The HER family has an important role in driving breast cancer. Epidermal growth factor receptor (EGFR)

overexpression has been demonstrated as prognostic factors in IBC. Overexpression of epidermal growth factor receptor 2 (HER2) occurs during the stage of advanced tumor but whether the overexpression has a prognostic role in IBC has yet to be established [7, 8]. Anti-HER2 therapies have shown benefit in IBC patients with HER2 amplification, which accounts for approximately 40% of IBC [9]. However, therapeutic options for patients with ER-negative and HER2 non-amplified IBC are very limited. IBCs are predominantly basal-like or triple-negative (TN) as characterized by the estrogen receptor (ER)-negative, progesterone receptor (PgR)-negative and HER2 non-amplified status [10].

EGFR is overexpressed in 30% of IBCs and 50% of TNIBCs [2, 11]. IBC patients with EGFR-positive tumors have Crenigacestat a lower overall survival rate than patients with EGFR-negative tumors, and EGFR overexpression in IBC is frequently associated with an increased risk of recurrence [9]. EGFR overexpression is also correlated with large tumor size, aggressiveness and poor prognosis [12, 13]. Thus, EGFR could be a potential therapeutic target in IBC and, in particular, in patients with EGFR-overexpressed IBC that currently has very limited treatment options. Currently there are few human IBC cell lines available for studying this complex disease. Although available cell lines were derived from IBC patients, the molecular signatures among IBC cell lines are very distinct. SUM149 was developed Bucladesine chemical structure from the primary tumor of IBC patient, but in vivo xenograft model

are unable to recapitulate the tumor emboli that are the signature of IBC in humans. We have recently developed a new IBC cell line, FC-IBC-02 that was derived from the pleural effusion fluid of a woman with secondary metastatic IBC [14, 15]. FC-IBC-02 cells form tumor spheroids in suspension culture, a characteristic of cancer stem cells, and recapitulate the tumor emboli in Acetophenone vivo xenograft models. SUM149 and FC-IBC-02 could be different representative models for studying the biology of IBC, both SUM149 and FC-IBC-02 cell lines are basal-like and ER/Pgr(-), EGFR-overexpressed and HER2 non-amplified. AZD8931 was developed with the hypothesis that combined inhibition of EGFR, HER2, and HER3-mediated signaling may be more effective for clinical cancer treatment [16]. Pharmacological profiling has shown that AZD8931 is a novel, equipotent, reversible small-molecule ATP competitive inhibitor of EGFR, HER2, and HER3 signaling. Previous results showed that AZD8931 was significantly more potent against EGFR, HER2 and HER3 signaling than other EGFR inhibitors such as lapatinib or gefitinib in vitro. AZD8931 has shown greater Selleck CH5183284 antitumor activity in a range of xenografted models compared with lapatinib or gefitinib [16].