MYBsuppresses differentiation and apoptosis of human breast cancer cells
© Drabsch et al.; licensee BioMed Central Ltd. 2010
Received: 22 March 2010
Accepted: 26 July 2010
Published: 26 July 2010
MYB is highly expressed in estrogen receptor positive (ER + ve) breast tumours and tumour cell lines. We recently demonstrated that MYB is essential for the proliferation of ER + ve breast cancer cells, and have now investigated its role in mammary epithelial differentiation.
MCF-7 breast cancer cells were treated with sodium butyrate, vitamin E succinate or 12-O-tetradecanoylphorbol-13-acetate to induce differentiation as measured by Nile Red staining of lipid droplets and β-casein expression. The non-tumorigenic murine mammary epithelial cell (MEC) line, HC11, was induced to differentiate with lactogenic hormones. MYB levels were manipulated by inducible lentiviral shRNA-mediated knockdown and retroviral overexpression.
We found that MYB expression decreases following chemically-induced differentiation of the human breast cancer cell line MCF-7, and hormonally-induced differentiation of a non-tumorigenic murine mammary epithelial cell (MEC) line, HC11. We also found that shRNA-mediated MYB knockdown initiated differentiation of breast cancer cells, and greatly sensitised them to the differentiative and pro-apoptotic effects of differentiation-inducing agents (DIAs). Sensitisation to the pro-apoptotic effects DIAs is mediated by decreased expression of BCL2, which we show here is a direct MYB target in breast cancer cells. Conversely, enforced expression of MYB resulted in the cells remaining in an undifferentiated state, with concomitant suppression of apoptosis, in the presence of DIAs.
Taken together, these data imply that MYB function is critical in regulating the balance between proliferation, differentiation, and apoptosis in MECs. Moreover, our findings suggest MYB may be a viable therapeutic target in breast cancer and suggest specific approaches for exploiting this possibility.
There is a critical balance between proliferation, differentiation, and apoptosis in the cellular composition of every tissue. In the hematopoietic system, MYB clearly plays a role in maintaining this balance. MYB is essential for hematopoiesis , is highly expressed in immature hematopoietic cells and its expression is down-regulated upon differentiation [2, 3]. Moreover, enforced expression of normal and activated forms of MYB can suppress differentiation and maintain proliferation of hematopoietic cells [4–6].
For these reasons, most work on MYB has focused on its role in normal and leukemic hematopoiesis. However, there is increasing evidence for a role of MYB in colonic epithelial cell differentiation and homeostasis, and notably, in colon cancer . The pattern of MYB expression in normal colonic crypts suggests that, similarly to the hematopoietic system, expression is high in immature, rapidly proliferating cells, and decreases with differentiation and maturation [8, 9], whereas reduced MYB activity perturbs colonic epithelial proliferation, differentiation and viability [8, 9]. The involvement of MYB in epithelial tumors was first suggested by the amplification of MYB in certain colon carcinoma-derived cell lines , and by its expression in a substantial proportion of tumors [7, 11]. Moreover MYB expression in colon tumors correlates with poor clinical prognosis , and an important transcriptional regulatory region of MYB is frequently mutated in this disease [13, 14]. Furthermore, MYB is required for colon carcinoma cell proliferation [7, 15], and is down-regulated during differentiation of these cells  while, conversely, ectopic MYB expression can suppress their differentiation .
By contrast, much less is known about the functions of MYB in mammary epithelial cells. Nevertheless, it has been shown that MYB is expressed at relatively high levels in estrogen receptor (ER) positive breast cancers and tumor cell lines . Moreover we, and others  have previously shown that MYB is a direct target of estrogen/ER signaling, and that MYB expression in breast cancer cells is regulated by transcriptional attenuation within its first intron . Importantly, we have also recently shown that MYB is required for the proliferation of ER positive, but not ER negative, breast cancer cell lines , identifying for the first time a functional role for MYB in breast cancer. In addition, Fang et al  reported a prolactin-inducible association between MYB and Stat5a, and that a number of Stat5a-responsive promoters such as that of the CISH gene are further stimulated by MYB. Their results suggested that MYB may act as a coactivator for Stat5a, and also supported a proliferative function for MYB in human breast cancer.
