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Rho GTPase 信号通路的下调参与了 microRNA-138 介导的舌鳞癌细胞迁移和侵袭的抑制。

Downregulation of the Rho GTPase signaling pathway is involved in the microRNA-138-mediated inhibition of cell migration and invasion in tongue squamous cell carcinoma.

机构信息

Center for Molecular Biology of Oral Diseases, College of Dentistry, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

Int J Cancer. 2010 Aug 1;127(3):505-12. doi: 10.1002/ijc.25320.


DOI:10.1002/ijc.25320
PMID:20232393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2885137/
Abstract

Tumor metastasis is the dominant cause of death in cancer patients, including patients with oral tongue squamous cell carcinoma (TSCC). Previously, we reported that reduced miR-138 level is correlated with enhanced metastatic potential in TSCC cells. Here, we demonstrate that miR-138 suppresses TSCC cell migration and invasion by regulating 2 key genes in the Rho GTPase signaling pathway: RhoC and ROCK2. Direct targeting of miR-138 to specific sequences located in the 3'-untranslated regions of both RhoC and ROCK2 mRNAs was confirmed using luciferase reporter gene assays. Ectopic transfection of miR-138 reduced the expression of both RhoC and ROCK2 in TSCC cells. These reduced expressions, in consequence, led to the reorganization of the stress fibers and the subsequent cell morphology change to a round bleb-like shape as well as the suppression of cell migration and invasion. In contrast, knockdown of miR-138 in TSCC cells enhanced the expression of RhoC and ROCK2, which resulted in an altered, elongated cell morphology, enhanced cell stress fiber formation and accelerated cell migration and invasion. Taken together, our results suggest that miR-138 plays an important role in TSCC cell migration and invasion by concurrently targeting RhoC and ROCK2, and miR-138 may serve as a novel therapeutic target for TSCC patients at risk of metastatic disease.

摘要

肿瘤转移是癌症患者死亡的主要原因,包括口腔舌鳞状细胞癌(TSCC)患者。此前,我们报道 miR-138 水平降低与 TSCC 细胞转移潜能增强有关。在这里,我们证明 miR-138 通过调节 Rho GTPase 信号通路中的 2 个关键基因 RhoC 和 ROCK2 来抑制 TSCC 细胞的迁移和侵袭。通过荧光素酶报告基因检测证实了 miR-138 对 RhoC 和 ROCK2 mRNA 3'非翻译区特定序列的直接靶向作用。外源性转染 miR-138 可降低 TSCC 细胞中 RhoC 和 ROCK2 的表达。这些表达的降低导致应力纤维的重排,随后细胞形态发生变化,呈圆形泡状,并抑制细胞迁移和侵袭。相反,在 TSCC 细胞中敲低 miR-138 会增强 RhoC 和 ROCK2 的表达,导致细胞形态改变为拉长的形状,增强细胞应激纤维的形成,并加速细胞迁移和侵袭。综上所述,我们的研究结果表明,miR-138 通过同时靶向 RhoC 和 ROCK2 在 TSCC 细胞迁移和侵袭中发挥重要作用,miR-138 可能成为有转移疾病风险的 TSCC 患者的一种新的治疗靶点。

相似文献

[1]
Downregulation of the Rho GTPase signaling pathway is involved in the microRNA-138-mediated inhibition of cell migration and invasion in tongue squamous cell carcinoma.

Int J Cancer. 2010-8-1

[2]
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[5]
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[6]
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[7]
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[10]
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[4]
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[6]
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[10]
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本文引用的文献

[1]
MiR-21 is an EGFR-regulated anti-apoptotic factor in lung cancer in never-smokers.

Proc Natl Acad Sci U S A. 2009-7-21

[2]
MicroRNA-138 suppresses invasion and promotes apoptosis in head and neck squamous cell carcinoma cell lines.

Cancer Lett. 2009-6-21

[3]
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells.

FEBS J. 2009-6

[4]
MicroRNA-222 regulates cell invasion by targeting matrix metalloproteinase 1 (MMP1) and manganese superoxide dismutase 2 (SOD2) in tongue squamous cell carcinoma cell lines.

Cancer Genomics Proteomics. 2009

[5]
A functional screen implicates microRNA-138-dependent regulation of the depalmitoylation enzyme APT1 in dendritic spine morphogenesis.

Nat Cell Biol. 2009-6

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Rho-kinase 2 is frequently overexpressed in hepatocellular carcinoma and involved in tumor invasion.

Hepatology. 2009-5

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Rho signaling, ROCK and mDia1, in transformation, metastasis and invasion.

Cancer Metastasis Rev. 2009-6

[8]
microRNA-138 modulates cardiac patterning during embryonic development.

Proc Natl Acad Sci U S A. 2008-11-18

[9]
Most mammalian mRNAs are conserved targets of microRNAs.

Genome Res. 2009-1

[10]
Mature miR-184 as Potential Oncogenic microRNA of Squamous Cell Carcinoma of Tongue.

Clin Cancer Res. 2008-5-1

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