Key result
Combined use of ellagic acid and GDC-0941 significantly inhibited breast cancer cell growth, migration, invasion, tumor initiation, and metastasis in vitro and in vivo.
Why the study?
Does ellagic acid enhance the efficacy of PI3K inhibitor GDC-0941 in breast cancer cells?
Does ellagic acid enhance the efficacy of PI3K inhibitor GDC-0941 in breast cancer cells?
Ellagic acid may be a safe and effective agent to boost the efficacy of PI3K-directed breast cancer therapy.
May inform ellagic acid–PI3K inhibitor combinations in breast cancer; leaves open human efficacy and safety.
The fact that the phosphatidylinositol 3 kinase (PI3K) signaling pathway is one of the most frequently deregulated signaling networks has triggered intensive efforts in the development of PI3K pathway inhibitors. However, recent clinical trial data have shown only limited activity of PI3K inhibitors at tolerated doses. Thus, there is an urgent need to identify rational combination therapy to improve the efficacy of PI3K-targeted cancer treatment. In this study, we investigated if dietary compound ellagic acid (EA) could improve the therapeutic efficacy of PI3K inhibitor GDC-0941 in breast cancer. Specifically, using a panel of breast cancer cell lines, we showed that combined use of EA and GDC-0941 significantly inhibited cell growth under attached and detached conditions, blocked migration and invasion in vitro as well as tumor initiation and metastasis in vivo. Furthermore, we found that EA promoted apoptosis and further reduced AKT/mTOR activation in GDC-0941- treated breast cancer cells. Together, our data suggest that EA may be a safe and effective agent to boost the efficacy of PI3K-directed breast cancer therapy and that such drug combination may merit further clinical investigation.
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Shi et al. (2015) studied Breast cancer. Ellagic acid (EA) combined with GDC-0941 vs. GDC-0941 alone or control was evaluated on Cell growth, migration, invasion, tumor initiation, and metastasis. Combined use of ellagic acid and GDC-0941 significantly inhibited breast cancer cell growth, migration, invasion, tumor initiation, and metastasis in vitro and in vivo.
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