Introduction
Patients with triple-negative breast cancer (TNBC) lack estrogen receptors, progesterone receptors as well as HER2 gene amplification/overexpression. Consequently, these patients cannot be treated with 2 of the most effective therapies currently available for breast cancer, i.e. endocrine and anti-HER2 therapy. Indeed, until recently, the only form of systemic therapy available for patients with TNBC was cytotoxic chemotherapy [
1]. Recently, however, several non-cytotoxic treatments have been approved for TNBC including the monoclonal antibody-conjugate, sacituzumab govitecan; immunotherapy with immune checkpoint such as atezolizumab or pembrolizumab and PARP inhibitors (olaparib, talazoparib) for the approximate 10–20% of TNBC patients with germline BRCA1/2 mutations [
2,
3]. Although these therapies are improving outcome in some patients with TNBC, all are efficacious in only a proportion of patients with the disease. Clearly, therefore, additional forms of treatment are necessary for patients with TNBC [
2,
3].
One of the most successful forms of anti-cancer treatment introduced in recent years is the use of drugs for targeting cancer driver genes. The most frequently occurring driver gene in TNBC is mutations in p53 which are present in 80–90% of these patients [
4,
5]. Thus, mutant p53 is a highly attractive target for new anti-cancer drugs for the treatment of patients with TNBC.
Historically, however, mutant p53 has proved difficult to target and was thus frequently regarded as “undruggable” [
6,
7]. This traditional viewpoint, however, is changing as several new strategies have recently been identified for targeting the mutant protein [
8,
9]. Two of the most promising strategies include degradation of the mutant protein and reactivation of mutant protein back to its wild-type form (for reviews, see refs. [
8,
9]).
While mutant p53-reactivating compounds have been widely investigated [
8], less work has been devoted to compounds that promote degradation of the mutant protein. For mutant p53 to exert its oncogenic activity, it must be stabilized [
10]. Stabilization is achieved by interaction with heat shock proteins (HSP), especially HSP40, HSP70 and HSP90 [
11]. Preventing these interactions might be expected to result in mutant p53 degradation and thus suppression of cancer growth. Early evidence that destabilization of mutant p53 had anti-cancer activity was obtained with HSP inhibitors in a range of experimental models [
12]. However, in clinical trials, HSP inhibitors were found to be relatively toxic and lack efficacy [
13,
14]. Consequently, these trials were largely abandoned.
In addition to HSP inhibitors, a group of commonly used drugs known as statins, have also been shown to degrade mutant p53 but not WT p53 [
15,
16]. Statins which are widely used to treat patients with high levels of cholesterol act by inhibiting HMG-CoA, the rate-limiting enzyme in biosynthesis of the lipid [
16]. In addition to reducing cholesterol levels, treatment with statins also lowers levels of other intermediate metabolites in the cholesterol biosynthetic pathway, especially mevalonate phosphate (MVP). Recently, Parrales et al. [
15] reported that decreased MVP levels resulting from treatment with the statin, lovastatin led to reduced binding of mutant p53 to a specific form of HSP40 known as DNAJA1. As a result of the decreased binding to DNAJAI, mutant p53 underwent degradation with the ubiquitin ligase CHIP. Consistent with its ability to degrade mutant p53, lovastatin was found to inhibit the in vitro and in vivo growth of tumour cells expressing mutant p53 (conformational mutations) but not cells with wild-type p53, cell lines null for p53 or cell lines containing p53 contact mutations [
15]. In a more recent study, treatment with a different statin, i.e. cerivastatin resulted in the dissociation of mutant p53 from HSP90 and degradation by MDM2 [
16].
Based on the high prevalence of p53 mutations in TNBC, the ability of statins to degrade mutant p53, and thereby inhibit tumour cell proliferation, the aim of our study was to test the hypothesis that these drugs might provide a new treatment for patients with TNBC.
Materials and methods
Cell culture
All cell lines were originally sourced from the American Type Culture Collection (ATCC), apart from Hs578Ts(i8) which was supplied by Dr. Susan McDonnell, University College, Dublin. All cell lines were maintained in RPMI, supplemented with 10% fetal bovine serum and 1% penicillin–streptomycin. All cell culture reagents were purchased from Biosciences (Dun Laoghaire, Ireland) and Sigma-Aldrich (Arklow, Ireland). Cells were maintained at 37 °C in a 5% CO2 environment. The p53 mutation status of these cell lines is shown in Table
1.
Table 1
p53 mutational status of cell lines used in this study
MCF-7 | WT | – |
T47D | MUT | L194F |
ZR-75-1 | WT | – |
CAMA1 | MUT | R280T |
SKBR3 | MUT | R175H |
JIMT-1 | MUT | R248W |
Hs578T | MUT | V157F |
Hs578Ts(i)8 | MUT | V157F |
MDA-MB-231 | MUT | R280K |
MDA-MB-453 | MUT | H368delinsG |
MDA-MB-468 | MUT | R273H |
HCC1143 | MUT | R248Q |
BT-549 | MUT | R249S |
SUM159 | MUT | R273H |
CAL-85-1 | MUT | L132E |
Proliferation assays
Cell response to statins was assessed by seeding 96-well plates with 5,000 cells per well and allowing to adhere overnight. The following day, fresh media were added, containing statins at the indicated concentration or DMSO. Cells were incubated for 5 days, at which point viability was assessed by adding 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) (Sigma-Aldrich) to 10% of media volume and incubating for 2 h. Absorbance was measured at 570 nm. In some experiments, mevalonate was added at a concentration of 100 or 200 µM.
