Abstract
Angiotensin-II (AgII) is thought to be crucial for tumor growth and progression. Moreover, hydrogen sulfide (H2S) performs a controversial action in cancer pathology. Zofenopril (ZF) is an angiotensin-converting enzyme (ACE) inhibitor with H2S donating properties. Hence, this study aims at investigating the tumor suppressor activity of ZF and elucidating the involved trajectories in Ehrlich’s solid tumor (EST)-bearing mice. EST was induced by the intradermal injection of Ehrlich’s ascites carcinoma cells into femoral region. All parameters were assessed after 28 days post-inoculation or one-week thereafter. ZF treatment resulted in significant reduction of tumor weights with marked decrease in IL-6 and VEGF levels in serum, and tumor Ag II and CEA contents. Additionally, the administration of ZF downregulated the tumor gene expression of cyclin-D, ACE-1, and Bcl2 and upregulated the proapoptotic gene, BAX. Moreover, ZF increased CBS gene expression, which is a major contributor to cellular H2S production. In addition, ZF was able to reduce the protein expression of PI3K, pAKT, pGSK-3β, and NFκB. Our study has provided novel insights into the possible mechanisms by which ZF may produce its tumor defeating properties. These intersecting trajectories involve the interference between PI3K/Akt and CBS signaling pathways.
Keywords: Zofenopril; Angiotensin II; Cancer; PI3K/Akt; Hydrogen sulfide; Cystathionine beta synthase
INTRODUCTION
Angiotensin-II (Ag-II) is a key member of the renin angiotensin system (RAS) that is well known for its impacts on blood pressure control, vascular remodeling, angiogenesis, and inflammation. The components of RAS are upregulated in assortment of tumors involving breast (Rodrigues-Ferreira et al., 2012), endometrial (Nowakowska et al., 2016), lung (Cortez-Retamozo et al., 2013) and prostate (Dominska et al., 2017), affirming the important role of Ag-II in tumor progression and metastasis (Zhang,Wang, 2018). Ag-II expression is related to expanded protein tyrosine phosphorylation and activation of the mitogen-activated protein kinases (MAPK), which prompts the instigation of growth factors and cytokines (Kim, Iwao, 2000; Touyz, Berry, 2002). Numerous studies have demonstrated that RAS blockade hampers tumor development both in vitro (Attoub et al., 2008; Wilsdorf et al., 2001) and in vivo (Miyajima et al., 2002; Neo et al., 2010, 2007). However, some other studies have proposed that this inhibition is due to halting angiogenesis.
Vascular Endothelial Growth Factor (VEGF) is the most powerful proangiogenic inducer that can activate phosphoinositide 3-kinase (PI3K)/ serine-threonine kinase-1 (Akt) signaling pathways after binding to its receptor tyrosine kinase to encourage tumor cell expansion, migration and angiogenesis (Yan et al., 2019). The PI3K/Akt cascade is a main controller of cell survival and fate through various downstream cell targets. One of these targets is glycogen synthase kinase-3β (GSK3β), which results in upregulated cyclin D1 and Myc expression with considerable acceleration of cell cycle (Zhu et al., 2011). NFκB is another key signaling element affected by PI3K/Akt incitement. Akt surges the degradation of the inhibitor of κB (IκB) with ensuing release of NFκB, which is pivotal in the commencement and progression of the disease, as well as development of aggressive tumors resisting the effect of various drugs (Ahmad et al., 2013). Moreover, Akt can restrict cellular apoptosis and augment its survival through the deactivation of BAX and BAD, but it hoists the antiapoptotic B-cell lymphoma 2 (Bcl-2), Bcl-xl and myeloid cell leukemia 1 levels Atif, Yousuf, Stein, 2015).
Zofenopril (ZF) is an angiotensin-converting enzyme (ACE) inhibitor with sulphydryl groups. It is characterized by high lipophilicity, high tissue penetration and powerful antioxidant effects (Napoli et al., 2004). Studies have confirmed that hydrogen sulfide (H2S) is engaged in the mechanisms by which ZF autonomously improves the vascular function and performs its ACE inhibiting activity (Bucci et al., 2014; Donnarumma et al., 2016; Monti et al., 2016). Synthesis of H2S occurs naturally from cysteine through some enzymes including cystathionine-c lyase (CSE), cystathionine β-synthetase (CBS) and 3-mercaptosulfurtransferase (3-MST). The role of CBS-triggered endogenous H2S generation in cancer biology is disputable. On one hand, at low H2S levels, it has been proved that it aids tumor development by keeping up mitochondrial respiration and production of ATP, invigorating proliferation and survival, as well as, redox balance and vasodilation (Zhu et al., 2018). On the other hand, at higher concentrations, it works as a mitochondrial toxin by hampering cytochrome c oxidase with subsequent antitumor activity (Szabo et al., 2013b).
