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PIWIL2 interacting with IKK to regulate autophagy and apoptosis in esophageal squamous cell carcinoma

机译:Piwil2与IKK相互作用以调节食管鳞状细胞癌中的自噬和凋亡

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摘要

Total mRNAs and proteins were extracted from tissue samples of eight individual ESCC patients, and subjected to RT-PCR (a) and western blot (b) respectively. T, tumor tissues; P, paratumor tissues. c ESCC cell lines (KYSE150, KYSE180, KYSE510, and Eca-109) and normal esophageal epithelial cell line Het-1A were subjected to expression analysis of PIWIL2 using western blotting (WB). d Kaplan–Meier curve depicting the long-term survival of the ESCC patients (n = 109). The curves were stratified based on the PIWIL2 level scored by intensity (0–3) and area (0–4) of the staining with TMA and IH technology (Log-rank test, p = 0.005). e Patients were randomly selected from PIWIL2 high-expression group and low-expression group (two from each). Biomarkers of autophagy (LC3 and P62) were analyzed using immunohistochemistry. Scale bar, 20 µm. *p < 0.05; ***p < 0.001.
机译:从八个个体ESCC患者的组织样品中提取全MRNA和蛋白质,分别进行RT-PCR(A)和Western Blot(B)。 T,肿瘤组织; p,实体组织。 C ESCC细胞系(Kyse150,Kyse180,KySe510和ECA-109)和正常食管上皮细胞系HET-1A使用Western印迹(WB)对PiWil2的表达分析进行表达分析。 D Kaplan-Meier曲线描绘了ESCC患者的长期存活(n = 109)。基于由TMA和IH技术的染色强度(0-3)和面积(0-4)评分的PIWIL2水平分具有曲线(对数级测试,P = 0.005)。 e患者从piwil2高表达组和低表达组中随机选择(来自每次)。使用免疫组化分析自噬(LC3和P62)的生物标志物。秤杆,20μm。 * P <0.05; *** p <0.001。

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