Protein expression of the gp78 E3 ligase predicts poor breast cancer outcome based on race

Women of African ancestry suffer higher rates of breast cancer mortality compared with all other groups in the United States. Though the precise reasons for these disparities remain unclear, many recent studies have implicated a role for differences in tumor biology. Using an epitope-validated antibody against the endoplasmic reticulum-associated E3 ligase, gp78, we show that elevated levels of gp78 in patient breast cancer cells predict poor survival. Moreover, high levels of gp78 are associated with poor outcomes in both ER+ and ER- tumors, and breast cancers expressing elevated amounts of gp78 protein are enriched in gene expression pathways that influence cell cycle, metabolism, receptor-mediated signaling, and cell stress response pathways. In multivariate analysis adjusted for subtype and grade, gp78 protein is an independent predictor of poor outcomes in women of African ancestry. Furthermore, gene expression signatures, derived from patients stratified by gp78 protein expression, are strong predictors of recurrence and pathological complete response in retrospective clinical trial data and share many common features with gene sets previously identified to be overrepresented in breast cancers based on race. These findings implicate a prominent role for gp78 in tumor progression and offer insights into our understanding of racial differences in breast cancer outcomes.

Automated summary

Women of African ancestry have higher rates of breast cancer mortality, and differences in tumor biology may play a role in these disparities. The protein gp78, found in patient breast cancer cells, is associated with poor survival outcomes in both ER+ and ER- tumors. Breast cancers with high levels of gp78 are enriched in gene expression pathways related to cell cycle, metabolism, signaling, and stress response. Gp78 protein is an independent predictor of poor outcomes in women of African ancestry, and gene expression signatures stratified by gp78 expression are strong predictors of recurrence and treatment response.