AKT1 and AKT2 promote malignant transformation in human brain glioma LN229 cells View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-09

AUTHORS

Jian Zou, Kun Wang, Lei Han, An-ling Zhang, Zhen-dong Shi, Pei-yu Pu, Chun-sheng Kang

ABSTRACT

To confirm the role played by AKT1 and AKT2 in the β-catenin/ Tcf-4 signaling pathway in promoting malignant transformation of glioma cells. LN229 cells were divided into five groups: a control group, acetone (ACE)group, acetylsalicylic acid (ASA; aspirin) group, ASA+AKT1 plasmid group and ASA+AKT2 plasmid group. Western blot and PCR were used to detect the expression of AKT1 and AKT2 after dealing with ASA and transferring AKT1/2 genes into LN229 cells. Cell proliferation was determined by flow cytometry, cell invasion was evaluated by transwell assay and cell apoptosis was detected with annexin V staining. The molecules regulating proliferation and invasion were examined by western blot analysis. Aspirin down-regulates AKT1 and AKT2 expression by modulating b-catenin/Tcf-4 activity. AKT1 and AKT2 can enhance cell proliferation and invasion by up-regulating the expression of cyclin-D and matrix metalloprotein-9 (MMP-9) in LN229 glioma cells. AKT1 and AKT2 play an important role in the bcatenin/Tcf-4 signaling pathway promoting malignant transformation; AKT1 is more effective than AKT2. AKT1 and AKT2 may be potential targets for brain glioma therapy and an effective way to prevent metastasis of gliomas. More... »

PAGES

144

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11805-011-0573-9

DOI

http://dx.doi.org/10.1007/s11805-011-0573-9

DIMENSIONS

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