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10.7150/jca.18031 http://scihub22266oqcxt.onion/10.7150/jca.18031 C5479241!5479241!28638450     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       J+Cancer 2017 ; 8 (8): 1362-70 Nephropedia Template TP {{tp|p=28638450|t=2017. Osteopontin is Critical for Hyperactive mTOR-Induced Tumorigenesis in Oral Squamous Cell Carcinoma |pdf=|usr=}}{{28638450}} gab.com Text Osteopontin is Critical for Hyperactive mTOR-Induced Tumorigenesis in Oral Squamous Cell Carcinoma JO: J Cancer http://www.kidney.de/pget.php?&tw=1&pmid=28638450 #FOAvip Mechanistic target of rapamycin (mTOR) plays a critical role in the development of oral squamous cell carcinoma (OSCC), but the underlying mechanisms remain poorly understood. Here we have demonstrated that the expression of osteopontin (OPN) was dramatically up-regulated in OSCC tissues and cell lines. Moreover, reduction of OPN suppressed cell proliferation, colony formation, and in vivo tumorigenic ability of OSCC cell lines Tca8113. In addition, there was a strong positive correlation between mTORC1 activity and OPN expression in OSCC tissues and cell lines. Furthermore, mTOR complex 1 (mTORC1) enhanced OPN expression through up-regulation of ERR?. Therefore, OPN is a downstream target of mTORC1 and is crucial for OSCC development. mTORC1, ERR?, and OPN may be potential targets for treatment of OSCC with aberrant mTORC1 signaling. Twit Text FOAVip Osteopontin is Critical for Hyperactive mTOR-Induced Tumorigenesis in Oral Squamous Cell Carcinoma ????J Cancer http://www.kidney.de/pget.php?&tw=1&pmid=28638450 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28638450 #FOAvip English Wikipedia <ref>{{Cite pmid|28638450}}</ref> Osteopontin is Critical for Hyperactive mTOR-Induced Tumorigenesis in Oral Squamous Cell Carcinoma #MMPMID28638450 Gan N; Zou S; Hang W; Yang D; Zhang X; Yin Y J Cancer 2017[]; 8 (8): 1362-70 PMID28638450show ga Mechanistic target of rapamycin (mTOR) plays a critical role in the development of oral squamous cell carcinoma (OSCC), but the underlying mechanisms remain poorly understood. Here we have demonstrated that the expression of osteopontin (OPN) was dramatically up-regulated in OSCC tissues and cell lines. Moreover, reduction of OPN suppressed cell proliferation, colony formation, and in vivo tumorigenic ability of OSCC cell lines Tca8113. In addition, there was a strong positive correlation between mTORC1 activity and OPN expression in OSCC tissues and cell lines. Furthermore, mTOR complex 1 (mTORC1) enhanced OPN expression through up-regulation of ERR?. Therefore, OPN is a downstream target of mTORC1 and is crucial for OSCC development. mTORC1, ERR?, and OPN may be potential targets for treatment of OSCC with aberrant mTORC1 signaling. äOsteopontin is Critical for Hyperactive mTOR-Induced Tumorigenesis in (epmc).pdf DeepDyve Pubget Overpricing