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10.1530/ERC-16-0142 http://scihub22266oqcxt.onion/10.1530/ERC-16-0142 C4990486!4990486!27435064     free     free     free Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Endocr+Relat+Cancer 2016 ; 23 (9): 747-58 Nephropedia Template TP {{tp|p=27435064|t=2016. EMT Reversal in human cancer cells after IR knockdown in hyperinsulinemic mice |pdf=|usr=}}{{27435064}} gab.com Text EMT Reversal in human cancer cells after IR knockdown in hyperinsulinemic mice JO: Endocr Relat Cancer http://www.kidney.de/pget.php?&tw=1&pmid=27435064 #FOAvip Type 2 Diabetes (T2D) is associated with increased cancer risk and cancer-related mortality. Data herein show that we generated an immunodeficient hyperinsulinemic mouse by crossing the Rag1?/? mice, which have no mature B or T lymphocytes, with the MKR mouse model of T2D to generate the Rag1?/? (Rag/WT) and Rag1?/?/MKR+/+ (Rag/MKR) mice. The female Rag/MKR mice are insulin resistant and have significantly higher non-fasting plasma insulin levels compared to the Rag/WT controls. Therefore, we used these Rag/MKR mice to investigate the role of endogenous hyperinsulinemia on human cancer progression. In this study we show that hyperinsulinemia in the Rag/MKR mice increases the expression of mesenchymal transcription factors, TWIST1 and ZEB1, and increases the expression of the angiogenesis marker, vascular endothelial growth factor A (VEGFA). We also show that silencing the insulin receptor (IR) in the human LCC6 cancer cells leads to decreased tumor growth and metastases, suppression of mesenchymal markers Vimentin, SLUG, TWIST1, and ZEB1, suppression of angiogenesis markers, VEGFA and VEGFD, and re-expression of the epithelial marker, E-cadherin. The data in this paper demonstrate that IR knockdown in primary tumors partially reverses the growth promoting effects of hyperinsulinemia as well as highlighting the importance of the insulin receptor signaling pathway in cancer progression, and more specifically in epithelial-mesenchymal transition. Twit Text FOAVip EMT Reversal in human cancer cells after IR knockdown in hyperinsulinemic mice ????Endocr Relat Cancer http://www.kidney.de/pget.php?&tw=1&pmid=27435064 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27435064 #FOAvip English Wikipedia <ref>{{Cite pmid|27435064}}</ref> EMT Reversal in human cancer cells after IR knockdown in hyperinsulinemic mice #MMPMID27435064 Zelenko Z; Gallagher EJ; Antoniou IM; Sachdev D; Nayak A; Yee D; LeRoith D Endocr Relat Cancer 2016[Sep]; 23 (9): 747-58 PMID27435064show ga Type 2 Diabetes (T2D) is associated with increased cancer risk and cancer-related mortality. Data herein show that we generated an immunodeficient hyperinsulinemic mouse by crossing the Rag1?/? mice, which have no mature B or T lymphocytes, with the MKR mouse model of T2D to generate the Rag1?/? (Rag/WT) and Rag1?/?/MKR+/+ (Rag/MKR) mice. The female Rag/MKR mice are insulin resistant and have significantly higher non-fasting plasma insulin levels compared to the Rag/WT controls. Therefore, we used these Rag/MKR mice to investigate the role of endogenous hyperinsulinemia on human cancer progression. In this study we show that hyperinsulinemia in the Rag/MKR mice increases the expression of mesenchymal transcription factors, TWIST1 and ZEB1, and increases the expression of the angiogenesis marker, vascular endothelial growth factor A (VEGFA). We also show that silencing the insulin receptor (IR) in the human LCC6 cancer cells leads to decreased tumor growth and metastases, suppression of mesenchymal markers Vimentin, SLUG, TWIST1, and ZEB1, suppression of angiogenesis markers, VEGFA and VEGFD, and re-expression of the epithelial marker, E-cadherin. The data in this paper demonstrate that IR knockdown in primary tumors partially reverses the growth promoting effects of hyperinsulinemia as well as highlighting the importance of the insulin receptor signaling pathway in cancer progression, and more specifically in epithelial-mesenchymal transition. äEMT Reversal in human cancer cells after IR knockdown in hyperinsuline(epmc).pdf DeepDyve Pubget Overpricing