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Atlas of clinically distinct cell states and ecosystems across human solid tumors
Author(s) -
Bogdan Luca,
Chloé B. Steen,
Magdalena Matusiak,
Armon Azizi,
Sushama Varma,
Chunfang Zhu,
Joanna Przybył,
Almudena Espín-Pérez,
Maximilian Diehn,
Ash A. Alizadeh,
Matt van de Rijn,
Andrew J. Gentles,
Aaron M. Newman
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2021.09.014
Subject(s) - biology , multicellular organism , stromal cell , cell , cell type , single cell analysis , computational biology , gene expression profiling , cancer , evolutionary biology , neuroscience , genetics , gene , cancer research , gene expression
Determining how cells vary with their local signaling environment and organize into distinct cellular communities is critical for understanding processes as diverse as development, aging, and cancer. Here we introduce EcoTyper, a machine learning framework for large-scale identification and validation of cell states and multicellular communities from bulk, single-cell, and spatially resolved gene expression data. When applied to 12 major cell lineages across 16 types of human carcinoma, EcoTyper identified 69 transcriptionally defined cell states. Most states were specific to neoplastic tissue, ubiquitous across tumor types, and significantly prognostic. By analyzing cell-state co-occurrence patterns, we discovered ten clinically distinct multicellular communities with unexpectedly strong conservation, including three with myeloid and stromal elements linked to adverse survival, one enriched in normal tissue, and two associated with early cancer development. This study elucidates fundamental units of cellular organization in human carcinoma and provides a framework for large-scale profiling of cellular ecosystems in any tissue.

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