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fty720  (MedChemExpress)


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    Structured Review

    MedChemExpress fty720
    TRANS enhances tumoral T cell abundance and synergizes with immune checkpoint inhib itors. (A) UMAP visualization of lymphocytes in the TME following PBS or TRANS treatment. (B) UMAP visualization of lymphocyte clusters. (C) Proportional distribution of lymphocyte clusters. (D) Expression of cluster-specific marker genes. (E) Top 10 maker genes in CD8 + effector T cells (Teff). (F) Volcano plot of differentially expressed genes in CD8 + Teff between TRANS and PBS. (G) Dot plot showing upregulated pathways in IFN-γ + T cells (TRANS vs PBS), with dot size reflecting KEGG enrichment intensity. (H) Dot plot of ligand-receptor interactions between myeloid cells and T cells (TRANS vs PBS). Ligands (blue) and receptors (red) are labeled. (I) Experimental design of tumor therapy by TRANS combination with <t>FTY720.</t> (J) Tumor growth curve in mice treated with PBS, TRANS, and FTY720+TRANS; n = 5. (K – M) Tumor-infiltrating CD4 + and CD8 + T cells (K), Granzyme + CD8 + T or IFN-γ + CD8 + T cells counts (L), and Exhausted T cells (M) in TME; n = 5. (N) Scheme of tumor therapy by TRANS combined with immune checkpoint inhibitors (ICI). (O and P) Individual tumor changes (O) and Survival rate (Q) of tumor-bearing mice with different treatments; n = 5. (Q and R) Ex vivo IFN-γ expression (Q) and Quantification (R) in splenic CD8 + T cells with PMA/ionomycin stimulation; n = 3. (S) IFN-γ secretion by splenic T cells following αCD3/αCD28 stimulation; n = 3. Data are presented as mean ± SD, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. Significance was calculated using One-way ANOVA.
    Fty720, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 87 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fty720/Fingolimod+hydrochloride/pmc12996997-359-0-11
    Average 97 stars, based on 87 article reviews
    fty720 - by Bioz Stars, 2026-09
    97/100 stars

    Images

    1) Product Images from "Chronic inflammation-responsive hydrogel restores myeloid-T cell crosstalk to reinvigorate antitumor immunity against metastatic colorectal cancer"

    Article Title: Chronic inflammation-responsive hydrogel restores myeloid-T cell crosstalk to reinvigorate antitumor immunity against metastatic colorectal cancer

