Document Detail


MiR-34a inhibits lymphatic metastasis potential of mouse hepatoma cells.
MedLine Citation:
PMID:  21553024     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
MicroRNAs are small non-coding RNAs that regulate the expression of other genes in a post-transcriptional manner. MiR-34a can induce apoptosis, cell cycle arrest, and senescence. However, its role in tumor progress remains to be fully elucidated. In the present study, the role of miR-34a in lymphatic metastasis was investigated using mouse hepatocarcinoma cell lines Hca-F and Hepa1-6. MicroRNA profiling and Hairpin-RT-PCR analysis showed that the expression level of miR-34a was higher in Hepa1-6 cells (of no metastatic ability) than that in Hca-F cells (of high metastatic ability). Ectopic expression of miR-34a can inhibit cell growth and cell invasion in Hepa1-6 and Hca-F cells. Moreover, miR-34a triggers G1 arrest and down-regulates CyclinD1 and CDK6 in Hepa1-6 cells. Furthermore, we proved that miR-34a decreased adhesion of Hca-F cells to regional lymph node in vitro, reduced lymph nodes-metastasized burden, and inhibited tumor lymph node metastases in vivo. All these results suggest that miR-34a plays multiple tumor suppressive roles in murine hepatocarcinoma, not only inhibiting cell growth by cell cycle arrest, but also repressing metastasis, and may serve as a novel therapeutic target for hepatocarcinoma.
Authors:
Yanjie Guo; Sheng Li; Jianhua Qu; Shujing Wang; Yibing Dang; Jianhui Fan; Shengjin Yu; Jianing Zhang
Related Documents :
19870054 - Cellular reactions in the meninges of rabbits to tuberculo-lipoid, protein, and polysac...
19025454 - Photothermal bubbles as optical scattering probes for imaging living cells.
17942794 - Development of a ligand blot assay using biotinylated live cells.
8376464 - Synchrony of cell spreading and contraction force as phagocytes engulf large pathogens.
18155194 - Presence of egf growth factor ligands and their effects on cultured rat conjunctival go...
9124594 - Parathyroid hormone-related protein, an autocrine growth inhibitor of alveolar type ii ...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-5-7
Journal Detail:
Title:  Molecular and cellular biochemistry     Volume:  -     ISSN:  1573-4919     ISO Abbreviation:  -     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-5-9     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0364456     Medline TA:  Mol Cell Biochem     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Biochemistry, Institute of Glycobiology, Dalian Medical University, 9 South Lvshun Road Western Section, Dalian, 116044, Liaoning, China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  CXCR4 positive cells from Lewis lung carcinoma cell line have cancer metastatic stem cell characteri...
Next Document:  Reduced dosage of the modifiers of epigenetic reprogramming Dnmt1, Dnmt3L, SmcHD1 and Foxo3a has no ...