In light of the previous background, the present study has been carried out to explore the potential tumor suppressing ability of ZF in Ehrlich solid tumor (EST)-bearing mice. The study was also extended to elucidate some of the possibly involved trajectories that could be responsible for the obtained antitumor activity.
MATERIAL AND METHODS
Material
Animals
Male Swiss albino mice, weighing 20-30 g, were used in the present study. They were obtained from the animal house of the National Cancer Institute, Cairo, Egypt. Mice were housed in polyethylene cages under controlled laboratory conditions (25 ± 1°C temperature, constant relative humidity and normal dark/light cycle). They were acclimatized to the experimental conditions for at least 1 week prior to the start of the experiment. Animals were allowed free access to standardized laboratory balanced diet and water. The study was carried out under strict conditions in accordance with the recommendations of the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health (NIH publication No.85-23, 1996). The protocol was revised and approved by the Ethics Research Committee of Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt (REC-FPSPI-12/85). All efforts were exerted to minimize animal suffering during the experimental period. The duration of the experiment was as short as possible, and the number of animals was kept to a minimum. Unnecessary disturbance of animals was avoided. Tough maneuver was avoided, and all animals were sacrificed by an overdose of thiopental.
Drugs and Chemicals
Zofenopril calcium (ZF) was purchased from Sigma Aldrich®, MO, USA. ZF was kept at 2-8°C and freshly dissolved in saline. The concentration was adjusted so that each 10 g animal body weight would receive 0.1 ml solution. All other chemicals were of analytical grade or equal quality.
Methods
Ehrlich tumor cells inoculation
Mice were injected with fixed number of Ehrlich’s ascites carcinoma (EAC) cell line (0.2 mL EAC cells containing 2 x 106 cells/ mouse) suspended in saline. EAC cell line was obtained from the Tumor Biology Department, National Cancer Institute, Cairo University (Cairo, Egypt). They were prepared under sterile conditions. The viability of EAC cell line was tested using Trypan blue dye exclusion technique. Tumors were induced by intradermal injection into the femoral region of the recipient male mouse. Tumors were left for 7-10 days to grow big as its diameter achieved 0.7-1.2 cm (Abd-Alhaseeb et al., 2014; Calixto-Campos et al., 2013).
Experimental design
Animals were initially weighed and randomly divided into five groups (n=10): (1) Normal-Control group; (2) Positive-Control group (EST-bearing mice); (3) ZF-Control group received ZF (15 mg/kg/day; p.o.) for 1 month; (4) ZF-Protection group that administered ZF (15 mg/kg/day; p.o.) from the day of EAC cells inoculation (day 1) until the end of experiment on day 30; (5) ZF-Treatment group given ZF (15 mg/kg/day; p.o.) form day 7 of EAC cells inoculation to the end of the experiment on day 37.
By the end of the experiment, animals were weighed to estimate % weight gain, which was calculated using the following formula: (([final body weight - initial body weight]/ intial body weight) *100). Blood samples were withdrawn from each mouse from the orbital sinuses. Blood samples were allowed to stand for 15 min. at room temperature and then centrifuged at 3000 g for 10 min. Serum samples were then separated and stored at -80°C till used for biochemical parameters determination. Mice were sacrificed by a lethal dose injection of thiopental. Tumor discs were isolated from inoculated mice viz; groups 2, 4 and 5. The discs were weighed and processed for histopathological or molecular biology studies.
Biochemical studies
The serum levels of interleukin-6 (IL-6), vascular endothelial growth factor (VEGF) and angiotensin-II (Ag-II) were determined using ELISA kits according to the manufacturer’s instructions using monoclonal antibodies specific for mouse IL-6 and VEGF (R&D Systems, USA) and Ag-II (Sigma-Aldrich, Germany). The color intensity was measured at 450 nm using a microplate reader (Bio Tek Instruments, VT, USA). On the other hand, the level of carcinoembryonic antigen (CEA) was measured by a radioimmunoassay method using commercially available kits (Immunotech. A Beckman Coulter/ Ref.2121).
