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Int J Clin Exp Pathol. 2014 Sep 15;7(10):7131-41. eCollection 2014.
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MicroRNA-31 is overexpressed in cutaneous squamous cell carcinoma and regulates cell motility and colony formation ability of tumor cells.微小RNA-31在皮肤鳞状细胞癌中过表达,并调节肿瘤细胞的细胞运动性和集落形成能力。
PLoS One. 2014 Jul 28;9(7):e103206. doi: 10.1371/journal.pone.0103206. eCollection 2014.
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MiR-20a inhibits cutaneous squamous cell carcinoma metastasis and proliferation by directly targeting LIMK1.微小RNA-20a通过直接靶向LIMK1抑制皮肤鳞状细胞癌的转移和增殖。
Cancer Biol Ther. 2014 Oct;15(10):1340-9. doi: 10.4161/cbt.29821. Epub 2014 Jul 14.
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miR-365 promotes cutaneous squamous cell carcinoma (CSCC) through targeting nuclear factor I/B (NFIB).微小RNA-365通过靶向核因子I/B(NFIB)促进皮肤鳞状细胞癌(CSCC)。
PLoS One. 2014 Jun 20;9(6):e100620. doi: 10.1371/journal.pone.0100620. eCollection 2014.
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MiR-20a is upregulated in anaplastic thyroid cancer and targets LIMK1.miR-20a 在间变性甲状腺癌中上调并靶向 LIMK1。
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miR-20a promotes prostate cancer invasion and migration through targeting ABL2.miR-20a 通过靶向 ABL2 促进前列腺癌的侵袭和迁移。
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Effects of PTTG down-regulation on proliferation and metastasis of the SCL-1 cutaneous squamous cell carcinoma cell line.垂体肿瘤转化基因(PTTG)下调对SCL-1皮肤鳞状细胞癌细胞系增殖和转移的影响。
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Involvement of miR-20a in promoting gastric cancer progression by targeting early growth response 2 (EGR2).miR-20a 通过靶向早期生长反应因子 2(EGR2)促进胃癌进展。
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Serum microRNA expression levels can predict lymph node metastasis in patients with early-stage cervical squamous cell carcinoma.血清 microRNA 表达水平可预测早期宫颈鳞状细胞癌患者的淋巴结转移。
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微小RNA-20a表达降低促进皮肤鳞状细胞癌的肿瘤进展并预示不良预后。

Decreased expression of microRNA-20a promotes tumor progression and predicts poor prognosis of cutaneous squamous cell carcinoma.

作者信息

Zhang Li, Xiang Ping, Han Xuan, Wu Liyong, Li Xuwen, Xiong Zhuyou

机构信息

Department of Plastic and Reconstructive Surgery, First Affiliated Hospital of Bengbu Medical College Anhui, China.

Center for Laboratory Research, First Affiliated Hospital of Bengbu Medical College Anhui, China.

出版信息

Int J Clin Exp Pathol. 2015 Sep 1;8(9):11446-51. eCollection 2015.

PMID:26617873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4637689/
Abstract

BACKGROUND

MicroRNA-20a (miRNA-20a or miR-20a) plays a key role in tumorigenesis and progression. But the prognostic value of miR-20a in cutaneous squamous cell carcinoma (CSCC) remains unclear. The aim of this study was to identify the association of miR-20a and the prognosis of CSCC patients.

METHODS

The miR-20a expression was detected using quantitative real-time polymerase chain reaction (qRT-PCR) in 152 CSCC tissues and matched adjacent normal tissues. Kaplan-Meier and Cox regression analysis were utilized to determine the association of miR-20a with overall survival as well as the prognosis of CSCC patients.

RESULTS

The expression of miR-20a was lower in CSCC tissues compared with adjacent normal tissues (P=0.000). Moreover, the expression of miR-20a was closely correlated with TNM stage (P=0.013). Kaplan-Meier analysis showed that patients with low miR-20a expression had significantly poorer overall survival than those with high miR-20a expression (P<0.05). Multivariate analysis revealed that miR-20a expression (P=0.001, HR=3.262, 95% CI: 1.635-6.520) could influence the prognosis and might be an independent prognostic predictor in CSCC.

CONCLUSIONS

Our results indicated that low miR-20a expression was associated with tumor stage of CSCC and suggested that miR-20a expression would be a novel biomarker for predicting clinical outcomes in CSCC patients. The inhibition of miR-20a might even become a new therapeutic method for the treatment of CSCC.

摘要

背景

微小RNA-20a(miRNA-20a或miR-20a)在肿瘤发生和发展中起关键作用。但miR-20a在皮肤鳞状细胞癌(CSCC)中的预后价值仍不清楚。本研究的目的是确定miR-20a与CSCC患者预后的关系。

方法

采用定量实时聚合酶链反应(qRT-PCR)检测152例CSCC组织及配对的癌旁正常组织中miR-20a的表达。利用Kaplan-Meier和Cox回归分析确定miR-20a与总生存期以及CSCC患者预后的关系。

结果

与癌旁正常组织相比,CSCC组织中miR-20a的表达较低(P = 0.000)。此外,miR-20a的表达与TNM分期密切相关(P = 0.013)。Kaplan-Meier分析显示,miR-20a低表达患者的总生存期明显低于miR-20a高表达患者(P < 0.05)。多因素分析显示,miR-20a表达(P = 0.001,HR = 3.262,95%CI:1.635 - 6.520)可影响预后,可能是CSCC的独立预后预测指标。

结论

我们的结果表明,miR-20a低表达与CSCC的肿瘤分期相关,提示miR-20a表达可能是预测CSCC患者临床结局的新型生物标志物。抑制miR-20a甚至可能成为治疗CSCC的新方法。