To further understand the function of MYB in breast cancer and in mammary epithelial cells (MECs) generally, we have now investigated its role in the differentiation of these cells. Differentiation of human breast cancer cell lines (MCF-7 and ZR-75-1) and non-tumorigenic MEC (HC11) can be induced by chemical agents or lactogenic hormones, respectively, and results in morphological and molecular properties that are characteristic of mature ductal epithelial cells. We have found that mammary carcinoma cell lines in which MYB expression was 'knocked-down' by shRNA show changes that indicate differentiation has occurred in some of these cells. Moreover, these MYB knock-down cells are more sensitive to differentiation after exposure to low doses of differentiation-inducing agents, and can be driven into apoptosis with doses that would normally only induce differentiation. Conversely, ectopic expression of MYB suppressed differentiation and apoptosis induced by differentiation-inducing agents (DIAs). Taken together, our data show that MYB plays an important role in regulating the balance between proliferation, differentiation, and apoptosis in both normal and malignant mammary epithelial cells, and that this role is remarkably similar to that it plays in hematopoietic and colonic epithelial cells. Finally, our observation that DIAs and MYB inhibition synergize in killing breast tumor cells suggests an approach to developing new treatments for ER/MYB positive breast cancer.
Materials and methods
The breast cancer cell lines MCF-7 and ZR-75-1 were cultured in DMEM (Invitrogen, Mount Waverley, Vic, Australia) supplemented with 10% FBS, l-glutamine, penicillin G, and streptomycin sulfate (All from GIBCO/BRL, Grand Island, New York, USA). All cell lines were maintained at 37°C in a humidified 5% carbon dioxide/95% air incubator. Prior to reaching confluence, cells were trypsinized with a 0.05% trypsin/0.53 mM EDTA solution and resuspended in fresh growth medium before plating onto a new growth surface.
Sodium butyrate, vitamin E succinate, and 12-O-tetradecanoylphorbol-13-acetate were purchased from Invitrogen (Mount Waverley, Vic, Australia).
HC11 cells were grown in Roswell Park Memorial Institute medium (RPMI)-1640 (Invitrogen, Mount Waverley, Vic, Australia) medium containing 10% FBS, 5 μg/ml insulin, and 10 ng/ml epidermal growth factor (both from Sigma-Aldrich, Castle Hill, NSW, Australia). Differentiation was induced three days after reaching confluence in medium containing 5 μg/ml insulin, 1 μg/ml hydrocortisone and 5 μg/ml prolactin (Sigma-Aldrich, Castle Hill, NSW, Australia).
For lipid droplet staining, cells grown on glass cover slips were rinsed twice with PBS and fixed for 20 minutes with PBS containing 4% paraformaldehyde at 20°C. After another PBS rinse and staining for 15 minutes with Nile Red and 4',6-diamidino-2-phenylindole (DAPI) (Sigma-Aldrich, Castle Hill, NSW, Australia), the cells were PBS washed and mounted. Fluorescence imaging was performed by using automated excitation and emission filter wheels of a Fluorescent AxioSkop 2 plus Microscope (Carl Zeiss Pty Ltd, New South Wales, Australia). For flow cytometric analysis, cells not grown on glass cover slips were washed in PBS, and resuspended in PBS containing 0.01% Nile Red for 15 minutes at 37°C. After three washes in PBS, they were analyzed by flow cytometry using a FACS Calibur instrument (Becton Dickinson, San Jose, CA, USA), and the primary data were then processed using CellQuest software (Becton Dickinson, San Jose, CA, USA).
For siRNA transfection experiments, MCF-7 cells were plated and transfected the following day with 100 nM of BCL2 specific, or and control siRNAs (Dharmacon Research, Lafayette, CO, USA) by using lipofectamine 2000 (Invitrogen, Mount Waverley, Vic, Australia). Briefly, all transfections were performed in a mixture of Opti-MEM and complete media without antibiotics, as described previously . The transfection incubation time for siRNA/lipofectamine 2,000 complexes was 24 hours.
