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首页> 外文期刊>American Journal of Cancer Research >Quantitative DNA hypomethylation of ligand Jagged1 and receptor Notch1 signifies occurrence and progression of breast carcinoma
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Quantitative DNA hypomethylation of ligand Jagged1 and receptor Notch1 signifies occurrence and progression of breast carcinoma

机译:配体Jagged1和受体Notch1的定量DNA低甲基化指示乳腺癌的发生和发展

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Methylation alterations of Jagged1 and Notch1 genes have been reported in non-tumor lesions and a few cancers. However, methylation profiles of Jagged1 promoter and Notch1 exon25 in breast cancer and matched normal tissue and the association of methylation with clinicopathological characteristics still remain unclear. To explore the potential effects of aberrant DNA methylation of Jagged1 and Notch1 on occurrence and progression of breast cancer, we detected the quantitative DNA methylation of Jagged1 and Notch1 in 73 breast cancer (BC) and 20 adjacent normal breast tissues (ANBT) by using MassARRAY spectrometry. The methylation level of overall and majority individual CpG sites of the two genes were synergistically significantly lower in BC than in ANBT. The overall hypomethylation of the two genes, particularly of Jagged1 CpG_8.9.10 and Notch1 CpG_14.15.16 in primary tumors, were markedly associated with lymph node metastasis, advanced stage and high grade. The protein expressions of the both genes were examined by immunohistochemical staining in same cohorts. The expression was significantly inverse correlation with methylation. The two proteins in primary tumor were synergistically up-regulated and dramatically related to lymph node metastasis, advanced stage and high grade. Our findings suggest that the synergetic hypomethylation of Jagged1 and Notch1 genes, especially of Jagged1 CpG_8.9.10 and Notch1 CpG_14.15.16, may involve tumorigenesis and development of breast cancer. The negative relationship between methylation and expression indicates methylation role for expression regulation. The synergetic overexpression of the two proteins further indicates the effects on occurrence and progression of breast cancer.
机译:Jagged1和Notch1基因的甲基化改变已被报道在非肿瘤性病变和一些癌症中。然而,Jagged1启动子和Notch1 exon25在乳腺癌和匹配的正常组织中的甲基化概况以及甲基化与临床病理特征的关联仍不清楚。为了探索Jagged1和Notch1的异常DNA甲基化对乳腺癌发生和发展的潜在影响,我们使用MassARRAY检测了73个乳腺癌(BC)和20个相邻的正常乳腺组织(ANBT)中Jagged1和Notch1的定量DNA甲基化。光谱法。 BC中两个基因的总体CpG位点和大多数个体CpG位点的甲基化水平在协同作用下显着低于ANBT。这两个基因的总体甲基化不足,特别是原发性肿瘤中的Jagged1 CpG_8.9.10和Notch1 CpG_14.15.16基因,明显与淋巴结转移,晚期和高级别相关。在同一队列中通过免疫组织化学染色检查了这两个基因的蛋白质表达。该表达与甲基化显着负相关。原发性肿瘤中的两种蛋白协同上调,与淋巴结转移,晚期和高级别密切相关。我们的研究结果表明Jagged1和Notch1基因,特别是Jagged1 CpG_8.9.10和Notch1 CpG_14.15.16的协同低甲基化,可能涉及乳腺癌的发生和发展。甲基化与表达之间的负相关关系表明甲基化对表达调控的作用。两种蛋白的协同过量表达进一步表明对乳腺癌的发生和发展的影响。

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