Research Papers:

ERRF sensitizes ERBB2-positive breast cancer cells to lapatinib treatment likely by attenuating MCL1 and ERBB2 expression

PDF |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2017; 8:36054-36066. https://doi.org/10.18632/oncotarget.16425

Metrics: PDF 1985 views  |   HTML 1866 views  |   ?  

Leilei Qi, Baotong Zhang, Shiying Zhang, Xinpei Ci, Qiao Wu, Gui Ma, Ang Luo, Liya Fu, Jamie L. King, Rita Nahta and Jin-Tang Dong _


Leilei Qi1, Baotong Zhang2, Shiying Zhang1, Xinpei Ci1, Qiao Wu1, Gui Ma1, Ang Luo1, Liya Fu1, Jamie L. King2, Rita Nahta3, Jin-Tang Dong1,2

1Department of Genetics and Cell Biology, College of Life Sciences, Nankai University, Tianjin 300071, China

2Emory Winship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia 30322, USA

3Emory Winship Cancer Institute, Department of Pharmacology, Emory University School of Medicine, Atlanta, Georgia 30322, USA

Correspondence to:

Jin-Tang Dong, email: [email protected]

Keywords: ERRF, lapatinib, ERBB2, breast cancer, drug resistance

Received: December 28, 2016     Accepted: March 14, 2017     Published: March 21, 2017


Previously we found that the estrogen receptor (ER) related factor ERRF regulates cell proliferation and tumor growth, and its expression is positively associated with ER status and better survival but inversely associated with ERBB2 (also named HER2) status in breast cancer. Here we report that ERRF also plays an important role in the response of ERBB2-positive breast cancer cells to lapatinib, a dual tyrosine kinase inhibitor that interrupts the ERBB2 and EGFR pathway. In ERBB2-positive breast cancer cell lines, lower levels of ERRF expression correlated with lapatinib resistance, restoration of ERRF expression in lapatinib-resistant cell lines JIMT-1 and MDA-MB-453 enhanced their lapatinib responses, and knockdown of ERRF in lapatinib sensitive cell lines BT-474 and SK-BR-3 caused lapatinib resistance. ERRF-enhanced lapatinib sensitivity was also confirmed in xenograft tumors of JIMT-1 cells. In patients with ERBB2-positive breast cancer, higher level of ERRF expression correlated with both pathologic complete response (pCR) to lapatinib and better survival. Mechanistically, ERRF expression in resistant cells promoted lapatinib-induced apoptosis by attenuating MCL1 and ERBB2 expression. These results suggest that ERRF plays an important role in lapatinib response of ERBB2-positive breast cancer, and further study of ERRF could lead to improved prediction and sensitivity of lapatinib response.


The ERBB2-positive subtype of breast cancer is characterized by gene amplification or protein overexpression of ERBB2, a member of the human epidermal growth factor receptor family. ERBB2 protein is an important marker and therapeutic target for about 30% of breast cancer patients, and such patients tend to have a shorter disease free survival and overall survival [16]. In addition to the ERBB2-positive subtype of breast cancer (ER and PR negative), the luminal B subtype is also ERBB2 positive, but this subtype is ER and PR positive and has different clinical characteristics and prognosis [7, 8]. For example, the luminal B subtype cancers are treated with endocrine therapies in combination with ERBB2 targeted drugs [9, 10], because the crosstalk between ER and ERBB2 can lead to endocrine therapy resistance [1114], while ERBB2-positive subtype tumors can benefit from ERBB2 targeted drugs [1519]. Unfortunately, patients usually develop resistance to ERBB2 target therapies within several years [1921]. One of the targeted therapies is the Lapatinib, a dual tyrosine kinase inhibitor that interrupts the ERBB2 and EGFR pathway in the treatment of ERBB2 positive breast cancer, which is used as ditosylate and orally active [22]. Lapatinib is primarily used in patients with advanced-stage, ERBB2-positive breast cancer that has stopped responding to anthracyclines, taxanes, and herceptin [19, 23].

A number of studies have been published on the causes of lapatinib resistance, but the mechanisms are still not well understood, and effective therapies remain to be developed to overcome lapatinib resistance. For example, higher expression levels of several genes, including ABCG2 [24], PA2G4 [25], BECN1 [26], ATG5 [26], MCL1 [27], ER [28], MET [29, 30], SPOCK1 [31], SRC [32, 33], HIF1A [34], DUSP2 [34], MST1R [35], MAP2K1 [36], MAP2K2 [36], FOXM1 [36], AXL [37] and YBX1 [38], have been shown to correlate with lapatinib resistance, but none of them can be used as diagnostic markers and neither have any therapeutic strategies been developed based on these molecules.

The ER related nuclear factor ERRF (C1orf64) was first discovered in a genome-wide sequencing study as one of the more frequently mutated genes in breast cancer [39, 40]. In a more detailed study [41], whereas the mutation of ERRF was not as frequent as expected, ERRF expression was frequently elevated in breast cancer compared to normal tissues, ERRF expression positively correlated with ER and PR status but negatively correlated with ERBB2 status, and knockdown of ERRF expression reduced tumor growth of ER and PR-positive breast cancer cells [41]. An inverse correlation between ERRF expression and ERBB2 status was also evident in an expression profiling study of 2000 breast cancer specimens [42]. It is thus possible that ERRF also plays a role in the development of ERBB2 positive breast cancer and its resistance to ERBB2-targeted therapies.

In this study, we evaluated the relationship between ERRF expression and the sensitivity of breast cancer cells to lapatinib in the context of ERBB2 signaling. We found that ERRF expression positively correlated with lapatinib sensitivity. In cultured cells, ectopic expression of ERRF enhanced the effect of lapatinib on cell death of JIMT-1 and MDA MB-453 cells, which expressed lower levels of ERRF and are resistant to lapatinib, while knockdown of ERRF compromised the effect of lapatinib on BT-474 and SK-BR-3 cell lines, which were sensitive to the drug and expressed higher levels of ERRF. The effect of ERRF on lapatinib was also confirmed in a xenograft model at least for the JIMT-1 cell line. We also found that ERRF attenuated the expression of ERBB2, which likely mediated the effect of ERRF on lapatinib sensitivity.


