Identification and validation of Notch pathway activating compounds through a novel high‐throughput screening method

• Published in: Cancer Vol. 117; no. 7; pp. 1386 - 1398
• Main Authors: Pinchot, Scott N., Jaskula‐Sztul, Renata, Ning, Li, Peters, Noel R., Cook, Mackenzie R., Kunnimalaiyaan, Muthusamy, Chen, Herbert
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2011; Wiley-Blackwell
• Subjects: achaete‐scute complex‐like 1; Antineoplastic Agents - pharmacology; Biological and medical sciences; carcinoid; Carcinoid Tumor - drug therapy; Carcinoid Tumor - metabolism; Cell Line, Tumor; Dose-Response Relationship, Drug; High-Throughput Screening Assays; Humans; Medical sciences; neuroendocrine; Receptors, Notch - metabolism; resveratrol; Signal Transduction; Stilbenes - pharmacology; Tumors; Up-Regulation; Validation; Notch receptor; achaete-scute complex-like 1; neuroendocrine; Method; Medical screening; carcinoid; Stilbene derivatives; Polyphenol; Cancerology; Phytoalexin; Resveratrol; Phenols
• ISSN: 0008-543X; 1097-0142
• DOI: 10.1002/cncr.25652

BACKGROUND: Carcinoids are neuroendocrine (NE) tumors with limited treatment options. Notch activation has been shown to suppress growth and hormone production in carcinoid cells. METHODS: The purpose of this study was to provide a process for identifying Notch activating compounds via high‐throughput screening (HTS) and to validate the effects of the strongest hit from the 7264 compounds analyzed: resveratrol (RESV). RESULTS: Treatment of carcinoid cells with RESV resulted in up‐regulation of the Notch signaling pathway as measured by suppression of its downstream target achaete‐scute complex‐like 1. Luciferase reporter assays incorporating the centromere‐binding factor 1 binding site also confirmed the functional activity of RESV‐induced Notch. Because activation of the Notch pathway has been shown to suppress carcinoid proliferation, RESV treatment of carcinoid cells led to a dose‐dependent inhibition of cellular growth. Immunoblotting revealed phosphorylation of cdc2 (Tyr15) and up‐regulation of p21Cip1/Waf, markers of cell cycle arrest, with RESV treatment. Flow cytometry confirmed the mechanism of RESV‐induced growth inhibition is S phase cell cycle arrest. Furthermore, because Notch has been shown to inhibit bioactive hormone production from NE tumors, RESV also suppressed expression of the NE peptides/hormones chromogranin A and serotonin. RNA interference assays demonstrated that the hormone suppressing capacity of RESV was due to up‐regulation of the Notch2 isoform. CONCLUSIONS: HTS can be used to identify novel Notch activating compounds, which may have the potential to suppress carcinoid tumor growth and the associated endocrinopathies. Cancer 2011. © 2010 American Cancer Society. Notch activation has been shown to suppress growth and hormone production in carcinoid cells. The purpose of this study was to provide a process for identifying Notch activating compounds via high‐throughput screening and to validate the effects of the strongest hit from the 7264 compounds analyzed: resveratrol.