Quantitative real-time (qRT-PCR)
Total RNA Isolation system (Promega, Madison, WI, USA) was used for total RNA extraction from tumor tissues using SV and the purity of obtained RNA was verified spectrophotometrically at 260 nm. The extracted RNA was reverse transcribed into cDNA using RT-PCR kit (Stratagene, Santa Clara, CA) according to the manufacturer’s instructions. To assess the expression of the target genes, quantitative real-time PCR was performed using SYBR green PCR Master mix (Qiagen, Germany) as described by the manufacturer. Briefly, 25μL of QuntiFast SYBR Green PCR Master Mix, 22.5μL dH2O, 2μL primer pair mix (5 pmol/μL each primer), and 0.5μL cDNA to reach a final reaction volume of 50μL. The sequences of primers (ThermoFisher Scientific, MA, USA) of BAX, Bcl2, ACE-1, cyclin-D, CBS and housekeeping gene (β-actin) are listed in Table I. PCR reactions included 10 min at 95 °C for the activation of AmpliTaq DNA polymerase, followed by 40 cycles at 95°C for 15 s (denaturing) and 60°C for 1 min (annealing/extension). The data were expressed in cycle threshold (Ct), where the increased fluorescence curve passes across a threshold value. The relative expression of the target gene was obtained using the comparative Ct (ΔΔCt) method. The ΔCt was calculated by subtracting BAX, Bcl2, ACE-1, cyclin-D or CBS Ct from that of target gene, whereas ΔΔCt was obtained by subtracting the ΔCt of reference sample (internal control) from that of test sample. The relative expression ratios were calculated by the 2-ΔΔCt (Pfaffl, 2001).
Western blot analysis
Following tumor protein quantification (Bio-Rad Protein Assay Kit, CA, USA), 10 μg proteins of each sample were separated by SDS polyacrylamide gel electrophoresis and transferred to a nitrocellulose membrane using a semi-dry transfer apparatus (Bio-Rad, CA, USA). Membranes were then soaked in 5% non-fat dry milk to block non-specific binding sites. Later, the membrane was incubated with anti-pAkt (1:1000; cat#: 44-621G), anti-PI3K (1:500; cat#: MA5-17150), anti-NF-κB p-65 (cat#: PA1-186), anti-T-GSK3β (1:250; cat#: 39-9500), anti-pGSK3β (1:1000; cat#: MA5-14873) (ThermoFisher Scientific, MA, USA) overnight at 4˚C on a roller shaker. The membranes were then probed with horseradish peroxidase-conjugated goat anti-rat immunoglobulin (Dianova, Hamburg, Germany). Finally, the blots were developed with enhanced chemiluminescence detection reagent (Amersham Biosciences, IL, USA). The protein was quantified by densitometric analysis using a scanning laser densitometer (GS-800 system, Bio-Rad, CA, USA). The results were expressed as arbitrary units (AU) after normalization for β-actin protein expression.
Histopathological examinations
The tumor samples were fixed in 10% phosphate buffered formaldehyde. Subsequently, all the specimens were washed in tap water for half an hour and then dehydrated using ascending grades of alcohol (70%, 80%, 90% and finally absolute alcohol). The specimens were then cleared in xylene, impregnated in soft paraffin wax at 55ºC and embedded in hard paraffin. Sections of 6 µm thickness were cut using a slide microtome and then stained with hematoxylin and eosin (Bancroft, Gamble, 2008). Six random non overlapping fields were scanned and analyzed for the assessment of mean area % of necrotic tissue per tissue section of each sample. All obtained data and micrographs were analyzed by using Leica application module (Leica Microsystems GmbH, Germany) for tissue sections analysis. Moreover, scoring for tumor sections was carried out to determine tumor cells pleomorphism, newly formed blood vessels, inflammatory cells infiltration and skeletal muscle damage. The severity of these alterations was represented as: + mild, ++ moderate and +++ severe. All histopathological examinations were performed by an experienced pathologist who was blinded to the experimental groups.
Statistical methods
Data are expressed as mean ± standard error (SE). All statistical analyses were performed using Version 6 (GraphPad Software Inc., CA, USA). The comparison among groups was performed by using One-way ANOVA followed by Tukey-Kramer as a post hoc test at p< 0.05.
RESULTS
As depicted by Figure 1A, the administration of ZF to the normal mice resulted in marked increase in % body weight gain. On the other hand, the EST-bearing mice showed significant reduction in % body weight gain, as compared to the normal-control group. The treatment of tumor-bearing mice with ZF starting from the first day (Protection Group) of EAC inoculation or the first week (Treatment Group) thereafter markedly raised % body weight gain, as compared to the EST-control group.