Chromatin immunoprecipitation assay
MCF-7 cells were grown to 95% confluence in phenol-red-free DMEM supplemented with 10% charcoal-stripped FBS for 72 hours; at which time, 10 nM b-estradiol was added for 12 hours. Chromatin immunoprecipitation (ChIP) was performed as previously described  by using rabbit immunoglobulin (Ig) G (Sigma, Castle Hill, NSW, Australia) and 1.1 anti-Myb/5.1 anti-Myb or 1.1 anti-Myb/Thelma anti-Myb monoclonal antibodies . The resultant samples were used as real-time PCR templates to quantify binding of MYB to the various regions of BCL2, MYC or GAPDH. Primer sequences used in the PCR were: Myb binding sites (MBS) 1 F 5'-GCTCAGAGGAGGGCTCTTTC-3', MBS 1 R 5'-TTTCTCCTCCTCCTGGTCCT-3', MBS 2 F 5'-CCCGCCTCTTCACCTTTCAG-3', MBS 2 R 5'-CAATGGCACTTCAAGTCCCGA, MBS 3 F-5'-GGTCAGGTGGACCACAGGT- 3', MBS 3 R 5'-GTCCAAGAATGCAAAGCACA-3', MBS 4 F 5'-CACAGCGCCAACAGAACTAC-3', MBS 4 R 5'-ACAGGCCAGATGCCAGATAC-3', MYC F 5'-GCCTGCGATGATTTATACTCACAG-3', MYC R 5'-CGGAGATTAGCGAGAGAGGATC-3', GAPDH F 5'-ATCAATGGAAATCCCATCACCATCT-3', GAPDH R 5'-GGTTTTTCTAGACGGCAGGTCAG-3', Upstream Control F 5'-GCAGGTGCTCAACAGATGAA-3', Upstream Control R 5'-GGGATTGCCTTACAGGTGAA-3'.
Apoptosis-induced nuclear DNA fragmentation was detected using the TMR Red In Situ Cell Death Detection Kit (Roche Diagnostics Corp, Indianapolis, IN, USA) following the manufacturer's protocol. Briefly, 24 hours after DIA treatment, cells grown on glass cover slips were fixed. This was followed by incubation in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) reaction mix for 60 minutes at 37°C. Slides were washed three times in PBS/Triton X-100/BSA (0.3%) and visualized on a fluorescent microscope. Cells not grown on glass cover slips were washed in PBS, and resuspended in PBS and TUNEL reaction mix for 60 minutes at 37°C. Cells were washed three times in PBS, and analysed by flow cytometry on the FACS Calibur as described earlier.
Total RNA was prepared by using a RNeasy MiniKit (Qiagen, Valencia, CA, USA) according to the manufacturer's instructions. One microgram of total RNA was reverse transcribed in a total of 20 μl by using SuperScript III (Invitrogen, Carlsbad, CA, USA). The resulting cDNA was then diluted to a total volume of 100 μl with sterile water. Each real-time PCR consisted of 1 μl of diluted reverse transcriptase product, iQ SYBR Green Supermix (Bio-Rad, Hercules, CA, USA), and 50 nM forward and reverse primers (see below). Reactions were carried out on a RotorGene 3000 (Corbett Research, Sydney, NSW, Australia) at 95°C for 10 minutes, followed by 40 cycles of 95°C for 20 seconds, 56°C for 15 seconds, and 72°C for 20 seconds. Fluorescence measurements analyzed by using the RotorGene 3000 software. The fold-change expression of each gene was calculated by using the ΔΔCT method, with cyclophilin A as an internal control. Primers used for real-time PCR were: MYB F, 5'-GCCAATTATCTCCCGAATCGA-3'; MYB R, 5'-ACCAACGTTTCGGACCGT A-3'; ß-casein F, 5'-CCCTCAAATCCCAAAACTCA-3'; ß-casein R, 5'-GAGCAGAAGGGCTTGAACAG-3'; BCL2 F, 5'-GTTCGGTGGGGTCATGTGTGTGGAGAGCG-3'; BCL2 R 5'-TAGCTGATTCGACGTTTTGCCTGA-3'; Cyclophilin A F, 5'-GGCAAATGCTGGACCCAACACAAA-3'; Cyclophilin A R, 5'-CTAGGCATGGGAGGGAACAAGGAA-3'.
