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姜浩, 宋鑫, 孙治国, 李娟. Wnt信号通路在ALDH1A1影响胃癌细胞生物学行为中作用[J]. 中国公共卫生, 2016, 32(10): 1333-1336. DOI: 10.11847/zgggws2016-32-10-10
引用本文: 姜浩, 宋鑫, 孙治国, 李娟. Wnt信号通路在ALDH1A1影响胃癌细胞生物学行为中作用[J]. 中国公共卫生, 2016, 32(10): 1333-1336. DOI: 10.11847/zgggws2016-32-10-10
JIANG Hao, SONG Xin, SUN Zhi-guo.et al, . Effect of ALDH1A1 on biological behavior of gastric cancer cells through Wnt signaling pathway[J]. Chinese Journal of Public Health, 2016, 32(10): 1333-1336. DOI: 10.11847/zgggws2016-32-10-10
Citation: JIANG Hao, SONG Xin, SUN Zhi-guo.et al, . Effect of ALDH1A1 on biological behavior of gastric cancer cells through Wnt signaling pathway[J]. Chinese Journal of Public Health, 2016, 32(10): 1333-1336. DOI: 10.11847/zgggws2016-32-10-10

Wnt信号通路在ALDH1A1影响胃癌细胞生物学行为中作用

Effect of ALDH1A1 on biological behavior of gastric cancer cells through Wnt signaling pathway

  • 摘要: 目的 探讨乙醛脱氢酶1A1(ALDH1A1)基因表达对胃癌细胞的生物学行为影响及机制。方法 通过脂质体将shRNA-ALDH1A1载体转染到胃癌MKN-45细胞,48 h后,采用RT-PCR及蛋白印迹(WB)法检测转染后MKN-45细胞中ALDH1A1蛋白及mRNA表达;四唑盐(MTT)法检测细胞活力;Transwell法检测胃癌细胞迁移及侵袭能力;WB检测细胞中基质金属蛋白酶2(MMP2)、MMP9及Wnt/β-catenin信号通路表达情况。结果 shRNA-ALDH1A1转染组MKN-45细胞中ALDH1A1蛋白及mRNA表达量分别为(0.09±0.01)、(0.08±0.01)明显低于对照组分别为(0.89±0.09)、(0.48±0.05); shRNA-ALDH1A1组MKN-45细胞活力(0.40±0.04)低于对照组(0.73±0.07),细胞迁移、侵袭数目分别为(39.78±3.24)、(42.53±4.25)个/视野少于对照组分别为(98.86±9.03)、(90.52±9.14)个/视野;shRNA-ALDH1A1组MKN-45细胞中MMP2、MMP9、Wnt1、Wnt5a及β-catenin表达水平分别为(0.10±0.01)、(0.10±0.01)、(0.28±0.03)、(0.12±0.01)、(0.19±0.02)明显低于对照组分别为(0.49±0.04)、(0.95±0.09)、(1.29±0.12)、(0.52±0.04)、(0.56±0.05),差异均具有统计学意义(P<0.01)。结论 ALDH1A1基因沉默可明显降低胃癌细胞MKN-45活力、抑制细胞迁移、侵袭能力,其机制可能与抑制Wnt/β-catenin信号通路有关。

     

    Abstract: Objective To explore the effect of aldehyde dehydrogenases 1A1 (ALDH1A1) on biological behavior of gastric cancer cell MKN-45 through wingless protein (Wnt) signaling pathway.Methods MKN-45 cells were transferred with the control and sh-RNA-ALDH1A1.The expression of ALDH1A1 in MK-45 cells was determined with reveres transcriptase-PCR (RT-PCR) and Western blot.The cell viability was detected with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay.The cell migration and invasion were detected with transwell method.The expressions of matrix metalloproteinase 2 (MMP2),matrix metalloproteinase 9 (MMP9),Wnt1,Wnt5a,and β-catenin were detected with Western blot.Results Compared with those of the control group,the ALDH1A1 transfected cells showed significantly down-regulated expressions of ALDH1A1 protein (0.89±0.09 vs. 0.09±0.01) and mRNA (0.48±0.05 vs. 0.08±0.01),decreased cell viability (0.73±0.07 vs. 0.40±0.04),inhibited cell migration (98.86±9.03 vs. 39.78±3.24) and invasion (90.52±9.14 vs. 42.53±4.25),and down-regulated expressions of MMP2 (0.49±0.04 vs. 0.10±0.01),MMP9 (0.95±0.09 vs. 0.10±0.01),Wnt1 (1.29±0.12 vs. 0.28±0.03),Wnt5a (0.52±0.04 vs. 0.12±0.01),and β-catenin (0.56±0.05 vs. 0.19±0.02) (P<0.01 for all).Conclusion ALDH1A1 silence could decrease cell viability and inhibit cell migration and invasion via regulation of Wnt signal pathway in MK-45 cells.

     

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