Induction of ERRF expression by lapatinib in lapatinib sensitive breast cancer cell lines and the correlation between ERRF expression and lapatinib sensitivities and better patient survival

Analysis of the Array Express database [43] showed that in the SK-BR-3 lapatinib-sensitive breast cancer cell line, treatment with lapatinib caused an upregulation in ERRF expression in a time-dependent manner (Figure 1A). We confirmed that lapatinib-mediated ERRF upregulation was also dose dependent in both SK-BR-3 and BT-474 cell lines (Figure 1B, 1C), the latter was also a lapatinib sensitive breast cancer cell line. Lapatinib resistant clones had been developed from both SK-BR-3 and BT-474 cell lines [44], and analysis of available genome-wide expression data for these resistant cells in the GEO database [44] indicates that ERRF mRNA expression was dramatically downregulated in the lapatinib resistant clones of SK-BR-3 and BT-474 cells (Figure 1D).

Lapatinib upregulates ERRF expression in SK-BR-3 and BT-474 breast cancer cell lines, and higher levels of ERRF correlate with lapatinib sensitivities and better patient survival.

Figure 1: Lapatinib upregulates ERRF expression in SK-BR-3 and BT-474 breast cancer cell lines, and higher levels of ERRF correlate with lapatinib sensitivities and better patient survival. (A) Illustration of ERRF expression after lapatinib treatment (100 nM) for 12 and 24 hours in SK-BR-3 cells based on the data from the Array Express database [43]. (B, C) Lapatinib upregulates ERRF expression in BT-474 and SK-BR-3 breast cancer cell lines, both express ERRF and respond to ERBB2 inhibition. Lapatinib treatment was at the indicated concentrations (μM) for 48 hours, and ERRF expression was measured by real-time RT-PCR. (D) Row signal of ERRF in SK-BR3 and BT-474 breast cancer cell lines and lapatinib resistant clones derived from them, as detected in a microarray study in the GEO database [44]. (E) Correlation of ERRF mRNA levels with sensitivities to ERBB2 inhibition in breast cancer cell lines, according to published information [45] and the CCLE database [58]. (F) Higher levels of ERRF expression are associated with better prognosis in ERBB2-positive breast cancer, as determined in the BreastMark database (HR = 0.5442, p = 0.028, n = 107).

To further test the correlation between ERRF expression and lapatinib sensitivity, we analyzed ERRF expression and sensitivities of breast cancer cell lines to ERBB2 drugs including lapatinib in a published study [45] and the CCLE, and found that lapatinib sensitive cell lines expressed significantly higher levels of ERRF than lapatinib resistant cell lines (Figure 1E).

We also tested whether ERRF expression correlates with prognosis in patients with ERBB2 positive breast cancer using the BreastMark Coexpression analysis tool. Interestingly, in 107 patients with known ERRF expression and disease-free survival (DFS) statuses, higher levels of ERRF expression significantly correlated with better DFS (Figure 1F).

Restoration of ERRF expression sensitizes lapatinib resistant ERBB2 positive breast cancer cells to lapatinib

To test whether ERRF is functionally involved in drug sensitivity, we restored ERRF expression by lentiviral infection in JIMT-1, a lapatinib resistant, ERBB2 positive breast cancer cell line that expressed a lower level of ERRF (Figure 1E), and measured cell survival in both 2-D and 3-D cultures. Ectopic expression of ERRF was confirmed by western blotting (Figure 2A). Stable ERFF expression clearly enhanced the killing effect of lapatinib on JIMT-1 cells in a dose dependent manner (Figure 2B). In 3-D culture, stable ERFF expression also decreased mammosphere formation of JIMT-1 cells after lapatinib treatment, although ERRF had no effect on sphere formation when lapatinib was absent (Figure 2C). Consistent results were obtained in the MDA-MB-453 breast cancer cell line, which was also lapatinib resistant and ERBB2 positive and expressed a lower level of ERRF (Figure 2D2F).

Ectopic expression of ERRF enhances lapatinib sensitivity in ERBB2-positive and lapatinib-resistant JIMT-1 and MDA-MB-453 breast cancer cell lines.

Figure 2: Ectopic expression of ERRF enhances lapatinib sensitivity in ERBB2-positive and lapatinib-resistant JIMT-1 and MDA-MB-453 breast cancer cell lines. Lentivirus-mediated stable expression of ERRF was confirmed by western blotting (A, D) and cell viability was determined by the CCK-8 assay (B, E) and the sphere formation assay was in matrigel or in ultralow attachment plates (C, F). Lapatinib treatment was for 6 days at indicated concentrations in the CCK-8 assay and for 6 days at 2 μM in sphere formation assays. *p < 0.05; **p < 0.01; ***p < 0.001; pLHCX, vector control.

Knockdown of ERRF expression desensitizes ERBB2 positive breast cancer cells to lapatinib

To further test the effect of ERRF on lapatinib sensitivity, we used two breast cancer cell lines that were ERBB2 positive and lapatinib sensitive [22, 46] and expressed higher levels of ERRF (Figure 1E), i.e., SK-BR-3 and BT-474. ERRF expression was knocked down by RNAi using two independent siRNAs [41], and the effect of knockdown was confirmed by real-time PCR (Figure 3A). CCK-8 analysis indicates that knockdown of ERRF expression compromised the killing effect of lapatinib on SK-BR-3 cells in a time- (Figure 3B) and dose-dependent manner (Figure 3C).

Knockdown of ERRF decreases lapatinib sensitivities in ERBB2-positive breast cancer cells.

Figure 3: Knockdown of ERRF decreases lapatinib sensitivities in ERBB2-positive breast cancer cells. SK-BR-3 (AC) and BT-474 (DI) cell lines were used, and the knockdown effect for siRNAs (#1 and #2) was confirmed by real-time PCR (A, F, H). The CCK-8 assay was used to detect cell viability (B, C, D, G, I), and sphere formation assay was also performed for BT-474 cells (E). Lapatinib treatments were at indicated times and doses (B, C, D). For BT-474 cells, different concentrations of siRNA were also applied (G, I) **p < 0.01; ***p < 0.001; C, negative control.

Similar results were obtained in BT-474 cells, where ERRF knockdown had no effect on cells treated with lower doses of lapatinib but significantly decreased drug sensitivities when higher doses of lapatinib were applied (Figure 3D). In 3-D culture, the effect was more profound, as ERRF knockdown increased sphere formation by several folds in lapatinib treated cells (Figure 3E). When we silenced ERRF by different concentrations of siRNA to simulate a range of expression levels similar to those in lapatinib resistant cell lines (Figure 3F, 3H), cell viability increased with increasing doses of ERRF siRNA in lapatinib treated cells in a time dependent manner (Figure 3G, 3I). The results from both SK-BR-3 and BT-474 cell lines indicate that ERRF downregulation causes a level of significantly reduced sensitivity to lapatinib treatment in ERBB2 positive breast cancer cells.

