Background
Breast cancer is a complex disease that results from a multi-stage process involving the deregulation of a number of different signalling cascades. About 212,930 new cases of breast cancer were diagnosed every year, of which 40,840 were related to deaths in the United States alone [
1]. This continuing magnitude of the breast cancer problem with respect to incidence, morbidity and mortality requires further studies involving novel approach to prevent this disease [
2]. Cisplatin, cis- [PtCl2(NHs)2], is a widely used anticancer drug, proved to be beneficial in the treatment of wide variety of solid tumours (head and neck, lung, bladder, colorectal and breast cancer) in various combination chemotherapy regimens [
3]. Higher doses of cisplatin are considered to be more efficacious for cancer chemotherapy; however these therapies manifest toxicities such as nephrotoxicity, despite its effectiveness which limits its use [
4,
5]. It was observed that after a single injection of cisplatin, around 28 to 36% of patients develop dose-dependent nephrotoxicity [
6]. However despite its toxicity, cisplatin remains to be one of the most commonly used chemotherapy drugs due to its therapeutic efficacy [
7]. Recent reports have shown that cisplatin induced nephrotoxicity is characterized by activation of pro-inflammatory cytokines and chemokines. TNF-α appears to play a central role in the cisplatin induced renal injury by activation of a large network of chemokines and cytokines in the kidney following cisplatin injection. Blockade of either TNF-α production or its activity prevents the activation of cytokine network and provides protection against cisplatin-induced renal dysfunction and structural damage [
8,
9].
Peroxisome proliferator-activated receptor-γ(PPARγ) is a member of the nuclear receptor superfamily of ligand-activated transcription factors [
10]. PPARγ forms a heterodimeric complex with the retinoid × receptor and then binds to the PPAR response element [
11]. This interaction can be responsible for the regulation of cellular events ranging from glucose and lipid homeostasis to cell differentiation and apoptosis [
12]. Ligands for PPARγ include natural compounds such as fatty acids and their derivatives and synthetic agents such as the antidiabetic drugs rosiglitazone (Avandia) and pioglitazone (Actos) [
13]. Although central role of PPAR-γ has been demonstrated in the differentiation of adipose cells, PPARγ has also been shown to regulate the growth, differentiation, and gene expression in number of different cancer cells [
14,
15]. Rosiglitazone has been shown to have anti-neoplastic activity in
in-vitro and
in-vivo breast cancer models [
16]. In addition, recently, several studies have demonstrated that PPARγ agonist's exhibit an anti-inflammatory effect
in-vitro and
in-vivo [
17,
18].
The eukaryotic genome is maintained as a nucleoprotein complex called chromatin, which consists, mainly of positively charged proteins called histones [
19]. Post-translational modification of histone proteins as well as non-histone proteins including nuclear receptors integrates signalling pathways mediating diverse biological processes. The influence exerted by the post-translational modifications of histones over the regulation of gene expression has been extensively studied in the past few years [
20]. Post-translational modification of histones provides a key mechanism of transcriptional regulation. Acetylation, phosphorylation and methylation of histone H3, modulate the activity of many genes by modifying both core histones and non-histone protein [
21]. Alterations in modifications of histones have been linked to deregulation of many genes which have important roles in cancer development and progression [
22]. Moreover, it has been reported that HER2-overexpressing breast cancer cells contained significantly higher levels of acetylated and phosphorylated histone H3 [
23]. So far there are no reports regarding the effect of rosiglitazone pretreatment on post-translational histone modifications in DMBA induced breast cancer in female SD rats.
Based upon above facts we hypothesize that pre-treatment of rosiglitazone along with cisplatin decreases its nephrotoxicity and may synergize or potentiate its anticancer activity. Understanding the mechanism of rosiglitazone and cisplatin treatment will help in initiating novel approach for cancer therapeutics.
Methods
Materials
Cisplatin and Rosiglitazone were kindly gifted by Dabur India Pvt. Ltd and Nicholas Piramal Research Centre, Mumbai, India, respectively. DMBA was obtained from Sigma (St. Louis, MO, USA). Blood urea nitrogen (BUN), creatinine and albumin kits were purchased from Accurex (Mumbai, India).
Animals
The guidelines of committee for the purpose of control and supervision of experiments on animals (CPCSEA), Government of India were followed and prior permission was sought from the institutional animal ethics committee (IAEC) for conducting the study. The female Sprague-Dawley rats (160–180 g) were procured from the central animal facility of the institute. They were maintained under standard environmental conditions and provided with feed and water ad libitum. All the animals were fed on normal pellet diet one week prior to the experimentation. Considering the animal ethical issues, all animals were kept under best hygienic conditions and the tumour bearing animals were inspected daily for any signs of pain, discomfort of distress.
Tumour induction
Female Sprague Dawley rats at the age of 8 weeks weighing 160–180 g were gavaged with 60 mg dimethylbenz [a]anthracene (DMBA)/kg body weight, a dose sufficient to cause 100% tumour incidence in the control group over the course of the study as described by Whitsett T
et al [
24]. The DMBA was dissolved in olive oil at a stock solution of 30 mg/ml. Animals were sacrificed when the tumour diameter reached three inch, animals became moribund or after the completion of experiment.
