Akt2 and acid ceramidase cooperate to induce cell invasion and resistance to apoptosis

被引:8
作者
Berndt, Norbert
Patel, Ronil
Yang, Hua
Balasis, Maria E.
Sebti, Said M. [1 ]
机构
[1] Univ S Florida, H Lee Moffitt Canc Ctr, Drug Discovery Dept, Tampa, FL 33682 USA
关键词
Akt; acid ceramidase; cell invasion; apoptosis; synthetic lethal interaction; drug synergy; TCN; MK-2206; B13; DEPRIVATION-INDUCED APOPTOSIS; PROTEIN PHOSPHATASE 2A; PROSTATE-CANCER; ENDOTHELIAL-CELLS; BREAST-CANCER; UP-REGULATION; ACTIVATION; PATHWAY; DEPHOSPHORYLATION; SPHINGOSINE;
D O I
10.4161/cc.25043
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Both Akt 2 and acid ceramidase (ASAH1) are found aberrantly overexpressed in cancer cells, but whether these two enzymes cooperate to induce malignant transformation is not known. We found that in immortalized, non-transformed cells, ectopic co-expression of Akt2 and ASAH1 is significantly more effective than expression of each gene alone at inducing cell invasion and at conferring resistance to apoptosis. Consistent with these observations, siRNA-mediated depletion of both Akt2 and ASAH1 is much more potent than depleting each alone at inhibiting cell viability/proliferation and cell invasion. Furthermore, pharmacological inhibitors of Akt (TCN or MK-2206) and ASAH1 (B13) synergize to inhibit cell viability/proliferation, and combinations of these drugs are more effective than single-agent treatments at inhibiting cell invasion. Taken together, the results suggest that these two enzymes cooperate to induce malignant transformation and warrant further preclinical studies to evaluate the potential of combining inhibitors of Akt and ASAH1 to treat cancer.
引用
收藏
页码:2024 / 2032
页数:9
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