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A Single Talent Immunogenic Membrane Antigen and Novel Prognostic Predictor: voltage-dependent anion channel 1 (VDAC1) in Pancreatic Cancer

机译:单一人才免疫原性膜抗原和新型预后预测:胰腺癌中的电压依赖性阴离子通道1(VDAC1)。

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摘要

Immunogenic membrane antigens associated with multiple biological functions of human cancer cells, have significant value in molecule diagnosis and targeted therapy. Here we screened immunogenic membrane antigens in pancreatic cancer by immunobloting IgG purified from sera of 66 pancreatic cancer patients with membrane proteins separated from two-dimensional PAGE of human pancreatic cancer cell line SWl990, and identified voltage-dependent anion channel 1 (VDAC1) as one of the potential immunogenic membrane antigens. Further studies focusing on VDAC1 demonstrated that VDAC1 mRNA and protein were significantly expressed in the tested pancreatic cancer cell lines. VDAC1 silencing with RNAi significantly decreased cell growth, invasion and migration in the pancreatic cancer cell line Capan-1. Additionally, VDAC1 expression was upregulated in pancreatic cancer tissue compared with normal pancreas samples and patients with low VDAC1 expression had a significantly greater median survival compared to those with high expression (27.0 months vs. 17.8 months, P = 0.039). In multivariable analysis, VDAC1 staining was an independent prognostic factor for survival [(Hazard-Ratio) HR = 1.544, 95% CI = 0.794–3.0, P = 0.021]. These results demonstrated that VDAC1 may be a candidate immunogenic membrane antigen for pancreatic cancer, a potential independent prognostic marker, and an ideal drug target.
机译:与人类癌细胞的多种生物学功能相关的免疫原性膜抗原在分子诊断和靶向治疗中具有重要价值。在这里,我们用从人胰腺癌细胞系SWl990的二维PAGE分离的膜蛋白对从66例胰腺癌患者血清中纯化的IgG进行免疫印迹,筛选了胰腺癌中的免疫原性膜抗原,并确定了电压依赖性阴离子通道1(VDAC1)潜在的免疫原性膜抗原。专注于VDAC1的进一步研究表明,VDAC1 mRNA和蛋白在受试胰腺癌细胞系中表达明显。用RNAi沉默VDAC1可显着降低胰腺癌细胞系Capan-1中的细胞生长,侵袭和迁移。此外,与正常胰腺样品相比,胰腺癌组织中的VDAC1表达上调,而低VDAC1表达的患者的中位生存期明显高于高表达胰腺癌的患者(27.0个月比17.8个月,P = 0.039)。在多变量分析中,VDAC1染色是生存的独立预后因素[(危险比)HR = 1.544,95%CI = 0.794-3.0,P = 0.021]。这些结果表明,VDAC1可能是胰腺癌的候选免疫原性膜抗原,潜在的独立预后标志物和理想的药物靶标。

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