作者
Matthew D. Young,Thomas J. Mitchell,Felipe A. Vieira Braga,Maxine Tran,Benjamin Stewart,John R. Ferdinand,Grace Collord,Rachel A. Botting,Dorin-Mirel Popescu,Kevin W. Loudon,Roser Vento‐Tormo,Emily Stephenson,Alex Cagan,Sarah J. Farndon,Martin Del Castillo Velasco‐Herrera,Charlotte Guzzo,Nathan Richoz,Lira Mamanova,Tevita Aho,James N. Armitage,Antony C.P. Riddick,Imran Mushtaq,Stephen Farrell,Dyanne Rampling,James C. Nicholson,Andrew Filby,Johanna Burge,Steven Lisgo,Patrick H. Maxwell,Susan Lindsay,Anne Y. Warren,Grant D. Stewart,Neil J. Sebire,Nicholas Coleman,Muzlifah Haniffa,Sarah A. Teichmann,Menna R. Clatworthy,Sam Behjati
摘要
Pediatric and adult kidney tumors differ Understanding tumor origins and the similarities and differences between organ-specific cancers is important for determining treatment options. Young et al. generated more than 72,000 single-cell transcriptomes from healthy and cancerous human kidneys. From these data, they determined that Wilms tumor, a pediatric kidney cancer, originates from aberrant fetal cells, whereas adult kidney cancers are likely derived from a specific subtype of proximal convoluted tubular cell. Science , this issue p. 594