Regarding the effect on tumor weight, Figure 1B showed that the administration of ZF to both protection and treatment groups significantly reduced tumor weight, as compared to the EST-control mice.
As demonstrated in Figure 2A, IL-6 and VEGF levels in serum were obviously greater in the EST-control mice, as compared to the normal ones. However, the treatment with ZF starting from the first day of EAC inoculation or the first week thereafter significantly reduced their levels, as compared to the EST-control mice (Figure 2A).
Similarly, the administration of ZF starting from first day of EAC inoculation or the first week thereafter resulted in pronounced reduction of tumor Ag-II and CEA contents, as compared to the EST-control mice (Figure 2 C & D).
ACE-1 gene expression was significantly reduced following the administration of ZF either starting from the first day of EAC inoculation or the first week thereafter, as compared to the EST-control mice (Figure 3 A).
On the other hand, the treatment with ZF markedly elevated intratumoral CBS gene expression of EST-bearing mice, as compared to the EST-control ones (Figure 3B).
Cyclin-D and Bcl2 gene expression were markedly decreased after the administration of ZF either starting from the first day of EAC inoculation or the first week thereafter, as compared to the EST-control mice (Figure 4A & 4C).
However, the treatment with ZF effectively increased intratumoral BAX gene expression of EST-bearing mice, as compared to the EST-control ones (Figure 4B).
As depicted in Figure 5, the administration of ZF in both treatment regimens suppressed the intratumoral protein expression of PI3K and p-Akt, as compared to EST-bearing mice.
Figure 6 shows that the treatment with ZF for 1 month either from the first day of EAC inoculation or the first week thereafter significantly reduced the intratumoral protein expression of p-GSK-3β and NfκB, as compared to EST-bearing mice.
The histopathological findings demonstrated in Figure 6 show that EST-bearing control mice have extensive subcutaneous infiltration of viable tumor cells [A], with marked pleomorphism, anaplasia [B] and newly formed blood vessels with hyperchromatsia [C], in addition to massive infiltration of viable tumor cells between degenerated skeletal muscle fibers [D].
On the other hand, the administration of ZF starting from the day of EAC inoculation resulted in marked reduction in tumor mass as manifested by wide diffuse areas of necrotic tumor tissue with smaller areas of inflammatory cells [E], [G] and [H], in addition to intact skeletal muscle fibers in the outer tumor zones [F].
The treatment of EST-bearing mice with ZF starting from 7th day post-inoculation resulted in moderate reduction in tumor mass as demonstrated by the wider outer viable zone of tumor cells with diffuse areas of necrotic tissue in the deeper zones with viable sheets of tumor cells with many small blood vessels [I] and [J]. Many of tumor cells showed 1 or 2 prominent nucleoli with many mitotic figures and few scattered lymphocytes [K] and [L]. These data are summarized in Table II.
Effect of oral administration of zofenopril (15 mg/kg/day) on severity of histopathological alterations in tumors isolated from EST-bearing mice
DISCUSSION
This investigation affords novel insights into the antitumor activity of ZF in EST-bearing mice. ESTs are quite similar to human tumors and are utilized in numerous investigations as experimental models to examine the antitumor activity of drugs or natural compounds. In this regard, the results of this work have shown that the administration of ZF starting from the 1st day of tumor inoculation or one week thereafter resulted in marked reduction in tumor masses with wide diffuse areas of necrosis. Such findings are consistent with some other findings reached by many authors who confirmed that the central role of RAS in cancer pathology and the anticancer activity of drugs cause RAS blockade (Abd-Alhaseeb et al., 2014; Araújo et al., 2015; Zhang,Wang, 2018).
The increased expression of Ag-II is in part associated with the release of inflammatory cytokines such IL-6 (Nakaigawa et al., 2006; Nakamura et al., 2018) and NfκB (Zhao et al., 2014) and the rise in tyrosine phosphorylation is associated with ensuing instigation of growth factors such as VEGF (Abd-Alhaseeb et al., 2014; Nakamura et al., 2018). They were all reported to promote chief components in cancer pathology. We found that administration of ZF was accompanied by marked reduction in serum levels of Ag-II and VEGF, and intratumoral gene expression of NfκB as well.
