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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and <t>Apilimod</t> + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.
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Image Search Results


Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and Apilimod + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.

Journal: Frontiers in Pharmacology

Article Title: IL-23 inhibitor enhances the effects of PTEN DNA-loaded lipid nanoparticles for metastatic CRPC therapy

doi: 10.3389/fphar.2024.1388613

Figure Lengend Snippet: Antitumor assays in vitro . (A) Cell viability of RM-1 cells after treatment with LNP@PTEN and Apilimod + LNP@PTEN for 24 h ( n = 3, means ± SD). ns: no significance, 2way ANOVA. (B, C) The statistical analysis of cells in nine fields of view of (B) anti-migration effects and (C) anti-invasion effects, respectively ( n = 9, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, ns: no significance, one-way ANOVA. (D) Microscope images of anti-migration effects and anti-invasion effects in each group (Apilimod: 10 nM, PTEN: 0.5 μg/mL), scale bars = 50 μm. (E) 3D tumor spheroid model. DiO-stained RM-1 cells and DiD-stained MC3T3-E1 cells. Blue fluorescence: DAPI, green fluorescence: DiO, red fluorescence: DiD, Scale bars = 100 μm. (F) The images of in vitro tumor spheroids penetration of each group were acquired by CLSM. DiO-stained LNPs (DiO: 20 μg/mL, Cy7-DNA: 0.5 μg/mL). Scale bars = 100 μm.

Article Snippet: Apilimod mesylate was purchased from MedChemExpress (United States).

Techniques: In Vitro, Migration, Microscopy, Staining, Fluorescence

In vivo study of LNPs. (A) Representative images of BmCRPC-bearing mice from each group were taken at 0–24 h after injection, with the tumor area marked by a red circle. (B) Fluorescence imaging of tumors and major organs. (C) The semiquantitative fluorescence intensity in major organs of each group ( n = 3, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, multiple t -test. (D) The in vivo study protocol of Apilimod + LNP@PTEN (PTEN DNA: 700 μg/kg, Apilimod: 10 mg/kg). (E) The five groups’ tumor volume curves ( n = 5, mean ± SD). (F) The five groups’ weight curves ( n = 5, mean ± SD). (G) Mice growth curves for body weight among the five groups ( n = 5, mean ± SD). (H) RT-qPCR results of the expression of PTEN in different treatment groups (n = 3, mean ± SD), *** p < 0.001, **** p < 0.0001, one-way ANOVA. (I) Survival curve of mice in different treatment groups ( n = 5, mean ± SD). **** p < 0.0001, ns: no significance, one-way ANOVA.

Journal: Frontiers in Pharmacology

Article Title: IL-23 inhibitor enhances the effects of PTEN DNA-loaded lipid nanoparticles for metastatic CRPC therapy

doi: 10.3389/fphar.2024.1388613

Figure Lengend Snippet: In vivo study of LNPs. (A) Representative images of BmCRPC-bearing mice from each group were taken at 0–24 h after injection, with the tumor area marked by a red circle. (B) Fluorescence imaging of tumors and major organs. (C) The semiquantitative fluorescence intensity in major organs of each group ( n = 3, mean ± SD), * p < 0.05, ** p < 0.01, *** p < 0.001, multiple t -test. (D) The in vivo study protocol of Apilimod + LNP@PTEN (PTEN DNA: 700 μg/kg, Apilimod: 10 mg/kg). (E) The five groups’ tumor volume curves ( n = 5, mean ± SD). (F) The five groups’ weight curves ( n = 5, mean ± SD). (G) Mice growth curves for body weight among the five groups ( n = 5, mean ± SD). (H) RT-qPCR results of the expression of PTEN in different treatment groups (n = 3, mean ± SD), *** p < 0.001, **** p < 0.0001, one-way ANOVA. (I) Survival curve of mice in different treatment groups ( n = 5, mean ± SD). **** p < 0.0001, ns: no significance, one-way ANOVA.

Article Snippet: Apilimod mesylate was purchased from MedChemExpress (United States).

Techniques: In Vivo, Injection, Fluorescence, Imaging, Quantitative RT-PCR, Expressing