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10.18240/ijo.2017.08.02

http://scihub22266oqcxt.onion/10.18240/ijo.2017.08.02
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suck abstract from ncbi


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pmid28861342      Int+J+Ophthalmol 2017 ; 10 (8): 1195-202
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  • MiR-200c suppresses the migration of retinoblastoma cells by reversing epithelial mesenchymal transition #MMPMID28861342
  • Shao XL; Chen Y; Gao L
  • Int J Ophthalmol 2017[]; 10 (8): 1195-202 PMID28861342show ga
  • AIM: To analyze the relationship between clinical features and epithelial mesenchymal transition (EMT) in retinoblastoma (RB), further to investigate whether miR-200c regulates the EMT and migration of RB cells. METHODS: Expression of EMT-related markers and tumor-related factors were detected by immuno-histochemistry analysis in RB tissue from 29 cases. Correlations between their expression and clinical characteristics were analyzed. The regulation effects of miR-200c on EMT-related markers, tumor-related factors were observed in mRNA level and protein level by real-time polymerase chain reaction (PCR) and Western blot, respectively, in Y79 and Weri-rb1 cells. Its effects on migration force of these RB cell lines were also detected with Transwell test. RESULTS: Lower expression of E-cadherin was present in the cases with malignant prognosis. MiR-200c promoted the expression of E-cadherin and decreased the expression of Vimentin and N-cadherin in Y79 and Weri-rb1 cells. Migration force of RB cells could be inhibited by miR-200c. CONCLUSION: EMT might be associated with bad prognosis in RB. MiR-200c suppresses the migration of retinoblastomatous cells by reverse EMT.
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