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HBXIP表达可预测乳腺癌患者的预后。

HBXIP expression predicts patient prognosis in breast cancer.

作者信息

Cheng Daye, Liang Bin, Li Yunhui

机构信息

Department of Transfusion, The First Hospital of China Medical University, North Nanjing Street, No. 155, Shenyang, People's Republic of China,

出版信息

Med Oncol. 2014 Oct;31(10):210. doi: 10.1007/s12032-014-0210-6. Epub 2014 Sep 2.

DOI:10.1007/s12032-014-0210-6
PMID:25178941
Abstract

Emerging evidence demonstrated that hepatitis B virus X-interacting protein (HBXIP) has broad roles in cancers. The aim of the study is to investigate the association between HBXIP expression and clinicopathological features of breast cancer patients so as to determine whether HBXIP protein may be correlated with poor prognosis in breast cancer patients. HBXIP protein expression was assessed in a well-characterized series of breast cancer (n=196) with long-term follow-up, using immunohistochemistry method. Correlation between HBXIP expression and clinicopathological factors was analyzed. The effects of several variables on survival were tested by a Cox proportional hazards regression analysis. High HBXIP expression was predominantly observed in breast cancer tissues but not the adjacent normal breast tissues. The expression of HBXIP was high in 125 (63.8%) of the 196 cancer patients and low in 71 (36.2%) of the 196 patients, respectively. High HBXIP expression was positively correlated with TNM stage (P=0.001), lymph node metastasis (P<0.001), and Ki67 expression (P=0.002). The patients with high HBXIP expression had lower 5-year overall survival (OS) and disease-free survival (DFS) rates than those with low HBXIP expression as determined using the Kaplan-Meier method (OS: P=0.006; DFS: P=0.022). In Cox regression analysis, both HBXIP expression (P=0.002 and P=0.009, respectively) and lymph node metastasis (P<0.001 and P=0.008, respectively) were associated with poor OS and DFS. Our study suggested that high HBXIP is associated with the progression of breast cancer. HBXIP could be a valuable prognostic marker as well as a potential molecular therapy target for breast cancer patients.

摘要

新出现的证据表明,乙型肝炎病毒X相互作用蛋白(HBXIP)在癌症中具有广泛作用。本研究的目的是调查HBXIP表达与乳腺癌患者临床病理特征之间的关联,以确定HBXIP蛋白是否可能与乳腺癌患者的不良预后相关。采用免疫组织化学方法,对一系列特征明确且有长期随访的196例乳腺癌患者评估HBXIP蛋白表达。分析HBXIP表达与临床病理因素之间的相关性。通过Cox比例风险回归分析测试几个变量对生存的影响。主要在乳腺癌组织中观察到高HBXIP表达,而在相邻的正常乳腺组织中未观察到。在196例癌症患者中,125例(63.8%)的HBXIP表达高,71例(36.2%)的HBXIP表达低。高HBXIP表达与TNM分期(P=0.001)、淋巴结转移(P<0.001)和Ki67表达(P=0.002)呈正相关。使用Kaplan-Meier方法确定,HBXIP表达高的患者5年总生存率(OS)和无病生存率(DFS)低于HBXIP表达低的患者(OS:P=0.006;DFS:P=0.022)。在Cox回归分析中,HBXIP表达(分别为P=0.002和P=0.009)和淋巴结转移(分别为P<0.001和P=0.008)均与不良的OS和DFS相关。我们的研究表明,高HBXIP与乳腺癌进展相关。HBXIP可能是乳腺癌患者有价值的预后标志物以及潜在的分子治疗靶点。

