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Increased expression of PDIA3 and its association with cancer cell proliferation and poor prognosis in hepatocellular carcinoma

机译:肝细胞癌中PDIA3表达的增加及其与癌细胞增殖和不良预后的关系

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The prognosis of hepatocellular carcinoma (HCC) is unfavorable following complete tumor resection. The aim of the present study was to identify a molecule able to predict HCC prognosis through comprehensive protein profiling and to elucidate its clinicopathological significance. Comprehensive protein profiling of HCC was performed by liquid chromatography-tandem mass spectrometry. Through the bioinformatic analysis of proteins expressed differentially in HCC and non-HCC tissues, protein disulfide-isomerase A3 (PDIA3) was identified as a candidate for the prediction of prognosis. PDIA3 expression was subsequently examined in 86 cases of HCC by immunostaining and associations between PDIA3 expression levels and clinicopathological characteristics were evaluated. The Ki-67 index and apoptotic cell death of carcinoma cells were examined by immunostaining and terminal deoxynucleotidyl transferase dUTP nick-end labeling assay in 24 cases. The results demonstrated that PDIA3 was expressed in all 86 HCC cases; 56 HCC cases (65%) exhibited high expression of PDIA3 and 30 (35%) exhibited low expression. The disease-free and overall survival times of HCC patients with high PDIA3 expression were significantly shorter than in HCC patients with low expression. Furthermore, increased expression of PDIA3 was associated with an elevated Ki-67 index, indicating increased cancer cell proliferation and a reduction in apoptotic cell death. Taken together, these results suggest that PDIA3 expression is associated with tumor proliferation and decreased apoptosis in HCC, and that increased expression of PDIA3 predicts poor prognosis. PDIA3 may therefore be a key molecule in the development of novel targeting therapies for patients with HCC.
机译:完全切除肿瘤后,肝细胞癌(HCC)的预后不良。本研究的目的是鉴定一种能够通过全面的蛋白质谱分析预测HCC预后的分子,并阐明其临床病理意义。通过液相色谱-串联质谱法对肝癌进行全面的蛋白质分析。通过对在HCC和非HCC组织中差异表达的蛋白质进行生物信息学分析,蛋白质二硫键异构酶A3(PDIA3)被确定为预测预后的候选者。随后通过免疫染色检查了86例HCC患者的PDIA3表达,并评估了PDIA3表达水平与临床病理特征之间的关联。通过免疫染色和末端脱氧核苷酸转移酶dUTP缺口末端标记法检测了24例癌细胞的Ki-67指数和凋亡细胞死亡。结果表明PDIA3在所有86例HCC病例中均有表达。 56例HCC病例(65%)表现出PDIA3高表达,30例(35%)表现出低表达。 PDIA3高表达的HCC患者的无病生存期和总体生存时间明显短于低表达的HCC患者。此外,PDIA3的表达增加与Ki-67指数升高有关,表明癌细胞增殖增加和凋亡细胞死亡减少。综上所述,这些结果表明PDIA3表达与HCC中的肿瘤增殖和凋亡减少有关,并且PDIA3表达的增加预示了不良的预后。因此,PDIA3可能是开发针对HCC患者的新型靶向疗法的关键分子。

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