Cell cycle analysis
Cells treated with statins for 24 h were harvested and fixed by resuspending in 500 µL PBS followed by slowly adding 4.5 mL ice-cold 70% ethanol. Cells were prepared for cell cycle analysis using FxCycle™ PI/RNase Staining Solution (Thermo-Fisher), following manufacturer’s protocol. Fluorescence was measured on a BD FACSCanto II, using a 488 nm excitation source and a 576 nm emission filter. Cell cycle percentages were calculated using Flowjo software.
Apoptosis detection
Cells treated with statins for 48 h were harvested and prepared for analysis using the FITC Annexin V Apoptosis Detection Kit with 7-AAD (Medical Supply Company, Mulhuddart, Ireland) following manufacturer’s guidelines. Fluorescence intensity of FITC and 7-AAD was measured on a BD FACSCanto II, using a 488 nm excitation source and a 525 nm or 695 nm emission filter, respectively.
Membrane array for detection of apoptosis-associated proteins
Expression of apoptotic proteins was analysed using the Raybiotech Human Apoptosis Array following manufacturer’s guidelines. Briefly, protein was isolated from SUM159 cells following treatment for 24 h with 10 µM simvastatin or vehicle control, using the provided lysis buffer. Membranes were blocked and incubated with protein samples overnight at 4 °C. After washing with the provided buffers, membranes were incubated overnight again at 4 °C with detection antibody. Membranes were incubated at room temperature with HRP-Streptavidin for 2 h. Following a final wash stage, membranes were incubated with detection buffer and imaged using a Licor C-DiGit Blot Scanner. ImageJ software was used to generate densitometry values which were then normalised to the internal controls on the membrane.
Western blotting
Protein was isolated and prepared for analysis by Western blotting as previously described [
17]. Primary incubations were carried out overnight at 4 °C with the following antibodies; IGFBP4 (R&D Systems, Abingdon, UK. 1:1000), GAPDH (Sigma, 1:4000). Secondary incubation was performed for 1 h at room temperature using HRP-conjugated IgG kappa binding protein (Santa-Cruz Biotech, Heidelberg, Germany. 1:5000). Blots were imaged using SuperSignal West Pico PLUS substrate (Biosciences) and a Licor C-DiGit Blot Scanner.
Drug combination assays
Efficacy of drug combinations was performed following the same protocol as proliferation assays. Drugs were tested as both single agents and in combination. Combination index (CI) values were calculated using Compusyn software [
18]. CI values below 1 are indicative of drug synergy.
Statistics
All experiments were repeated at least 3 times. All statistical analysis was performed using GraphPad Prism 8 software. Significance was determined using Student t tests or ANOVA post-hoc analysis. A p value of less than 0.05 was deemed statistically significant.
Discussion
Here, we show that although 2 widely used statins decreased the proliferation of breast cancer cell lines representing the main molecular subtypes of breast cancer, their inhibitory impact was significantly more potent in TNBC than in non-TNBC cell lines. A possible explanation for the enhanced sensitivity of the TNBC versus the non-TNBC cell lines may relate to the higher prevalence of p53 mutations in this breast cancer subtype. Indeed, as mentioned in the Introduction above, our findings are consistent with previous observations in which treatment with statins was reported to result in the degradation of mutant but not wild-type p53 [
15,
16]. Previously, Chou et al. found that lung cancer cell lines containing mutant p53 were also more sensitive to statins than cells with wild-type p53 [
20]. The effects of the statins on reduced cell proliferation in our study appeared to be mediated by induction of cell cycle arrest and promotion of apoptosis.
Previously, Parrales et al. reported that lovastatin degraded p53 with conformational mutations but had minimal effects on contact mutations [
15]. Based on this finding, it might be expected that cell lines expressing conformational mutations would be more sensitive to growth inhibition than cell lines expressing mutant p53 with contact mutations. However, our work using a larger panel of cell lines found similar IC50 values, irrespective of the type of p53 mutation.
Although our results show that two different statins reduced the proliferation of TNBC cell lines, these drugs are unlikely to be used alone for the treatment of this form of breast cancer. We therefore evaluated the effects of combining simvastatin with two frequently used drugs to treat TNBC, i.e. docetaxel and doxorubicin. Both these cytotoxic drugs in combination with simvastatin synergistically enhanced growth inhibition in the 2 TNBC cell lines investigated, suggesting that combined treatment with simvastatin and docetaxel or doxorubicin might be investigated in a clinical trial.
