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Nat Rev Immunol. 2018 May;18(5):309-324. doi: 10.1038/nri.2017.142. Epub 2018 Jan 22.
2
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Future Oncol. 2018 Feb;14(5):461-469. doi: 10.2217/fon-2017-0490. Epub 2018 Jan 12.
3
The interaction of TAK1 and TAB1 enhances LPS-induced cytokine release via modulating NF-κB activation (Larimichthys crocea).TAK1 和 TAB1 的相互作用通过调节 NF-κB 激活增强 LPS 诱导的细胞因子释放(大黄鱼)。
Fish Shellfish Immunol. 2018 Mar;74:450-458. doi: 10.1016/j.fsi.2018.01.005. Epub 2018 Jan 8.
4
Early esophageal cancer with epidermization diagnosed and treated with endoscopic resection.经内镜切除诊断和治疗的伴有表皮化生的早期食管癌。
Clin J Gastroenterol. 2018 Feb;11(1):29-33. doi: 10.1007/s12328-017-0792-6. Epub 2017 Oct 27.
5
Medical expenditure for esophageal cancer in China: a 10-year multicenter retrospective survey (2002-2011).中国食管癌医疗费用:一项为期10年的多中心回顾性调查(2002 - 2011年)
Chin J Cancer. 2017 Sep 7;36(1):73. doi: 10.1186/s40880-017-0242-3.
6
Takinib, a Selective TAK1 Inhibitor, Broadens the Therapeutic Efficacy of TNF-α Inhibition for Cancer and Autoimmune Disease.他泽司他丁,一种选择性 TAK1 抑制剂,拓宽了 TNF-α 抑制剂在癌症和自身免疫性疾病治疗中的疗效。
Cell Chem Biol. 2017 Aug 17;24(8):1029-1039.e7. doi: 10.1016/j.chembiol.2017.07.011.
7
Expression and function of transforming growth factor‑β‑activated protein kinase 1 in gastric cancer.转化生长因子-β激活蛋白激酶1在胃癌中的表达及功能
Mol Med Rep. 2017 Sep;16(3):3103-3110. doi: 10.3892/mmr.2017.6998. Epub 2017 Jul 15.
8
Cancer of the esophagus and esophagogastric junction: an 8 edition staging primer.食管癌和食管胃交界癌:第8版分期指南
J Thorac Dis. 2017 Mar;9(3):E282-E284. doi: 10.21037/jtd.2017.03.39.
9
GEPIA: a web server for cancer and normal gene expression profiling and interactive analyses.GEPIA:一个用于癌症和正常基因表达谱分析及交互式分析的网络服务器。
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10
MiR-143 Targeting TAK1 Attenuates Pancreatic Ductal Adenocarcinoma Progression via MAPK and NF-κB Pathway In Vitro.靶向TAK1的MiR-143通过MAPK和NF-κB通路在体外减弱胰腺导管腺癌进展
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[TAK1和TAB1在食管癌中的表达及其与预后的相关性]

[Expressions of TAK1 and TAB1 in esophageal cancer and their correlation with prognosis].

作者信息

Cao Sai, Cheng Meirong, Liu Sue, Duan Xiaole, Li Mei

机构信息

Department of Thoracic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Department of Cardiovascular Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2018 Jul 30;38(7):895-900. doi: 10.3969/j.issn.1673-4254.2018.07.21.

DOI:10.3969/j.issn.1673-4254.2018.07.21
PMID:33168518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6765533/
Abstract

OBJECTIVE

To detect the expressions of transforming growth factor-β (TGF-β)-activated kinase (TAK1) and TGF-β- activated protein kinase 1 (TAB1) in esophageal cancer tissues and explore their correlations with the clinicopathological features and prognosis of the patients.

METHODS

The expressions of TAK1 and TAB1 in 84 esophageal cancer tissues and paired adjacent tissues was detected using immunohistochemical staining. The correlations of different patterns of TAK1 and TAB1 expressions (TAK1 alone, TAB1 alone, and both) with the clinicopathological features of the patients were analyzed. The correlation between TAK1 and TAB1 was assessed based on GEPIA datasets. Kaplan-Meier survival analysis was used to analyze the recurrence-free survival of the patients in relation with TAK1 and TAB1 expressions.

RESULTS

TAK1 and TAB1 were highly expressed in 65.5% (55/84) and 52.4% (44/84) of the esophageal cancer tissues, respectively. The expression of TAK1, TAB1 and their co-expression were all correlated with tumor invasion depth, lymph node metastasis, and TNM staging ( < 0.05). A strong correlation was found between TAK1 and TAB1 expressions. A high expression of TAK1 and TAK1/TAB1 co-expression both predicted a poor recurrence-freed survival of the patients ( < 0.05).

CONCLUSIONS

TAK1 and TAB1 are associated with the progression and prognosis of esophageal cancer and can serve as new prognostic biomarkers for esophageal cancer and as potential molecular targets for therapies.

摘要

目的

检测食管癌组织中转化生长因子-β(TGF-β)激活激酶(TAK1)和TGF-β激活蛋白激酶1(TAB1)的表达,探讨其与患者临床病理特征及预后的相关性。

方法

采用免疫组织化学染色法检测84例食管癌组织及配对癌旁组织中TAK1和TAB1的表达。分析TAK1和TAB1不同表达模式(单独TAK1、单独TAB1及两者均有)与患者临床病理特征的相关性。基于GEPIA数据集评估TAK1与TAB1之间的相关性。采用Kaplan-Meier生存分析法分析患者无复发生存率与TAK1和TAB1表达的关系。

结果

TAK1和TAB1在65.5%(55/84)和52.4%(44/84)的食管癌组织中高表达。TAK1、TAB1的表达及其共表达均与肿瘤浸润深度、淋巴结转移及TNM分期相关(P<0.05)。TAK1与TAB1表达之间存在强相关性。TAK1高表达及TAK1/TAB1共表达均提示患者无复发生存率较差(P<0.05)。

结论

TAK1和TAB1与食管癌的进展及预后相关,可作为食管癌新的预后生物标志物及潜在的治疗分子靶点。