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1.
Journal of Southern Medical University ; (12): 1810-1816, 2010.
Article in Chinese | WPRIM | ID: wpr-330836

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of radiosensitivity and X-ray dose on the expression of miR-7 in nasopharyngeal carcinoma (NPC) cells.</p><p><b>METHODS</b>Low radiosensitive NPC cells CNE-1 and high radiosensitive NPC cells CNE-2 were exposed to 0, 2 and 8 Gy X-ray. The total RNAs of the cell lines were extracted 10 h after radiation for reverse transcription of miR-7 and 18S rRNA by stem-loop primer and random hexamers, respectively. The non-irradiated CNE-1 cells served as the control sample and the relative quantity of the expression level was calculated after real-time PCR using SyBR green.</p><p><b>RESULTS</b>miR-7 expression differed significantly between CNE-1 and CNE-2 cells (4.49-/+3.62 vs 1.29-/+1.10, F=135.483, P<0.001). The radiation dose also significantly affected the expression of miR-7 in NPC cells (F=39.565, P<0.001). CNE-1 cells with a 2 Gy exposure had the highest expression level of miR-7, while the non-irradiated CNE-1 cells had the lowest expression. CNE-2 cells exposed to 2 Gy X-ray had the lowest expression level of miR-7 and the non-irradiated CNE-2 cells had the highest.</p><p><b>CONCLUSION</b>Radiosensitivity and radiation dose of X-ray have significant effect on the expression of miR-7 in NPC cells, indicating that miR-7 plays an important role in radioresistance of NPC cells to X-ray, and suppressed miR-7 expression may elevate the radiosensitivity of NPC cells.</p>


Subject(s)
Humans , Apoptosis , Radiation Effects , Carcinoma , Cell Line, Tumor , Dose-Response Relationship, Radiation , Gene Expression Regulation, Neoplastic , Radiation Effects , MicroRNAs , Genetics , Nasopharyngeal Neoplasms , Genetics , Radiation Tolerance , Genetics , X-Rays
2.
Journal of Southern Medical University ; (12): 1522-1525, 2010.
Article in Chinese | WPRIM | ID: wpr-336152

ABSTRACT

<p><b>OBJECTIVE</b>To study the protective effect of ginsenoside Rg1 on cultured rat hippocampal neurons against radiation injury and explore new therapies for preventing radiation encephalopathy.</p><p><b>METHODS</b>Rat hippocampal neurons cultured for 12 days were subjected to a single-dose X-ray exposure of 30 Gy. 4',6-diamidino-2-phenylindole (DAPI) staining was used to detect the neuronal apoptosis and NOS activity kit utilized to evaluate NOS activity in the cells after the exposure.</p><p><b>RESULTS</b>Nuclear condensation was detected in (25.3-/+3.57)% of the neurons 24 h after 30 Gy X-ray exposure, a rate significantly higher than that in the control cells [(1.95-/+0.78)%, P<0.01]. In the neurons pretreated with ginsenoside Rg1, only (7.43-/+1.51)% of the cells presented with nuclear condensation after the exposure, significantly different from the rates in the control cultures and the exposed cultures (P<0.01). The NOS activity of exposed cultures was 6.46-/+0.95 U/ml, significantly higher than that in the control cultures (3.20-/+0.70 U/ml, P<0.01). The NOS activity of the neurons pretreated with ginsenoside Rg1 was 3.85-/+0.69 U/ml, significantly different from that in the control cultures (P<0.05) and the exposed cultures (P<0.01).</p><p><b>CONCLUSION</b>Ginsenoside Rg1 offers significant protective effect on rat hippocampal neurons from radiation-induced apoptosis by reducing the activity of NOS.</p>


Subject(s)
Animals , Rats , Cells, Cultured , Ginsenosides , Pharmacology , Hippocampus , Cell Biology , Radiation Effects , Neurons , Radiation Effects , Neuroprotective Agents , Pharmacology , Nitric Oxide , Metabolism , Nitric Oxide Synthase , Metabolism , Radiation Injuries , Metabolism , Rats, Sprague-Dawley
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