Background
Breast cancer is a leading cancer in women. In 2015, 231,840 new cases of female invasive cases were diagnosed in the US (American Cancer Society, Surveillance Research, 2015). Traditionally, there are three clinical subtypes of breast cancer: estrogen or progesterone receptor-positive (ER+ or PR+), human epidermal growth factor receptor 2 positive (HER2+), and triple negative (ER−, PR−, HER2−). Recently, based on genetic profiling, revised clinical classifications suggested five subtypes: luminal A, luminal B, basal, claudin-low, and HER2 [
1].
Invasive ductal carcinoma (IDC) is the most prevalent type of breast cancer. For this study, we chose to use MCF7 (ER+, PR+, or luminal A) and MDA-MB-231 (triple-negative or claudin-low) cells due to their prevalence in contemporary cancer research, well-defined characteristics, and similarity to in vivo IDC development when cultured. These two cell lines, along with T-47D, account for over two-thirds of all abstracts on breast cancer growth studies [
2]. The MCF7 cell line has become the most widely-used breast cancer line since its establishment in 1973. MDA-MB-231 cells exhibit a more aggressive phenotype in contrast to MCF7 cells [
3] and are therefore a model of intractable IDC.
Bioelectrical potentials depend on ion flux in biological cells. Due to an asymmetrical distribution of ions across the plasma membrane, ions constantly flow in and out of cell membranes through their transporters: ion channels, pumps and exchangers [
4]. Gating of ion channels results in changes in resting membrane potential which is essential for both normal cell and cancer development [
4]. The roles of voltage-gated calcium channels, sodium channels, and potassium channels in cancer cell proliferation, invasion, and metastasis have only recently been demonstrated [
4‐
9].
Breast cancer cells isolated from patients have a resting membrane potential of −13 mV [
10]. In normal human mammary epithelial cells (HMEC), the resting membrane potential is −60 mV [
10]. Membrane depolarization has been hypothesized to stimulate cell proliferation [
4]. Membrane depolarization activates voltage-gated calcium channels and causes an influx of Ca
2+ through T-type voltage-gated calcium channels in human breast cancer cells [
11]. Calcium channels play a pivotal role in proliferation and tumorigenesis of the cell, yet the underlying mechanism is not completely understood [
12]. T-type voltage-gated calcium channels have been reported to be overexpressed in MCF7 and play an important role in cell proliferation [
13]. Potassium channel blockers such as 4-aminopyridine mimic the effects of calcium channel activators and provide an influx of calcium into the cell [
14].
Calcium-triggered apoptosis is a principle pathway that regulates cell growth and death [
15]. Apoptosis is mainly but not exclusively triggered by caspases [
16]. Breast cancer cells express various isoforms of caspases. Caspase-3 is present in MDA-MB-231, but not in MCF7 cells [
17], which express other isoforms such as caspase-9 [
18,
19].
To test the hypothesis that altered bioelectricity in cell membranes may be independent of breast cancer subtypes, we investigated the effects of voltage-gated potassium and calcium channel blockers on proliferation of two different breast cancer cell lines, MCF7 and MDA-MB-231. Particularly, we focused on cell death induced by verapamil, a clinically used calcium channel blocker in treatment of hypertension, and its underlying mechanisms.
Methods
Cell culture
Human breast adenocarcinoma cells (ER-positive MCF7 and triple-negative MDA-MB-231) were routinely cultured in Dulbecco’s modified eagle’s medium (DMEM, invitrogen) containing 10 % fetal bovine serum, 100 IU/mL penicillin, and 100 g/L streptomycin. Normal HMEC (ATCC) were grown in mammary epithelial cell basal medium (MEC), supplemented with MEC growth kit (ATCC). Cells were washed with PBS and media was replaced daily until 90 % confluence was reached. After addition of TEA or verapamil, cells were monitored every 24 h for cell growth and death.
Whole-cell patch clamp measurement of resting membrane potential
For resting membrane potential measurement using whole-cell patch clamp technique, cells were transferred to polylysine-coated coverslips. These were placed in a lucite bath with the temperature maintained at 35–37 °C using a temperature control unit (TC2BIP, Cell MicroControls). Resting membrane potential (Em) was recorded using the whole cell patch clamp technique with an Axopatch–700B amplifier. Em was measured with normal Tyrode’s and pipette solutions. The Tyrode’s solution contained (in mM): 143 NaCl, 5.4 KCl, 1.8 CaCl2, 0.5 MgCl2, 0.25 NaH2PO4, and 5 HEPES; pH was adjusted to 7.4 by NaOH. The pipette solution contained (in mM): 120 KCl, 1 CaCl2, 5 MgCl2, 5 Na2ATP, 11 EGTA, 10 HEPES, and 11 glucose; pH was adjusted to 7.3 by KOH.
Live cell imaging
Cells in 6-well plates were imaged daily using a Zeiss fluorescent microscope equipped with an AxioCam HRc camera and AxioVision 4.6 imaging software.
Quantification of cells using ImageJ
Fiji ImageJ was used for cell quantification. The image threshold range was set manually for all images using the ‘Dark Background’ setting. When using the ‘Analyze Particles’ plugin, a minimum size value of 0.001 pixels2 was set to prevent miscounting cell debris as live cells.
Immunoblotting
Protein extracts were prepared after 90 % death was observed. Floating cells were pelleted from the media by centrifugation (3000×g for 5 min) and then resuspended in lysis buffer (fresh protease and phosphatase inhibitors (Sigma), 20 mM Tris, 150 mM NaCl, 10 mM EGTA and 10 mM EDTA at pH 7.4). Buffer was then added to culture dishes and a cell scraper was used to detach cells. The dishes were allowed to sit for 5 min before cellular debris was centrifuged out of solution. Supernatants were placed into new tubes and protein concentrations were recorded using Bradford’s method on an Eppendorf biophotometer.
