TY - JOUR
T1 - Mapping the Single-Cell Differentiation Landscape of Osteosarcoma
AU - Truong, Danh D.
AU - Weistuch, Corey
AU - Murgas, Kevin A.
AU - Admane, Prasad
AU - King, Bridgette L.
AU - Lee, Jes Chauviere
AU - Lamhamedi-Cherradi, Salah E.
AU - Swaminathan, Jyothishmathi
AU - Daw, Najat C.
AU - Gordon, Nancy
AU - Gopalakrishnan, Vidya
AU - Gorlick, Richard G.
AU - Somaiah, Neeta
AU - Deasy, Joseph O.
AU - Mikos, Antonios G.
AU - Tannenbaum, Allen
AU - Ludwig, Joseph
N1 - Publisher Copyright:
© 2024 American Association for Cancer Research.
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Purpose: The genetic intratumoral heterogeneity observed in human osteosarcomas poses challenges for drug development and the study of cell fate, plasticity, and differentiation, which are processes linked to tumor grade, cell metastasis, and survival. Experimental Design: To pinpoint errors in osteosarcoma differentiation, we transcriptionally profiled 31,527 cells from a tissue-engineered model that directs mesenchymal stem cells toward adipogenic and osteoblastic fates. Incorporating preexisting chondrocyte data, we applied trajectory analysis and non-negative matrix factorization to generate the first human mesenchymal differentiation atlas. Results: This “roadmap” served as a reference to delineate the cellular composition of morphologically complex osteosarcoma tumors and quantify each cell’s lineage commitment. Projecting a bulk RNA-sequencing osteosarcoma dataset onto this roadmap unveiled a correlation between a stem-like transcriptomic phenotype and poorer survival outcomes. Conclusions: Our study quantifies osteosarcoma differentiation and lineage, a prerequisite to better understanding lineage-specific differentiation bottlenecks that might someday be targeted therapeutically.
AB - Purpose: The genetic intratumoral heterogeneity observed in human osteosarcomas poses challenges for drug development and the study of cell fate, plasticity, and differentiation, which are processes linked to tumor grade, cell metastasis, and survival. Experimental Design: To pinpoint errors in osteosarcoma differentiation, we transcriptionally profiled 31,527 cells from a tissue-engineered model that directs mesenchymal stem cells toward adipogenic and osteoblastic fates. Incorporating preexisting chondrocyte data, we applied trajectory analysis and non-negative matrix factorization to generate the first human mesenchymal differentiation atlas. Results: This “roadmap” served as a reference to delineate the cellular composition of morphologically complex osteosarcoma tumors and quantify each cell’s lineage commitment. Projecting a bulk RNA-sequencing osteosarcoma dataset onto this roadmap unveiled a correlation between a stem-like transcriptomic phenotype and poorer survival outcomes. Conclusions: Our study quantifies osteosarcoma differentiation and lineage, a prerequisite to better understanding lineage-specific differentiation bottlenecks that might someday be targeted therapeutically.
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U2 - 10.1158/1078-0432.CCR-24-0563
DO - 10.1158/1078-0432.CCR-24-0563
M3 - Article
C2 - 38775859
AN - SCOPUS:85200424024
SN - 1078-0432
VL - 30
SP - 3259
EP - 3272
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 15
ER -