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10.3892/ol.2016.4910

http://scihub22266oqcxt.onion/10.3892/ol.2016.4910
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C4998577!4998577!27602169
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suck abstract from ncbi


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pmid27602169      Oncol+Lett 2016 ; 12 (3): 2232-8
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  • Aloe-emodin suppresses esophageal cancer cell TE1 proliferation by inhibiting AKT and ERK phosphorylation #MMPMID27602169
  • Chang X; Zhao J; Tian F; Jiang Y; Lu J; Ma J; Zhang X; Jin G; Huang Y; Dong Z; Liu K; Dong Z
  • Oncol Lett 2016[Sep]; 12 (3): 2232-8 PMID27602169show ga
  • Aberrant AKT and extracellular signal-regulated kinase (ERK) activation is often observed in various human cancers. Both AKT and ERK are important in the phosphoinositide 3-kinase/AKT and mitogen-activated protein kinase kinase/ERK signaling pathways, which play vital roles in cell proliferation, differentiation and survival. Compounds that are able to block these pathways have therefore a promising use in cancer treatment and prevention. The present study revealed that AKT and ERK are activated in esophageal cancer TE1 cells. Aloe-emodin, an anthraquinone present in aloe latex, can suppress TE1 cell proliferation and anchor-independent cell growth. Aloe-emodin can also reduce the number of TE1 cells in S phase. Protein analysis indicated that aloe-emodin inhibits the phosphorylation of AKT and ERK in a dose-dependent manner. Overall, the present data indicate that aloe-emodin can suppress TE1 cell growth by inhibiting AKT and ERK phosphorylation, and suggest its clinical use for cancer therapy.
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