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Targeting LRRC25 enhances antitumor immunity of tumor-associated macrophages through CD8+ T cells [scRNA-seq]

GSE264446 Mus musculus Expression profiling by high throughput sequencing 4 samples Submitted 2025/01/01 Platform GPL24247
Summary
Leucine-rich repeat containing 25 (LRRC25), a type I membrane protein, is specifically expressed in myeloid cells. The anti-inflammatory function of LRRC25 has been established in multiple sterile and pathogenic models, however, its role in cancer remains largely unexplored. In this study, we demonstrated that LRRC25 is highly expressed in tumor-associated macrophages (TAMs) across human and mouse tumors. Lrrc25 deficiency in mice suppressed various tumor types by reprogramming TAMs toward an antitumoral phenotype and enhancing CD8+ T cell activation. Lrrc25 deficiency facilitated the reprogramming of TAMs through activation of the Nox2-ROS-Nlrp3-Il1β signaling pathway. Additionally, our findings confirmed the host safety of Lrrc25 deficiency. Overall, our results elucidate the role of LRRC25 in orchestrating TAMs and suggest that LRRC25 could serve as an effective and safe immunotherapy target for cancer treatment.
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Direct links to NCBI, no account and no request form: the whole study as GSE264446_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 4 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1102424 and SRA study SRP502935. Searching any of these in the dataset finder brings you back here.

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