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本文引用的文献

1
Downregulation of GLTSCR2 expression is correlated with breast cancer progression.GLTSCR2 表达下调与乳腺癌的进展相关。
Pathol Res Pract. 2013 Nov;209(11):700-4. doi: 10.1016/j.prp.2013.07.010. Epub 2013 Aug 27.
2
The diverse distribution of risk factors between breast cancer subtypes of ER, PR and HER2: a 10-year retrospective multi-center study in China.雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(HER2)乳腺癌亚型之间危险因素的多样分布:一项在中国进行的为期10年的回顾性多中心研究
PLoS One. 2013 Aug 20;8(8):e72175. doi: 10.1371/journal.pone.0072175. eCollection 2013.
3
The oncoprotein HBXIP upregulates PDGFB via activating transcription factor Sp1 to promote the proliferation of breast cancer cells.
癌蛋白HBXIP通过激活MMP15表达促进肝癌细胞转移。
Cancer Manag Res. 2019 May 16;11:4529-4540. doi: 10.2147/CMAR.S198783. eCollection 2019.
4
Oncoprotein LAMTOR5 Activates GLUT1 Via Upregulating NF-κB in Liver Cancer.癌蛋白LAMTOR5通过上调肝癌中的NF-κB来激活葡萄糖转运蛋白1。
Open Med (Wars). 2019 Feb 26;14:264-270. doi: 10.1515/med-2019-0022. eCollection 2019.
5
Oncogenic HBXIP enhances ZEB1 through Sp1 to accelerate breast cancer growth.致癌 HBXIP 通过 Sp1 增强 ZEB1 以加速乳腺癌生长。
Thorac Cancer. 2018 Dec;9(12):1664-1670. doi: 10.1111/1759-7714.12878. Epub 2018 Oct 1.
6
Elevated HBXIP expression is associated with aggressive phenotype and poor prognosis in esophageal squamous cell carcinoma.HBXIP表达升高与食管鳞状细胞癌的侵袭性表型和不良预后相关。
Am J Cancer Res. 2017 Nov 1;7(11):2190-2198. eCollection 2017.
7
Clinical study on the relationship between hepatitis B virus infection and risk of breast cancer: a large sized case-control and single center study in southwest of China.乙型肝炎病毒感染与乳腺癌风险关系的临床研究:中国西南部一项大型单中心病例对照研究
Oncotarget. 2017 Jul 10;8(42):72044-72053. doi: 10.18632/oncotarget.19132. eCollection 2017 Sep 22.
8
The prevalence and clinicopathological features of breast cancer patients with hepatitis B virus infection in China.中国乙型肝炎病毒感染乳腺癌患者的患病率及临床病理特征
Oncotarget. 2017 Mar 14;8(11):18185-18190. doi: 10.18632/oncotarget.15305.
9
Hepatitis B X-interacting protein promotes cisplatin resistance and regulates CD147 via Sp1 in ovarian cancer.乙型肝炎病毒X相互作用蛋白促进卵巢癌顺铂耐药并通过Sp1调节CD147。
Exp Biol Med (Maywood). 2017 Mar;242(5):497-504. doi: 10.1177/1535370216685007. Epub 2017 Jan 5.
癌蛋白 HBXIP 通过激活转录因子 Sp1 上调 PDGFB 以促进乳腺癌细胞的增殖。
Biochem Biophys Res Commun. 2013 May 3;434(2):305-10. doi: 10.1016/j.bbrc.2013.02.123. Epub 2013 Mar 26.
4
Prognostic value of TMPRSS4 expression in patients with breast cancer.TMPRSS4 表达在乳腺癌患者中的预后价值。
Med Oncol. 2013 Jun;30(2):497. doi: 10.1007/s12032-013-0497-8. Epub 2013 Feb 19.
5
The oncoprotein HBXIP up-regulates Skp2 via activating transcription factor E2F1 to promote proliferation of breast cancer cells.癌蛋白 HBXIP 通过激活转录因子 E2F1 上调 Skp2 以促进乳腺癌细胞的增殖。
Cancer Lett. 2013 Jun 1;333(1):124-32. doi: 10.1016/j.canlet.2013.01.029. Epub 2013 Jan 22.
6
Relationship between NF-κB, ER, PR, Her2/neu, Ki67, p53 expression in human breast cancer.人乳腺癌中NF-κB、雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(Her2/neu)、Ki67、p53表达之间的关系
Exp Oncol. 2012 Dec;34(4):358-63.
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The oncoprotein HBXIP activates transcriptional coregulatory protein LMO4 via Sp1 to promote proliferation of breast cancer cells.癌蛋白 HBXIP 通过 Sp1 激活转录共激活蛋白 LMO4 促进乳腺癌细胞的增殖。
Carcinogenesis. 2013 Apr;34(4):927-35. doi: 10.1093/carcin/bgs399. Epub 2013 Jan 5.
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The oncoprotein HBXIP uses two pathways to up-regulate S100A4 in promotion of growth and migration of breast cancer cells.癌蛋白 HBXIP 通过两种途径上调 S100A4,促进乳腺癌细胞的生长和迁移。
J Biol Chem. 2012 Aug 31;287(36):30228-39. doi: 10.1074/jbc.M112.343947. Epub 2012 Jun 27.
9
HBXIP upregulates CD46, CD55 and CD59 through ERK1/2/NF-κB signaling to protect breast cancer cells from complement attack.HBXIP 通过 ERK1/2/NF-κB 信号上调 CD46、CD55 和 CD59,从而保护乳腺癌细胞免受补体攻击。
FEBS Lett. 2012 Mar 23;586(6):766-71. doi: 10.1016/j.febslet.2012.01.039. Epub 2012 Jan 27.
10
miR-520b regulates migration of breast cancer cells by targeting hepatitis B X-interacting protein and interleukin-8.miR-520b 通过靶向乙型肝炎 X 相互作用蛋白和白细胞介素-8 调节乳腺癌细胞的迁移。
J Biol Chem. 2011 Apr 15;286(15):13714-22. doi: 10.1074/jbc.M110.204131. Epub 2011 Feb 22.