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Status |
Public on Sep 06, 2022 |
Title |
Single-Cell Sequencing Reveals the Overall Changes in Tumor Microenvironment Mediated by CD39i |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Here we identified the ecto-enzyme, CD39 (encoded by ENTPD1), as a potential therapeutic target for BC via single-cell transcriptome analysis of BC and para-cancer tissues. In a subcutaneous model, inhibition of CD39 (CD39i) is able to limit the growth of BC and improve overall survival of tumor-bearing mice. Via single-cell sequencing of tumor infiltrated immune cells, we found that CD39i with POM-1 increased the intratumor NK cells, conventional type 1 dendritic cells (cDC1) and CD8+ T cells, along with decreased Treg abundance. The anti-tumor effect and reprogram of tumor microenvironment are blockade in a cDC1-deficient Batf3−/− model.
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Overall design |
Comparing changes in TME caused by CD39i.
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Contributor(s) |
Liu L, Hou Y |
Citation(s) |
36347860 |
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Submission date |
Nov 18, 2021 |
Last update date |
Nov 29, 2022 |
Contact name |
Junyi Hu |
Organization name |
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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Department |
Urology
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Street address |
No. 1277 Liberation Avenue
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City |
Wu Han |
ZIP/Postal code |
430022 |
Country |
China |
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Platforms (1) |
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Samples (6)
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Relations |
BioProject |
PRJNA781604 |
SRA |
SRP346770 |