Experimental design
Female SD rats were divided initially into two different groups namely, normal control (Group I) received olive oil and DMBA treated group received DMBA (60 mg/kg). After three months mammary carcinoma was confirmed by histological examination and breast palpation. Twelve weeks later, DMBA treated rats were grouped into four different groups on the basis of their tumour volume. DMBA treated rats received normal saline (Group II). Mammary carcinoma induced rats treated with rosiglitazone (8 mg/kg) suspended in 0.5% CMC through oral gavage (Group III). Mammary carcinoma induced rats treated with cisplatin (7.5 mg/kg) dissolved in normal saline by intraperitoneal route (Group IV). Mammary carcinoma induced rats first pre-treated with rosiglitazone (8 mg/kg) suspended in 0.5% CMC for five days through oral gavage and then on fifth day single dose of cisplatin (7.5 mg/kg) dissolved in normal saline (0.9% w/v) by intra-peritoneal route (Group V). These animals were maintained on standard diet and water for 3 months prior to drug ingestion.
Estimation of plasma glucose, albumin, blood urea nitrogen and creatinine
Blood samples were collected from rat tail vein under light ether anesthesia in heparinized centrifuge tubes and immediately centrifuged at 2300 g for the separation of plasma. Plasma was stored at -80° until assayed. The plasma was used for the estimation of albumin, blood urea nitrogen (BUN) and creatinine as described previously [
25].
Measurement of TNF-α level
The level of TNF-α in serum was determined by using enzyme-linked immunosorbent assay (ELISA) kits (Endogen, Woburn, MA, USA), according to the manufacturer's instructions. In all the cases, a standard curve was constructed from standards provided by the manufacturer.
Measurement of tumour volume
The measurements were done for visible tumours; two diameters that is shortest and longest diameter of the tumours were measured. The volume of the tumour was calculated as: Π/6.(a)
2(b), where a is the smallest and b is the longest length of the tumour [
26].
Histopathology of Mammary and kidney
Histopathology of kidneys and mammary tumours were done as described previously [
27,
28]. Briefly rats were anesthetized under light ether anesthesia, after surgery circulating blood was removed by cardiac perfusion with 0.1 M PBS (pH 7.4; 20–50 ml). After clearance of circulating blood, 4% paraformaldehyde in 0.1 M phosphate buffer (pH 7.4) was perfused for another 5 min (100–200 ml of fixative) to fix the tissues. Kidneys and mammary tumours were removed from the animal, decapsulated, sliced transversely, and paraffin embedded for light microscopic evaluation. Histopathological changes in these tissues were assessed in at least 25 randomly selected tissue sections from each group studied. Sections were stained with Meyer's hematoxylin and eosin to examine cell structure. Slides were observed under Olympus microscope (Model no. BX51). For histological quantification 100 renal tubules were randomly examined from each animal and scored as 0, 1, 2, and 3 (No damage, Mild, Moderate, and extensive damage) depending on the extent of damage observed. The no. of tubules under each score was multiplied with the respective scores and the sum obtained to get the final renal tubules damage score. For histological quantification of mammary tumours the histological grades were assessed as proposed by Elston and Ellis[
29]. Briefly histological grade was obtained by summing the scores of three parameters: tubular formation, nuclear pleomorphism and mitotic counts and then classified as follows: 3–5 points: grade I, well differentiated; 6–7 points: grade II, moderately differentiated; 8–9 points: grade III, poorly differentiated.
Protein isolation and western blotting
Nuclei, histone isolation and western blotting were performed in kidney tissues as described previously [
25,
27,
28]. Immunoblot analysis was performed by using Anti phospho-Histone H3 (ser-10) (rabbit 1:2000, Santa Cruz, CA), Anti acetyl-Histone H3 (lysine 14) (rabbit 1:2000, Santa Cruz, CA), Anti Histone H3 (rabbit 1:5000, Upstate, Lake Placid, NY), Anti PPARγ (rabbit 1:500, Santa Cruz, CA), Anti p38 (rabbit 1:500, Santa Cruz, CA), Anti-actin (rabbit 1:2500, Sigma, St. Louis, MO) and HRP-conjugated secondary antibodies (anti-rabbit) from Santa Cruz. Proteins were detected with the enhanced chemiluminescence system and ECL Hyperfilm (Amersham Pharmacia Biotech, UK Ltd, Little Chalfont, Buckinghamshire, UK).
Statistical analysis
Experimental values are expressed as mean ± SEM. Comparison of mean values between various groups was performed by one way-analysis of variance (one way-ANOVA) followed by multiple comparisons by Turkey test. P-value < 0.05 is considered to be significant.