ERRF expression enhances lapatinib’s therapeutic effect in a preclinical model and correlates with improved clinical response to lapatinib in patients

To test whether ERRF expression improves the therapeutic response of ERBB2 positive breast cancer to lapatinib, JIMT-1 cells stably expressing ERRF and the vector control were subcutaneously injected into nude mice, lapatinib treatment was applied subsequently, and tumor growth was analyzed. During the 3 weeks of tumor growth before lapatinib administration, ERRF expression had no detectable effect on tumor volumes (Figure 4A). After lapatinib treatment began, tumor growth in the ERRF-overexpressing group was arrested or significantly slowed from day 7 after lapatinib administration (Figure 4A), but tumors in the control group kept growing at the same rate before treatment. Tumor weights (Figure 4B) and tumor images (Figure 4C) at excision confirmed the effect of ERRF expression on the therapeutic effects of lapatinib in JIMT-1 cells. Cell proliferation rate, indicated by Ki67 IHC staining, was decreased in the group of ERRF overexpression under lapatinib treatment (Figure 4D).

ERRF expression sensitizes xenograft breast cancer to the therapeutic effect of lapatinib and predicts response to lapatinib in breast cancer patients.

Figure 4: ERRF expression sensitizes xenograft breast cancer to the therapeutic effect of lapatinib and predicts response to lapatinib in breast cancer patients. Lapatinib resistant and ERBB2-positive JIMT-1 cells expressing ERRF or vector control (pLHCX) were injected subcutaneously into nude mice, lapatinib treatment was started at day 21, and tumor volumes (A) weights at excision (B) and images (C) are shown. (D). Detection of Ki67 in tumor sections by IHC staining. (E) Correlation of higher levels of ERRF expression with pathologic complete response (pCR) in patients treated with chemotherapy combined with lapatinib, as determined using a publically available data in the GEO database. NS, not significant; *P < 0.05; **P < 0.01.

In a phase II randomized study where drug activity and safety were evaluated in ERBB2 positive operable breast cancer, patients were treated with chemotherapy as a neoadjuvant therapy and lapatinib as a targeted therapy [47]. Analysis of available data in this study indicates that ERRF expression was higher in patients with pathologic complete response (pCR) than those without (Figure 4E). In this study, ERRF was identified in the list of 50 genes whose expression states predicted pCR in 93% of the test tumor samples [48], suggesting that patients with ERBB2 positive breast cancer, higher ERRF expression predicts a benefit from lapatinib treatment.

ERRF expression enhances lapatinib-mediated apoptotic response

Lapatinib treatment induces apoptosis [49], so we examined the effect of ERRF on lapatinib-mediated apoptosis by flow cytometry in lapatinib sensitive BT-474 cells with the knockdown of ERRF (Figure 5A) and lapatinib resistant JIMT-1 cells with ectopic expression of ERRF (Figure 5D). Without lapatinib treatment, stable overexpression or knockdown of ERRF had no significant effect on apoptosis (Figure 5C, 5F). When lapatinib treatment was applied, knockdown of ERRF in BT-474 cells decreased the ratio of apoptotic cells (annexin V stained) from 43.2% for control siRNA to 11.1% for siRNA #1 and 23.1% for siRNA #2 (Figure 5B, 5C). In JIMT-1 cells treated with lapatinib, the vector control had 19.7% of annexin V positive cells, while cells overexpressing ERRF increased the ratio to 41.2% (Figure 5E, 5F). Therefore, ERRF expression influences the apoptotic response of ERBB2 positive breast cancer cells to lapatinib.

ERRF enhances lapatinib-mediated apoptosis.

Figure 5: ERRF enhances lapatinib-mediated apoptosis. BT-474 cells with RNAi-mediated knockdown of ERRF (AC) and JIMT-1 cells overexpressing ERRF (DF) were treated with 10 μM lapatinib for 24 h, stained with annexin V, and then subjected to flow cytometry to detect apoptotic cells. The knockdown of ERRF was confirmed by real–time PCR, while ectopic expression of ERRF was confirmed by western blotting. C, control; #1 and #2, siRNAs against ERRF. **p < 0.01; ***p < 0.001.

ERBB2 and MCL1 appear to mediate ERRF’s effect on lapatinib sensitivity

Lapatinib can inhibit tyrosine kinase activity of ERBB2/EGFR to inactivate the downstream signaling pathway. In this study, we found no correlation between ERRF and AKT and MAPK’s phosphorylation levels (Supplementary Figure 1A). Using real-time PCR analysis, we tested the expression levels of genes that have been shown to correlate with lapatinib resistance in previous studies (Supplementary Figure 1B), and found that MCL1 was one of the genes that were upregulated by ERRF knockdown. Considering that ERRF enhances lapatinib-induced apoptosis (Figure 5), ERRF expression inversely correlates with ERBB2 status [41], and MCL1 is not only an anti-apoptotic gene that mediates lapatinib resistance in HCT116 cells [50] but also an upstream regulator of ERBB2 [51], we evaluated whether ERBB2 and MCL1 are related to ERRF in any way in breast cancer cells. We queried breast cancer samples in the TCGA database for those with expression information for both ERRF and MCL1 (Supplementary Table 1), and found a significant inverse correlation between ERRF and MCL1 (Figure 6A).

ERBB2 and MCL1 are involved in ERRF mediated sensitization to lapatinib treatment.

Figure 6: ERBB2 and MCL1 are involved in ERRF mediated sensitization to lapatinib treatment. (A) Expression of ERRF inversely correlates with that of MCL1 in breast cancer samples, as determined by the Pearson correlation analysis using data from the TCGA database (Supplementary Table 1). (B) Overexpression of ERRF inhibits ERBB2 and MCL1 expression in the JIMT-1 ERBB2 positive breast cancer cell line, as determined by western blotting. (C, D). Knockdown of ERRF in the BT-474 breast cancer cell line, as confirmed by real-time PCR (C), increases ERBB2 and MCL1 expression, as determined by western blotting (D). (E, F) Knockdown of MCL1 by siRNA transfection (50 nM) rescued decreased sensitivity of BT-474 cells to lapatinib mediated by ERRF knockdown (12.5 nM and 25 nM siRNA). ERRF and MCL1 expression levels were examined by real-time PCR or western blotting. Con, control; #1 and #2, siRNAs against ERRF.

We further tested whether there was a relationship between ERRF, MCL1, ERBB2 and lapatinib response. In JIMT-1 cells with ERRF overexpression, we found that treatment with 1 μM lapatinib for three days downregulated both MCL-1 and ERBB2 compared to cells without ERRF overexpression (Figure 6B). Consistently, silencing ERRF with siRNAs in BT-474 cells treated with lapatinib increased the expression of both MCL-1 and ERBB2 when compared to the negative control (Figure 6C, 6D). In BT-474 cells transfected with ERRF siRNA, insensitivity to lapatinib was rescued by knocking down MCL1 (Figure 6E, 6F), further implicating MCL1 in ERRF-mediated lapatinib sensitivity.


