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本文引用的文献

1
Zinc transporter-2 (ZnT2) variants are localized to distinct subcellular compartments and functionally transport zinc.锌转运蛋白2(ZnT2)变体定位于不同的亚细胞区室,并在功能上转运锌。
Biochem J. 2009 Jul 29;422(1):43-52. doi: 10.1042/BJ20081189.
2
Prolactin regulates ZNT2 expression through the JAK2/STAT5 signaling pathway in mammary cells.催乳素通过乳腺细胞中的JAK2/STAT5信号通路调节锌转运体2(ZNT2)的表达。
Am J Physiol Cell Physiol. 2009 Aug;297(2):C369-77. doi: 10.1152/ajpcell.00589.2008. Epub 2009 Jun 3.
3
The Znt4 mutation inlethal milk mice affects intestinal zinc homeostasis through the expression of other Zn transporters.致死奶鼠的 Znt4 突变通过其他锌转运蛋白的表达影响肠道锌稳态。
Genes Nutr. 2006 Mar;1(1):61-70. doi: 10.1007/BF02829937.
4
ZIP7-mediated intracellular zinc transport contributes to aberrant growth factor signaling in antihormone-resistant breast cancer Cells.ZIP7介导的细胞内锌转运促成抗激素耐药性乳腺癌细胞中异常的生长因子信号传导。
Endocrinology. 2008 Oct;149(10):4912-20. doi: 10.1210/en.2008-0351. Epub 2008 Jun 26.
5
Lost in translation? A systematic database of gene expression in breast cancer.迷失在翻译中?乳腺癌基因表达的系统数据库。
Pathobiology. 2008;75(2):112-8. doi: 10.1159/000123849. Epub 2008 Jun 10.
6
The hereditary hemochromatosis protein, HFE, inhibits iron uptake via down-regulation of Zip14 in HepG2 cells.遗传性血色素沉着症蛋白HFE通过下调HepG2细胞中的Zip14来抑制铁摄取。
J Biol Chem. 2008 Aug 1;283(31):21462-8. doi: 10.1074/jbc.M803150200. Epub 2008 Jun 4.
7
The human zinc transporter SLC39A8 (Zip8) is critical in zinc-mediated cytoprotection in lung epithelia.人类锌转运蛋白SLC39A8(Zip8)在锌介导的肺上皮细胞保护中起关键作用。
Am J Physiol Lung Cell Mol Physiol. 2008 Jun;294(6):L1127-36. doi: 10.1152/ajplung.00057.2008. Epub 2008 Apr 4.
8
Concordant correlation of LIV-1 and E-cadherin expression in human breast cancer cell MCF-7.人乳腺癌细胞MCF-7中LIV-1与E-钙黏蛋白表达的一致性相关性
Mol Biol Rep. 2009 Apr;36(4):653-9. doi: 10.1007/s11033-008-9225-4. Epub 2008 Mar 11.
9
Zip6 (LIV-1) regulates zinc uptake in neuroblastoma cells under resting but not depolarizing conditions.Zip6(LIV-1)在静息而非去极化条件下调节神经母细胞瘤细胞对锌的摄取。
Brain Res. 2008 Mar 14;1199:10-9. doi: 10.1016/j.brainres.2008.01.015. Epub 2008 Jan 18.
10
Slc39a14 gene encodes ZIP14, a metal/bicarbonate symporter: similarities to the ZIP8 transporter.Slc39a14基因编码ZIP14,一种金属/碳酸氢盐共转运蛋白:与ZIP8转运蛋白的相似性。
Mol Pharmacol. 2008 May;73(5):1413-23. doi: 10.1124/mol.107.043588. Epub 2008 Feb 12.

乳腺的锌代谢:调节与失调。

Mammary gland zinc metabolism: regulation and dysregulation.

机构信息

Department of Nutritional Sciences, The Pennsylvania State University, 222 Chandlee Laboratory, University Park, PA, 16802, USA,

出版信息

Genes Nutr. 2009 Jun;4(2):83-94. doi: 10.1007/s12263-009-0119-4. Epub 2009 Apr 2.

DOI:10.1007/s12263-009-0119-4
PMID:19340474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2690727/
Abstract

Zinc (Zn) is required for numerous metabolic processes serving both a structural and catalytic role. The mammary gland has a unique Zn requirement resulting from the need to also transfer an extraordinary amount of Zn into milk (~0.5-1 mg Zn/day) during lactation. Impairments in this process can result in severe Zn deficiency in the nursing offspring which has adverse consequences with respect to growth and development. Moreover, dysregulated mammary gland Zn metabolism has recently been implicated in breast cancer transition, progression and metastasis, thus there is a critical need to understand the molecular mechanisms which underlie these observations. Tight regulation of Zn transporting mechanisms is critical to providing an extraordinary amount of Zn for secretion into milk as well as maintaining optimal cellular function. Expression of numerous Zn transporters has been detected in mammary gland or cultured breast cells; however, understanding the molecular mechanisms which regulate mammary Zn metabolism as well as the etiology and downstream consequences resulting from their dysregulation is largely not understood. In this review, we will summarize the current understanding of the regulation of mammary gland Zn metabolism and its regulation by reproductive hormones, with a discussion of the dysregulation of this process in breast cancer.

摘要

锌(Zn)是许多代谢过程所必需的,具有结构和催化作用。乳腺具有独特的锌需求,这是因为在哺乳期还需要将大量的锌转移到乳汁中(~0.5-1 mg Zn/天)。如果这个过程受损,哺乳后代可能会出现严重的缺锌,这对其生长和发育会产生不利影响。此外,最近乳腺中锌代谢的失调与乳腺癌的转变、进展和转移有关,因此迫切需要了解这些观察结果背后的分子机制。严格调控锌转运机制对于为分泌到乳汁中提供大量的锌以及维持最佳的细胞功能至关重要。在乳腺或培养的乳腺细胞中已经检测到许多锌转运体的表达;然而,对于调节乳腺锌代谢的分子机制以及其失调的病因和下游后果,人们的理解还很有限。在这篇综述中,我们将总结目前对乳腺锌代谢的调节及其受生殖激素调节的理解,并讨论该过程在乳腺癌中的失调。