    Journal: Bioactive Materials

    doi: 10.1016/j.bioactmat.2026.03.012

    TRANS enhances tumoral T cell abundance and synergizes with immune checkpoint inhib itors. (A) UMAP visualization of lymphocytes in the TME following PBS or TRANS treatment. (B) UMAP visualization of lymphocyte clusters. (C) Proportional distribution of lymphocyte clusters. (D) Expression of cluster-specific marker genes. (E) Top 10 maker genes in CD8 + effector T cells (Teff). (F) Volcano plot of differentially expressed genes in CD8 + Teff between TRANS and PBS. (G) Dot plot showing upregulated pathways in IFN-γ + T cells (TRANS vs PBS), with dot size reflecting KEGG enrichment intensity. (H) Dot plot of ligand-receptor interactions between myeloid cells and T cells (TRANS vs PBS). Ligands (blue) and receptors (red) are labeled. (I) Experimental design of tumor therapy by TRANS combination with FTY720. (J) Tumor growth curve in mice treated with PBS, TRANS, and FTY720+TRANS; n = 5. (K – M) Tumor-infiltrating CD4 + and CD8 + T cells (K), Granzyme + CD8 + T or IFN-γ + CD8 + T cells counts (L), and Exhausted T cells (M) in TME; n = 5. (N) Scheme of tumor therapy by TRANS combined with immune checkpoint inhibitors (ICI). (O and P) Individual tumor changes (O) and Survival rate (Q) of tumor-bearing mice with different treatments; n = 5. (Q and R) Ex vivo IFN-γ expression (Q) and Quantification (R) in splenic CD8 + T cells with PMA/ionomycin stimulation; n = 3. (S) IFN-γ secretion by splenic T cells following αCD3/αCD28 stimulation; n = 3. Data are presented as mean ± SD, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. Significance was calculated using One-way ANOVA.
    Figure Legend Snippet: TRANS enhances tumoral T cell abundance and synergizes with immune checkpoint inhib itors. (A) UMAP visualization of lymphocytes in the TME following PBS or TRANS treatment. (B) UMAP visualization of lymphocyte clusters. (C) Proportional distribution of lymphocyte clusters. (D) Expression of cluster-specific marker genes. (E) Top 10 maker genes in CD8 + effector T cells (Teff). (F) Volcano plot of differentially expressed genes in CD8 + Teff between TRANS and PBS. (G) Dot plot showing upregulated pathways in IFN-γ + T cells (TRANS vs PBS), with dot size reflecting KEGG enrichment intensity. (H) Dot plot of ligand-receptor interactions between myeloid cells and T cells (TRANS vs PBS). Ligands (blue) and receptors (red) are labeled. (I) Experimental design of tumor therapy by TRANS combination with FTY720. (J) Tumor growth curve in mice treated with PBS, TRANS, and FTY720+TRANS; n = 5. (K – M) Tumor-infiltrating CD4 + and CD8 + T cells (K), Granzyme + CD8 + T or IFN-γ + CD8 + T cells counts (L), and Exhausted T cells (M) in TME; n = 5. (N) Scheme of tumor therapy by TRANS combined with immune checkpoint inhibitors (ICI). (O and P) Individual tumor changes (O) and Survival rate (Q) of tumor-bearing mice with different treatments; n = 5. (Q and R) Ex vivo IFN-γ expression (Q) and Quantification (R) in splenic CD8 + T cells with PMA/ionomycin stimulation; n = 3. (S) IFN-γ secretion by splenic T cells following αCD3/αCD28 stimulation; n = 3. Data are presented as mean ± SD, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. Significance was calculated using One-way ANOVA.

    Techniques Used: Inhibition, Expressing, Marker, Labeling, Ex Vivo

    Related Articles

    Injection:

    Article Title: Notch Signaling Exacerbates Pulmonary Fibrosis by Regulating the Differentiation of CD4 + Tissue-Resident Memory T Cells
    Article Snippet: .. To investigate the origin of lung T RM cells in PF, FTY720 (MCE, Monmouth Junction, NJ, USA, Cat#: HY-12005, 1 mg/kg) or vehicle was administered via intraperitoneal injection starting three days before BLM exposure and continued daily thereafter. ..

    Article Title: Notch Signaling Exacerbates Pulmonary Fibrosis by Regulating the Differentiation of CD4 + Tissue-Resident Memory T Cells.
    Article Snippet: .. A midline cervical incision was made to expose the trachea, followed by intratracheal injection of BLM (MCE, Monmouth Junction, NJ, USA, Cat#: HY-17565A, 2 mg/kg) or an equal volume of PBS as a control. https://doi.org/10.3390/biom16020328 To investigate the origin of lung TRM cells in PF, FTY720 (MCE, Monmouth Junction, NJ, USA, Cat#: HY-12005, 1 mg/kg) or vehicle was administered via intraperitoneal injection starting three days before BLM exposure and continued daily thereafter. ..

    Saline:

    Article Title: Liver-directed AAV-IL-10 therapy enhances CD8 + T cell-mediated immunity against hepatocellular carcinoma.
    Article Snippet: .. 7–9 weeks old male C57BL/6 mice were treated with intraperitoneal injections of FTY720 (Fingolimod; MCE, HY- 12005, 0.025 mg in 100 μL normal saline) beginning 1 day prior to Hep55.1c- OVA cell inoculation. ..