In this study, we tested whether ERRF plays a role in the development of resistance to ERBB2-targeted therapies in ERBB2-positive breast cancer. We evaluated the expression of ERRF in breast cancer in publically available databases, and correlated ERRF expression to responses to both ERBB2-targeted therapies and patient survival. We also tested whether ERRF functionally modulates the responses of ERBB2-positive breast cancer cells to the lapatinib ERBB2 inhibitor. Finally, we explored cellular and molecular mechanisms that underlie the effect of ERRF on lapatinib-mediated cell killing. Results from these analyses established ERRF as an important regulator of ERBB2 function and the effectiveness of ERBB2-targeted therapy.

ERRF expression predicts the sensitivity to lapatinib in ERBB2 positive breast cancer. This conclusion is supported by several lines of evidence, including the upregulation of ERRF by lapatinib in lapatinib-sensitive SK-BR-3 and BT-474 breast cancer cell lines (Figure 1A1C), downregulation of ERRF in lapatinib-resistant clones derived from SK-BR-3 and BT-474 cells (Figure 1D) [44], and the association of ERRF expression with lapatinib sensitivities in breast cancer cell lines (Figure 1E) [44]. In patients with breast cancer, although no data is currently available for correlating ERRF expression and lapatinib sensitivities, higher levels of ERRF expression significantly correlated with better DFS (Figure 1F), and ERRF was among a panel of 50 genes predicting treatment benefit from a combination of chemotherapy and lapatinib treatment [47].

Functionally, ERRF indeed sensitizes ERBB2 positive breast cancer to the therapeutic effects of lapatinib. This conclusion was supported by in vitro and in vivo experiments using both lapatinib resistant and lapatinib sensitive cell lines with modulated ERRF expression. In both 2-D and 3-D cell culture models, expression of ERRF sensitizes intrinsically resistant ERBB2 positive breast cancer cells to lapatinib (Figure 2); and in vivo tumorigenesis assay confirmed the effect (Figure 4). On the other hand, knockdown of ERRF in two lapatinib-sensitive ERBB2-positive breast cancer cell lines compromised the effect of lapatinib on cell survival in 2-D and 3-D cultures (Figure 3), further indicating a necessary role of ERRF in breast cancer’s sensitivity to lapatinib.

Mechanistically, ERRF promotes lapatinib-induced apoptosis likely by attenuating the expression of ERBB2 and its upstream regulator MCL-1. As expected, ectopic expression of ERRF increased, while knockdown of ERRF expression decreased, cell death induced by lapatinib in different breast cancer cell lines (Figure 5). Drug resistant cells usually have active anti-apoptotic signaling, while drug sensitive cells have more active pro-apoptotic signaling [49, 52]. MCL1 is a member of the anti-apoptotic BCL-2 family that is upregulated in tumors, and its upregulation leads to drug resistance [27, 50, 53]. MCL1 has been shown to upregulate ERBB2 expression in breast cancer cells [27]. Although the relationship between ERBB2 expression and lapatinib resistance has not been reported, mitochondrial ERBB2 (mtERBB2) appears to regulate cellular metabolism and therapeutic resistance [54]. There was a correlation between ERRF and MCL1 expression in breast cancer (Figure 6A); and ectopic expression of ERRF decreased while the knockdown of ERRF increased the expression of MCL1 in breast cancer cells (Figure 6), suggesting that ERRF could directly downregulate MCL1 expression. Taken together with the result that knockdown of MCL1 compromised lapatinib resistance mediated by ERRF knockdown (Figure 6E, 6F), it is possible that ERRF downregulates MCL1 expression to promote apoptosis in breast cancer’s response to lapatinib. ERRF expression decreased while its knockdown increased ERBB2 expression in breast cancer cells as well (Figure 6), it is also possible that ERRF loss upregulates ERBB2 including mtERBB2 to decrease lapatinib sensitivity. Nevertheless, how ERRF regulates lapatinib sensitivity in breast cancer cells largely remains unknown.

ERRF is a novel regulator of breast carcinogenesis involved in both the ER signaling and the ERBB2 signaling. We previously reported that ERRF expression positively correlates with ER and PR statuses but negatively associated with ERBB2 status [41], and knockdown of ERRF inhibits the proliferation and tumorigenesis of ER- and PR-positive breast cancer cells [41]. In addition, ERRF is transcriptionally regulated by the E2-ER signaling pathway in ER/PR-positive but ERBB2-negative breast cancer cells [55]. Our current study demonstrated that in ERBB2-positive breast cancer, ERRF also plays an important role, as ERRF sensitized such cells to lapatinib treatment, and higher levels of ERRF expression correlated with increased lapatinib sensitivity and better patient survival. These findings suggest that ERRF could be useful not only in the prediction of lapatinib responses but also in the improvement of lapatinib-based therapies of ERBB2-positive breast cancer.


Cell lines and other materials

BT-474, SK-BR-3 and MDA-MB-453 breast cancer cell lines and HEK293T cells were purchased from the American Type Culture Collection (ATCC, Manassas, VA) and propagated according to ATCC’s instructions. The JIMT-1 cell line was kindly provided by Dr. Rita Nahta of Emory University.

Lapatinib was purchased from LC Laboratories (Woburn, MA), hygromycin B was from Roche (Basel, Switzerland), and Matrigel was from BD Biosciences (Bedford, MA).

Retroviral expression of ERRF

Polymerase chain reaction (PCR) was performed to amplify the coding region of ERRF from genomic DNA with forward primer 5′–GGAAGCTTATGGCCCCGTCAGAAG–3′ and reverse primer 5′–CCATCGATCTAATCGGCCTGCCCA–3′. PCR products were digested with Hind III and Cla I, purified, and cloned into the pLHCX vector (Clontech, Mountain View, CA). After sequencing verification, the ERRF plasmids or the empty vector was cotransfected with the envelope vector VSV-G and the gal/pol expression vector Ecopac (Clontech) into HEK293T cells (ATCC) using the Lipofectamine 2000 reagent (Invitrogen, Carlsbad, CA). Viruses were harvested 72 hours after transfection and filtered with 0.45 μm filters (Millipore, Billerica, MA). Cells infected with viruses were selected in medium containing hygromycin B at 200 μg/ml (Roche) for 14 days before use.