Western blot analysis was conducted as described previously . Briefly, extracts prepared in SDS loading buffer were resolved in SDS/10% PAGE gels and transferred to PVDF membranes. These were incubated overnight in the presence of anti-c-Myb antibody 1.1  and were developed by using ECL western blotting substrates (Pierce Biotechnology, Rockford, IL, USA).
Characterization of, and MYBexpression during, the differentiation of human mammary carcinoma cell lines
As mammary epithelial cells undergo differentiation there is an increase in the transcription of the gene encoding the milk protein ß-casein ; as such, this can be used as a molecular marker for differentiation. Indeed, quantitative RT-PCR showed that ß-casein message was significantly increased after treatment of MCF-7 cells with increasing concentrations of DIAs for 72 hours (Figure 1c).
Previous studies have shown that differentiation of a number of different cell types, notably hematopoietic [2, 3] and colonic epithelial cells [8, 9, 11, 14, 16], is associated with a reduction in MYB expression. Therefore, we asked whether the level of MYB would also be reduced when mammary carcinoma cells underwent differentiation. The MYB message was, as expected, readily detectable in control MCF-7 cells by quantitative RT-PCR, but treatment with increasing concentrations of NaBu for 72 hours induced a dose-dependent decrease in the level of MYB message (Figure 1d). Western blot analysis of total cell lysates showed a corresponding profile for the MYB protein (Figure 1e).
MYBexpression decreases with differentiation of non-tumorigenic mammary epithelial cells
MYBknockdown promotes differentiation of mammary carcinoma cells
We have previously used a doxycycline (Dox)-inducible lentiviral siRNA system targeting MYB to show that MYB is required for the proliferation of ER positive cell lines . To examine the effect of MYB knockdown on differentiation, MCF-7 cells stably transduced with this vector, or appropriate controls, were treated with Dox for 72 hours. The cells were then stained for lipid droplet accumulation using Nile Red. Approximately 35% of MYB knockdown cells stained positively for lipid droplet accumulation in contrast to approximately 20% of control cells [see Additional file 2]. This is a modest, yet statistically significant (Student's t test, n = 6, P < 0.05), increase. It should be noted that the intensity of Nile Red staining was greater in the MYB knockdown cells, and the number of droplets/cell and droplet size in the MYB knockdown cells were greater than those seen in the control cells as visualized by fluorescence microscopy [see Figure S2A in Additional file 2]. In addition, ß-casein mRNA levels rose by approximately 3 fold following MYB knockdown [see Figure S2C in Additional file 2]. These experiments were repeated using ZR-75-1 cells, and a similar result was observed [see Additional file 3]. These data suggest that MYB knockdown induces breast tumor cells to initiate the process of differentiation in the absence of DIAs, albeit with limited efficiency.
Synergy between DIA treatment and MYBknockdown
BCL2 is regulated by MYBin breast cancer cells
Although BCL2 is a direct target of MYB in T and myeloid cells [32–34] (Zhao et al: Defining the MYB Transcriptional Program by Genome-Wide Chromatin Occupancy and Expression Analyses, submitted) this has not been shown in other cell types. To determine whether MYB acts directly on the BCL2 gene in breast cancer cells, we performed ChIP assays using MCF-7 cells. Potential MBS in BCL2 promoters 1 and 2 were identified based on binding sites previously mapped in other cell types [34, 35] in conjunction with the established consensus sequence YAACN(G/T) for MYB protein binding [36, 37]. Additional sites examined corresponded to those detected by ChIP-Seq in murine myeloid cells (Zhao et al, Defining the MYB Transcriptional Program by Genome-Wide Chromatin Occupancy and Expression Analyses, submitted), which are located within intron 2 and downstream of exon 3 (Figure 4c). Following immunoprecipitation of chromatin from MCF-7 cells with anti-MYB antibody, PCR products were detected with the primers for regions in BCL2 containing the above-mentioned potential MBS. Quantitative RT-PCR showed substantial enrichment for all four regions and the positive control MYC, but not primers corresponding to the GAPDH gene or a region 6 kb upstream of BCL2, with the anti-Myb antibody (Figure 4d). These results demonstrate that endogenous MYB binds in situ to the BCL2 gene and, combined with the data of Figures 4a, b and 5a (see also below), imply that MYB directly regulates BCL2 expression in mammary carcinoma cells.
