Faculty, Staff and Student Publications
Publication Date
9-1-2024
Journal
Advanced Science
Abstract
Although hypoxia is known to be associated with immune resistance, the adaptability to hypoxia by different cell populations in the tumor microenvironment and the underlying mechanisms remain elusive. This knowledge gap has hindered the development of therapeutic strategies to overcome tumor immune resistance induced by hypoxia. Here, bulk, single-cell, and spatial transcriptomics are integrated to characterize hypoxia associated with immune escape during carcinogenesis and reveal a hypoxia-based intercellular communication hub consisting of malignant cells, ALCAM
Keywords
Tumor Microenvironment, Immunotherapy, Macrophages, Mice, Animals, Humans, CD8-Positive T-Lymphocytes, Hypoxia-Inducible Factor 1, alpha Subunit, Hypoxia, Disease Models, Animal, Cell Line, Tumor, Neoplasms, ALCAM + macrophage, cancer immunotherapy, exhausted T cell, hypoxia, spatial transcriptomics
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Medical Sciences Commons, Oncology Commons
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Associated Data
PMID: 38956900