The impact of multi-omics in medicine

Cracking the code of cancer through spatial multi-omics Recent advances in spatial multi-omics and molecular imaging technologies have transformed our ability to study cancer.These platforms, combined with advanced bioinformatics, offer exceptional capabilities for profiling cancer cells and the tumor microenvironment (TME).Among their many potential applications, they show a unique advantage in investigating the spatial organization of various cell types in tissue environments and dissecting their complex interactions with neighboring cells.A cell's phenotype and function can be significantly shaped by interactions with its neighbors.The organization and interactions of cells in the TME are not random but intricately orchestrated in ways we don't yet fully understand.Studies have identified recurrent spatial organization patterns of cells that form distinct cellular neighborhoods within the TME, creating microenvironments with unique properties that influence the fates, phenotypic states, and functions of resident cells.For instance, tumor-infiltrating T cells or cancer-associated fibroblasts across different neighborhoods within the same tumor may display markedly distinct organizational and transcriptomic features and cell interactions.Future advancements in single-cell spatial platforms with greater gene coverage or whole-transcriptome capabilities will enable more comprehensive analyses of cancer cells and the TME.These advancements could decode cell interactions and link cell spatial organization patterns and communication circuits to their phenotypic and functional properties.With advanced machine-learning approaches, we may predict a cell's fate, phenotype, function, and response to a treatment based on these spatial features and interactions.Such advancements may facilitate the translation of spatial profiling discoveries into clinically informative insights and therapeutic strategies.

Authors

Publication Details

Journal
Cell Reports Medicine
Published
2024-09-01
DOI
https://doi.org/10.1016/j.xcrm.2024.101742
Citations
5
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
1.17
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article

The impact of multi-omics in medicine

Suvi Linna-Kuosmanen, Oscar Harari, Linghua Wang, Justin A. Boddey et al.
5 citations
Cell Reports Medicine
Bioinformatics and Genomic Networks
1.17
article

The impact of multi-omics in medicine

Suvi Linna-Kuosmanen, Oscar Harari, Linghua Wang, Justin A. Boddey, Jing Qu, Zhang Wang
article en
5 citations

Abstract

Cracking the code of cancer through spatial multi-omics Recent advances in spatial multi-omics and molecular imaging technologies have transformed our ability to study cancer.These platforms, combined with advanced bioinformatics, offer exceptional capabilities for profiling cancer cells and the tumor microenvironment (TME).Among their many potential applications, they show a unique advantage in investigating the spatial organization of various cell types in tissue environments and dissecting their complex interactions with neighboring cells.A cell's phenotype and function can be significantly shaped by interactions with its neighbors.The organization and interactions of cells in the TME are not random but intricately orchestrated in ways we don't yet fully understand.Studies have identified recurrent spatial organization patterns of cells that form distinct cellular neighborhoods within the TME, creating microenvironments with unique properties that influence the fates, phenotypic states, and functions of resident cells.For instance, tumor-infiltrating T cells or cancer-associated fibroblasts across different neighborhoods within the same tumor may display markedly distinct organizational and transcriptomic features and cell interactions.Future advancements in single-cell spatial platforms with greater gene coverage or whole-transcriptome capabilities will enable more comprehensive analyses of cancer cells and the TME.These advancements could decode cell interactions and link cell spatial organization patterns and communication circuits to their phenotypic and functional properties.With advanced machine-learning approaches, we may predict a cell's fate, phenotype, function, and response to a treatment based on these spatial features and interactions.Such advancements may facilitate the translation of spatial profiling discoveries into clinically informative insights and therapeutic strategies.

Cell Reports MedicineVol. 5(9)
Openalex Percentile: Top 22%
Bioinformatics and Genomic Networks
1.17
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