Cytotoxicity assay

After transfecting with control siRNA or ERRF siRNA for 48 hours or selecting with hygromycin B for 2 weeks after viral infection, cells were dissociated with trypsin and seeded onto 96-well plates (5000 cells per well). After adhesion overnight, cells were incubated with lapatinib at a range of concentrations for 4 or 6 days. The cell counting kit-8 (CCK-8, Dojindo, Munich, Germany) was used to measure the total cell numbers. Following manufacturer instructions, 10 μL CCK-8 solution was added to each well, incubated for 1.5 hours, and, optical density (OD) was measured at the 450 nm wavelength.

Apoptosis assay

Apoptosis was measured by staining cells with Annexin V-FITC and PI. After incubation with lapatinib for 48 hours, cells were collected, washed with cold PBS, resuspended in 100 μL of 1 × Annexin V binding buffer, stained with Annexin V and PI (BD Pharmingen) by adding 5 μL of each to a tube and incubating for 15 min in the dark at room temperature, and analyzed by flow cytometry using the FlowJo 7.6 software.

Western blotting

Antibodies used in this study included: ERRF (1:1000 dilution, Sigma-Aldrich, St Louis, MO), ERBB2 (1:1000 dilution, OriGene, Rockville, MD), β-actin (1:5000 dilution, Sigma-Aldrich), and MCL1 (1:1000 dilution, Cell Signaling Technology, Danvers, MA). Western blotting was performed following standard protocols using WesternBright ECL (Advansta, Menlo Park, CA), and blots were photographed with the Image Quant LAS 4000 luminescent image analyzer (General Electric, Fairfield, CT). All Western blots were quantified using the ImageJ program.

Mammosphere culture

For 2-D culture, cells were plated in ultralow attachment plates (Corning, Corning, NY) at a density of 5,000 viable cells/mL and grown in DMEM/F-12 medium supplemented with B27 (Invitrogen), 20 ng/mL EGF (Promega, WI), 20 ng/mL bFGF (BD Biosciences), and 10 μg/mL heparin (Sigma-Aldrich). For 3-D culture, cells were seeded into 8-well glass chamber slides containing 40 μL growth factor-reduced matrigel per well and cultured in the same medium as in 2-D culture. The number of spheres containing at least 15 cells was counted under a microscope following a published procedure [56].

Tumorigenesis assay

Three to four week old female athymic BALB/c nude mice (vitalriver Beijing, China) were used. JIMT-1 cells in PBS:matrigel mixture (1:1 ratio) were injected subcutaneously into the flanks of mice at 2 × 105 cells/ml and 100 μL/site. Eight mice were used in each group. When tumors reached a volume of approximately 100 mm3, mice were treated with either vehicle (2% DMSO with 30% PEG300 in water) or lapatinib (100 mg/kg ) twice daily by oral gavage for 21 days [22]. Tumor volumes were measured every other day, and tumors were surgically isolated from mice and weighed at the end of tumorigenesis experiments.


After excision, tumors were formalin-fixed, paraffin-embedded, deparaffinized and rehydrated; and tissue sections were prepared following standard procedure. Antigen retrieval was carried out by heating in sodium citrate buffer using a pressure cooker for 3 min at full pressure. Sections were incubated overnight at 4°C with Ki67 antibody (1:2000 dilution, Abcam, Cambridge, UK) and the HRP solution (Dako, Santa Clarita, CA) for 1 hour. The DAB-chromogen (Maxim, Fuzhou, China) was used for staining.

Bioinformatics analysis

The BreastMark Breast Cancer Survival Analysis Tool (http://glados.ucd.ie/BreastMark/), an algorithm that integrates gene expression and survival data from 26 datasets on 12 different microarray platforms, was used to associate ERRF expression with patient survival with known ERBB2 status. The number of samples used for analysis depends on how many platforms have probes for a gene of interest and the availability of relevant clinical data [57].

We also used the Broad-Novartis Cancer Cell Line Encyclopedia (CCLE; http://www.broadinstitute.org/ccle/home) to evaluate ERRF expression and lapatinib sensitivity in breast cancer cell lines. Microarray or RNA-Seq-based expression data was available for all genes in this resource. We used the Gene Expression Omnibus (GEO) Database (data set GSE51889) to compare SK-BR-3 and BT-474 lapatinib resistant clones to control untreated cancer cells.

Statistical analysis

All experimental readings were expressed as mean ± standard errors. Differences between two groups were determined by using the unpaired Student t-test, and p-values less than 0.05 were considered as statistically different.

Novelty and impact

Development of resistance and sometimes lack of response to ERBB2-targetted therapy constitute a significant problem in the treatment of ERBB2-positive breast cancer. In this study, we found that expression of ERRF, an estrogen receptor related factor, predicted the sensitivity of ERBB2-positive breast cancers to lapatinib, a drug used in combination with other drugs to treat either ERBB2-positive breast cancers that have received prior therapy or metastatic, hormone receptor positive and ERBB2-postive breast cancer in postmenopausal women. Functionally, overexpression of ERRF sensitizes ERBB2-positive breast cancer cells to lapatinib in both in vitro and in vivo assays, and the underlying mechanism involved ERRF-mediated expression change of ERBB2. These findings implicate ERRF in the ERBB2 pathway and the response of ERBB2-positive breast cancer to lapatinib, and further studies in this area could lead to improved detection and/or treatment of ERBB2-positive breast cancer.

Authors’ contributions

LQ, RN and JTD conceived the project; LQ, BZ and JTD designed all experiments and analyzed all data; LQ, SZ, XC, QW, GM and AL performed experiment; LQ, BZ, JLK and JTD prepared the manuscript.


We thank Dr. Dan Zhao, Dr. Zhengmao Zhu, Ms. Ang Gao and Mr. Xing Fu of Nankai University for helpful comments and assistance during the study.


The authors declare they have no conflicts of interest.


This work was supported by grant 81472464 from the National Natural Science Foundation of China.


1. Ravdin PM, Chamness GC. The c-erbB-2 proto-oncogene as a prognostic and predictive marker in breast cancer: a paradigm for the development of other macromolecular markers—a review. Gene. 1995; 159:19–27.

2. Seshadri R, Firgaira FA, Horsfall DJ, McCaul K, Setlur V, Kitchen P. Clinical significance of HER-2/neu oncogene amplification in primary breast cancer. The South Australian Breast Cancer Study Group. J Clin Oncol. 1993; 11: 1936–42. doi: 10.1200/JCO.1993.11.10.1936.

3. Press MF, Pike MC, Chazin VR, Hung G, Udove JA, Markowicz M, Danyluk J, Godolphin W, Sliwkowski M, Akita R. Her-2/neu expression in node-negative breast cancer: direct tissue quantitation by computerized image analysis and association of overexpression with increased risk of recurrent disease. Cancer Res. 1993; 53:4960–70.

