Effect of miR-215 on the Expression of Tumor Suppressor Gene Rb1 in Retinoblastoma Cell Lines

Effect of miR-215 on the expression of tumor suppressor gene retinoblastoma (Rb)1 in Rb cell lines was investigated. A total of 128 patients were selected. The expression of miR-215 in cancer and adjacent healthy tissues of the 128 patients was detected by reverse transcription-quantitative PCR (RT-...

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Veröffentlicht in:Iranian journal of public health 2020-07, Vol.49 (7), p.1298-1306
Hauptverfasser: Shao, Liqin, Sheng, Zhangxing, Zhu, Yuefeng, Li, Jianchao, Meng, Rufa
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Sprache:eng
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Zusammenfassung:Effect of miR-215 on the expression of tumor suppressor gene retinoblastoma (Rb)1 in Rb cell lines was investigated. A total of 128 patients were selected. The expression of miR-215 in cancer and adjacent healthy tissues of the 128 patients was detected by reverse transcription-quantitative PCR (RT-qPCR). HXO-Rb44 and Y79 cell lines were transfected with miR-215 analogs or miR-215 inhibitors, and the expression of Rb1 protein in the cell lines was detected by western blotting. The expression of miR-215 in the adjacent healthy tissues of patients was significantly lower than that in cancer tissues ( 0.001). The expression of miR-215 in Y79 and HXO-Rb44 cells was significantly higher than that in APRE-19 cells ( 0.001). The expression of miR-215 in HXO-Rb44 cells was significantly higher than that in Y79 cells ( 0.001). The expression of miR-215 was statistically different from the degree of differentiation and nerve infiltration ( 0.05). The expression of Rb1 in cancer tissues was significantly lower than that in adjacent tissues ( 0.001), the expression of APRE-19 was significantly higher than that in Y79 and HXO-Rb44 cells ( 0.001), and the expression of Rb1 in HXO-Rb44 cells was significantly higher than that in Y79 cells ( 0.05). There was a negative correlation between miR-215 and Rb1 in the tissues of patients, and Rb1 expression decreased with the increase of miR-215 (r=-0.576, 0.001). miR-215 is highly expressed in Rb cell lines, and is related to the clinicopathological features of this disease.
ISSN:2251-6085
2251-6093
DOI:10.18502/ijph.v49i7.3583