BCL2knockdown sensitizes breast cancer cells to DIA-induced apoptosis
The data presented above are all consistent with the proposal that differentiation-associated apoptosis is due in part to loss of BCL2 function. To further investigate this hypothesis, siRNAs targeting BCL2 were transiently transfected into MCF-7 cells, which were subsequently treated with NaBu. BCL2 knockdown was verified by western blot analysis (Figure 4e). When assayed for apoptosis with TUNEL, BCL2 knockdown induced 60 to 70% apoptosis in the presence of a level (1 mM) of NaBu that normally would only induce differentiation, whereas only about 20% of cells were TUNEL positive when treated with BCL2 siRNA alone (Figure 4f). Thus BCL2 knockdown in MCF-7 cells resulted in similar sensitivity to DIA-induced apoptosis to that seen when MYB was knocked down using shRNA (Figure 3).
Enforced expression of MYBsuppresses differentiation and apoptosis of MECs
To further examine the role of MYB in the differentiation of MECs, MCF-7 cells were stably transduced with retroviral vectors expressing either wild type (WT) MYB, a truncated, activated form of MYB (CT3) , or the empty pMYs-IRES-GFP vector. Overexpression of MYB was verified by western blot analysis (Figure 5a). The cells were then treated for 72 hours with NaBu. Although MYB overexpression had no effect on proliferation of untreated cells (Figure 5c), Figure 5d shows that overexpression of WT or CT3-MYB allowed the cells to continue proliferating, and prevented differentiation in the presence of NaBu (Figure 5b). As expected, the parental and vector control cells ceased proliferating and underwent differentiation as quantitated by Nile Red staining. These data indicate that overexpression of MYB is capable of preventing induced differentiation of MCF-7 cells.
Overexpression of MYBprotects mammary carcinoma cell lines from DIA-induced apoptosis
Given that MYB overexpression results in an increase in the level of BCL2 (Figure 5a), and protects MCF-7 s from differentiation-induced apoptosis (Figure 7b), we next sought to investigate whether BCL2 was required for this activity of MYB. MCF-7 cells overexpressing WT MYB, or transduced with the empty vector only, were transiently transfected with two of the siRNAs targeting BCL2 used previously (Figure 4). These cells were then treated with 0 or 100 mM NaBu for 24 hours before TUNEL assay for apoptotic cells. Figure 7c shows that the protective effect of MYB overexpression on cells treated with high levels of NaBu is almost completely abolished when BCL2 expression is suppressed.
Anti-estrogen and DIA treatments synergize to induce differentiation and apoptosis of breast cancer cells
MYBregulation of mammary epithelial cell differentiation
The studies reported here have shown that MYB has an important role in the control of MEC differentiation and in the resistance of mammary carcinoma cells to apoptosis. As we will discuss further, this role appears to parallel that played by MYB in other cell systems where MYB expression and function has been extensively characterized - hematopoietic cells and colonic epithelium [4–6, 42]. We have confirmed that, like some other cancer cells, mammary carcinoma cells can be induced to differentiate and shown that MYB expression decreases during this process. Similarly to the haemopoietic and colonic epithelial cell systems, decreased MYB expression on differentiation is not limited to tumor cell lines, as we have shown here for the non-tumorigenic murine MEC line HC11.
A functional role for MYB in MEC differentiation is implied by the effects of MYB knockdown on breast cancer cell lines. Although a small degree of differentiation was observed with an inducible MYB shRNA alone, a more dramatic effect was apparent from the synergy between MYB knockdown and (otherwise) marginally-effective concentrations of DIAs, which resulted in essentially complete differentiation. Conversely, enforced MYB expression was able to block differentiation of both carcinoma cells and non-tumorigenic HC11 cells, again strikingly paralleling the activities of MYB in other cell systems [6, 16, 43–45].