    Selection:

    Article Title: A genome-wide CRISPR/Cas9 screen reveals novel positive regulators of FTY720 sensitivity in acute lymphoblastic leukemia cells.
    Article Snippet: Jurkat cells stably expressing Cas9 (4 x 10 6 cells, Genecopoeia) were transduced with the GeCKOv2 lentivirus library (17,18) to achieve a total AR TIC LE IN PR ES S Fisher Scientific, Waltham, MA, catalog no. A1113803) was added 24 h post-transduction for 7 days. .. After puromycin selection, the cells were divided into two groups (4 x 10 6 cells/plate) and cultured in either the presence of FTY720 [8 μM] (MedChem Express, Monmouth Junction, NJ) or absence (DMSO [8 μM] vehicle control) for 48 h. Two rounds of 48-hour FTY720 or DMSO treatment were performed. .. After treatment, genomic DNA was extracted using the Blood and Cell Culture Midi Kit (Qiagen, Germantown, MD, catalog no. 13343).

    Cell Culture:

    Article Title: A genome-wide CRISPR/Cas9 screen reveals novel positive regulators of FTY720 sensitivity in acute lymphoblastic leukemia cells.
    Article Snippet: Jurkat cells stably expressing Cas9 (4 x 10 6 cells, Genecopoeia) were transduced with the GeCKOv2 lentivirus library (17,18) to achieve a total AR TIC LE IN PR ES S Fisher Scientific, Waltham, MA, catalog no. A1113803) was added 24 h post-transduction for 7 days. .. After puromycin selection, the cells were divided into two groups (4 x 10 6 cells/plate) and cultured in either the presence of FTY720 [8 μM] (MedChem Express, Monmouth Junction, NJ) or absence (DMSO [8 μM] vehicle control) for 48 h. Two rounds of 48-hour FTY720 or DMSO treatment were performed. .. After treatment, genomic DNA was extracted using the Blood and Cell Culture Midi Kit (Qiagen, Germantown, MD, catalog no. 13343).

    Control:

    Article Title: A genome-wide CRISPR/Cas9 screen reveals novel positive regulators of FTY720 sensitivity in acute lymphoblastic leukemia cells.
    Article Snippet: Jurkat cells stably expressing Cas9 (4 x 10 6 cells, Genecopoeia) were transduced with the GeCKOv2 lentivirus library (17,18) to achieve a total AR TIC LE IN PR ES S Fisher Scientific, Waltham, MA, catalog no. A1113803) was added 24 h post-transduction for 7 days. .. After puromycin selection, the cells were divided into two groups (4 x 10 6 cells/plate) and cultured in either the presence of FTY720 [8 μM] (MedChem Express, Monmouth Junction, NJ) or absence (DMSO [8 μM] vehicle control) for 48 h. Two rounds of 48-hour FTY720 or DMSO treatment were performed. .. After treatment, genomic DNA was extracted using the Blood and Cell Culture Midi Kit (Qiagen, Germantown, MD, catalog no. 13343).

    Article Title: Notch Signaling Exacerbates Pulmonary Fibrosis by Regulating the Differentiation of CD4 + Tissue-Resident Memory T Cells.
    Article Snippet: .. A midline cervical incision was made to expose the trachea, followed by intratracheal injection of BLM (MCE, Monmouth Junction, NJ, USA, Cat#: HY-17565A, 2 mg/kg) or an equal volume of PBS as a control. https://doi.org/10.3390/biom16020328 To investigate the origin of lung TRM cells in PF, FTY720 (MCE, Monmouth Junction, NJ, USA, Cat#: HY-12005, 1 mg/kg) or vehicle was administered via intraperitoneal injection starting three days before BLM exposure and continued daily thereafter. ..

    Article Title: Decreased PP2A expression and activity represent a therapeutic target for plexiform neurofibroma.
    Article Snippet: .. The four groups were administered the following treatments: (1) vehicle control; (2) the MEK inhibitor selumetinib (AZD6244, HY50706, MedChemExpress); (3) FTY720 (HY-12005, MedChemExpress); and (4) a combination of the above two reagents. ..



