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ATCC
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ATCC
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ATCC
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European Collection of Authenticated Cell Cultures
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HORIBA Ltd
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Johns Hopkins HealthCare
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STEMCELL Technologies Inc
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Makoto USA Inc
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STREX Inc
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Federation of European Neuroscience Societies
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National Centre for Cell Science
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Muegge GmbH
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Image Search Results
Journal: Frontiers in Oncology
Article Title: Anti-secretory and anti-proliferative actions of next-generation dual subtype 2 and 5 somatostatin receptor ligands in neuroendocrine tumor models
doi: 10.3389/fonc.2026.1766563
Figure Lengend Snippet: Effect of the test and control SRLs on ACTH secretion in AtT-20 cells. Effect of the test and control SRLs on ACTH secretion in AtT-20 cells. (A, B) AtT-20 cells were seeded at a density of 3500 cells/well and then were treated with the indicated concentrations of (A) the control SRLs octreotide, pasireotide or (B) the test peptides, i.e. 5nM, 10nM, and 50nM. After 72h, supernatants were collected, and ACTH levels were determined by means of the mouse/Rat ACTH ELISA Kit (Abcam). The experiment was repeated 3 times with similar results. Data shown are the average of two technical replicates ± standard deviation (SD). (C, D) The decrease in ACTH secretion upon treatment with the test peptides is here compared with that obtained with (C) octreotide or (D) pasireotide. NT, untreated. In red are the comparisons where the test peptides performed better than the reference drugs, in black are the comparisons where the reference drugs performed better than the test peptides. (A-D) Statistical analyses were carried out in GraphPad Prism using one-way ANOVA: *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001; ****p ≤ 0.0001.
Article Snippet:
Techniques: Control, Enzyme-linked Immunosorbent Assay, Standard Deviation
Journal: Frontiers in Oncology
Article Title: Anti-secretory and anti-proliferative actions of next-generation dual subtype 2 and 5 somatostatin receptor ligands in neuroendocrine tumor models
doi: 10.3389/fonc.2026.1766563
Figure Lengend Snippet: Effect of the test and control SRLs on the proliferation of AtT-20 cells. Effect of the test and control SRLs on the proliferation of AtT-20 cells. (A, B) AtT-20 cells were seeded at a density of 3500 cells/well and then were treated with the indicated concentrations (1nM, 2, 5nM, 5nM, 10nM, 50nM) of (A) the control SRLs octreotide or pasireotide, or with (B) the test peptides, for 72h. Cell viability was then carried out with WST-1 colorimetric assay. The experiment was repeated 3 times with similar results. Data shown are the average of 3 technical replicates ± SD. NT, untreated. (C, D) The decrease in cell proliferation upon treatment with the test peptides is here compared with that obtained with (C) octreotide or (D) pasireotide. NT, untreated. In red are the comparisons where the test peptides performed better than the reference drugs, in black are the comparisons where the reference drugs performed better than the test peptides. (A-D) Statistical analyses were carried out in GraphPad Prism using one-way ANOVA: *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001; ****p ≤ 0.0001.
Article Snippet:
Techniques: Control, Colorimetric Assay
Journal: Frontiers in Oncology
Article Title: Anti-secretory and anti-proliferative actions of next-generation dual subtype 2 and 5 somatostatin receptor ligands in neuroendocrine tumor models
doi: 10.3389/fonc.2026.1766563
Figure Lengend Snippet: Effect of SMTR-002 and control SRLs on forskolin-induced cAMP production in AtT-20 cells. (A, B) AtT-20 cells were seeded at a density of 3500 cells/well and then treated with the indicated concentrations (10nM, 50nM, 100nM) of (A) the control SRLs octreotide or pasireotide, or with (B) SMTR-002 for 72 hours. Cells were induced with 10 µM forskolin 3 hours prior to performing the assay. The levels of cAMP were then quantified with the cAMP-Glo luminescent assay. The experiment was repeated 3 times with similar results. Data shown are the average of 3 technical replicates ± SD. Data shown are the average of 3 technical replicates ± SD. Statistical analyses were carried out in GraphPad Prism using one-way ANOVA: ***p ≤ 0.001; ****p ≤ 0.0001.
Article Snippet:
Techniques: Control, Luminescence Assay