How MYB exerts its effects on differentiation in this system is unknown. One might suspect that the G1 phase growth arrest that accompanies MYB knockdown  and differentiation  [see Additional file 1] in mammary carcinoma cells may be important but is unlikely to be sufficient, because only limited differentiation was observed following MYB knockdown alone [see Additional file 2]. In fact, rather less is known about the transcriptional network that regulates differentiation of MECs than in other systems such as hematopoiesis. Thus, our findings suggest that studies to identify MYB target genes in MECs would shed light not only on MYB function but also on MEC differentiation per se. Such targets may be directly bound by MYB (as shown here for BCL2) or as in the case of Stat5a-regulated genes, by MYB functioning as a co-activator .
MYBand apoptosis of mammary carcinoma cells
When MYB knockdown was induced in the presence of DIAs at concentrations that normally induce efficient differentiation but little cell death, apoptosis in over 80% of cells resulted. This was true for all three DIAs (NaBu, VES and TPA) and both cell lines tested, implying that it is a general phenomenon and not the property of one agent or cell line. In any case this observation, taken together with the ability of DIAs at higher concentrations to induce apoptosis by themselves [41, 46, 47] (Figure 7a), and the ability of MYB overexpression to protect against apoptosis, supports the following model. We suggest that DIAs induce pro-apoptotic signals that, at normal differentiation-inducing concentrations, are countered by MYB activity, whereas either increased DIA concentrations and hence stronger apoptotic signaling, or reduced MYB activity leads to apoptosis. Conversely, increased MYB expression overcomes the pro-apoptotic activity of higher DIA concentrations.
Our data and this model raise the question of what the apoptotic signals induced by DIAs are, and how MYB protects against them. NaBu has histone deactetylase inhibitor (HDI) activity , and indeed our unpublished data show that the HDI suberoylanilide hydroxamic acid (SAHA/Vorinistat) also acts as a DIA in our system. Several mechanisms have been reported for apoptosis induction by HDIs , including enhanced expression of pro-apoptotic BH3-only proteins . Furthermore, VES has also been reported to trigger the intrinsic apoptotic pathway, in this case via activation of Bax [51, 52]. It is interesting to note that MCF-7 cells are known to be deficient in the apoptotic 'executioner' caspase 3 . However, further work is needed to define the mechanism of DIA-induced apoptosis of breast cancer cells.
BCL2 suppresses apoptosis via the intrinsic pathway, and thus regulation of BCL2 is a plausible mechanism for the anti-apoptotic function of MYB in mammary carcinoma cells. Indeed we have shown here that BCL2, a known MYB target gene in other cell types, is directly regulated by MYB in breast cancer cells, and have identified multiple MBS within the BCL2 gene. Moreover we have shown that BCL2 is necessary for the ability of MYB to protect such cells against DIA-induced apoptosis.
A common role for MYBin multiple tissues and cancers?
As briefly reviewed in the Introduction, and more extensively elsewhere [4–6], MYB is essential for the proliferation of multiple cancer and normal cell types, including haemopoietic, colonic and mammary epithelial. Similarly, with the data presented in this report, there is now strong evidence that MYB can antagonize differentiation in all three cell systems. MYB is also involved in vascular smooth muscle cell proliferation  and there are reports of MYB down-regulation during differentiation in this system too . Moreover, c-myb expression in developing and adult mice has been characterized using in situ hybridization and correlated with stage-specific differentiation and mitotic activity .
MYB can also suppress apoptosis in the hematopoietic and colonic epithelial systems [8, 32, 57], and, as reported here, in mammary epithelial cells. Data in these systems and those presented here have implicated BCL2 as a common effector, although probably not the only one. Whether the other 'MYB phenotypes' of proliferation and differentiation suppression are mediated by common or specific factors needs to be elucidated. However, it is likely that some tissue-specific factors are involved in effects on differentiation, and indeed this is supported by our recent data in the haemopoietic system (Zhao et al: Defining the MYB Transcriptional Program by Genome-Wide Chromatin Occupancy and Expression Analyses, submitted).