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    TRANS enhances tumoral T cell abundance and synergizes with immune checkpoint inhib itors. (A) UMAP visualization of lymphocytes in the TME following PBS or TRANS treatment. (B) UMAP visualization of lymphocyte clusters. (C) Proportional distribution of lymphocyte clusters. (D) Expression of cluster-specific marker genes. (E) Top 10 maker genes in CD8 + effector T cells (Teff). (F) Volcano plot of differentially expressed genes in CD8 + Teff between TRANS and PBS. (G) Dot plot showing upregulated pathways in IFN-γ + T cells (TRANS vs PBS), with dot size reflecting KEGG enrichment intensity. (H) Dot plot of ligand-receptor interactions between myeloid cells and T cells (TRANS vs PBS). Ligands (blue) and receptors (red) are labeled. (I) Experimental design of tumor therapy by TRANS combination with FTY720. (J) Tumor growth curve in mice treated with PBS, TRANS, and FTY720+TRANS; n = 5. (K – M) Tumor-infiltrating CD4 + and CD8 + T cells (K), Granzyme + CD8 + T or IFN-γ + CD8 + T cells counts (L), and Exhausted T cells (M) in TME; n = 5. (N) Scheme of tumor therapy by TRANS combined with immune checkpoint inhibitors (ICI). (O and P) Individual tumor changes (O) and Survival rate (Q) of tumor-bearing mice with different treatments; n = 5. (Q and R) Ex vivo IFN-γ expression (Q) and Quantification (R) in splenic CD8 + T cells with PMA/ionomycin stimulation; n = 3. (S) IFN-γ secretion by splenic T cells following αCD3/αCD28 stimulation; n = 3. Data are presented as mean ± SD, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. Significance was calculated using One-way ANOVA.

    Journal: Bioactive Materials

    Article Title: Chronic inflammation-responsive hydrogel restores myeloid-T cell crosstalk to reinvigorate antitumor immunity against metastatic colorectal cancer

    doi: 10.1016/j.bioactmat.2026.03.012

    Figure Lengend Snippet: TRANS enhances tumoral T cell abundance and synergizes with immune checkpoint inhib itors. (A) UMAP visualization of lymphocytes in the TME following PBS or TRANS treatment. (B) UMAP visualization of lymphocyte clusters. (C) Proportional distribution of lymphocyte clusters. (D) Expression of cluster-specific marker genes. (E) Top 10 maker genes in CD8 + effector T cells (Teff). (F) Volcano plot of differentially expressed genes in CD8 + Teff between TRANS and PBS. (G) Dot plot showing upregulated pathways in IFN-γ + T cells (TRANS vs PBS), with dot size reflecting KEGG enrichment intensity. (H) Dot plot of ligand-receptor interactions between myeloid cells and T cells (TRANS vs PBS). Ligands (blue) and receptors (red) are labeled. (I) Experimental design of tumor therapy by TRANS combination with FTY720. (J) Tumor growth curve in mice treated with PBS, TRANS, and FTY720+TRANS; n = 5. (K – M) Tumor-infiltrating CD4 + and CD8 + T cells (K), Granzyme + CD8 + T or IFN-γ + CD8 + T cells counts (L), and Exhausted T cells (M) in TME; n = 5. (N) Scheme of tumor therapy by TRANS combined with immune checkpoint inhibitors (ICI). (O and P) Individual tumor changes (O) and Survival rate (Q) of tumor-bearing mice with different treatments; n = 5. (Q and R) Ex vivo IFN-γ expression (Q) and Quantification (R) in splenic CD8 + T cells with PMA/ionomycin stimulation; n = 3. (S) IFN-γ secretion by splenic T cells following αCD3/αCD28 stimulation; n = 3. Data are presented as mean ± SD, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001. Significance was calculated using One-way ANOVA.

    Article Snippet: FTY720, AMG 487, TAK-779, D-Mannitol, and hydroxypropyl-β-cyclodextrin (HP-β-CD) were provided by MedChemExpress (USA).

    Techniques: Inhibition, Expressing, Marker, Labeling, Ex Vivo