Tracing and Targeting the Origins of Childhood Cancer

Author:

Coorens Tim H.H.12,Behjati Sam134

Affiliation:

1. Wellcome Sanger Institute, Hinxton, United Kingdom;

2. Current affiliation: Broad Instituted of MIT and Harvard, Cambridge, Massachusetts, USA;

3. Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom

4. Department of Paediatrics, University of Cambridge, Cambridge, United Kingdom

Abstract

Despite the success of treating childhood cancers with cytotoxic agents, novel therapeutic strategies are required to achieve the next leap in cure rates. A promising avenue may be to target the origin of childhood cancers. Here, we review recent advances in tracing the origins of pediatric tumors. Cancer-to-normal cell comparisons by single-cell mRNA sequencing reveal the fetal state of cancer cells, as well as their cell of origin. Recent phylogenetic analyses have uncovered large tissue-resident precursor clones to childhood cancers, which already possess key genomic alterations leading to tumor formation. Both the transcriptional fetalness and genomic status of the premalignant tissue bed provide further avenues for targeted therapy. Overall, these advances begin to describe the precise origins of pediatric tumors and pave the way for novel methods in detecting, treating, and perhaps even preventing childhood cancers. Expected final online publication date for the Annual Review of Cancer Biology, Volume 6 is April 2022. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

Publisher

Annual Reviews

Subject

Cancer Research,Cell Biology,Oncology

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