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首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Manganese superoxide dismutase in breast cancer: From molecular mechanisms of gene regulation to biological and clinical significance
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Manganese superoxide dismutase in breast cancer: From molecular mechanisms of gene regulation to biological and clinical significance

机译:乳腺癌中的锰超氧化物歧化酶:从基因调控分子机制到生物学和临床意义

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摘要

Breast cancer is one of the most common malignancies of all cancers in women worldwide. Many difficulties reside in the prediction of tumor metastatic progression because of the lack of sufficiently reliable predictive biological markers, and this is a permanent preoccupation for clinicians. Manganese superoxide dismutase (MnSOD) may represent a rational candidate as a predictive biomarker of breast tumor metastatic progression, because its gene expression is profoundly altered between early and advanced breast cancer, in contrast to expression in the normal mammary gland. In this review, we report the characterization of some gene polymorphisms and molecular mechanisms of SOD2 gene regulation, which allows a better understanding of how MnSOD is decreased in early breast cancer and increased in advanced breast cancer. Several studies display the biological significance of MnSOD level in proliferation as well as in invasive and angiogenic abilities of breast tumor cells by controlling superoxide anion radical (Or) and hydrogen peroxide (H2O2). Particularly, they report how these reactive oxygen species may activate some signaling pathways involved in breast tumor growth. Emerging understanding of these findings provides an interesting framework for guiding translational research and suggests a way to define precisely the clinical interest of MnSOD as a prognostic and/or predicting marker in breast cancer, by associating with some regulators involved in SOD2 gene regulation and other well-known biomarkers, in addition to the typical clinical parameters. (C) 2014 Elsevier Inc. All rights reserved.
机译:乳腺癌是全球妇女所有癌症中最常见的恶性肿瘤之一。由于缺乏足够可靠的预测性生物学标志物,许多困难在预测肿瘤转移性进展中,这是临床医生的永久性关注。锰超氧化物歧化酶(MNSOD)可以代表理性候选者作为乳腺肿瘤转移性进展的预测生物标志物,因为其基因表达在早期和晚期乳腺癌之间是深刻的,与正常乳腺的表达相反。在该综述中,我们报告了SOD2基因调节一些基因多态性和分子机制的表征,这允许更好地了解早期乳腺癌中的MNSOD如何降低,并且在晚期乳腺癌中增加。几项研究通过控制超氧化物阴离子(或)和过氧化氢(H2O2),显示出胃癌患者的增殖水平的生物学意义以及乳腺肿瘤细胞的侵袭性和血管生成能力。特别是,他们报告这些反应性氧气物种如何激活乳腺肿瘤生长中涉及的一些信号通路。对这些调查结果的新兴了解提供了一个有趣的框架,用于指导翻译研究,并表明一种方法可以通过与参与SOD2基因调节和其他良好的一些调节剂相关联 - 除了典型的临床参数之外,已知的生物标志物。 (c)2014年elsevier Inc.保留所有权利。

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