4. Slamon DJ, Clark GM, Wong SG, Levin WJ, Ullrich A, McGuire WL. Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science. 1987; 235:177–82.

5. Slamon DJ, Godolphin W, Jones LA, Holt JA, Wong SG, Keith DE, Levin WJ, Stuart SG, Udove J, Ullrich A. Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. Science. 1989; 244:707–12.

6. Slamon DJ, Leyland-Jones B, Shak S, Fuchs H, Paton V, Bajamonde A, Fleming T, Eiermann W, Wolter J, Pegram M, Baselga J, Norton L. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med. 2001; 344:783–92. doi: 10.1056/NEJM200103153441101.

7. Garcia Fernandez A, Gimenez N, Fraile M, Gonzalez S, Chabrera C, Torras M, Gonzalez C, Salas A, Barco I, Cirera L, Cambra MJ, Veloso E, Pessarrodona A. Survival and clinicopathological characteristics of breast cancer patient according to different tumour subtypes as determined by hormone receptor and Her2 immunohistochemistry. a single institution survey spanning 1998 to 2010. Breast. 2012; 21:366–73. doi: 10.1016/j.breast.2012.03.004.

8. Blows FM, Driver KE, Schmidt MK, Broeks A, van Leeuwen FE, Wesseling J, Cheang MC, Gelmon K, Nielsen TO, Blomqvist C, Heikkila P, Heikkinen T, Nevanlinna H, et al. Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies. PLoS Med. 2010; 7:e1000279. doi: 10.1371/journal.pmed.1000279.

9. Prat A, Cheang MC, Galvan P, Nuciforo P, Pare L, Adamo B, Munoz M, Viladot M, Press MF, Gagnon R, Ellis C, Johnston S. Prognostic Value of Intrinsic Subtypes in Hormone Receptor-Positive Metastatic Breast Cancer Treated With Letrozole With or Without Lapatinib. JAMA Oncol. 2016; 2:1287–94. doi: 10.1001/jamaoncol.2016.0922.

10. Johnston S, Pippen J Jr, Pivot X, Lichinitser M, Sadeghi S, Dieras V, Gomez HL, Romieu G, Manikhas A, Kenedy MJ, Press MF, Maltzman J, Florance A, et al. Lapatinib combined with letrozole versus letrozole and placebo as first-line therapy for postmenopausal hormone receptor-positive metastatic breast cancer. J Clin Oncol. 2009; 27:5538–46. doi: 10.1200/JCO.2009.23.3734.

11. Gutierrez MC, Detre S, Johnston S, Mohsin SK, Shou J, Allred DC, Schiff R, Osborne CK, Dowsett M. Molecular changes in tamoxifen-resistant breast cancer: relationship between estrogen receptor, HER-2, and p38 mitogen-activated protein kinase. J Clin Oncol. 2005; 23:2469–76. doi: 10.1200/JCO.2005.01.172.

12. Knowlden JM, Hutcheson IR, Jones HE, Madden T, Gee JM, Harper ME, Barrow D, Wakeling AE, Nicholson RI. Elevated levels of epidermal growth factor receptor/c-erbB2 heterodimers mediate an autocrine growth regulatory pathway in tamoxifen-resistant MCF-7 cells. Endocrinology. 2003; 144:1032–44. doi: 10.1210/en.2002–220620.

13. Arpino G, Wiechmann L, Osborne CK, Schiff R. Crosstalk between the estrogen receptor and the HER tyrosine kinase receptor family: molecular mechanism and clinical implications for endocrine therapy resistance. Endocr Rev. 2008; 29:217–33. doi: 10.1210/er.2006–0045.

14. Shou J, Massarweh S, Osborne CK, Wakeling AE, Ali S, Weiss H, Schiff R. Mechanisms of tamoxifen resistance: increased estrogen receptor-HER2/neu cross-talk in ER/HER2-positive breast cancer. J Natl Cancer Inst. 2004; 96: 926–35.

15. Gianni L, Pienkowski T, Im YH, Roman L, Tseng LM, Liu MC, Lluch A, Staroslawska E, de la Haba-Rodriguez J, Im SA, Pedrini JL, Poirier B, Morandi P, et al. Efficacy and safety of neoadjuvant pertuzumab and trastuzumab in women with locally advanced, inflammatory, or early HER2-positive breast cancer (NeoSphere): a randomised multicentre, open-label, phase 2 trial. Lancet Oncol. 2012; 13:25–32. doi: 10.1016/S1470-2045(11)70336-9.

16. Romond EH, Perez EA, Bryant J, Suman VJ, Geyer CE Jr, Davidson NE, Tan-Chiu E, Martino S, Paik S, Kaufman PA, Swain SM, Pisansky TM, Fehrenbacher L, et al. Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer. N Engl J Med. 2005; 353: 1673–84. doi: 10.1056/NEJMoa052122.

17. Piccart-Gebhart MJ, Procter M, Leyland-Jones B, Goldhirsch A, Untch M, Smith I, Gianni L, Baselga J, Bell R, Jackisch C, Cameron D, Dowsett M, Barrios CH, et al. Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. N Engl J Med. 2005; 353:1659–72. doi: 10.1056/NEJMoa052306.

18. Baselga J, Bradbury I, Eidtmann H, Di Cosimo S, de Azambuja E, Aura C, Gomez H, Dinh P, Fauria K, Van Dooren V, Aktan G, Goldhirsch A, Chang TW, et al. Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial. Lancet. 2012; 379:633–40. doi: 10.1016/S0140–6736(11)61847–3.

19. Geyer CE, Forster J, Lindquist D, Chan S, Romieu CG, Pienkowski T, Jagiello-Gruszfeld A, Crown J, Chan A, Kaufman B, Skarlos D, Campone M, Davidson N, et al. Lapatinib plus capecitabine for HER2-positive advanced breast cancer. N Engl J Med. 2006; 355:2733–43. doi: 10.1056/NEJMoa064320.

20. Tripathy D, Slamon DJ, Cobleigh M, Arnold A, Saleh M, Mortimer JE, Murphy M, Stewart SJ. Safety of treatment of metastatic breast cancer with trastuzumab beyond disease progression. J Clin Oncol. 2004; 22: 1063–70. doi: 10.1200/JCO.2004.06.557.

21. Smith I, Procter M, Gelber RD, Guillaume S, Feyereislova A, Dowsett M, Goldhirsch A, Untch M, Mariani G, Baselga J, Kaufmann M, Cameron D, Bell R, et al. 2-year follow-up of trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer: a randomised controlled trial. The Lancet. 2007; 369:29–36. doi: 10.1016/S0140–6736(07)60028–2.

