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Metallothionein 1E mRNA is highly expressed in oestrogen receptor-negative human invasive ductal breast cancer

机译:金属硫蛋白1E mRNA在雌激素受体阴性的人类浸润性导管癌中高表达

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摘要

Metallothioneins (MTs), a group of ubiquitous metalloproteins, comprise isoforms encoded by ten functional genes in humans. Different MT isoforms possibly play different functional roles during development or under various physiological conditions. The MT-1E isoform mRNA has been recently shown to be differentially expressed in oestrogen receptor (OR)-positive and OR-negative breast cancer cell lines. In this study, we evaluated MT-1E mRNA expression via semi-quantitative RT-PCR in 51 primary invasive ductal breast cancer tissues, concurrently with OR-positive and progesterone receptor (PR)-positive MCF7 cells, OR-negative and PR-negative MDA-MB-231 cells and PR-transfected MDA-MB-231 breast cancer cells (ABC28). We demonstrated significantly higher MT-1E mRNA expression in OR-negative compared with OR-positive breast cancer tissues (P= 0.026). MCF7 cells lacked MT-1E mRNA expression, while both OR- and PR-negative MDA-MD-231 cells exhibited a high level of MT-1E mRNA expression. The level of MT-1E mRNA expression in progesterone-treated and -untreated ABC28 cells remained similar as the parental cell line MDA-MB-231-C2 cells. The results suggest that MT-1E may have specific and functional roles in OR-negative invasive ductal breast cancers, possibly mediated via effector genes downstream of the oestrogen receptor, but not through the PR pathway. © 2000 Cancer Research Campaign
机译:金属硫蛋白(MTs)是一组普遍存在的金属蛋白,包含人类十种功能基因编码的同工型。在发育过程中或在各种生理条件下,不同的MT同工型可能发挥不同的功能作用。最近已显示MT-1E亚型mRNA在雌激素受体(OR)阳性和OR阴性乳腺癌细胞系中差异表达。在这项研究中,我们通过半定量RT-PCR评价了51例原发性导管癌组织中MT-1E mRNA的表达,并与OR阳性和孕激素受体(PR)阳性的MCF7细胞,OR阴性和PR阴性同时进行MDA-MB-231细胞和PR转染的MDA-MB-231乳腺癌细胞(ABC28)。我们证明与OR阳性乳腺癌组织相比,OR阴性的MT-1E mRNA表达明显更高(P = 0.026)。 MCF7细胞缺乏MT-1E mRNA表达,而OR和PR阴性的MDA-MD-231细胞均表现出高水平的MT-1E mRNA表达。孕酮处理和未处理的ABC28细胞中MT-1E mRNA表达水平与亲本细胞系MDA-MB-231-C2细胞相似。结果表明,MT-1E在OR阴性浸润性导管癌中可能具有特异性和功能性作用,可能是通过雌激素受体下游的效应基因介导的,而不是通过PR途径介导的。 ©2000癌症研究运动

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