10.1038/ng.2653

10.1016/j.cell.2011.01.004

10.1016/j.ccr.2006.03.030

10.1093/neuonc/nor195

10.1146/annurev-pathol-011110-130324

10.1016/j.ccr.2011.11.005

10.1073/pnas.1219817110

10.1593/neo.101744

10.1038/srep04223

10.1016/j.celrep.2014.02.014

10.1126/science.1155998

10.1002/jso.10180

10.1016/j.cell.2010.04.020

10.1038/nature09557

10.1038/nature09624

10.1073/pnas.1016030108

10.1101/gad.216804.113

10.1016/j.cell.2014.02.030

10.1016/j.ccr.2010.03.017

10.1186/gb-2009-10-3-r25

10.1186/1471-2105-12-323

10.1523/JNEUROSCI.4178-07.2008

10.1038/nn.3599

10.1152/physiolgenomics.00186.2002