SpatialCells: Automated Profiling of Tumor Microenvironments with Spatially Resolved Multiplexed Single-Cell Data.

Bioinformatics Immune infiltration Multiplexed imaging Region-based profiling Single-cell data Spatial analysis Tumor microenvironment

Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
14 Nov 2023
Historique:
pubmed: 28 11 2023
medline: 28 11 2023
entrez: 28 11 2023
Statut: epublish

Résumé

Cancer is a complex cellular ecosystem where malignant cells coexist and interact with immune, stromal, and other cells within the tumor microenvironment. Recent technological advancements in spatially resolved multiplexed imaging at single-cell resolution have led to the generation of large-scale and high-dimensional datasets from biological specimens. This underscores the necessity for automated methodologies that can effectively characterize the molecular, cellular, and spatial properties of tumor microenvironments for various malignancies. This study introduces SpatialCells, an open-source software package designed for region-based exploratory analysis and comprehensive characterization of tumor microenvironments using multiplexed single-cell data. SpatialCells efficiently streamlines the automated extraction of features from multiplexed single-cell data and can process samples containing millions of cells. Thus, SpatialCells facilitates subsequent association analyses and machine learning predictions, making it an essential tool in advancing our understanding of tumor growth, invasion, and metastasis.

Sections du résumé

Background UNASSIGNED
Cancer is a complex cellular ecosystem where malignant cells coexist and interact with immune, stromal, and other cells within the tumor microenvironment. Recent technological advancements in spatially resolved multiplexed imaging at single-cell resolution have led to the generation of large-scale and high-dimensional datasets from biological specimens. This underscores the necessity for automated methodologies that can effectively characterize the molecular, cellular, and spatial properties of tumor microenvironments for various malignancies.
Results UNASSIGNED
This study introduces SpatialCells, an open-source software package designed for region-based exploratory analysis and comprehensive characterization of tumor microenvironments using multiplexed single-cell data.
Conclusions UNASSIGNED
SpatialCells efficiently streamlines the automated extraction of features from multiplexed single-cell data and can process samples containing millions of cells. Thus, SpatialCells facilitates subsequent association analyses and machine learning predictions, making it an essential tool in advancing our understanding of tumor growth, invasion, and metastasis.

Identifiants

pubmed: 38014067
doi: 10.1101/2023.11.10.566378
pmc: PMC10680639
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAMS NIH HHS
ID : K23 AR080791
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM142879
Pays : United States

Auteurs

Guihong Wan (G)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.

Zoltan Maliga (Z)

Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.

Boshen Yan (B)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.

Tuulia Vallius (T)

Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.
Ludwig Center for Cancer Research at Harvard, Harvard Medical School, Boston, MA.

Yingxiao Shi (Y)

Department of Medicine, Dana-Farber Cancer Institute, Boston, MA, USA.

Sara Khattab (S)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Crystal Chang (C)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Ajit J Nirmal (AJ)

Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.
Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Kun-Hsing Yu (KH)

Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

David Liu (D)

Department of Medicine, Dana-Farber Cancer Institute, Boston, MA, USA.

Christine G Lian (CG)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Mia S DeSimone (MS)

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Peter K Sorger (PK)

Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.

Yevgeniy R Semenov (YR)

Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Laboratory of Systems Pharmacology, Program in Therapeutic Science, Harvard Medical School, Boston, MA.

Classifications MeSH