Tumor to normal single cell mRNA comparisons reveal a pan-neuroblastoma cancer cell

Author:

Kildisiute Gerda,Kholosy Waleed M.,Young Matthew D.,Roberts Kenny,Elmentaite Rasa,van Hooff Sander R.,Khabirova Eleonora,Piapi Alice,Thevanesan Christine,Blanco Eva Bugallo,Burke Christina,Mamanova Lira,Lijnzaad Philip,Margaritis Thanasis,Holstege Frank C.P.,Tas Michelle L.,Wijnen Marc H.W.A.,van Noesel Max M.,del Valle Ignacio,Barone Giuseppe,van der Linden Reinier,Duncan Catriona,Anderson John,Achermann John C.,Haniffa Muzlifah,Teichmann Sarah A.,Rampling Dyanne,Sebire Neil J.,He Xiaoling,de Krijger Ronald R.,Barker Roger A.,Meyer Kerstin B.ORCID,Bayraktar Omer,Straathof Karin,Molenaar Jan J.,Behjati Sam

Abstract

AbstractNeuroblastoma is an embryonal childhood cancer that arises from aberrant development of the neural crest, mostly within the fetal adrenal medulla. It is not established what developmental processes neuroblastoma cancer cells represent. Here, we sought to reveal the phenotype of neuroblastoma cancer cells by comparing cancer (n=16,591) with fetal adrenal single cell transcriptomes (n=57,972). Our principal finding was that the neuroblastoma cancer cell resembled fetal sympathoblasts, but no other fetal adrenal cell type. The sympathoblastic state was a universal feature of neuroblastoma cells, transcending cell cluster diversity, individual patients and clinical phenotypes. We substantiated our findings in 652 neuroblastoma bulk transcriptomes and by integrating canonical features of the neuroblastoma genome with transcriptional signals. Overall, our observations indicate that there exists a pan-neuroblastoma cancer cell state which may be an attractive target for novel therapeutic avenues.

Publisher

Cold Spring Harbor Laboratory

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