For western blotting procedures, protein concentrations were normalized between samples to 20 μg and mixed with non-reducing lane marker (Thermo Fisher) with 5 % β-mercaptoethanol. After heating in a water bath to 95 °C for 5 min, samples were cooled to 4 °C then loaded into a 4–12 % bis–tris gels (invitrogen). Electrophoresis was carried out at 80 V for 30 min then 160 V for the remainder.
Proteins were transferred to pre-wetted nitrocellulose membranes (0.2 μm pore size) at 30 V for 1 h. Blots were blocked with 3 % bovine serum albumin (BSA) in tris-buffered saline with 0.1 % tween-20 (TBS-T) for 1 h before primary caspase-3 or caspase-9 antibody (1:1000 dilution; cell signaling) was added on a shaker at 4 °C overnight. Primary antibody solution was replaced with fresh 3 % BSA in TBS-T containing secondary antibodies at 1:10,000 dilution for 1 h at room temperature on a shaker. After five washes with TBS-T, blots were developed with a standard ECL kit (Life Technologies) on x-ray film or using a G:BOX digital imaging system (Syngene).
Statistical analysis
Data were presented as mean ± SEM. Student’s t test was used to calculate the statistical significance between two groups. ANOVA was used to calculate the statistical significance among multiple groups. Data were considered as statistically significant when p < 0.05.
Discussion
Depolarized membrane potential has recently been recognized as a potential novel bioelectrical marker of cancer cells [
22,
23]. In this study, we explored the notion that the intrinsic association of membrane potential and breast cancer growth is independent of breast cancer subtypes. We tested the idea using two different types of human breast cancer cell lines, an ER+ MCF7 and a triple-negative MDA-MB-231. We attempted to address a specific question: if membrane depolarization is indeed associated with cell growth of breast cancer cells, what mediates the membrane depolarization and proliferation of breast cancer cells? Alterations of ion channel expression and activities are associated with the initiation, proliferation, and metastasis of cancer cells [
5,
8]. Voltage-gated calcium channels are present in human breast cancer cells but not in normal human mammary epithelial cells [
13]. Therefore, we focused on voltage-gated potassium and calcium channels as potential underlying mechanisms that link membrane depolarization and breast cancer growth.
We showed that membrane potentials of MCF7 and MDA-MB-231 are depolarized in comparison to that of normal human mammary epithelial cells. HMEC grew much slower compared to MCF7 and MDA-MB-231. These results are consistent with previous reports that demonstrated the association between membrane potential and breast cancer patients [
10].
Second, we showed that membrane depolarization, induced by increasing external potassium concentration or blocking voltage-gated potassium channels, stimulated growth of MCF7 and MDA-MB-231 cells. Third, we demonstrated that calcium is essential for growth of MCF7 and MDA-MB-231 since removing external calcium led to death of both types of cells. These results are consistent with the essential role of calcium in cell growth and cancer development [
24]. Fourth, we observed reduced proliferation and death of MCF7 and MDA-MB-231 cells by verapamil, reinforcing the role of calcium entry through voltage-gated calcium channels during the growth of breast cancer cells. We noticed that verapamil inhibited growth of MDA-MB-231 to the similar degree at days 2 and 3 (Fig.
4c), but it appears there is time-dependent inhibition of verapamil on cell growth of MCF7 (Fig.
4d).
To understand the underlying mechanisms of verapamil-induced cell death in breast cancer cells, we explored the potential role of caspase signaling, known to be integral in calcium- induced apoptosis [
15]. We found that the caspase-3 levels in MDA-MB-231 cells were significantly increased during chronic exposure to verapamil. In MCF7, no protein expression of caspase-3 was detected (Fig.
6a). Rather, caspase-9 protein levels are increased in response to verapamil treatment (Fig.
6c). It is imperative to emphasize that caspase-9 may not be the main mechanism that mediates the apoptotic effect of verapamil on MCF7, since the increase in its protein levels is small (Fig.
6d) compared to verapamil-induced increase in caspase-3 in MDA-MB-231 (Fig.
6b). Other caspases, such as caspase-6 and caspase-7, might be more important in mediating the verapamil-induced cell death in MCF7 [
18,
19]. Additionally, there exists caspase-independent apoptosis in both MCF7 and MDA-MB-231 cells [
25‐
27]. Therefore, the exact mechanisms that mediate verapamil-induced apoptosis require more investigation.
A recent study demonstrated that depolarized membrane potential increases the clustering of phosphatidylserine lipids and K-Ras, promoting RAF-MAPK signaling, which is known to induce proliferation of cancer cells [
22,
28,
29]. This mechanism has yet to be validated with regard to intracellular calcium homeostasis in the breast cancer cell culture models used in our study.
Conclusions
Collectively, we showed that membrane potential depolarization occurs in breast cancer cells, independent of subtypes. Verapamil, a voltage-gated calcium channel blocker which is clinically used to treat hypertensive patients can induce cell death in both MCF7 and MDA-MB-231. However, cellular mechanisms that mediate verapamil-induced inhibition of breast cancer cells are different and likely subtype-specific.
Authors’ contributions
SB and MN performed experiments and data analysis, and provided critical reading and editing the manuscript. HGY designed the experiments and wrote the manuscript. All authors read and approved the final manuscript.