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核结合蛋白2信使核糖核酸的高表达:前列腺癌患者总生存的独立预后因素

High expression of nucleobindin 2 mRNA: an independent prognostic factor for overall survival of patients with prostate cancer.

作者信息

Zhang Hongtuan, Qi Can, Wang Andi, Li Liang, Xu Yong

机构信息

National Key Clinical Specialty of Urology, Second Affiliated Hospital of Tianjin Medical University, Tianjin Key Institute of Urology, 23 Pingjiang Road, Hexi District, Tianjin, 300211, China.

出版信息

Tumour Biol. 2014 Mar;35(3):2025-8. doi: 10.1007/s13277-013-1268-z. Epub 2013 Oct 4.

DOI:10.1007/s13277-013-1268-z
PMID:24092574
Abstract

Nucleobindin 2 (NUCB2) has been demonstrated to play critical roles in tumorigenesis and tumor development of breast cancer. The expression change of nucleobindin 2 at mRNA level in prostate cancer (PCa) tissues compared with adjacent benign prostate tissues was detected by using real-time quantitative reverse transcriptase-polymerase chain reaction analysis in our previous study. The data suggests that NUCB2 is a cancer-related gene associated with the aggressive progression and biochemical recurrence-free survival predictor of PCa patients. However, the correlation between the expression of the NUCB2 mRNA and the overall survival of patients with PCa was not analyzed. Thus, the association of NUCB2 mRNA expression with overall survival of PCa patients was analyzed in this study. Kaplan-Meier analysis and Cox proportional hazards regression models were used to investigate the correlation between NUCB2 mRNA expression and prognosis of PCa patients. The Kaplan-Meier survival analysis showed that the high expression of NUCB2 was related to the poor overall survival of patients with PCa. Multivariate Cox analysis showed that NUCB2 mRNA was an independent prognostic factor for overall survival of patients with PCa. In conclusion, we demonstrated that high NUCB2 mRNA expression correlated with poor overall survival in patients with PCa.

摘要

核结合蛋白2(NUCB2)已被证明在乳腺癌的肿瘤发生和肿瘤发展中起关键作用。在我们之前的研究中,通过实时定量逆转录聚合酶链反应分析检测了前列腺癌(PCa)组织与相邻良性前列腺组织相比核结合蛋白2在mRNA水平的表达变化。数据表明,NUCB2是一个与PCa患者的侵袭性进展和无生化复发生存预测相关的癌症相关基因。然而,未分析NUCB2 mRNA表达与PCa患者总生存期之间的相关性。因此,本研究分析了NUCB2 mRNA表达与PCa患者总生存期的关联。采用Kaplan-Meier分析和Cox比例风险回归模型来研究NUCB2 mRNA表达与PCa患者预后的相关性。Kaplan-Meier生存分析表明,NUCB2的高表达与PCa患者较差的总生存期相关。多变量Cox分析表明,NUCB2 mRNA是PCa患者总生存期的独立预后因素。总之,我们证明了PCa患者中NUCB2 mRNA的高表达与较差的总生存期相关。

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circ_001504 promotes the development of renal cell carcinoma by sponging microRNA-149 to increase NUCB2.环状RNA_001504通过吸附微小RNA-149以增加核结合蛋白2来促进肾细胞癌的发展。

本文引用的文献

1
Clinical significance of NUCB2 mRNA expression in prostate cancer.前列腺癌中 NUCB2 mRNA 表达的临床意义。
J Exp Clin Cancer Res. 2013 Aug 16;32(1):56. doi: 10.1186/1756-9966-32-56.
2
Association of methylenetetrahydrofolate dehydrogenase 1 polymorphisms with cancer: a meta-analysis.亚甲基四氢叶酸脱氢酶 1 多态性与癌症的关联:一项荟萃分析。
PLoS One. 2013 Jul 19;8(7):e69366. doi: 10.1371/journal.pone.0069366. Print 2013.
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CYP1B1 polymorphisms and susceptibility to prostate cancer: a meta-analysis.CYP1B1 多态性与前列腺癌易感性的关系:一项荟萃分析。
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Nucleobindin-2 enhances the epithelial-mesenchymal transition in renal cell carcinoma.核结合蛋白-2促进肾细胞癌的上皮-间质转化。
Oncol Lett. 2020 Jun;19(6):3653-3664. doi: 10.3892/ol.2020.11526. Epub 2020 Apr 10.
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High expression of NUCB2 promotes papillary thyroid cancer cells proliferation and invasion.NUCB2的高表达促进甲状腺乳头状癌细胞的增殖和侵袭。
Onco Targets Ther. 2019 Feb 18;12:1309-1318. doi: 10.2147/OTT.S184560. eCollection 2019.
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Nesfatin-1/Nucleobindin-2 Is a Potent Prognostic Marker and Enhances Cell Proliferation, Migration, and Invasion in Bladder Cancer.神经降压素-1/核蛋白结合蛋白-2 是一种强有力的预后标志物,并增强膀胱癌中的细胞增殖、迁移和侵袭。
Dis Markers. 2018 Sep 19;2018:4272064. doi: 10.1155/2018/4272064. eCollection 2018.
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High NUCB2 expression level is associated with metastasis and may promote tumor progression in colorectal cancer.高NUCB2表达水平与转移相关,可能促进结直肠癌的肿瘤进展。
Oncol Lett. 2018 Jun;15(6):9188-9194. doi: 10.3892/ol.2018.8523. Epub 2018 Apr 18.
8
A novel function of NUCB2 in promoting the development and invasion of renal cell carcinoma.NUCB2在促进肾细胞癌发展和侵袭方面的新功能。
Oncol Lett. 2018 Feb;15(2):2425-2430. doi: 10.3892/ol.2017.7563. Epub 2017 Dec 8.
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Sci Rep. 2017 Nov 22;7(1):16013. doi: 10.1038/s41598-017-16357-7.
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PLoS One. 2013 Jul 4;8(7):e68634. doi: 10.1371/journal.pone.0068634. Print 2013.
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CA Cancer J Clin. 2011 Jul-Aug;61(4):212-36. doi: 10.3322/caac.20121. Epub 2011 Jun 17.
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