Inferred developmental origins of brain tumors from single-cell RNA-sequencing data

被引:0
作者
Wang, Su [1 ]
Curry, Rachel Naomi [2 ,3 ]
McDonald, Malcolm F. [3 ,4 ,5 ]
Koh, Hyun Yong [6 ]
Erickson, Anders W. [7 ,8 ,9 ]
Kleinman, Claudia L. [10 ,11 ]
Taylor, Michael D. [12 ,13 ]
Rao, Ganesh [1 ,14 ]
Deneen, Benjamin [1 ,3 ,14 ]
Harmanci, Arif O. [15 ]
Harmanci, Akdes Serin [1 ,14 ]
机构
[1] Baylor Coll Med, Dept Neurosurg, 1250 Moursund St, Houston, TX 77030 USA
[2] Baylor Coll Med, Grad Sch Biomed Sci, Houston, TX USA
[3] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX USA
[4] Baylor Coll Med, Med Scientist Training Program, Houston, TX USA
[5] Baylor Coll Med, Program Dev Dis Models & Therapeut, Houston, TX USA
[6] Baylor Coll Med, Dept Pediat & Neurol, Houston, TX USA
[7] Hosp Sick Children, Arthur & Sonia Labatt Brain Tumor Res Ctr, Toronto, ON, Canada
[8] Hosp Sick Children, Dev & Stem Cell Biol Program, Toronto, ON, Canada
[9] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[10] Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ, Canada
[11] McGill Univ, Dept Human Genet, Montreal, PQ, Canada
[12] Texas Childerens Hosp, Texas Childrens Canc Ctr, Hematol Oncol Sect, Houston, TX USA
[13] Baylor Coll Med, Dept Pediat Hematol Oncol & Neurosurg, Houston, TX USA
[14] Baylor Coll Med, Ctr Canc Neurosci, Houston, TX USA
[15] Univ Texas Hlth Sci Ctr, McWilliams Sch Biomed Informat, 7000 Fannin St, Houston, TX 77030 USA
关键词
artificial neural network model; brain tumor; cell of origin; scRNA-Seq; UNIPOLAR BRUSH CELLS; RHOMBIC LIP; RADIAL GLIA; MEDULLOBLASTOMA; DIFFERENTIATION; HETEROGENEITY; CEREBELLUM; EXPRESSION; LANDSCAPE; PROGRAMS;
D O I
10.1093/noajnl/vdaf016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The reactivation of neurodevelopmental programs in cancer highlights parallel biological processes that occur in both normal development and brain tumors. Achieving a deeper understanding of how dysregulated developmental factors play a role in the progression of brain tumors is therefore crucial for identifying potential targets for therapeutic interventions. Single-cell RNA-sequencing (scRNA-Seq) provides an opportunity to understand how developmental programs are dysregulated and reinitiated in brain tumors at single-cell resolution. The aim of this study is to identify the developmental origins of brain tumors using scRNA-Seq data.Methods Here, we introduce COORS (Cell Of ORigin like CellS), a computational tool trained on developmental human brain single-cell datasets that annotates "developmental-like" cell states in brain tumors. COORS leverages cell type-specific multilayer perceptron models and incorporates a developmental cell type tree that reflects hierarchical relationships and models cell type probabilities.Results Applying COORS to various brain cancer datasets, including medulloblastoma (MB), glioma, and diffuse midline glioma (DMG), we identified developmental-like cells that represent putative cells of origin in these tumors. Our method provides both cell of origin classification and cell age regression, offering insights into the developmental cell types of tumor subgroups. COORS identified outer radial glia developmental cells within IDHWT glioma cells whereas oligodendrocyte precursor cells (OPCs) and neuronal-like cells in IDHMut. Interestingly, IDHMut subgroup cells that map to OPC show bimodal distributions that are both early and late weeks in development. Furthermore, COORS offers a valuable resource by providing novel markers linked to developmental states within MB, glioma, and DMG tumor subgroups.Conclusions Our work adds to our cumulative understanding of brain tumor heterogeneity and helps pave the way for tailored treatment strategies.
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页数:13
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