Vascular tumors have increased p70 S6-kinase activation and are inhibited by topical rapamycin
- PMID: 23938603
- DOI: 10.1038/labinvest.2013.98
Vascular tumors have increased p70 S6-kinase activation and are inhibited by topical rapamycin
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.
Similar articles
-
mTORC1-S6K1 inhibition or mTORC2 activation improves hippocampal synaptic plasticity and learning in Angelman syndrome mice.Cell Mol Life Sci. 2016 Nov;73(22):4303-4314. doi: 10.1007/s00018-016-2269-z. Epub 2016 May 12. Cell Mol Life Sci. 2016. PMID: 27173058 Free PMC article.
-
Different patterns of Akt and ERK feedback activation in response to rapamycin, active-site mTOR inhibitors and metformin in pancreatic cancer cells.PLoS One. 2013;8(2):e57289. doi: 10.1371/journal.pone.0057289. Epub 2013 Feb 21. PLoS One. 2013. PMID: 23437362 Free PMC article.
-
A comparison of Ku0063794, a dual mTORC1 and mTORC2 inhibitor, and temsirolimus in preclinical renal cell carcinoma models.PLoS One. 2013;8(1):e54918. doi: 10.1371/journal.pone.0054918. Epub 2013 Jan 22. PLoS One. 2013. PMID: 23349989 Free PMC article.
-
The Enigma of Rapamycin Dosage.Mol Cancer Ther. 2016 Mar;15(3):347-53. doi: 10.1158/1535-7163.MCT-15-0720. Epub 2016 Feb 25. Mol Cancer Ther. 2016. PMID: 26916116 Free PMC article. Review.
-
Multifaceted role of mTOR (mammalian target of rapamycin) signaling pathway in human health and disease.Signal Transduct Target Ther. 2023 Oct 2;8(1):375. doi: 10.1038/s41392-023-01608-z. Signal Transduct Target Ther. 2023. PMID: 37779156 Free PMC article. Review.
Cited by
-
Analysis of PI3K pathway components in human cancers.Oncol Lett. 2016 Apr;11(4):2913-2918. doi: 10.3892/ol.2016.4309. Epub 2016 Mar 8. Oncol Lett. 2016. PMID: 27073576 Free PMC article.
-
Genetic context of oncogenic drivers dictates vascular sarcoma development in aP2-Cre mice.J Pathol. 2022 May;257(1):109-124. doi: 10.1002/path.5873. Epub 2022 Feb 15. J Pathol. 2022. PMID: 35066877 Free PMC article.
-
CD44-tropic polymeric nanocarrier for breast cancer targeted rapamycin chemotherapy.Nanomedicine. 2014 Aug;10(6):1221-30. doi: 10.1016/j.nano.2014.02.015. Epub 2014 Mar 15. Nanomedicine. 2014. PMID: 24637218 Free PMC article.
-
Identification of novel potential biomarkers in infantile hemangioma via weighted gene co-expression network analysis.BMC Pediatr. 2022 May 1;22(1):239. doi: 10.1186/s12887-022-03306-1. BMC Pediatr. 2022. PMID: 35501731 Free PMC article.
-
Ponatinib Combined With Rapamycin Causes Regression of Murine Venous Malformation.Arterioscler Thromb Vasc Biol. 2019 Mar;39(3):496-512. doi: 10.1161/ATVBAHA.118.312315. Arterioscler Thromb Vasc Biol. 2019. PMID: 30626204 Free PMC article.
Publication types
MeSH terms
Substances
Supplementary concepts
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous