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Status |
Public on Jun 24, 2022 |
Title |
Tissue-resident CXCR4+ macrophage as a poor prognosis signature promotes pancreatic ductal adenocarcinoma progression |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
In this study, we explored the CXCR4+ macrophages subset on its prognosis value, immune profile and distinct function in pancreatic cancer progression. RNA-seq analysis is performed to find the distinct characters of mouse tumor-derived Cxcr4+ macrophages.
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Overall design |
RNA-seq analysis is performed to find the distinct characters of mouse tumor-derived Cxcr4+ macrophages (three Cxcr4+ macrophage samples and three Cxcr4- macrophage samples).
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Contributor(s) |
Liao Z, Ye L, Li T |
Citation missing |
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Submission date |
Jun 21, 2022 |
Last update date |
Jun 24, 2022 |
Contact name |
Zhenyu Liao |
E-mail(s) |
liaozhenyu@fudanpci.org
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Organization name |
Fudan University Shanghai Cancer Centre
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Street address |
No.270 Dongan Road
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City |
Shanghai |
ZIP/Postal code |
200040 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA851389 |