Abstract
Vascular tumors are endothelial cell neoplasms whose cellular and molecular mechanisms, leading to tumor formation, are poorly understood, and current therapies have limited efficacy with significant side effects. We have investigated mechanistic (mammalian) target of rapamycin (mTOR) signaling in benign and malignant vascular tumors, and the effects of mTOR kinase inhibitor as a potential therapy for these lesions. Human vascular tumors (infantile hemangioma and angiosarcoma) were analyzed by immunohistochemical stains and western blot for the phosphorylation of p70 S6-kinase (S6K) and S6 ribosomal protein (S6), which are activated downstream of mTOR complex-1 (mTORC1). To assess the function of S6K, tumor cells with genetic knockdown of S6K were analyzed for cell proliferation and migration. The effects of topical rapamycin, an mTOR inhibitor, on mTORC1 and mTOR complex-2 (mTORC2) activities, as well as on tumor growth and migration, were determined. Vascular tumors showed increased activation of S6K and S6. Genetic knockdown of S6K resulted in reduced tumor cell proliferation and migration. Rapamycin fully inhibited mTORC1 and partially inhibited mTORC2 activities, including the phosphorylation of Akt (serine 473) and PKCα, in vascular tumor cells. Rapamycin significantly reduced vascular tumor growth in vitro and in vivo. As a potential localized therapy for cutaneous vascular tumors, topically applied rapamycin effectively reduced tumor growth with limited systemic drug absorption. These findings reveal the importance of mTOR signaling pathways in benign and malignant vascular tumors. The mTOR pathway is an important therapeutic target in vascular tumors, and topical mTOR inhibitors may provide an alternative and well-tolerated therapy for the treatment of cutaneous vascular lesions.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Administration, Topical
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Adolescent
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Adult
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Aged
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Animals
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Antibiotics, Antineoplastic / administration & dosage
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Antibiotics, Antineoplastic / pharmacology
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Antibiotics, Antineoplastic / therapeutic use*
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Cell Line, Tumor
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Child
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Female
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Hemangioma, Capillary / drug therapy*
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Hemangioma, Capillary / epidemiology
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Hemangioma, Capillary / metabolism
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Hemangioma, Capillary / pathology
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Hemangiosarcoma / drug therapy*
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Hemangiosarcoma / epidemiology
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Hemangiosarcoma / metabolism
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Hemangiosarcoma / pathology
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Humans
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Infant
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Male
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Mechanistic Target of Rapamycin Complex 1
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Mechanistic Target of Rapamycin Complex 2
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Mice
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Mice, Nude
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Multiprotein Complexes / antagonists & inhibitors
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Multiprotein Complexes / metabolism
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Neoplasm Proteins / antagonists & inhibitors
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Neoplasm Proteins / genetics
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Neoplasm Proteins / metabolism
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Neoplastic Syndromes, Hereditary / drug therapy*
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Neoplastic Syndromes, Hereditary / epidemiology
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Neoplastic Syndromes, Hereditary / metabolism
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Neoplastic Syndromes, Hereditary / pathology
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Protein Kinase Inhibitors / administration & dosage
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Protein Kinase Inhibitors / pharmacology
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Protein Kinase Inhibitors / therapeutic use*
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Ribosomal Protein S6 Kinases, 70-kDa / antagonists & inhibitors*
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Ribosomal Protein S6 Kinases, 70-kDa / genetics
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Ribosomal Protein S6 Kinases, 70-kDa / metabolism
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Signal Transduction / drug effects*
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Sirolimus / administration & dosage
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Sirolimus / pharmacology
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Sirolimus / therapeutic use*
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TOR Serine-Threonine Kinases / antagonists & inhibitors
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TOR Serine-Threonine Kinases / metabolism
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Tumor Cells, Cultured
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Xenograft Model Antitumor Assays
Substances
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Antibiotics, Antineoplastic
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Multiprotein Complexes
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Neoplasm Proteins
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Protein Kinase Inhibitors
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Mechanistic Target of Rapamycin Complex 1
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Mechanistic Target of Rapamycin Complex 2
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Ribosomal Protein S6 Kinases, 70-kDa
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TOR Serine-Threonine Kinases
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Sirolimus
Supplementary concepts
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Hemangioma, capillary infantile