Besides, the current work has demonstrated that the administration of ZF resulted in significant decrease in phosphorylation of PI3K and Akt with consequent reduction in their downstream signaling pathways including GSK-3β, NfκB and cyclin-D. The PI3K/Akt signaling cascade is believed to stand out amongst chief oncogenic trajectories in human malignancy. An increasing body of evidence has shown that this pathway is commonly hyperactivated in many cancer types ( Crowell, Steele, Fay, 2007; Song et al., 2019). PI3K transmits impulses from various growth factors, cytokines and oncoproteins to multiple targets including Akt, which in turn, controls various cellular functions, including cell survival, proliferation and development ( Crowell, Steele, Fay, 2007). GSK-3β, a serine/threonine kinase is phosphorylated and deactivated by Akt that accordingly augments cyclin D1 and Myc expression (Zhu et al., 2011). In addition, Akt-induced suppression of forkhead box O1 (FOXO1) diminishes p27 and p21 levels and sequentially enhanced cyclin-dependent kinase expression. Consequently, the enhancement of these molecules significantly encouraged progression of the cell cycle. Hence, inhibiting the PI3K/Akt signaling trajectories could be one of the imperative factors by which ZF produces its antitumor activity.
Moreover, NfκB is an additional signaling molecule activated by Akt. It is crucial for the initiation and progress of cancers, and for gaining of drug resistance in aggressive cancers (Ahmad et al., 2013b; Zhang et al., 2015). Once NFκB turns free under the influence of Akt, it can quickly translocate to the nucleus and trigger the transcription of several target genes. Moreover, Akt may hamper cellular programmed cell death. It is able to debilitate pro-apoptotic Bad and Bax activities, and strengthen anti-apoptotic Bcl2, Bcl-xl though ( Atif, Yousuf, Stein, 2015). Thus, the global power of PI3K/Akt signaling is about enhancing cellular replication and survival and lessening apoptosis, that are in whole hallmarks for carcinogenesis. ZF was able to suppress PI3K/Akt signaling cascade either directly by inhibiting their trajectories or indirectly by inhibiting ACE-1 with subsequent reduction in Ag-II, cytokines such as IL-6 or growth factors like VEGF.
Another prime target that may explain the observed tumor suppressing activity of ZF is its H2S donating properties. Supporting body of evidence has proposed the association of H2S as yet another mechanism by which ZF improves peripheral vascular function (Bucci et al., 2014). Our findings showed that ZF use was accompanied by marked increase in intratumoral CBS gene expression, a key enzyme involved in H2S biosynthesis, suggesting a pronounced increase in intratumoral H2S contents. Diminished CBS activity was also reported in a mouse-hepatocellular carcinoma tumor model (Avila et al., 2000). However, it is now obvious that CBS activity plays a controversial role in cancer pathology. Under normal circumstances, CBS-prompted endogenous H2S production was accounted to support tumor growth by preserving mitochondrial respiration and ATP synthesis, and to stimulate cell proliferation and survival (Lagoutte et al., 2010; Szabo et al., 2013a). Additionally, H2S may stimulate cellular replication through augmentation of specific kinase pathways such as PI3K/Akt (CAI et al., 2007; Manna, Jain, 2011). Further, H2S induces the sulfhydration of NFκB, which appeared to repress apoptosis and might be of specific importance to cancer cell growth and survival (Sen et al., 2012).
Despite what might be expected, at higher concentrations, H2S goes about as a mitochondrial poison by means of the concealment of cytochrome c oxidase in mitochondrial complex IV. H2S acts as a mitochondrial poison via the suppression of cytochrome c oxidase in mitochondrial complex IV. Additional cytotoxic effects may involve calcium and iron mobilization, mitochondrial uncoupling, pore opening, DNA damage, release of excitatory amino acids and intracellular acidification (Szabo et al., 2013b). H2S-donating compounds, such as sulfhydryl ACEI as ZF possess biphasic response, deliver H2S exogenously in which low H2S levels boost cellular proliferation and cell viability. However, high H2S concentrations cause malicious/unfavorable impacts in cells (Hellmich et al., 2015; Szabo et al., 2013b). Our findings have demonstrated that ZF upregulated CBS intratumoral gene expression, confirming the significant rise in intratumoral H2S contents with subsequent cytotoxicity.
In conclusion, this study has highlighted the beneficial tumor defeating properties of ZF. Such favorable effects could be achieved via modulating the crosstalk between PI3K/Akt and H2S signaling pathways. Further investigations are however necessary to determine the likelihood of incorporating ZF in the treatment of malignant tumors.
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Publication Dates
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Publication in this collection
15 July 2022 -
Date of issue
2022
History
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Received
13 Nov 2019 -
Accepted
23 Apr 2020