Article

LRRC4 Inhibits Glioma Cell Growth and Invasion Through a miR-185- Dependent Pathway.

Cancer Research Institute, Central South University, Changsha 410078 Hunan, P.R. China. .
Current cancer drug targets (impact factor: 5.13). 07/2012; 12(8):1032-42. pp.1032-42
Source: PubMed

ABSTRACT Leucine-rich repeat (LRR) genes encode transmembrane proteins that are essential for normal brain development and are often dysregulated in central nervous system tumors. Leucine-rich repeat C4 (LRRC4) is a member of the LRR protein superfamily and specifically expressed in brain tissue. Importantly it acts as a tumor suppressor in the pathogenesis of malignant gliomas. However, the molecular mechanisms by which LRRC4 regulates glioma tumorigenesis are largely unknown. In this report, we found that miR-185 is markedly upregulated by LRRC4. We also found that miR-185 was downregulated in glioma, and overexpression of miR-185 inhibited glioma cell invasion. Low expressions of LRRC4 and miR-185 were associated with a poor outcome in glioma patients. Further investigation revealed that LRRC4 mediated its tumor suppressor function by regulating miR-185 targets CDC42 and RhoA. LRRC4 overexpression inhibited glioma cell invasion through miR-185-mediated CDC42 and RhoA direct regulation and VEGFA indirect regulation. Together, our findings suggest that the altered expression of the tumor suppressor LRRC4 may be an important event that leads to the dysregulation of miR-185 in human gliomas. LRRC4 and miR-185 may also be good prognostic markers and therapeutic targets in glioma.

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Keywords

altered expression
 
central nervous system tumors
 
glioma patients
 
human gliomas
 
Leucine-rich repeat C4
 
Low expressions
 
LRR protein superfamily
 
LRRC4 overexpression inhibited glioma cell invasion
 
LRRC4 regulates glioma tumorigenesis
 
malignant gliomas
 
miR-185 inhibited glioma cell invasion
 
miR-185-mediated CDC42
 
normal brain development
 
overexpression
 
regulating miR-185 targets CDC42
 
RhoA direct regulation
 
tumor suppressor
 
tumor suppressor function
 
tumor suppressor LRRC4
 
VEGFA indirect regulation
 

Hailin Tang