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

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Associated Data

PMID: 38956900

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