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Oncotarget ; 7(41): 66558-66568, 2016 Oct 11.
Article in English | MEDLINE | ID: mdl-27589685

ABSTRACT

Perfluorooctanoic acid (PFOA) is a common environmental pollutant that has been associated with various diseases, including cancer. We explored the molecular mechanisms underlying PFOA-induced endometrial cancer cell invasion and migration. PFOA treatment enhanced migration and invasion by human Ishikawa endometrial cancer cells, which correlated with decreased E-cadherin expression, a marker of epithelial-mesenchymal transition. PFOA also induced activation of ERK1/2/mTOR signaling. Treatment with rapamycin, an mTOR inhibitor, antagonized the effects of PFOA and reversed the effects of PFOA activation in a xenograft mouse model of endometrial cancer. Consistent with these results, pre-treatment with rapamycin abolished PFOA-induced down-regulation of E-cadherin expression. These results indicate that PFOA is a carcinogen that promotes endometrial cancer cell migration and invasion through activation of ERK/mTOR signaling.


Subject(s)
Caprylates/toxicity , Cell Movement/drug effects , Endometrial Neoplasms/pathology , Fluorocarbons/toxicity , MAP Kinase Signaling System/drug effects , TOR Serine-Threonine Kinases/drug effects , Animals , Carcinogens/toxicity , Cell Line, Tumor , Endometrial Neoplasms/metabolism , Enzyme Activation/drug effects , Epithelial-Mesenchymal Transition/drug effects , Female , Heterografts , Humans , Mice , Mice, Inbred BALB C , Mice, Nude , Neoplasm Invasiveness/pathology , Signal Transduction/drug effects , TOR Serine-Threonine Kinases/metabolism
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