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10.1038/cddis.2017.203 http://scihub22266oqcxt.onion/10.1038/cddis.2017.203 C5520722!5520722 !28492544     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28492544 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Cell+Death+Dis 2017 ; 8 (5 ): e2789 Nephropedia Template TP {{tp|p=28492544 |t=2017. Halofuginone dually regulates autophagic flux through nutrient-sensing pathways in colorectal cancer |pdf=|usr=}}{{28492544 }} gab.com Text Halofuginone dually regulates autophagic flux through nutrient-sensing pathways in colorectal cancer JO: Cell Death Dis http://www.kidney.de/pget.php?&tw=1&pmid=28492544 #FOAvip Autophagy has a key role in metabolism and impacts on tumorigenesis. Our previous study found that halofuginone (HF) exerts anticancer activity in colorectal cancer (CRC) by downregulating Akt/mTORC1 (mechanistic target of rapamycin complex 1) signaling pathway. But whether and how HF regulates autophagy and metabolism to inhibit cancer growth remains an open question. Here, we unveil that HF activates ULK1 by downregulation of its phosphorylation site at Ser757 through Akt/mTORC1 signaling pathway, resulting in induction of autophagic flux under nutrient-rich condition. On the other hand, HF inactivates ULK1 by downregulation of its phosphorylation sites at Ser317 and Ser777 through LKB1/AMPK signaling pathway, resulting in autophagic inhibition under nutrient-poor condition. Furthermore, Atg7-dependent autophagosome formation is also induced under nutrient-rich condition or blocked in nutrient-poor environment, respectively, upon HF treatment. More interestingly, we also found that HF inhibits glycolysis under nutrient-rich condition, whereas inhibits gluconeogenesis under nutrient-poor condition in an Atg7-dependent manner, suggesting that autophagy has a pivotal role of glucose metabolism upon HF treatment. Subsequent studies showed that HF treatment retarded tumor growth in xenograft mice fed with either standard chow diet or caloric restriction through dual regulation of autophagy in vivo. Together, HF has a dual role in autophagic modulation depending on nutritional conditions for anti-CRC. Twit Text FOAVip Halofuginone dually regulates autophagic flux through nutrient-sensing pathways in colorectal cancer ????Cell Death Dis http://www.kidney.de/pget.php?&tw=1&pmid=28492544 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28492544 #FOAvip English Wikipedia <ref>{{Cite pmid|28492544 }}</ref> Halofuginone dually regulates autophagic flux through nutrient-sensing pathways in colorectal cancer #MMPMID28492544 Chen GQ ; Gong RH ; Yang DJ ; Zhang G ; Lu AP ; Yan SC ; Lin SH ; Bian ZX Cell Death Dis 2017[May]; 8 (5 ): e2789 PMID28492544 show ga Autophagy has a key role in metabolism and impacts on tumorigenesis. Our previous study found that halofuginone (HF) exerts anticancer activity in colorectal cancer (CRC) by downregulating Akt/mTORC1 (mechanistic target of rapamycin complex 1) signaling pathway. But whether and how HF regulates autophagy and metabolism to inhibit cancer growth remains an open question. Here, we unveil that HF activates ULK1 by downregulation of its phosphorylation site at Ser757 through Akt/mTORC1 signaling pathway, resulting in induction of autophagic flux under nutrient-rich condition. On the other hand, HF inactivates ULK1 by downregulation of its phosphorylation sites at Ser317 and Ser777 through LKB1/AMPK signaling pathway, resulting in autophagic inhibition under nutrient-poor condition. Furthermore, Atg7-dependent autophagosome formation is also induced under nutrient-rich condition or blocked in nutrient-poor environment, respectively, upon HF treatment. More interestingly, we also found that HF inhibits glycolysis under nutrient-rich condition, whereas inhibits gluconeogenesis under nutrient-poor condition in an Atg7-dependent manner, suggesting that autophagy has a pivotal role of glucose metabolism upon HF treatment. Subsequent studies showed that HF treatment retarded tumor growth in xenograft mice fed with either standard chow diet or caloric restriction through dual regulation of autophagy in vivo. Together, HF has a dual role in autophagic modulation depending on nutritional conditions for anti-CRC. |AMP-Activated Protein Kinase Kinases [MESH] |AMP-Activated Protein Kinases [MESH] |Animals [MESH] |Autophagy/*drug effects/genetics [MESH] |Cell Line, Tumor [MESH] |Colorectal Neoplasms/drug therapy/*metabolism/pathology [MESH] |Humans [MESH] |Male [MESH] |Mechanistic Target of Rapamycin Complex 1/genetics/metabolism [MESH] |Mice [MESH] |Mice, Inbred BALB C [MESH] |Mice, Nude [MESH] |Piperidines/*pharmacology [MESH] |Protein Kinases/genetics/metabolism [MESH] |Protein Serine-Threonine Kinases/genetics/metabolism [MESH] |Proto-Oncogene Proteins c-akt/genetics/metabolism [MESH] |Quinazolinones/*pharmacology [MESH] |Signal Transduction/*drug effects/genetics [MESH]Halofuginone dually regulates autophagic flux through nutrient-sensing(epmc).pdf DeepDyve Pubget Overpricing