TY - JOUR
T1 - Xanthohumol inhibits the neuroendocrine transcription factor achaete-scute complex-like 1, suppresses proliferation, and induces phosphorylated ERK1/2 in medullary thyroid cancer
AU - Cook, Mackenzie R.
AU - Luo, Jie
AU - Ndiaye, Mary
AU - Chen, Herbert
AU - Kunnimalaiyaan, Muthusamy
N1 - Funding Information:
Supported by the Howard Hughes Medical Research Institute (M.R.C.), NIH − R 21 CA117117 (H.C.), NIH − R01 CA109053 (H.C.), NIH – RO1 CA121115 (H.C.), American College of Surgeons , George H.A. Clowes Jr Memorial Research Career Development Award (H.C.), and Carcinoid Cancer Foundation Research Award (H.C.).
PY - 2010/3
Y1 - 2010/3
N2 - Background: Achaete-scute complex-like 1 (ASCL1) is a transcription factor important in the malignant development of medullary thyroid cancer (MTC). Activation of Raf-1 signaling is associated with ASCL1 suppression and growth inhibition. Xanthohumol, a natural compound, has recently been shown to have anticancer properties. We thus hypothesized that xanthohumol would suppress growth by activating Raf-1 signaling, thus altering the malignant phenotype of MTC. Methods: Human MTC cells were treated with xanthohumol (0-30 μmol/L) for up to 6 days. Proliferation was measured by a methylthiazolyldiphenyl-tetrazolium bromide (MTT) colorimetric assay. Western blot analysis was performed for ASCL1 and markers of Raf-1 pathway activation. Results: Treatment of MTC cells with xanthohumol resulted in a dose dependent inhibition of growth. Additionally, induction of phosphorylated ERK1/2 and a reduction of ASCL1 protein was noted. Conclusions: Xanthohumol is a potent Raf-1 activator in MTC cells. This compound suppresses MTC growth, alters the malignant phenotype, and warrants further preclinical study.
AB - Background: Achaete-scute complex-like 1 (ASCL1) is a transcription factor important in the malignant development of medullary thyroid cancer (MTC). Activation of Raf-1 signaling is associated with ASCL1 suppression and growth inhibition. Xanthohumol, a natural compound, has recently been shown to have anticancer properties. We thus hypothesized that xanthohumol would suppress growth by activating Raf-1 signaling, thus altering the malignant phenotype of MTC. Methods: Human MTC cells were treated with xanthohumol (0-30 μmol/L) for up to 6 days. Proliferation was measured by a methylthiazolyldiphenyl-tetrazolium bromide (MTT) colorimetric assay. Western blot analysis was performed for ASCL1 and markers of Raf-1 pathway activation. Results: Treatment of MTC cells with xanthohumol resulted in a dose dependent inhibition of growth. Additionally, induction of phosphorylated ERK1/2 and a reduction of ASCL1 protein was noted. Conclusions: Xanthohumol is a potent Raf-1 activator in MTC cells. This compound suppresses MTC growth, alters the malignant phenotype, and warrants further preclinical study.
KW - Achaete-scute complex-like 1
KW - Medullary thyroid cancer
KW - Neuroendocrine tumor
KW - Phosphorylated ERK1/2
KW - Xanthohumol
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U2 - 10.1016/j.amjsurg.2009.08.034
DO - 10.1016/j.amjsurg.2009.08.034
M3 - Article
C2 - 20226902
AN - SCOPUS:77649300540
SN - 0002-9610
VL - 199
SP - 315
EP - 318
JO - American Journal of Surgery
JF - American Journal of Surgery
IS - 3
ER -