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Soft Tissue Sarcoma Cancer Stem Cells: An Overview.

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Date
2018-01
Authors
Genadry, Katia C
Pietrobono, Silvia
Rota, Rossella
Linardic, Corinne M
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Abstract
Soft tissue sarcomas (STSs) are an uncommon group of solid tumors that can arise throughout the human lifespan. Despite their commonality as non-bony cancers that develop from mesenchymal cell precursors, they are heterogeneous in their genetic profiles, histology, and clinical features. This has made it difficult to identify a single target or therapy specific to STSs. And while there is no one cell of origin ascribed to all STSs, the cancer stem cell (CSC) principle-that a subpopulation of tumor cells possesses stem cell-like properties underlying tumor initiation, therapeutic resistance, disease recurrence, and metastasis-predicts that ultimately it should be possible to identify a feature common to all STSs that could function as a therapeutic Achilles' heel. Here we review the published evidence for CSCs in each of the most common STSs, then focus on the methods used to study CSCs, the developmental signaling pathways usurped by CSCs, and the epigenetic alterations critical for CSC identity that may be useful for further study of STS biology. We conclude with discussion of some challenges to the field and future directions.
Type
Journal article
Subject
cancer stem cells
developmental pathways
epigenetic plasticity
sarcoma
soft tissue sarcoma
stemness
Permalink
https://hdl.handle.net/10161/17677
Published Version (Please cite this version)
10.3389/fonc.2018.00475
Publication Info
Genadry, Katia C; Pietrobono, Silvia; Rota, Rossella; & Linardic, Corinne M (2018). Soft Tissue Sarcoma Cancer Stem Cells: An Overview. Frontiers in Oncology, 8. pp. 475. 10.3389/fonc.2018.00475. Retrieved from https://hdl.handle.net/10161/17677.
This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.
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Scholars@Duke

Linardic

Corinne Mary Linardic

Associate Professor of Pediatrics
Pediatric Sarcomas: Sarcomas are among the most difficult-to-treat cancers in pediatric oncology, with metastatic forms having the highest mortality. We have established genetically defined human cell-based models and genetically engineered murine models for the pediatric skeletal muscle cancer known as rhabdomyosarcoma. Using these models, we can study the causative role of certain genetic changes (e.g. chromosomal translocations and oncogenic RAS) in rhabdomyosarcoma formation
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