Atlas of clinically distinct cell states and ecosystems across human solid tumors.
|
IF: 66.850
|
Cited by: 77
|

Abstract

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.

Keywords

Spatial Omics
Seurat
Spatial Transcriptomics
LCM-seq
Spatial Gene Expression
CIBERSORTx
EcoTyper
cancer genomics
cell states
cellular communities
ecosystems
ecotypes
expression deconvolution
tumor immunology
tumor microenvironment

MeSH terms

Cell Survival
Gene Expression Regulation, Neoplastic
Humans
Immunotherapy
Inflammation
Ligands
Neoplasms
Phenotype
Prognosis
Transcription, Genetic
Tumor Microenvironment

Authors

Luca, Bogdan A
Steen, Chloé B
Matusiak, Magdalena
Azizi, Armon
Varma, Sushama
Zhu, Chunfang
Przybyl, Joanna
Espín-Pérez, Almudena
Diehn, Maximilian
Alizadeh, Ash A
van de Rijn, Matt
Gentles, Andrew J
Newman, Aaron M

Recommend literature





Similar data