A novel finding in this report was that simvastatin upregulated levels of IGBPF4. Although we did not investigate the mechanism of this upregulation or its possible implication for statin actions, previous studies showed that IGFBP4 binds and sequesters IGF-1 ligands, thus acting to dampen IGFR1 signalling [
24]. Consistent with this observation, administration of a high dose of atorvastatin decreased serum IGF-1 levels in diabetic patients [
25,
26]. Furthermore, statins were reported to downregulate expression of the IGF1R [
27,
28]. Theoretically, therefore, statin-induced upregulation of IGBP4 could lead to sequestration of IGF1 which in turn could downregulate IGF1R signalling. Decreased IGF1R signalling might be expected to result in inhibition of cell line growth and/or promotion of apoptosis as this signalling system has been has been shown to promote breast cancer cell proliferation and survival [
29]. Modulation of IGFBP4 expression has previously been suggested as a therapeutic strategy, with a degradation-resistant form of the protein demonstrating significant effects on tumour growth and angiogenesis in both in vitro and in vivo models [
30,
31].
We should state however, that there are several other mechanisms other than via upregulation of IGBP4 by which statins could decrease cell proliferation or promote apoptosis. These include a reduction in different cell signalling systems such as from RAS, RHO, Hedgehog, YAP or TAZ (for review, see Ref. [
32]). Furthermore, statins have been shown to reduce N-glycosylation of specific membrane proteins and suppress epithelial–mesenchymal transition (EMT) [
33]. Indeed, the reduced levels of cholesterol following statin treatment have also been associated with decreased cancer cell growth [
34]. All of these actions of statins, like that of mutant p53 degradation, appear to result from inhibition of HMG-CoA and blockage of the MVA pathway [
32].
Consistent with our preclinical studies, several clinical studies have shown that the use of statins was associated with improved outcome in breast cancer patients. Thus following a systematic review of the literature and meta-analysis, Manthravadi et al. [
35] identified 10 studies containing 75,684 women with breast, that compared outcome in statin-users versus non-users. Statin use was found to be associated with both improved recurrence-free survival (HR 0.64; 95% CI 0.53–0.79), improved overall survival (HR 0.66; 95% CI 0.44–0.99) and improved cancer-specific survival (HR 0.70; 95% CI 0.46–1.06). Furthermore, in a large population-based study carried out in Denmark, statin use was associated with a reduced risk of breast cancer recurrence in postmenopausal women receiving adjuvant aromatase inhibitors (following multivariate analysis, HR 0.72; 95% CI 0.50–1.04) [
36]. Also, in a large randomized phase III double blind clinical trial (BIG 1–98) in which hormone receptor-positive patients were undergoing endocrine treatment, receipt of statins was related to longer disease-free-survival (HR 0.79; 95% CI 0.66–0.95;
p = 0.01), longer breast cancer-free interval (HR 0.76; 95% CI 0.60–0.97;
p = 0.02) and longer distant recurrence-free interval (HR 0.74; 95% CI 0.56–0.97;
p = 0.03) [
37].
Of particular relevance to our study was the recent report showing a significant benefit of statins in patients with TNBC but not in those with non-triple-negative disease [
38]. Thus, in a large population-based study that included women with stage I-III breast cancer, Nowakowska et al. found that use of statins improved breast cancer-specific survival (HR 0.42; 95% CI 0.20–0.88;
p = 0.022) and overall survival (HR 0.70; 95% CI 0.50–0.99;
p = 0.046) in patients with TNBC (
n = 1534). In contrast, there was no association with breast cancer-specific survival (HR 0.99; 95% CI 0.71–1.39;
p = 0.97) or overall survival (HR 1.04; 95% CI 0.92–1.17;
p = 0.55) in those without TN disease (
n = 15,979). Since cell lines containing mutant p53 appear to be more sensitive to statins than p53 wild-type cells [
20] theoretically, the benefit of statins in the tripe-negative cohort relative to the non-TN patients could be a least partly due to the considerable greater prevalence of p53 mutations in the former subtype of breast cancer [
5]. In addition to breast cancer, use of statins has also been associated with improved outcome in several other types of malignancy, although contradictory data have also been published including contradictory results in breast cancer (for review, see ref. [
39]).
Despite the multiplicity of preclinical and epidemiological studies linking statin use with anti-cancer activity across different types of cancer, there are little data from randomized clinical trials that treatment with these drugs improves outcome for patients with cancer. Statins however, are one of the most commonly prescribed classes of drug worldwide, with well-established safety and dosage profiles [
40]. Their limited toxicity, low cost, and ease of use make them an ideal choice for repurposing as anti-cancer drugs.
In conclusion, our data described in this article may be informative with respect to the design of clinical trials involving statins for the treatment of breast cancer. We show that the anti-proliferative effect of simvastatin is enhanced by combination with docetaxel or doxorubicin. Furthermore, our preliminary finding when combined with that of others [
20] suggests that statins are more potent cell-growth inhibitors in mutant than in wild-type p53 cells, implying that the mutational status of p53 might be a predictive biomarker for statin sensitivity. Thus, the mutational status of p53 should be investigated in any clinical trial using statins. Finally, while this work was in progress, 2 clinical trials investigating statins in the neoadjuvant treatment of TNBC began recruiting patients (ClinicalTrials.gov Identifier: NCT03358017 and NCT03872388).
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.