首页> 外文期刊>British Journal of Cancer >The prolyl 3-hydroxylases P3H2 and P3H3 are novel targets for epigenetic silencing in breast cancer
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The prolyl 3-hydroxylases P3H2 and P3H3 are novel targets for epigenetic silencing in breast cancer

机译:脯氨酸3-羟基酶P3H2和P3H3是乳腺癌表观遗传沉默的新靶标

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摘要

Expression of P3H2 (Leprel1) and P3H3 (Leprel2) but not P3H1 (Leprecan) is down-regulated in breast cancer by aberrant CpG methylation in the 5′ regulatory sequences of each gene. Methylation of P3H2 appears specific to breast cancer as no methylation was detected in a range of cell lines from other epithelial cancers or from primary brain tumours or malignant melanoma. Methylation in P3H2, but not P3H3, was strongly associated with oestrogen-receptor-positive breast cancers, whereas methylation in P3H3 was associated with higher tumour grade and Nottingham Prognostic Index. Ectopic expression of P3H2 and P3H3 in cell lines with silencing of the endogenous gene results in suppression of colony growth. This is the first demonstration of epigenetic inactivation of prolyl hydroxylases in human cancer, implying that this gene family represents a novel class of tumour suppressors. The restriction of silencing in P3H2 to breast carcinomas, and its association with oestrogen-receptor-positive cases, suggests that P3H2 may be a breast-cancer-specific tumour suppressor.
机译:在乳腺癌中,由于每个基因的5'调控序列中异常的CpG甲基化作用,乳腺癌中的P3H2(Leprel1)和P3H3(Leprel2)的表达被下调。 P3H2的甲基化似乎是乳腺癌特有的,因为在其他上皮癌或原发性脑瘤或恶性黑色素瘤的一系列细胞系中未检测到甲基化。 P3H2(而非P3H3)中的甲基化与雌激素受体阳性乳腺癌密切相关,而P3H3中的甲基化与较高的肿瘤等级和诺丁汉预后指数相关。 P3H2和P3H3在细胞系中异位表达且内源基因沉默导致集落生长受到抑制。这是人类癌症中脯氨酰羟化酶的表观遗传失活的首次证明,这表明该基因家族代表了一类新型的肿瘤抑制因子。 P3H2沉默对乳腺癌的局限性及其与雌激素受体阳性病例的关系表明,P3H2可能是乳腺癌特异性的肿瘤抑制因子。

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