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Nuclear Localization of Catechol-O-Methyltransferase in Neoplastic and Nonneoplastic Mammary Epithelial Cells

机译:赘生物和非赘生性乳腺上皮细胞中邻苯二酚-O-甲基转移酶的核定位

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摘要

Catechol->O-methyltransferase (COMT) plays both a regulatory and protective role in catechol homeostasis. It contributes to the regulation of tissue levels of catecholamines and catecholestrogens (CEs) and, by blocking oxidative metabolism of catechols, prevents endogenous and exogenous catechols from becoming a source of potentially mutagenic electrophiles. Evidence implicating CEs in carcinogenesis, in particular in the hamster kidney model of estrogen-induced cancer, has focused attention on the protective role of COMT in estrogen target tissues. We have previously reported that treating hamsters with estrogens causes translocation of COMT to nuclei of epithelial cells in the renal cortex, the site of CE biosynthesis and where the cancers arise. This finding suggested that nuclear COMT may be a marker of a threat to the genome by catechols, including CEs. It is postulated that CEs play a role in the genesis of breast cancer by contributing to a state of chronic oxidative stress that is presumed to underlie the high incidence of this disease in the United States. Therefore, here we used immunocytochemistry to re-examine human breast parenchyma for nuclear COMT. In addition to confirming previous reports of cytoplasmic COMT in mammary epithelial cells, we identified nuclear COMT in foci of mammary epithelial cells in histologically normal breast tissue of virtually all control (macromastia) and cancer patients and in breast cancer cells. There was no correlation between tissue histology and the numbers of cells with nuclear COMT, the size of foci containing such cells, or intensity of nuclear COMT immunostaining. The focal nature of the phenomenon suggests that nuclear COMT does not serve a housekeeping function but that it reflects a protective response to an increased local catechol load, presumably of CEs and, as such, that it may be a characteristic of the population of women studied who share the same major risk factor for developing breast cancer, that of living in the industrialized West.
机译:儿茶酚-> O -甲基转移酶(COMT)在儿茶酚体内平衡中起调节和保护作用。它有助于调节儿茶酚胺和儿茶酚雌激素(CEs)的组织水平,并通过阻断儿茶酚的氧化代谢,防止内源和外源儿茶酚成为潜在诱变亲电试剂的来源。涉及CEs致癌作用的证据,特别是在雌激素诱导的癌症的仓鼠肾脏模型中,已将注意力集中在COMT在雌激素靶组织中的保护作用上。我们以前曾报道过用雌激素治疗仓鼠会导致COMT易位到肾皮质上皮细胞核,CE生物合成的部位以及发生癌症的地方。这一发现表明,核COMT可能是儿茶酚(包括CE)对基因组构成威胁的标志。据推测,CEs通过促进慢性氧化应激状态而在乳腺癌的发生中发挥作用,据推测,慢性氧化应激是美国这种疾病高发的基础。因此,这里我们使用免疫细胞化学重新检查人的乳房实质是否存在核COMT。除了确认以前关于乳腺上皮细胞中细胞质COMT的报道外,我们还在几乎所有对照(巨乳腺),癌症患者和乳腺癌患者的组织学正常乳腺组织中的乳腺上皮细胞灶中鉴定了核COMT。组织组织学与具有核COMT的细胞数量,包含此类细胞的病灶大小或核COMT免疫染色强度之间没有相关性。这种现象的重点性质表明,核COMT不能起到管家的作用,但是它反映了对局部邻苯二酚负荷(可能是CE)增加的保护性反应,因此,它可能是受研究妇女群体的特征。他们患乳腺癌的主要危险因素是生活在工业化的西方。

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