Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors

Matthew D. Young(Wellcome Sanger Institute), Thomas J. Mitchell(University of Cambridge), Felipe A. Vieira Braga(Wellcome Sanger Institute), Maxine Tran(The Royal Free Hospital), Benjamin J. Stewart(MRC Laboratory of Molecular Biology), John R. Ferdinand(MRC Laboratory of Molecular Biology), Grace Collord(University of Cambridge), Rachel A. Botting(Newcastle University), Dorin-Mirel Popescu(Newcastle University), Kevin W. Loudon(MRC Laboratory of Molecular Biology), Roser Vento‐Tormo(Wellcome Sanger Institute), Emily Stephenson(Newcastle University), Alex Cagan(Wellcome Sanger Institute), Sarah J. Farndon(Great Ormond Street Hospital), Martin Del Castillo Velasco‐Herrera(Wellcome Sanger Institute), Charlotte Guzzo(Wellcome Sanger Institute), Nathan Richoz(MRC Laboratory of Molecular Biology), Lira Mamanova(Wellcome Sanger Institute), Tevita Aho(Cambridge University Hospitals NHS Foundation Trust), James N. Armitage(University of Cambridge), Antony C. P. Riddick(University of Cambridge), Imran Mushtaq(Great Ormond Street Hospital for Children NHS Foundation Trust), Stephen Farrell(Cambridge University Hospitals NHS Foundation Trust), Dyanne Rampling(Great Ormond Street Hospital for Children NHS Foundation Trust), James C. Nicholson(University of Cambridge), Andrew Filby(Newcastle University), Johanna Burge(Cambridge University Hospitals NHS Foundation Trust), Steven Lisgo(Newcastle University), Patrick H. Maxwell(University of Cambridge), Susan Lindsay(Newcastle University), Anne Y. Warren(Cambridge University Hospitals NHS Foundation Trust), Grant D. Stewart(University of Cambridge), Neil J. Sebire(Great Ormond Street Hospital), Nicholas Coleman(University of Cambridge), Muzlifah Haniffa(Royal Victoria Infirmary), Sarah A. Teichmann(Wellcome Sanger Institute), Menna R. Clatworthy(MRC Laboratory of Molecular Biology), Sam Behjati(University of Cambridge)
Science
August 10, 2018
Cited by 819Open Access
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Abstract

Messenger RNA encodes cellular function and phenotype. In the context of human cancer, it defines the identities of malignant cells and the diversity of tumor tissue. We studied 72,501 single-cell transcriptomes of human renal tumors and normal tissue from fetal, pediatric, and adult kidneys. We matched childhood Wilms tumor with specific fetal cell types, thus providing evidence for the hypothesis that Wilms tumor cells are aberrant fetal cells. In adult renal cell carcinoma, we identified a canonical cancer transcriptome that matched a little-known subtype of proximal convoluted tubular cell. Analyses of the tumor composition defined cancer-associated normal cells and delineated a complex vascular endothelial growth factor (VEGF) signaling circuit. Our findings reveal the precise cellular identities and compositions of human kidney tumors.


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