| Source: |
| Type: |
| FoxP3+ refers to cells that express the FoxP3 protein. Immune Suppression: FOXP3+ Tregs are known for their ability to suppress immune responses. In the context of cancer, they can inhibit the activity of effector T cells and other immune cells, allowing tumors to evade immune detection. Tumor Microenvironment: The presence of FOXP3+ Tregs in the tumor microenvironment is often associated with an immunosuppressive environment, which can facilitate tumor growth and metastasis. FOXP3+ Tregs in Specific Cancers Breast Cancer: Expression: FOXP3+ Tregs are present in the tumor microenvironment. Prognosis: High levels of FOXP3+ Tregs are often linked to better prognosis, indicating a potential anti-tumor immune response. Lung Cancer: Expression: FOXP3+ Tregs are found in the tumor microenvironment. Prognosis: Increased FOXP3+ Tregs can correlate with poor prognosis, suggesting immune evasion. So expression is high, but prognosis can vary. |
| 560- | ART/DHA, | Dihydroartemisinin shift the immune response towards Th1, inhibit the tumor growth in vitro and in vivo |
| - | in-vivo, | NA, | NA |
| 562- | ART/DHA, | Artesunate exerts an anti-immunosuppressive effect on cervical cancer by inhibiting PGE2 production and Foxp3 expression |
| - | in-vivo, | NA, | HeLa |
| 561- | ART/DHA, | Antitumor and immunomodulatory properties of artemether and its ability to reduce CD4+ CD25+ FoxP3+ T reg cells in vivo |
| - | in-vivo, | NA, | NA |
| 451- | CUR, | The effect of Curcumin on multi-level immune checkpoint blockade and T cell dysfunction in head and neck cancer |
| - | vitro+vivo, | HNSCC, | SCC15 | - | vitro+vivo, | HNSCC, | SNU1076 | - | vitro+vivo, | HNSCC, | SNU1041 |
Query results interpretion may depend on "conditions" listed in the research papers. Such Conditions may include : -low or high Dose -format for product, such as nano of lipid formations -different cell line effects -synergies with other products -if effect was for normal or cancerous cells
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