22. Rusnak DW, Lackey K, Affleck K, Wood ER, Alligood KJ, Rhodes N, Keith BR, Murray DM, Knight WB, Mullin RJ, Gilmer TM. The effects of the novel, reversible epidermal growth factor receptor/ErbB-2 tyrosine kinase inhibitor, GW2016, on the growth of human normal and tumor-derived cell lines in vitro and in vivo. Mol Cancer Ther. 2001; 1:85–94.

23. Burris HA 3rd. Dual kinase inhibition in the treatment of breast cancer: initial experience with the EGFR/ErbB-2 inhibitor lapatinib. Oncologist. 2004; 9:10–5.

24. Dai CL, Tiwari AK, Wu CP, Su XD, Wang SR, Liu DG, Ashby CR Jr, Huang Y, Robey RW, Liang YJ, Chen LM, Shi CJ, Ambudkar SV, et al. Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2. Cancer Res. 2008; 68:7905–14. doi: 10.1158/0008–5472.CAN-08–0499.

25. Awasthi S, Ezelle H, Hassel BA, Hamburger AW. The ErbB3-binding protein EBP1 modulates lapatinib sensitivity in prostate cancer cells. Mol Cell Biochem. 2015; 405: 177–86. doi: 10.1007/s11010–015–2409-z.

26. Huang HL, Chen YC, Huang YC, Yang KC, Pan H, Shi SP, Chen YJ. Lapatinib induces autophagy, apoptosis and megakaryocytic differentiation in chronic myelogenous leukemia K562 cells. PLoS One. 2011; 6:e29014. doi: 10.1371/journal.pone.0029014.

27. Martin AP, Mitchell C, Rahmani M, Nephew KP, Grant S, Dent P. Inhibition of MCL-1 enhances lapatinib toxicity and overcomes lapatinib resistance via BAK-dependent autophagy. Cancer Biol Ther. 2009; 8:2084–96.

28. Xia W, Bacus S, Hegde P, Husain I, Strum J, Liu L, Paulazzo G, Lyass L, Trusk P, Hill J, Harris J, Spector NL. A model of acquired autoresistance to a potent ErbB2 tyrosine kinase inhibitor and a therapeutic strategy to prevent its onset in breast cancer. Proc Natl Acad Sci USA. 2006; 103:7795–800. doi: 10.1073/pnas.0602468103.

29. Lee YY, Kim HP, Kang MJ, Cho BK, Han SW, Kim TY, Yi EC. Phosphoproteomic analysis identifies activated MET-axis PI3K/AKT and MAPK/ERK in lapatinib-resistant cancer cell line. Exp Mol Med. 2013; 45:e64. doi: 10.1038/emm.2013.115.

30. Chen CT, Kim H, Liska D, Gao S, Christensen JG, Weiser MR. MET activation mediates resistance to lapatinib inhibition of HER2-amplified gastric cancer cells. Mol Cancer Ther. 2012; 11:660–9. doi: 10.1158/1535–7163.MCT-11–0754.

31. Kim HP, Han SW, Song SH, Jeong EG, Lee MY, Hwang D, Im SA, Bang YJ, Kim TY. Testican-1-mediated epithelial-mesenchymal transition signaling confers acquired resistance to lapatinib in HER2-positive gastric cancer. Oncogene. 2014; 33:3334–41. doi: 10.1038/onc.2013.285.

32. Hong YS, Kim J, Pectasides E, Fox C, Hong SW, Ma Q, Wong GS, Peng S, Stachler MD, Thorner AR, Van Hummelen P, Bass AJ. Src mutation induces acquired lapatinib resistance in ERBB2-amplified human gastroesophageal adenocarcinoma models. PLoS One. 2014; 9:e109440. doi: 10.1371/journal.pone.0109440.

33. Rexer BN, Ham AJ, Rinehart C, Hill S, Granja-Ingram Nde M, Gonzalez-Angulo AM, Mills GB, Dave B, Chang JC, Liebler DC, Arteaga CL. Phosphoproteomic mass spectrometry profiling links Src family kinases to escape from HER2 tyrosine kinase inhibition. Oncogene. 2011; 30: 4163–74. doi: 10.1038/onc.2011.130.

34. Karakashev SV, Reginato MJ. Hypoxia/HIF1alpha induces lapatinib resistance in ERBB2-positive breast cancer cells via regulation of DUSP2. Oncotarget. 2015; 6:1967–80. doi: 10.18632/oncotarget.2806.

35. Wang Q, Quan H, Zhao J, Xie C, Wang L, Lou L. RON confers lapatinib resistance in HER2-positive breast cancer cells. Cancer Lett. 2013; 340:43–50. doi: 10.1016/j.canlet.2013.06.022.

36. Gayle SS, Castellino RC, Buss MC, Nahta R. MEK inhibition increases lapatinib sensitivity via modulation of FOXM1. Curr Med Chem. 2013; 20:2486–99.

37. Liu L, Greger J, Shi H, Liu Y, Greshock J, Annan R, Halsey W, Sathe GM, Martin AM, Gilmer TM. Novel mechanism of lapatinib resistance in HER2-positive breast tumor cells: activation of AXL. Cancer Res. 2009; 69: 6871–8. doi: 10.1158/0008–5472.CAN-08–4490.

38. Shibata T, Kan H, Murakami Y, Ureshino H, Watari K, Kawahara A, Kage M, Hattori S, Ono M, Kuwano M. Y-box binding protein-1 contributes to both HER2/ErbB2 expression and lapatinib sensitivity in human gastric cancer cells. Mol Cancer Ther. 2013; 12:737–46. doi: 10.1158/1535–7163.MCT-12–1125.

39. Bardeesy N, Cheng KH, Berger JH, Chu GC, Pahler J, Olson P, Hezel AF, Horner J, Lauwers GY, Hanahan D, DePinho RA. Smad4 is dispensable for normal pancreas development yet critical in progression and tumor biology of pancreas cancer. Genes Dev. 2006; 20:3130–46. doi: 10.1101/gad.1478706.

40. Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, et al. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc Natl Acad Sci USA. 2002; 99:16899–903. doi: 10.1073/pnas.242603899.

41. Su D, Fu X, Fan S, Wu X, Wang XX, Fu L, Dong XY, Ni JJ, Fu L, Zhu Z, Dong JT. Role of ERRF, a novel ER-related nuclear factor, in the growth control of ER-positive human breast cancer cells. Am J Pathol. 2012; 180:1189–201. doi: 10.1016/j.ajpath.2011.11.025.

