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Status |
Public on Jun 04, 2024 |
Title |
Tumor cell intrinsic type I interferon signaling dictates CD47-SIRPα blockade immunotherapy via metabolic reprograming [dataset 1] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Innate immune checkpoint has emerging as a highly potential target for cancer immunotherapy in recent years. The CD47-SIRPα axis is the best-studied innate checkpoint in cancer. However, the transcription profile of tumor cell duiring CD47-SIRPα blockade therapy remains unclear.
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Overall design |
C57BL/6 mice (n=3 per group) transplanted s.c. with 5×10E5 MC38 cells were treated i.t. with 50 μg CV-1 or hIgG every three days. Two days after the third treatment, CD45- cells were sorted for the generation of RNA-seq libraries.
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Contributor(s) |
Zhou H, Wang W, Ding J, Zhu M |
Citation(s) |
38982116 |
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Submission date |
Jun 16, 2023 |
Last update date |
Aug 08, 2024 |
Contact name |
Mingzhao Zhu |
E-mail(s) |
zhumz@ibp.ac.cn
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Phone |
8610-64888775
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Organization name |
Institute of Biophysics, Chinese Academy of Sciences
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Department |
Key Laboratory of Infection and Immunity
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Street address |
15 Da Tun Rd, Chaoyang District
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City |
Beijing |
ZIP/Postal code |
100101 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (5)
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This SubSeries is part of SuperSeries: |
GSE235113 |
Tumor cell intrinsic type I interferon signaling dictates CD47-SIRPα blockade immunotherapy via metabolic reprograming. |
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Relations |
BioProject |
PRJNA984610 |