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10.1186/s13046-016-0350-y http://scihub22266oqcxt.onion/10.1186/s13046-016-0350-y C4855705!4855705!27141829     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27141829&cmd=llinks): Failed to open stream: HTTP request failed! 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TET3 inhibits TGF-?1-induced epithelial-mesenchymal transition by demethylating miR-30d precursor gene in ovarian cancer cells |pdf=|usr=}}{{27141829}} gab.com Text TET3 inhibits TGF- 1-induced epithelial-mesenchymal transition by demethylating miR-30d precursor gene in ovarian cancer cells JO: J Exp Clin Cancer Res http://www.kidney.de/pget.php?&tw=1&pmid=27141829 #FOAvip Background: Abnormal DNA methylation/demethylation is recognized as a hallmark of cancer. TET (ten-eleven translocation) family members are novel DNA demethylation related proteins that dysregulate in multiple malignances. However, their effects on ovarian cancer remain to be elucidated. Methods: The changes of TET family members during TGF-?1-induced epithelial-mesenchymal transition (EMT) in SKOV3 and 3AO ovarian cancer cells were detected. TET3 was ectopically expressed in TGF-?1-treated ovarian cancer cells to examine its effect on TGF-?1-induced EMT phenotype. The downstream target of TET3 was further identified. Finally, the relationships of TET3 expression to clinic-pathological parameters of ovarian cancer were investigated with a tissue microarray using immunohistochemistry. Results: TET3 was downregulated during TGF-?1-initiatd epithelial-mesenchymal transition (EMT) in SKOV3 and 3AO ovarian cancer cells. Overexpression of TET3 reversed TGF-?1-induced EMT phenotypes including the expression pattern of molecular markers (E-cadherin, Vimentin, N-cadherin, Snail) and migratory and invasive capabilities of ovarian cancer cells. miR-30d was identified as a downstream target of TET3, and TET3 overexpression resumed the demethylation status in the promoter region of miR-30d precursor gene, resulting in restoration of miR-30d (an EMT suppressor of ovarian cancer cells proven in our previous study) level in TGF-?1-induced EMT. We further found that TET3 expression was decreased in ovarian cancer tissues, especially in serous ovarian cancers. The overall positivity of TET3 was inversely correlated with the grade of differentiation status of ovarian cancer. Conclusion: Our results revealed that TET3 acted as a suppressor of ovarian cancer by demethylating miR-30d precursor gene promoter to block TGF-?1-induced EMT. Electronic supplementary material: The online version of this article (doi:10.1186/s13046-016-0350-y) contains supplementary material, which is available to authorized users. Twit Text FOAVip TET3 inhibits TGF- 1-induced epithelial-mesenchymal transition by demethylating miR-30d precursor gene in ovarian cancer cells ????J Exp Clin Cancer Res http://www.kidney.de/pget.php?&tw=1&pmid=27141829 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27141829 #FOAvip English Wikipedia <ref>{{Cite pmid|27141829}}</ref> TET3 inhibits TGF-?1-induced epithelial-mesenchymal transition by demethylating miR-30d precursor gene in ovarian cancer cells #MMPMID27141829 Ye Z; Li J; Han X; Hou H; Chen H; Zheng X; Lu J; Wang L; Chen W; Li X; Zhao L J Exp Clin Cancer Res 2016[]; 35 (ä): ä PMID27141829show ga Background: Abnormal DNA methylation/demethylation is recognized as a hallmark of cancer. TET (ten-eleven translocation) family members are novel DNA demethylation related proteins that dysregulate in multiple malignances. However, their effects on ovarian cancer remain to be elucidated. Methods: The changes of TET family members during TGF-?1-induced epithelial-mesenchymal transition (EMT) in SKOV3 and 3AO ovarian cancer cells were detected. TET3 was ectopically expressed in TGF-?1-treated ovarian cancer cells to examine its effect on TGF-?1-induced EMT phenotype. The downstream target of TET3 was further identified. Finally, the relationships of TET3 expression to clinic-pathological parameters of ovarian cancer were investigated with a tissue microarray using immunohistochemistry. Results: TET3 was downregulated during TGF-?1-initiatd epithelial-mesenchymal transition (EMT) in SKOV3 and 3AO ovarian cancer cells. Overexpression of TET3 reversed TGF-?1-induced EMT phenotypes including the expression pattern of molecular markers (E-cadherin, Vimentin, N-cadherin, Snail) and migratory and invasive capabilities of ovarian cancer cells. miR-30d was identified as a downstream target of TET3, and TET3 overexpression resumed the demethylation status in the promoter region of miR-30d precursor gene, resulting in restoration of miR-30d (an EMT suppressor of ovarian cancer cells proven in our previous study) level in TGF-?1-induced EMT. We further found that TET3 expression was decreased in ovarian cancer tissues, especially in serous ovarian cancers. The overall positivity of TET3 was inversely correlated with the grade of differentiation status of ovarian cancer. Conclusion: Our results revealed that TET3 acted as a suppressor of ovarian cancer by demethylating miR-30d precursor gene promoter to block TGF-?1-induced EMT. Electronic supplementary material: The online version of this article (doi:10.1186/s13046-016-0350-y) contains supplementary material, which is available to authorized users. äTET3 inhibits TGF-?1-induced epithelial-mesenchymal transition by deme(epmc).pdf DeepDyve Pubget Overpricing