Discussion
In this study, we provide evidence that rosiglitazone significantly increases the level of PPARγ in mammary tumours, leading to significant reduction in tumour volume. Moreover, combination of rosiglitazone with cisplatin led to remarkable reduction in nephropathy. Cytokines, particularly tumour necrosis factor-α (TNF-α), appears to contribute to cisplatin-induced renal injury and coordinate the activation of a large network of chemokines and cytokines in the kidney following cisplatin injection [
9]. Agonists of the peroxisome proliferator-activated receptor-γ (PPARγ), such as rosiglitazone, have been recently reported to regulate inflammation by modulating the production of inflammatory mediators and adhesion molecules [
17].
Plasma albumin, creatinine and blood urea nitrogen parameters are considered as an index of nephrotoxicity [
37]. Our combination of rosiglitazone pretreatment with cisplatin significantly reduced cisplatin induced nephrotoxicity by lowering the levels of nephrotoxicity markers, BUN and creatinine. Histopathological examination also supports that rosiglitazone pre-treatment prevents cisplatin nephrotoxicity which is clearly evident from the reduced glomerular thickening and vacuolation. In line with the protective effect of rosiglitazone on cisplatin induced nephrotoxicity rosiglitazone pre-treatment also showed significant decrease in TNF-α level. TNFα leads to activation of NFκB which further activates phosphorylation and consequent degradation of inhibitory protein IκBα, leading to release of inflammatory mediators [
8]. Thus, reduction in TNFα levels confirms the protection observed in nephrotoxicity and supports our biochemical and histopathological data.
PPARγ is a transcription factor belonging to the nuclear receptor superfamily and forms functional heterodimers with the retinoid × receptor [
38,
39]. Recently, it has been shown that activation of PPARγ by J2 series cyclopentenone prostaglandins (cyPGs), especially 15-deoxy-D
12,14-prostaglandin J2 (15d-PGJ2) or synthetic agents, such as antidiabetic thiazolidinediones, causes anti-proliferation, apoptosis, differentiation, and anti-inflammation of certain types of cancer cells [
40]. In breast tissue, agonists of PPARγ have been shown to inhibit cell growth, reduce oestrogen production by adipose tissue, inhibit oestrogen receptor (ER) activity and play a role in tumour regression [
41,
42]. In our study, the PPARγ agonist rosiglitazone activated PPARγ and inhibited progression of breast cancer. Moreover, pretreatment of rosiglitazone with cisplatin showed maximum increase in PPARγ expression which was well correlated with maximum percentage of tumour inhibition.
Deregulated growth signaling pathways and acquired resistance toward apoptosis constitute two hallmarks of most, if not all, human tumours [
43]. Activity of MAPkinase p38 is regulated through Akt and is deregulated partly due to Akt activation in human cancer. Activation of Akt antagonizes p38 activation while inactivation of Akt results in p38 activation [
33]. Mice deficient in p38α are prone to cancer development using carcinogen or oncogene-induced cancer models. p38α can suppress cell proliferation by antagonizing the JNK/c-Jun pathway, which is an important regulator of proliferation and apoptosis [
32]. Our data indicates a significant decrease in expression of p38 in breast cancer control animals. However, increase in p38 expression by pretreatment of rosiglitazone, suggests an increase in apoptosis of breast cancer cells.
Post-translational modification of histones alters chromatin structure, facilitating the binding of nuclear factors that mediate DNA repair, transcription, and other processes. The modification of the lysine groups of core histones by multiple post-translational events including phosphorylation and acetylation coincident with activation of mitogenic signalling [
36]. Increase in acetylation and phosphorylation of histone H3 in cancer cells shows increased cell proliferation and decreased cell differentiation. Breast cancer control animals showed increased phosphorylation and acetylation of histone H3. But rosiglitazone pre-treatment prevented an increase in acetylation and phosphorylation of histone H3. This is first report which shows that rosiglitazone directly or indirectly can induce change in histone H3 modification. Phosphorylation of histone H3 is known to be involved in cell proliferation. Decrease in histone H3 phosphorylation and acetylation by cisplatin and rosiglitazone pretreatment therapy supports our earlier data of maximum tumour volume reduction in the combination therapy. Lys4 methylation of histone H3 is found to be increased in cancer cell which leads to transcription of various oncogenes, our data also showed high level of Lys4 methylation of histone H3 in cancer control animals. However, pretreatment of rosiglitazone with cisplatin showed decreased level of lys4 methylation of histone H3 which suggests that there is decrease in transcription of proto-oncogenes in mammary tumours.
Acknowledgements
We thank Anil Gaikwad, Idrish Ali and Durga Nand Tripathi for providing their help in the initial stages of this work. Cisplatin and Rosiglitazone were kindly gifted by Dabur India Pvt. Ltd and Nicholas Piramal Research Centre, Mumbai, India, respectively. This work was supported by funds from Department of Science and Technology and National Institute of Pharmaceutical Education and Research (NIPER).
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
KT planned and supervised the project and has given final approval of the version to be published. PCB planned and performed all the in vivo experiments and has made substantial contributions to analysis and interpretation of data. JG has carried out immunoblotting experiments and its analysis and also involved in drafting the manuscript.