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A novel validated enzyme-linked immunosorbent assay to quantify soluble hemojuvelin in mouse serum.一种新型经验证的酶联免疫吸附测定法,用于定量检测小鼠血清中的可溶性血红素结合蛋白。
Haematologica. 2013 Feb;98(2):296-304. doi: 10.3324/haematol.2012.070136. Epub 2012 Aug 8.
2
Is hemojuvelin a possible new player in iron metabolism in hemodialysis patients?在血液透析患者的铁代谢中,血红素结合蛋白是否是一个可能的新角色?
Int Urol Nephrol. 2012 Dec;44(6):1805-11. doi: 10.1007/s11255-011-0084-x. Epub 2011 Dec 1.
3
Control of systemic iron homeostasis by the hemojuvelin-hepcidin axis.血红素结合蛋白-铁调素轴对系统性铁稳态的调控。
Adv Nutr. 2010 Nov;1(1):38-45. doi: 10.3945/an.110.1009. Epub 2010 Nov 16.
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Pharmacologic inhibition of hepcidin expression reverses anemia of chronic inflammation in rats.药物抑制铁调素表达可逆转大鼠慢性炎症性贫血。
Blood. 2011 Nov 3;118(18):4977-84. doi: 10.1182/blood-2011-03-345066. Epub 2011 Jul 5.
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Iron-refractory iron deficiency anemia.铁难治性缺铁性贫血
Semin Hematol. 2009 Oct;46(4):378-86. doi: 10.1053/j.seminhematol.2009.06.006.
6
Anaemia of cancer: an overview of mechanisms involved in its pathogenesis.癌症贫血:其发病机制概述
Med Oncol. 2008;25(1):12-21. doi: 10.1007/s12032-007-9000-8. Epub 2007 Sep 2.
7
Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin.可溶性和细胞相关的血色素沉着症相关蛋白对铁调素mRNA的竞争性调节
Blood. 2005 Oct 15;106(8):2884-9. doi: 10.1182/blood-2005-05-1845. Epub 2005 Jul 5.
8
Time-course analysis of hepcidin, serum iron, and plasma cytokine levels in humans injected with LPS.注射脂多糖的人体中,铁调素、血清铁和血浆细胞因子水平的时间进程分析。
Blood. 2005 Sep 1;106(5):1864-6. doi: 10.1182/blood-2005-03-1159. Epub 2005 May 10.
9
Regulation of hepcidin transcription by interleukin-1 and interleukin-6.白细胞介素-1和白细胞介素-6对铁调素转录的调节
Proc Natl Acad Sci U S A. 2005 Feb 8;102(6):1906-10. doi: 10.1073/pnas.0409808102. Epub 2005 Jan 31.
10
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization.铁调素通过与铁转运蛋白结合并诱导其内化来调节细胞铁外流。
Science. 2004 Dec 17;306(5704):2090-3. doi: 10.1126/science.1104742. Epub 2004 Oct 28.

乳腺癌组织和血清中铁调素与铁转运蛋白的表达及其与贫血的关系。

Hepcidin and ferroportin expression in breast cancer tissue and serum and their relationship with anemia.

作者信息

Pan X, Lu Y, Cheng X, Wang J

机构信息

The First Affiliated Hospital of Suzhou University, Taicang, Jiangsu, P.R.C.

出版信息

Curr Oncol. 2016 Feb;23(1):e24-6. doi: 10.3747/co.23.2840. Epub 2016 Feb 18.

DOI:10.3747/co.23.2840
PMID:26966409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4754065/
Abstract

OBJECTIVE

Our correlation study investigated the relationships of the expression of hepcidin and ferroportin (fpn) in tissues and serum from breast cancer (bca) patients and the relationships of hepcidin and fpn with anemia.

METHODS

We used elisa and immunohistochemistry to detect the expression of hepcidin and fpn in tissue and serum from 62 individuals with bca, and we analyzed correlations between hepcidin and fpn expression in tissue and in serum. At the same time, we evaluated the relationships between hepcidin, fpn, and anemia.

RESULTS

Mean serum hepcidin was 8.18 ± 3.75 μg/L in bca patients with anemia and 4.53 ± 2.07μg/L in those without anemia, a statistically significant difference (t = 3.7090, p < 0.01). Mean serum fpn was obviously lower in the anemia group than in the non-anemia group (1.77 ± 0.51 μg/L vs. 2.46 ± 0.52 μg/L, t = 3.5115, p < 0.01). Serum hepcidin and hemoglobin were negatively correlated (r = -0.502, p < 0.01); however, serum fpn was positively correlated with hemoglobin, and serum hepcidin was negatively correlated with fpn. The rates of hepcidin and fpn expression in bca tissues were 50.0% and 61.2% respectively, but no association with anemia was observed. We also observed no relationship between expression of hepcidin and fpn in serum and in tissue.

CONCLUSIONS

In bca patients, expression of hepcidin in serum was high, but expression of fpn was low, suggesting that serum hepcidin plays a major role in anemia in those patients. Expression of hepcidin and fpn in bca tissue showed no correlation with their expression in serum and no clear relationship with anemia.

摘要

目的

我们的相关性研究调查了乳腺癌(BCA)患者组织和血清中hepcidin和铁转运蛋白(Fpn)的表达关系,以及hepcidin和Fpn与贫血的关系。

方法

我们使用酶联免疫吸附测定(ELISA)和免疫组织化学方法检测了62例BCA患者组织和血清中hepcidin和Fpn的表达,并分析了组织和血清中hepcidin与Fpn表达之间的相关性。同时,我们评估了hepcidin、Fpn与贫血之间的关系。

结果

贫血的BCA患者血清hepcidin平均水平为8.18±3.75μg/L,无贫血患者为4.53±2.07μg/L,差异有统计学意义(t = 3.7090,p < 0.01)。贫血组血清Fpn明显低于非贫血组(1.77±0.51μg/L对2.46±0.52μg/L,t = 3.5115,p < 0.01)。血清hepcidin与血红蛋白呈负相关(r = -0.502,p < 0.01);然而,血清Fpn与血红蛋白呈正相关,血清hepcidin与Fpn呈负相关。BCA组织中hepcidin和Fpn的表达率分别为50.0%和61.2%,但未观察到与贫血有关联。我们还观察到血清和组织中hepcidin与Fpn的表达之间无关系。

结论

在BCA患者中,血清hepcidin表达高,但Fpn表达低,表明血清hepcidin在这些患者的贫血中起主要作用。BCA组织中hepcidin和Fpn的表达与它们在血清中的表达无相关性,与贫血也无明确关系。