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Association of Wwox with ErbB4 in breast cancer
Rami I Aqeilan1, Valentina Donati, Eugenio Gaudio
1Department of Molecular Virology, Immunology and Medical Genetics, Human Cancer Genetics Program, Comprehensive Cancer Center, Ohio State University, Columbus, Ohio 43210, USA. rami.aqeilan@osumc.edu
Abstract:
WWOX, WW domain-containing oxidoreductase, is a tumor suppressor that is altered in many human cancers, including breast cancer. Wwox interacts with the ErbB4 receptor, reduces nuclear translocation of the cleaved intracellular domain of ErbB4, and inhibits its transactivation function mediated through Yes-associated protein. Here, we assessed the clinical significance of the Wwox-ErbB4 association. We determined Wwox protein expression by immunohistochemistry in a series of 556 breast cancers. Wwox expression was absent in 36% of the cancers, and loss of Wwox expression was associated with unfavorable outcome (P = 0.02). Membranous location of ErbB4 was associated with favorable survival compared with women whose cancer lacked such ErbB4 expression (P = 0.02). Wwox expression was strongly associated with membranous ErbB4 localization (P = 0.0003) and with overall ErbB4 expression (P = 0.0002). Coexpression of membranous ErbB4 and Wwox was associated with favorable outcome compared with cases with membranous ErbB4 and no Wwox immunoreactivity (P = 0.002). In vitro, Wwox associated with the two ErbB4 isoforms, JM-a CYT-1 and JM-a CYT-2, expressed in breast cancer. Moreover, expression of Wwox both in vitro and in vivo led to accumulation of total full-length membrane-associated ErbB4. These results suggest that expression of Wwox is associated with ErbB4 expression and that their coexpression has prognostic significance in breast cancer.
Insights
WW domain-containing oxidoreductase (Wwox) loss in breast cancer correlates with poor prognosis. Coexpression of Wwox and membranous ErbB4 indicates a favorable outcome, suggesting a joint prognostic role.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- WW domain-containing oxidoreductase (WWOX) functions as a tumor suppressor implicated in various human cancers.
- WWOX interacts with the ErbB4 receptor, modulating its nuclear translocation and transactivation functions.
Purpose of the Study:
- To investigate the clinical significance of the WWOX-ErbB4 association in breast cancer.
- To determine the prognostic value of WWOX and ErbB4 expression and their coexpression in breast cancer patients.
Main Methods:
- Immunohistochemistry was used to assess WWOX protein expression in 556 breast cancer samples.
- Analysis of the association between WWOX expression, ErbB4 localization (membranous vs. absent), and patient survival outcomes.
- In vitro studies to examine WWOX interaction with ErbB4 isoforms and its effect on full-length ErbB4 accumulation.
Main Results:
- Loss of WWOX expression was observed in 36% of breast cancers and was linked to unfavorable outcomes (P = 0.02).
- Membranous ErbB4 localization was associated with favorable survival (P = 0.02) and strongly correlated with WWOX expression (P = 0.0003).
- Coexpression of membranous ErbB4 and WWOX significantly predicted a favorable prognosis (P = 0.002).
Conclusions:
- WWOX expression is clinically significant in breast cancer and is associated with ErbB4 expression.
- The coexpression of WWOX and membranous ErbB4 holds prognostic value, indicating a potential therapeutic target.
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