Objective
The majority of women with advanced-stage epithelial ovarian cancer (OVCA) ultimately develop chemo-resistant, recurrent disease. Therefore, a great need exists to develop new, more active, and less toxic agents and/or to optimize the efficacy of existing agents.
Methods
In this study, we investigated the activity of Avemar®, a natural, non-toxic, fermented wheat germ extract (FWGE), against a range of OVCA cell lines, both alone and in combination with cisplatin chemotherapy, and delineated the molecular signaling pathways that underlie FWGE activity at a genome-wide level.
Results
We found that FWGE exhibited significant anti-proliferative effects against 12 human OVCA cell lines and potentiated cisplatin-induced apoptosis. Pearson’s correlation of FWGE sensitivity and gene expression data identified 2,142 genes (FDR<0.2) representing 27 biological pathways (p<0.05) to be significantly associated with FWGE sensitivity. A parallel analysis of genomic data for 59 human cancer cell lines matched to chemo-sensitivity data for 2,6-dimethoxy-p-benzoquinone, a proposed active component of FWGE, identified representation of 13 pathways common to both FWGE and 2,6-dimethoxy-p-benzoquinone sensitivity.
Conclusions
Our findings confirm the value of FWGE as a natural product with anti-cancer properties that may also enhance the activity of existing therapeutic agents. Furthermore, our findings provide substantial insights into the molecular basis of FWGE’s effect on human cancer cells.