42. Curtis C, Shah SP, Chin SF, Turashvili G, Rueda OM, Dunning MJ, Speed D, Lynch AG, Samarajiwa S, Yuan Y, Graf S, Ha G, Haffari G, et al. The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups. Nature. 2012; 486:346–52. doi: 10.1038/nature10983.

43. Paroni G, Fratelli M, Gardini G, Bassano C, Flora M, Zanetti A, Guarnaccia V, Ubezio P, Centritto F, Terao M, Garattini E. Synergistic antitumor activity of lapatinib and retinoids on a novel subtype of breast cancer with coamplification of ERBB2 and RARA. Oncogene. 2012; 31:3431–43. doi: 10.1038/onc.2011.506.

44. Chen YJ, Yeh MH, Yu MC, Wei YL, Chen WS, Chen JY, Shih CY, Tu CY, Chen CH, Hsia TC, Chien PH, Liu SH, Yu YL, et al. Lapatinib-induced NF-kappaB activation sensitizes triple-negative breast cancer cells to proteasome inhibitors. Breast Cancer Res. 2013; 15:R108. doi: 10.1186/bcr3575.

45. O’Brien NA, Browne BC, Chow L, Wang Y, Ginther C, Arboleda J, Duffy MJ, Crown J, O’Donovan N, Slamon DJ. Activated phosphoinositide 3-kinase/AKT signaling confers resistance to trastuzumab but not lapatinib. Mol Cancer Ther. 2010; 9:1489–502. doi: 10.1158/1535–7163.MCT-09–1171.

46. Konecny GE, Pegram MD, Venkatesan N, Finn R, Yang G, Rahmeh M, Untch M, Rusnak DW, Spehar G, Mullin RJ, Keith BR, Gilmer TM, Berger M, et al. Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells. Cancer Res. 2006; 66:1630–9. doi: 10.1158/0008–5472.CAN-05–1182.

47. Guarneri V, Frassoldati A, Bottini A, Cagossi K, Bisagni G, Sarti S, Ravaioli A, Cavanna L, Giardina G, Musolino A, Untch M, Orlando L, Artioli F, et al. Preoperative chemotherapy plus trastuzumab, lapatinib, or both in human epidermal growth factor receptor 2-positive operable breast cancer: results of the randomized phase II CHER-LOB study. J Clin Oncol. 2012; 30:1989–95. doi: 10.1200/JCO.2011.39.0823.

48. Guarneri V, Dieci MV, Frassoldati A, Maiorana A, Ficarra G, Bettelli S, Tagliafico E, Bicciato S, Generali DG, Cagossi K, Bisagni G, Sarti S, Musolino A, et al. Prospective Biomarker Analysis of the Randomized CHER-LOB Study Evaluating the Dual Anti-HER2 Treatment With Trastuzumab and Lapatinib Plus Chemotherapy as Neoadjuvant Therapy for HER2-Positive Breast Cancer. Oncologist. 2015; 20:1001–10. doi: 10.1634/theoncologist.2015–0138.

49. Xia W, Mullin RJ, Keith BR, Liu LH, Ma H, Rusnak DW, Owens G, Alligood KJ, Spector NL. Anti-tumor activity of GW572016: a dual tyrosine kinase inhibitor blocks EGF activation of EGFR/erbB2 and downstream Erk1/2 and AKT pathways. Oncogene. 2002; 21:6255–63. doi: 10.1038/sj.onc.1205794.

50. Martin AP, Miller A, Emad L, Rahmani M, Walker T, Mitchell C, Hagan MP, Park MA, Yacoub A, Fisher PB, Grant S, Dent P. Lapatinib resistance in HCT116 cells is mediated by elevated MCL-1 expression and decreased BAK activation and not by ERBB receptor kinase mutation. Mol Pharmacol. 2008; 74:807–22. doi: 10.1124/mol.108.047365.

51. Bashari MH, Fan F, Vallet S, Sattler M, Arn M, Luckner-Minden C, Schulze-Bergkamen H, Zornig I, Marme F, Schneeweiss A, Cardone MH, Opferman JT, Jager D, et al. Mcl-1 confers protection of Her2-positive breast cancer cells to hypoxia: therapeutic implications. Breast Cancer Res. 2016; 18:26. doi: 10.1186/s13058–016–0686–4.

52. Tanizaki J, Okamoto I, Fumita S, Okamoto W, Nishio K, Nakagawa K. Roles of BIM induction and survivin downregulation in lapatinib-induced apoptosis in breast cancer cells with HER2 amplification. Oncogene. 2011; 30: 4097–106. doi: 10.1038/onc.2011.111.

53. Mitchell C, Yacoub A, Hossein H, Martin AP, Bareford MD, Eulitt P, Yang C, Nephew KP, Dent P. Inhibition of MCL-1 in breast cancer cells promotes cell death in vitro and in vivo. Cancer Biol Ther. 2010; 10:903–17. doi: 10.4161/cbt.10.9.13273.

54. Ding Y, Liu Z, Desai S, Zhao Y, Liu H, Pannell LK, Yi H, Wright ER, Owen LB, Dean-Colomb W, Fodstad O, Lu J, LeDoux SP, et al. Receptor tyrosine kinase ErbB2 translocates into mitochondria and regulates cellular metabolism. Nat Commun. 2012; 3:1271. doi: 10.1038/ncomms2236.

55. Luo A, Su D, Zhang X, Qi L, Fu L, Dong JT. Estrogen-estrogen receptor signaling suppresses the transcription of ERRF in breast cancer cells. J Genet Genomics. 2016; 43: 565–7. doi: 10.1016/j.jgg.2016.06.003.

56. Dontu G, Abdallah WM, Foley JM, Jackson KW, Clarke MF, Kawamura MJ, Wicha MS. In vitro propagation and transcriptional profiling of human mammary stem/progenitor cells. Genes Dev. 2003; 17:1253–70. doi: 10.1101/gad.1061803.

57. Madden SF, Clarke C, Gaule P, Aherne ST, O’Donovan N, Clynes M, Crown J, Gallagher WM. BreastMark: an integrated approach to mining publicly available transcriptomic datasets relating to breast cancer outcome. Breast Cancer Res. 2013; 15: R52. doi: 10.1186/bcr3444.

58. Barretina J, Caponigro G, Stransky N, Venkatesan K, Margolin AA, Kim S, Wilson CJ, Lehar J, Kryukov GV, Sonkin D, Reddy A, Liu M, Murray L, et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature. 2012; 483:603–7. doi: 10.1038/nature11003.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 16425