Data from 5-Fluorouracil Enhances the Antitumor Activity of the Glutaminase Inhibitor CB-839 against <i>PIK3CA</i>-Mutant Colorectal Cancers

Abstract

<div>Abstract<p><i>PIK3CA</i> encodes the p110α catalytic subunit of PI3K and is frequently mutated in human cancers, including ∼30% of colorectal cancer. Oncogenic mutations in <i>PIK3CA</i> render colorectal cancers more dependent on glutamine. Here we report that the glutaminase inhibitor CB-839 preferentially inhibits xenograft growth of <i>PIK3CA</i>-mutant, but not wild-type (WT), colorectal cancers. Moreover, the combination of CB-839 and 5-fluorouracil (5-FU) induces <i>PIK3CA</i>-mutant tumor regression in xenograft models. CB-839 treatment increased reactive oxygen species and caused nuclear translocation of Nrf2, which in turn upregulated mRNA expression of uridine phosphorylase 1 (UPP1). UPP1 facilitated the conversion of 5-FU to its active compound, thereby enhancing the inhibition of thymidylate synthase. Consistently, knockout of UPP1 abrogated the tumor inhibitory effect of combined CB-839 and 5-FU administration. A phase I clinical trial showed that the combination of CB-839 and capecitabine, a prodrug of 5-FU, was well tolerated at biologically-active doses. Although not designed to test efficacy, an exploratory analysis of the phase I data showed a trend that <i>PIK3CA</i>-mutant patients with colorectal cancer might derive greater benefit from this treatment strategy as compared with <i>PIK3CA</i> WT patients with colorectal cancer. These results effectively demonstrate that targeting glutamine metabolism may be an effective approach for treating patients with <i>PIK3CA</i>-mutant colorectal cancers and warrants further clinical evaluation.</p>Significance:<p>Preclinical and clinical trial data suggest that the combination of CB-839 with capecitabine could serve as an effective treatment for <i>PIK3CA</i>-mutant colorectal cancers.</p></div>