首页> 外文期刊>The Journal of Pathology: Clinical Research >High CerS5 expression levels associate with reduced patient survival and transition from apoptotic to autophagy signalling pathways in colorectal cancer
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High CerS5 expression levels associate with reduced patient survival and transition from apoptotic to autophagy signalling pathways in colorectal cancer

机译:高CerS5表达水平与大肠癌患者生存率降低以及从凋亡信号通路向自噬信号通路的过渡有关

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AbstractCeramide synthase 5 is involved in the de novo synthesis of ceramide, a sphingolipid involved in cell death and proliferation. In this study, we investigated the role of ceramide synthase 5 in colorectal cancer by examining ceramide synthase 5 expression, clinico-pathological parameters and association with survival/death signalling pathways in cancer. Immunohistochemical analysis of CerS5 was performed on 102 colorectal cancer samples using tissue microarrays constructed from formalin-fixed and paraffin-embedded tissues. We found strong membranous ceramide synthase 5 staining in 57 of 102 (56%) colorectal cancers. A multivariate Cox regression analysis of ceramide synthase 5 expression adjusted for disease stage, differentiation and lymphovascular invasion revealed reduced 5-year overall survival (p = 0.001) and 5-year recurrence-free survival (p = 0.002), with hazard ratios of 4.712 and 4.322, respectively. The effect of ceramide synthase 5 expression on tumourigenic processes was further characterised by reverse phase protein array analysis. Reverse phase protein arrays were generated from laser capture microdissection-enriched carcinoma cells from 19 fresh-frozen colorectal cancer tissues. Measurements of phosphorylation and total levels of signalling proteins involved in apoptosis, autophagy and other cancer-related pathways revealed two distinct signalling networks; weak membranous ceramide synthase 5 intensity was associated with a proteomic network dominated by signalling proteins linked to apoptosis, whereas strong ceramide synthase 5 intensity was associated with a proteomic sub-network mostly composed of proteins linked to autophagy. In conclusion, high ceramide synthase 5 expression was found in colorectal cancer tissue and was associated with poorer patient outcomes. Our findings suggest that this may be mediated by a transition from apoptotic to autophagy signalling pathways in ceramide synthase 5 High expressing tumours, thus implicating ceramide synthase 5 in the progression of colorectal cancer.
机译:摘要神经酰胺合酶5参与神经酰胺的从头合成,神经酰胺是一种参与细胞死亡和增殖的鞘脂。在这项研究中,我们通过检查神经酰胺合酶5的表达,临床病理参数以及与癌症生存/死亡信号通路的关系,研究了神经酰胺合酶5在大肠癌中的作用。使用由福尔马林固定和石蜡包埋的组织构建的组织微阵列,对102个结直肠癌样品进行了CerS5的免疫组织化学分析。我们在102个(56%)结直肠癌中的57个中发现了强烈的膜神经酰胺合酶5染色。针对疾病阶段,分化和淋巴管浸润进行调整的神经酰胺合酶5表达的多变量Cox回归分析显示,降低的5年总生存期(p = 0.001)和5年无复发生存期(p = 0.002),危险比为4.712和4.322分别。通过反相蛋白质阵列分析进一步表征了神经酰胺合酶5表达对致瘤性过程的影响。从富集了19个新鲜冷冻结直肠癌组织的激光捕获显微解剖的癌细胞中生成了反相蛋白质阵列。对凋亡,自噬和其他与癌症相关的途径中涉及的磷酸化和信号蛋白总水平的测量揭示了两个不同的信号网络。弱的膜状神经酰胺合酶5强度与蛋白质组学网络相关,该蛋白组学网络由与凋亡相关的信号蛋白主导,而强的神经酰胺合酶5强度与蛋白质组学子网络相关,该子组网络主要由与自噬相关的蛋白组成。总之,在结肠直肠癌组织中发现了高神经酰胺合酶5表达,并且与患者预后较差有关。我们的研究结果表明,这可能是由神经酰胺合酶5高表达肿瘤中的凋亡信号转为自噬信号通路所介导的,因此,神经酰胺合酶5参与了结直肠癌的发展。

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