Pediatric Tumors as Disorders of Development: The Case for In Vitro Modeling Based on Human Stem Cells

Author:

Clairmont Cullen D.12ORCID,Gell Joanna J.1234,Lau Ching C.1234

Affiliation:

1. University of Connecticut School of Medicine, Farmington, CT, USA

2. The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA

3. Connecticut Children’s Medical Center, Center for Cancer and Blood Disorders, Hartford, CT, USA

4. Division of Pediatric Hematology-Oncology, Department of Pediatrics, UConn Health, Farmington, CT, USA

Abstract

Despite improvements in patient outcomes, pediatric cancer remains a leading cause of non-accidental death in children. Recent genetic analysis of patients with pediatric cancers indicates an important role for both germline genetic predisposition and cancer-specific somatic driver mutations. Increasingly, evidence demonstrates that the developmental timepoint at which the cancer cell-of-origin transforms is critical to tumor identity and therapeutic response. Therefore, future therapeutic development would be bolstered by the use of disease models that faithfully recapitulate the genetic context, cell-of-origin, and developmental window of vulnerability in pediatric cancers. Human stem cells have the potential to incorporate all of these characteristics into a pediatric cancer model, while serving as a platform for rapid genetic and pharmacological testing. In this review, we describe how human stem cells have been used to model pediatric cancers and how these models compare to other pediatric cancer model modalities.

Funder

CCMC Martin J Gavin Endowment

West Family Trust

CureSearch for Childrens Cancer

JAX Director Innovation Fund

National Human Genome Research Institute

Congressionally Directed Medical Research Program

Publisher

SAGE Publications

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