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 |
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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. |
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ISSN: | 2251-6085 2251-6093 |
DOI: | 10.18502/ijph.v49i7.3583 |