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Differential expression of p42.3 in low- and high-grade gliomas

机译:p42.3在低度和高度神经胶质瘤中的差异表达

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Background Malignant gliomas are the most common form of primary malignant brain tumor. It has recently been suggested that genetic changes are involved in the progression of malignant gliomas. In previous studies, a novel gene, p42.3 , was characterized as a tumor-specific gene that encodes a mitosis phase–dependent expression protein which is expressed in gastric cancer, but not in matched normal tissues. Methods In a series of 200 human brain gliomas and 13 normal tissues, we performed RT-PCR and mRNA in situ hybridization for analysis of p42.3 gene expression in gliomas, including astrocytoma (grade 2), oligoastrocytomas (grade 2), anaplastic oligoastrocytomas (grade 3), glioblastomas (grade 4) and normal tissues. Also, the mRNA expression was detected in gliomas by in situ hybridization. After producing polyclonal antibody to p42.3, we further tested p42.3 protein expression in astrocytomas and glioblastomas by immunohistochemistry and Western blot analysis. Results Our results demonstrated that overexpression of the p42.3 gene is detected in gliomas, but not in normal brain tissues. Importantly, p42.3 mRNA expression is correlated with the pathological features of gliomas. In addition, p42.3 protein is expressed in both the cytoplasm and the nucleus in astrocytomas, whereas this protein appeared in the cytoplasm in glioblastomas. Conclusions These results indicate that p42.3 might be involved in carcinogenesis as a potential molecular marker for malignant gliomas.
机译:背景恶性神经胶质瘤是原发性恶性脑肿瘤的最常见形式。最近已经提出,遗传改变与恶性神经胶质瘤的发展有关。在先前的研究中,一个新基因p42.3被表征为一种肿瘤特异性基因,该基因编码有丝分裂期依赖性表达蛋白,该蛋白在胃癌中表达,但在匹配的正常组织中不表达。方法在200例人脑神经胶质瘤和13例正常组织中,我们进行了RT-PCR和mRNA原位杂交,以分析神经胶质瘤中p42.3基因的表达,包括星形细胞瘤(2级),少星形细胞瘤(2级),间变性少星形细胞瘤。 (3级),胶质母细胞瘤(4级)和正常组织。另外,通过原位杂交在神经胶质瘤中检测到mRNA表达。产生针对p42.3的多克隆抗体后,我们通过免疫组织化学和Western印迹分析进一步测试了星形细胞瘤和胶质母细胞瘤中p42.3蛋白的表达。结果我们的结果表明,在神经胶质瘤中检测到p42.3基因的过表达,但在正常脑组织中未检测到。重要的是,p42.3 mRNA表达与神经胶质瘤的病理特征有关。另外,星形细胞瘤中p42.3蛋白在细胞质和细胞核中都有表达,而在胶质母细胞瘤中,该蛋白出现在细胞质中。结论这些结果表明,p42.3可能参与了癌变,成为恶性神经胶质瘤的潜在分子标记。

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