Targeting MYBin breast cancer
As discussed above, our data  (and that reported here) imply that MYB is required in ER positive mammary carcinoma cells for three key 'hallmarks of cancer'  - continued proliferation, suppression of differentiation, and resistance to apoptosis. This could potentially make MYB an excellent therapeutic target in breast cancer, particularly under conditions where MYB activity is limiting for one or more of these processes. The attractiveness of MYB as a target in this disease is reinforced by the fact that 60 to 70% of all human breast tumors express MYB [17, 19] (see also [6, 19, 59]).
Treating tumors by inducing cancer cell differentiation has been discussed for some time; although an attractive concept, it has rarely proved to be an effective approach by itself. However, the combination of DIAs and other agents can be highly effective; for example, the combination of the DIA all-trans retinoic acid with arsenic trioxide is now the accepted treatment modality for patients with acute promyelocytic leukemia . Our studies have identified the combination of MYB inhibition with DIA treatment as a potentially effective combination therapy for ER positive breast cancer that not only suppresses proliferation but induces extensive tumor cell death. Further development will require the identification of more appropriate DIAs for clinical use, and of a feasible approach for inhibiting MYB activity in breast tumors. The studies shown here together with our unpublished work suggest that VES and HDIs are both good candidate DIAs for clinical use. Importantly, both have been used in patients and, indeed, the HDI SAHA/Vorinistat is approved for treating cutaneous T-cell lymphoma.
Our observation that fulvestrant, which is in clinical use for breast cancer treatment, appears to substitute in this regard for MYB knockdown suggests that the combination of this agent with clinically acceptable DIAs might be one approach to bring this approach to clinical application. This is in apparent contradiction with the data from De los Santos et al. , which showed that 2.5 mM NaBu induced about 60% of MCF-7 cells to undergo apoptosis, and that there was no synergistic effect of adding fulvestrant. It must be pointed out that the experiments of De los Santos et al. were carried out in under estrogen-free conditions. It is likely that the addition of an anti-estrogenic compound would not synergize with a histone deactetylase inhibitor in an already estrogen-free environment. This is further strengthened by the studies by Chopin et al , which show less than 20% of MCF-7 s cells are apoptotic with 2.5 mM NaBu at 48 hours when in complete (i.e. not estrogen-free) medium. It seems, therefore, that there is clear evidence for a potential chemotherapeutic effect of combining a suitable anti-estrogen and a DIA.
Although we have discussed a number of approaches to targeting MYB itself in breast cancer , it may instead be possible to target specifically the anti-apoptotic effectors of MYB to induce tumor cell killing by DIAs. Our data show that BCL2 is a relevant MYB target in this regard, raising the possibility of using recently-developed inhibitors of BCL2 , such as ABT-737  and its more bioavailable analogue ABT-263 , in combination with DIAs. Interestingly, such a combination has recently shown efficacy in a mouse lymphoma model . Further laboratory and animal model studies to assess the effectiveness and potential toxicities of these approaches in vitro and in vivo are clearly warranted.
This study has shown that MYB knockdown sensitizes breast cancer cells to induced differentiation and apoptosis. Conversely, ectopic MYB expression blocks induced growth arrest and differentiation of BC cells. Furthermore, ectopic MYB expression blocks apoptosis of breast cancer cells by directly upregulating BCL2. These data highlight the potential of combining differentiation inducers and MYB inhibition to lead to new breast cancer therapies.
Dulbecco's Modified Eagle's Medium
epidermal growth factor
fetal bovine serum
histone deactetylase inhibitor
Myb binding sites
mammary epithelial cell
reverse-transcription polymerase chain reaction
suberoylanilide hydroxamic acid
Terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling
Roswell Park Memorial Institute medium
vitamin E succinate
We thank Dr Juliet French, and Dr Chanel Smart, from the laboratory of Dr Melissa Brown, University of Queensland, for assistance with cell lines. We thank Professor Nancy Hynes for permission to use the HC11 cell lines. We thank Dr Ibtissam Abdul Jabbar and Michael Rist for advice and assistance with flow cytometry. YD was supported by a University of Queensland Sister Janet Mylonas Memorial scholarship. RGR is supported by a National Health and Medical Research Council of Australia Fellowship. This work was supported in part by a grant from The Cancer Council Queensland to TJG and RGR.
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