TY - JOUR
T1 - Tautomycetin and tautomycin suppress the growth of medullary thyroid cancer cells via inhibition of glycogen synthase kinase-3β
AU - Adler, Joel T.
AU - Cook, Mackenzie
AU - Luo, Yinggang
AU - Pitt, Susan C.
AU - Ju, Jianhua
AU - Li, Wenli
AU - Shen, Ben
AU - Kunnimalaiyaan, Muthusamy
AU - Chen, Herbert
PY - 2009/4/1
Y1 - 2009/4/1
N2 - Medullary thyroid cancer (MTC) is a relatively uncommon neuroendocrine tumor that arises from the calcitonin-secreting parafollicular cells of the thyroid gland. Unfortunately, MTC frequently metastasizes, precluding curative surgical resection and causing significant morbidity. Thus, there is an urgent need for new treatment modalities. Tautomycin and tautomycetin are antifungal antibiotics isolated from Streptomyces spiroverticillatus and Streptomyces griseochromogens, respectively. Glycogen synthase kinase-3β is a serine/threonine protein kinase that regulates multiple cellular processes and is important in various cancers, including MTC. Treatment with tautomycin and tautomycetin decreased neuroendocrine markers, suppressed hormonal secretion, and inhibited growth through apoptosis in MTC cells. Importantly, we describe a novel action of these compounds: inhibition of glycogen synthase kinase-3β.
AB - Medullary thyroid cancer (MTC) is a relatively uncommon neuroendocrine tumor that arises from the calcitonin-secreting parafollicular cells of the thyroid gland. Unfortunately, MTC frequently metastasizes, precluding curative surgical resection and causing significant morbidity. Thus, there is an urgent need for new treatment modalities. Tautomycin and tautomycetin are antifungal antibiotics isolated from Streptomyces spiroverticillatus and Streptomyces griseochromogens, respectively. Glycogen synthase kinase-3β is a serine/threonine protein kinase that regulates multiple cellular processes and is important in various cancers, including MTC. Treatment with tautomycin and tautomycetin decreased neuroendocrine markers, suppressed hormonal secretion, and inhibited growth through apoptosis in MTC cells. Importantly, we describe a novel action of these compounds: inhibition of glycogen synthase kinase-3β.
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U2 - 10.1158/1535-7163.MCT-08-0712
DO - 10.1158/1535-7163.MCT-08-0712
M3 - Article
C2 - 19372564
AN - SCOPUS:66449115520
SN - 1535-7163
VL - 8
SP - 914
EP - 920
JO - Molecular Cancer Therapeutics
JF - Molecular Cancer Therapeutics
IS - 4
ER -