Details

Autor(en) / Beteiligte

• Singhal, Sandeep K
• Byun, Jung S
• Yan, Tingfen
• Yancey, Ryan
• Caban, Ambar
• Gil Hernandez, Sara
• Bufford, Sediqua
• Hewitt, Stephen M
• Winfield, Joy
• Pradhan, Jaya Sarin
• Mustkov, Vesco
• McDonald, Jasmine A
• Pérez-Stable, Eliseo J
• Napoles, Anna Maria
• Vohra, Nasreen
• De Siervi, Adriana
• Yates, Clayton
• Davis, Melissa B
• Yang, Mei
• Tsai, Yien Che
• Weissman, Allan M
• Gardner, Kevin

Titel

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

Ist Teil von

• JCI insight, 2022-07, Vol.7 (13)

Ort / Verlag

United States: American Society for Clinical Investigation

Erscheinungsjahr

2022

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• Women of African ancestry suffer higher rates of breast cancer mortality compared to 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 degradation (ERAD) E3 ubiquitin 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-positive and ER-negative 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 new insights into our understanding of racial differences in breast cancer outcomes.