AZD1480 blocks growth and tumorigenesis of RET- activated thyroid cancer cell lines Journal Article
| Authors: | Couto, J. P.; Almeida, A.; Daly, L.; Sobrinho-Simões, M.; Bromberg, J. F.; Soares, P. |
| Article Title: | AZD1480 blocks growth and tumorigenesis of RET- activated thyroid cancer cell lines |
| Abstract: | Persistent RET activation is a frequent event in papillary thyroid carcinoma (PTC) and medullary thyroid carcinoma (MTC). In these cancers, RET activates the ERK/MAPK, the PI3K/AKT/mTOR and the JAK/STAT3 pathways. Here, we tested the efficacy of a JAK1/2- inhibitor, AZD1480, in the in vitro and in vivo growth of thyroid cancer cell lines expressing oncogenic RET. Thyroid cancer cell lines harboring RET/PTC1 (TPC-1), RET M918T (MZ-CRC1) and RET C634W (TT) alterations, as well as TPC-1 xenografts, were treated with JAK inhibitor, AZD1480. This inhibitor led to growth inhibition and/or apoptosis of the thyroid cancer cell lines in vitro, as well as to tumor regression of TPC-1 xenografts, where it efficiently blocked STAT3 activation in tumor and stromal cells. This inhibition was associated with decreased proliferation, decreased blood vessel density, coupled with increased necrosis. However, AZD1480 repressed the growth of STAT3- deficient TPC-1 cells in vitro and in vivo, demonstrating that its effects in this cell line were independent of STAT3 in the tumor cells. In all cell lines, the JAK inhibitor reduced phospho-Y1062 RET levels, and mTOR effector phospho-S6, while JAK1/2 downregulation by siRNA did not affect cell growth nor RET and S6 activation. In conclusion, AZD1480 effectively blocks proliferation and tumor growth of activated RET- thyroid cancer cell lines, likely through direct RET inhibition in cancer cells as well as by modulation of the microenvironment (e.g. via JAK/phospho-STAT3 inhibition in endothelial cells). Thus, AZD1480 should be considered as a therapeutic agent for the treatment of RET- activated thyroid cancers. © 2012 Couto et al. |
| Keywords: | signal transduction; protein kinase b; controlled study; protein phosphorylation; human cell; janus kinase 2; drug targeting; protein localization; stat3 protein; apoptosis; small interfering rna; in vivo study; cancer cell culture; in vitro study; tumor regression; phosphatidylinositol 3 kinase; carcinogenesis; cancer inhibition; gene activation; mammalian target of rapamycin; cellular distribution; down regulation; thyroid cancer; ic 50; stroma cell; protein ret; tumor microenvironment; oncogene ret; protein s6; selumetinib; janus kinase 1; 5 chloro n2 [1 (5 fluoro 2 pyrimidinyl)ethyl] n4 (5 methyl 1h pyrazol 3 yl) 2,4 pyrimidinediamine |
| Journal Title: | PLoS ONE |
| Volume: | 7 |
| Issue: | 10 |
| ISSN: | 1932-6203 |
| Publisher: | Public Library of Science |
| Date Published: | 2012-01-01 |
| Start Page: | e46869 |
| Language: | English |
| DOI: | 10.1371/journal.pone.0046869 |
| PROVIDER: | scopus |
| PMCID: | PMC3462763 |
| PUBMED: | 23056499 |
| DOI/URL: | |
| Notes: | --- - "Export Date: 2 November 2012" - "Source: Scopus" |
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