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本文引用的文献

1
Thymosin beta 10 is a key regulator of tumorigenesis and metastasis and a novel serum marker in breast cancer.胸腺素β10是肿瘤发生和转移的关键调节因子,也是乳腺癌中的一种新型血清标志物。
Breast Cancer Res. 2017 Feb 8;19(1):15. doi: 10.1186/s13058-016-0785-2.
2
Medical treatment of renal cancer: new horizons.肾癌的医学治疗:新视野
Br J Cancer. 2016 Aug 23;115(5):505-16. doi: 10.1038/bjc.2016.230. Epub 2016 Aug 4.
3
The prospect of precision therapy for renal cell carcinoma.精准治疗肾癌的前景。
Cancer Treat Rev. 2016 Sep;49:37-44. doi: 10.1016/j.ctrv.2016.07.003. Epub 2016 Jul 12.
4
Current management and future directions in the treatment of advanced renal cell carcinoma-a latin american perspective: 10 years in review.晚期肾细胞癌治疗的当前管理与未来方向——拉丁美洲视角:十年回顾
Int Braz J Urol. 2015 Sep-Oct;41(5):835-43. doi: 10.1590/S1677-5538.IBJU.2014.0651.
5
Combined Proteomics and Transcriptomics Identifies Carboxypeptidase B1 and Nuclear Factor κB (NF-κB) Associated Proteins as Putative Biomarkers of Metastasis in Low Grade Breast Cancer.蛋白质组学与转录组学相结合鉴定羧肽酶B1和核因子κB(NF-κB)相关蛋白为低级别乳腺癌转移的潜在生物标志物。
Mol Cell Proteomics. 2015 Jul;14(7):1814-30. doi: 10.1074/mcp.M114.041335. Epub 2015 Apr 22.
6
Thymosin β4 promotes hepatoblastoma metastasis via the induction of epithelial-mesenchymal transition.胸腺素β4通过诱导上皮-间质转化促进肝母细胞瘤转移。
Mol Med Rep. 2015 Jul;12(1):127-32. doi: 10.3892/mmr.2015.3359. Epub 2015 Feb 16.
7
Thymosin beta 10 correlates with lymph node metastases of papillary thyroid carcinoma.胸腺素β10与甲状腺乳头状癌的淋巴结转移相关。
J Surg Res. 2014 Dec;192(2):487-93. doi: 10.1016/j.jss.2014.05.066. Epub 2014 May 27.
8
Hypomethylation of the thymosin β(10) gene is not associated with its overexpression in non-small cell lung cancer.胸腺素β(10)基因低甲基化与非小细胞肺癌中其过表达无关。
Mol Cells. 2011 Oct;32(4):343-8. doi: 10.1007/s10059-011-0073-z. Epub 2011 Oct 17.
9
Thymosins β-4 and β-10 are expressed in bovine ovarian follicles and upregulated in cumulus cells during meiotic maturation.胸腺素β-4和β-10在牛卵巢卵泡中表达,并在减数分裂成熟过程中在卵丘细胞中上调。
Reprod Fertil Dev. 2010;22(8):1206-21. doi: 10.1071/RD10015.
10
Evaluation of thymosin β4 in the regulation of epithelial-mesenchymal transformation in urothelial carcinoma.评价胸腺肽β4 在尿路上皮癌上皮-间充质转化中的调控作用。
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TMSB10促进癌细胞的迁移和侵袭,是肾细胞癌的一种新型预后标志物。

TMSB10 promotes migration and invasion of cancer cells and is a novel prognostic marker for renal cell carcinoma.

作者信息

Xiao Ruihai, Shen Shaochen, Yu Yi, Pan Qiufeng, Kuang Renrui, Huang Hongwei

机构信息

Department of Urology, The Second Affiliated Hospital of Nanchang University Nanchang, Jiangxi Province, People's Republic of China.

出版信息

Int J Clin Exp Pathol. 2019 Jan 1;12(1):305-312. eCollection 2019.

PMID:31933746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6944031/
Abstract

OBJECTIVE

The study aims to examine the effect of thymosin β10 (TMSB10) on renal cell carcinoma (RCC) progression and metastasis.

METHODS

Real-time PCR and immunohistochemistry analysis were used to evaluate TMSB10 expression in RCC tissue samples and renal cancer cells. Statistical analyses were applied to investigate the association between TMSB10 expression and the clinicopathological characteristics and prognosis of RCC patients. In vitro migration and invasion assays were performed in 786-O and ACHN cells.

RESULTS

The expression of TMSB10 was significantly higher in renal cancer cells and tissues compared with normal kidney cells and tissues. TMSB10 expression was significantly related to tumor stage (P=0.002), lymph node metastasis (P=0.034), and distant metastasis (P=0.039). Kaplan-Meier analysis suggested that high TMSB10 expression was significantly associated with unfavorable overall (P=0.004) and recurrent-free survival (P=0.025) of RCC patients. Furthermore, TMSB10 knockdown inhibited the migration and invasion abilities of renal cancer cells in vitro.

CONCLUSION

TMSB10 is overexpressed in RCC and regulates malignant cell metastasis by inducing epithelial-mesenchymal transition, which makes TMSB10 a candidate therapeutic target for RCC.

摘要

目的

本研究旨在探讨胸腺素β10(TMSB10)对肾细胞癌(RCC)进展和转移的影响。

方法

采用实时荧光定量PCR和免疫组织化学分析评估RCC组织样本及肾癌细胞中TMSB10的表达。应用统计学分析研究TMSB10表达与RCC患者临床病理特征及预后的相关性。在786-O和ACHN细胞中进行体外迁移和侵袭实验。

结果

与正常肾细胞和组织相比,肾癌细胞和组织中TMSB10的表达显著更高。TMSB10表达与肿瘤分期(P = 0.002)、淋巴结转移(P = 0.034)和远处转移(P = 0.039)显著相关。Kaplan-Meier分析表明,高TMSB10表达与RCC患者不良的总生存期(P = 0.004)和无复发生存期(P = 0.025)显著相关。此外,TMSB10基因敲低抑制了肾癌细胞的体外迁移和侵袭能力。

结论

TMSB10在RCC中过表达,并通过诱导上皮-间质转化调节恶性细胞转移,这使得TMSB10成为RCC的一个候选治疗靶点。