首页|长链非编码RNA SNHG1对结直肠癌增殖、迁移的影响及调控机制

长链非编码RNA SNHG1对结直肠癌增殖、迁移的影响及调控机制

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目的:探讨长链非编码RNA小核仁RNA宿主基因1(SNHG1)对结直肠癌(CRC)增殖、迁移的影响及其调控机制.方法:采用实时荧光定量PCR检测人正常结直肠上皮细胞(FHC)、结直肠腺癌细胞系(HT29)细胞中IncRNA SNHG1的表达水平.将HT29细胞分为干扰组(si-SNHG1)和对照组(si-NC),分别转染SNHG1 siRNA和NC siRNA,采用MTT检测细胞增殖活力,Transwell实验检测细胞迁移能力,Western blot检测JAK-STAT信号通路相关蛋白表达.结果:HT29 细胞中SNHG1的表达明显高于FHC细胞,差异有统计学意义(t=17.045,P<0.05);si-SNHGI组细胞增值活性、迁移细胞数均降低,差异有统计学意义(t=16.317、12.714,P<0.05),STAT3蛋白表达差异无统计学意义(t=1.063,P>0.05),P-STAT3蛋白表达减少(t=15.473,P<0.05).结论:SNHG1在CRC细胞中呈高表达,可促进CRC细胞增殖、迁移,其机制可能与SNHG1上调P-STAT3蛋白的表达促进JAK-STAT信号通路活化有关.
Effects of Long Non-coding RNA SNHG1 on Proliferation and Migration of Colorectal Cancer and its Regulatory Mechanism
Objective:To investigate the effects of long non-coding RNA SNHG1 on Proliferation and migration of colorectal cancer and its regulatory mechanisms.Methods:Real-time fluorescence quantitative PCR was used to detect the expression level of IncRNA SNHG1 in human normal colorectal ePithelial cells(FHC)and colorectal adenocarcinoma cell line(HT29)cells.HT29 cells were divided into interference group(si-SNHG1)and control group(si-NC)and transfected with SNHG1 siRNA and NC siRNA,respectively.MTT was used to detect cell proliferation viability,transwell assay was used to detect cell migration ability,and Western blot was used to detect the exPression of proteins related to JAK-STAT signaling pathway.Results:The expression of SNHG1 in HT29 cells was significantly higher than that in FHC cells,and the difference was statistically significant(t=17.045,P<0.05).Compared with the control group,cell value-added activity and the number of migrating cells were reduced in the interference group,and the difference was statistically significant(t=16.317,12.714,P<0.05).The difference in STAT3 protein expression was not statistically significant(t=1.063,P>0.05).P-STAT3 Protein expression was reduced,and the difference was statistically significant(t=15.473,P<0.05).Conclusion:SNHG1 was highly expressed in CRC cells and could promote the proliferation and migration of CRC cells.The mechanism may be related to the upregulation of P-STAT3 protein expression by SNHG1 to promote the activation of JAK-STAT signaling pathway.

Long non-coding RNASNHG1Colorectal cancerProliferationMigration

曹强

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湘潭医卫职业技术学院,湖南 湘潭 411102

长链非编码RNA 小核仁RNA宿主基因1 结直肠癌 增殖 迁移

2024

黑龙江医学
中华医学会黑龙江分会

黑龙江医学

影响因子:0.714
ISSN:1004-5775
年,卷(期):2024.48(4)
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