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Breast. 2016 Dec;30:151-155. doi: 10.1016/j.breast.2016.09.015. Epub 2016 Oct 14.
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Androgen-induced miR-27A acted as a tumor suppressor by targeting MAP2K4 and mediated prostate cancer progression.雄激素诱导的miR-27A通过靶向MAP2K4发挥肿瘤抑制作用并介导前列腺癌进展。
Int J Biochem Cell Biol. 2016 Oct;79:249-260. doi: 10.1016/j.biocel.2016.08.043. Epub 2016 Sep 1.
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Global cancer statistics, 2012.全球癌症统计数据,2012 年。
CA Cancer J Clin. 2015 Mar;65(2):87-108. doi: 10.3322/caac.21262. Epub 2015 Feb 4.
4
Mitogen-activated protein kinase kinase 4 (MAP2K4) promotes human prostate cancer metastasis.丝裂原活化蛋白激酶激酶4(MAP2K4)促进人类前列腺癌转移。
PLoS One. 2014 Jul 14;9(7):e102289. doi: 10.1371/journal.pone.0102289. eCollection 2014.
5
MicroRNA-27a promotes proliferation, migration and invasion by targeting MAP2K4 in human osteosarcoma cells.微小RNA-27a通过靶向人骨肉瘤细胞中的丝裂原活化蛋白激酶激酶4促进细胞增殖、迁移和侵袭。
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Histopathology. 2013 Sep;63(3):362-70. doi: 10.1111/his.12176. Epub 2013 Jun 12.
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8
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A nation-wide multicenter 10-year (1999-2008) retrospective clinical epidemiological study of female breast cancer in China.中国一项全国范围的多中心十年(1999-2008 年)回顾性临床流行病学研究:女性乳腺癌。
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[丝裂原活化蛋白激酶激酶4和雌激素受体在浸润性乳腺癌中的表达及其临床意义]

[Expressions of MAP2K4 and estrogen receptor and their clinical significance in invasive breast cancer].

作者信息

Liu Shu, Liu Yi-Yi, Li Rong

机构信息

Guizhou Maternity and Child Health Hospital,Guiyang 550003, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2016 Apr 20;37(4):488-493. doi: 10.3969/j.issn.1673-4254.2017.04.11.

DOI:10.3969/j.issn.1673-4254.2017.04.11
PMID:28446401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6744108/
Abstract

OBJECTIVE

To explore the association of mitogen-activated protein kinase kinase-4 (MAP2K4) with the pathological features, prognosis and expression of estrogen receptor (ER) in patients with breast cancer.

METHODS

The expression of MAP2K4 was detected immunohistochemically in 102 breast cancer tissues. Chi square test was used to analyze the correlation of MAP2K4 expression with the clinicopathological features of the patients. Kaplan-Meier and log rank test were used for survival analysis of the patients. Multivariate survival analysis was performed using Cox proportional hazard regression model. The correlation between the expressionsof MAP2K4 and ER was investigated using Spearman rank correlation test.

RESULTS

Immunohistochemical analysis revealed low MAP2K4 expression in 55.9%(57/102) and high MAP2K4 expression in 44.1%(45/102) of the breast cancer tissues. The expression of MAP2K4 was significantly correlated with the pathological grades of breast cancer (P=0.011). Kaplan-Meier survival analysis showed that patients with a high expression of MAP2K4 had a shorter overall survival rate than those with low MAP2K4 expressions (P=0.009). Multivariate analysis identified high expression of MAP2K4 as the independent predictor of a poor outcome of patients with breast cancer. The expressions of MAP2K4 and ER were not significantly correlated, but ER-negative patients with a high MAP2K4 expressionshowed the shortest overall survival time.

CONCLUSION

Overexpression of MAP2K4 promotes the progression in breast cancer and is associated with a poor outcome of the patients. TheER-negativepatients with a high MAP2K4 expression have the shortest overall survival time, suggestingthe value of combined examination of MAP2K4 and ER in accurate estimation of the prognosis of breast cancer patients.

摘要

目的

探讨丝裂原活化蛋白激酶激酶4(MAP2K4)与乳腺癌患者病理特征、预后及雌激素受体(ER)表达的相关性。

方法

采用免疫组织化学法检测102例乳腺癌组织中MAP2K4的表达。采用卡方检验分析MAP2K4表达与患者临床病理特征的相关性。采用Kaplan-Meier法和对数秩检验对患者进行生存分析。使用Cox比例风险回归模型进行多因素生存分析。采用Spearman等级相关检验研究MAP2K4与ER表达之间的相关性。

结果

免疫组织化学分析显示,55.9%(57/102)的乳腺癌组织中MAP2K4表达低,44.1%(45/102)的乳腺癌组织中MAP2K4表达高。MAP2K4的表达与乳腺癌的病理分级显著相关(P = 0.011)。Kaplan-Meier生存分析表明,MAP2K4高表达的患者总生存率低于MAP2K4低表达的患者(P = 0.009)。多因素分析确定MAP2K4高表达是乳腺癌患者预后不良的独立预测因素。MAP2K4与ER的表达无显著相关性,但MAP2K4高表达的ER阴性患者总生存时间最短。

结论

MAP2K4过表达促进乳腺癌进展并与患者不良预后相关。MAP2K4高表达的ER阴性患者总生存时间最短,提示联合检测MAP2K4和ER对准确评估乳腺癌患者预后具有重要价值。