Phenotype IMMUNE_SYSTEME_MODULATION
IMMUNE_SYSTEME_MODULATION@default
References
PMID:19956757
Cancer associated fibroblasts promote tumor growth and metastasis by modulating the tumor immune microenvironment in a 4T1 murine breast cancer model
PMID:21051638
Depletion of FAP-expressing cells, which made up only 2% of all tumor cells in established Lewis lung carcinomas, caused rapid hypoxic necrosis of both cancer and stromal cells in immunogenic tumors by a process involving interferon-?? and tumor necrosis factor-??. Depleting FAP-expressing cells in a subcutaneous model of pancreatic ductal adenocarcinoma also permitted immunological control of growth. Therefore, FAP-expressing cells are a nonredundant, immune-suppressive component of the tumor microenvironment.
Modifications:
In compartment: default
- IMMUNE_SYSTEME_MODULATION@default
Participates in complexes:
Participates in reactions:
As Reactant or Product:- IL32@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- CLCF1@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- PGE2@default
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IMMUNE_SYSTEME_MODULATION@default
- IDO1@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- CYTOKINE_CHEMOKINE_PRODUCTION@default
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IMMUNE_SYSTEME_MODULATION@default
- PDL1*@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- PDL2*@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- MHC_class_II*@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- B7H3*@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- NT5E@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- OX40L*@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
- S100A4@Cytosol
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IMMUNE_SYSTEME_MODULATION@default
As Catalyser: