Elevated Expression of Cytosolic Phospholipase A2Delta Is Associated with Lipid Metabolism Dysregulation during Hepatocellular Carcinoma Progression

Maryam Ranjpour, S. Wajid, S. Jain
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引用次数: 3

Abstract

Objective Liver cancer is the third rank amongst the common malignancies, causing maximum death in the patients diagnosed with cancers. Currently available biomarkers are not enough sensitive for early diagnosis of hepatocellular carcinoma (HCC). This makes difficult management of HCC. With the aim of finding new generation of proteomic-based biomarkers, the represented study was designed to characterize the differentially expressed proteins at different stages of HCC initiation and at progression. This could lead to find potential biomarkers for early detection of HCC. Materials and Methods In this experimental study, we report induction of HCC by administrating chemical carcinogens in male Wistar rats. Disease progression was monitored by histological evaluation. Serum proteomic analyses such as 2 dimensional (2D)-electrophoresis, MALDI-TOF-MS/MS and Western blot have been used to analyze and characterize the differentially expressed proteins during HCC development. Results HCC initiation and tumorigenesis were observed at one and four months post carcinogen treatment, respectively. One of the differentially-expressed proteins, namely, cytosolic phospholipase A2delta was significantly up-regulated at very early stage of HCC development. Its expression continued to increase during cancer progression and hepatotumorigenesis stages. Its elevated expression has been confirmed by Western blot analysis. Consistent to this, analyses of the sera in the clinically confirmed liver cancer patients showed elevated expression of this protein, further validating our experimental results. Conclusion This study suggests that elevation in the expression of cytosolic phospholipase A2delta is associated with progression of HCC.
肝细胞癌进展过程中,胞质磷脂酶A2Delta表达升高与脂质代谢失调有关
目的肝癌是常见恶性肿瘤的第三大杀手,在癌症患者中死亡率最高。目前可用的生物标志物对肝细胞癌(HCC)的早期诊断不够敏感。这使得HCC的治疗变得困难。为了寻找新一代基于蛋白质组学的生物标志物,该代表性研究旨在表征HCC发生和发展不同阶段的差异表达蛋白。这可能会导致发现HCC早期检测的潜在生物标志物。材料与方法在本实验研究中,我们报道了化学致癌物在雄性Wistar大鼠中的诱导作用。通过组织学评估监测疾病进展。血清蛋白质组学分析,如二维电泳、MALDI-TOF-MS/MS和Western blot已被用于分析和表征HCC发展过程中的差异表达蛋白。结果肝癌起始和肿瘤发生分别在致癌物治疗后1个月和4个月。其中一种差异表达蛋白,即胞质磷脂酶a2 δ,在HCC发展的早期阶段显著上调。它的表达在癌症进展和肝肿瘤发生阶段持续增加。Western blot分析证实其表达升高。与此一致的是,对临床确诊的肝癌患者的血清分析显示该蛋白的表达升高,进一步验证了我们的实验结果。结论本研究提示胞质磷脂酶a2 δ的表达升高与HCC的进展有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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