Amplified intracellular Ca2+ for synergistic anti-tumor therapy of microwave ablation and chemotherapy
Developing new strategies to reduce the output power of microwave (MW) ablation while keeping anti-tumor effect are highly desirable for the simultaneous achievement of effective tumor killing and avoidance of complications. We find that mild MW irradiation can significantly increase intracellular Ca2+ concentration in the presence of doxorubicin hydrochloride (DOX) and thus induce massive tumor cell apoptosis. Herein, we designed a synergistic nanoplatform that not only amplifies the intracellular Ca2+ concentration and induce cell death under mild MW irradiation but also avoids the side effect of thermal ablation and chemotherapy.
The as-made NaCl–DOX@PLGA nanoplatform selectively elevates the temperature of tumor tissue distributed with nanoparticles under low-output MW, which further prompts the release of DOX from the PLGA nanoparticles and tumor cellular uptake of DOX. More importantly, its synergistic effect not only combines thermal ablation and chemotherapy, but also obviously increases the intracellular Ca2+ concentration. Changes of Ca2+ broke the homeostasis of tumor cells, decreased the mitochondrial inner membrane potential and finally induced the cascade of apoptosis under nonlethal temperature. As such, the NaCl–DOX@PLGA efficiently suppressed the tumor cell progression in vivo and in vitro under mild MW irradiation for the triple synergic effect.
This work provides a biocompatible and biodegradable nanoplatform with triple functions to realize the effective tumor killing in unlethal temperature. Those findings provide reliable solution to solve the bottleneck problem bothering clinics about the balance of thermal efficiency and normal tissue protection.
KeywordsIntracellular Ca2+ Synergistic therapy Ablation Chemotherapy
scanning electron microscopy
Hank's Balanced Salt Solution
3,4,5-trimethoxybenzoic acid 8-(diethylamino) octyl ester
reactive oxygen/nitrogen species
red blood cells
white blood cells
hematoxylin and eosin
Tumor therapies are developing quickly due to the development of modern technique and the unsatisfactory results of traditional therapies such as surgery and chemotherapy. Microwave (MW) ablation is a new and promising kind of thermal therapy with advantages of high efficiency, minimal invasion, and favorable efficacy . However, its long-term survival outcomes are still not fully satisfactory, mainly because of the high rates of tumor recurrence and progression [2, 3, 4]. Non-lethal and insufficient thermal delivery is the most common cause for tumor progression after MW ablation, especially in the peripheral tumor area with lower temperature [5, 6]. Recently, different kinds of MW-sensitive agents and combined therapies of MW ablation and chemotherapy have been developed to enhance the therapeutic outcomes of MW ablation [7, 8, 9, 10]. Nevertheless, all those efforts failed to solve the high recurrence in the peri-ablation areas of tumors. Solutions to induce tumor death in traditionally non-lethal temperature are highly desirable to achieve safe and effective antitumor therapy.
Typically, the best known biological response to MW therapy is thermal effect resulting from frictional heating of ions and polar molecules within cells in response to the oscillating electromagnetic field of MW . Nevertheless, its biologic influence on ions movements deserves more attention with lots of potential benefits.MW has electromagnetic wave with frequencies of ≥ 300 MHz. Dipole molecule rotation and ionic polarization in the electromagnetic field have been shown to enhance transmembrane movement and interfere homeostasis of ions inside or outside of cells [9, 12, 13, 14]. Of all the intracellular or extracellular ions, Ca2+ is crucial and attractive as a pleiotropic second messenger involved in controlling many important physiological functions including cell proliferation, migration, and survival [15, 16, 17]. Moreover, its antitumor effect has gained lots of attention as a promising approach to trigger apoptosis in tumor cells [15, 18]. When an imbalance of intracellular Ca2+ occurs, mitochondria will take in Ca2+ from the cytoplasm to keep the intracellular calcium homeostasis. Then the overloading of Ca2+ in mitochondria would be followed by the damage of outer mitochondrial membrane and decrease of mitochondrial membrane potential(MMP) [19, 20]. Mitochondria is a primary energy factory for cells to keep working and is critical among many signal pathways involved in cell apoptosis, lipids and amino acids metabolism and so on.. Therefore, cell death is inevitable once mitochondrial dysfunction constantly occurs . Studies focused on increasing the intracellular Ca2+ to trigger cell apoptosis have achieved promising results in many cancer treatments [22, 23, 24]. To the best of our knowledge, no systematic investigations have been conducted regarding regulation of intracellular Ca2+ concentration to enhance MW therapy under small thermal delivery.
Herein, a synergistic nanoplatform aimed at amplifying changes in intracellular Ca2+ was designed to investigate the synergic treatment of tumor cells by sensitizing them to MW irradiation under unlethal temperature conditions. Poly(lactic-co-glycolic acid) (PLGA) was selected as the carrier because it is one of the most common biodegradable polymeric compounds approved by the US FDA for use in drug delivery systems [25, 26]. Sodium chloride (NaCl), an ionic liquid with good MW sensitivity, was loaded into hollow PLGA nanoparticles to enhance MW efficiency by confining the collision of ions. Furthermore, DOX was loaded into the nanoparticles as we found that a low dose of DOX could significantly improve the intracellular Ca2+ concentration and induce massive tumor cell apoptosis under mild MW irradiation in low temperature. In this synergistic nanoplatform, DOX acted mainly as an accelerator of intracellular Ca2+ more than chemotherapy drugs. Additionally, a low dose of encapsulated DOX could reduce the toxic side effects.
Materials and methods
The mPEG–PLGA (mPEG, MW 1000, PLGA, lactide: glycolide 60:40, MW 100,000) were provided by Daigang Biomaterial Co., Ltd (Jinan, China). DOX·HCl was purchased from Huafeng United Technology Co., Ltd. Sodium chloride, Dimethyl sulfoxide (DMSO, 99%), and 1,4-dioxane were obtained from the Beijing Chemical Reagents Company. Polyvinylpyrrolidone (PVP, 95%) was purchased from Shantou Xilong Chemical Co., Ltd. Ethanol and aqueous ammonia were commercially available products. All reagents used in this work were of analytical grade without any further purification.
Preparation of NaCl–DOX@PLGA drug-loaded nanoplatforms
In 4 mL DCM, 200 mg mPEG-PLGA was dissolved. A 0.5 mL aliquot of an aqueous solution (inner water phase) containing 10 mg DOX·HCl and 3% NaCl was emulsified for 90 s in an ice bath. A probe type sonicator (180 W, 90 s) was used to form a homogeneous primary emulsion. 10 mL water containing 5% PVA was added to the emulsion, and the solution was emulsified for another 90 s in an ice bath by the sonicator (400 W, 90 s). Then the acquired emulsion is dropped into 40 mL water (outer water phase) containing 0.1% PVA agitated by a magnetic stirrer for 4 h to remove the DCM. Pure mPEG-PLGA nanoparticles (without DOX·HCl) were prepared under constant conditions with only the inner water phase components changing. Microcapsules were collected and washed by centrifugation at 12,000 rpm for 40 min.
The morphology and size of the NaCl@PLGA and NaCl–DOX@PLGA nanoparticles were measured using a model 4300 scanning electron microscope (Hitachi). A Zetasizer (Malvern Instruments Zetasizer Nano ZS90, UK) was used to measure the hydrodynamic zeta potential and size of the NaCl@PLGA and NaCl–DOX@PLGA nanoparticles at a temperature of 25 °C. The absorption spectra of DOX were acquired via a UV–vis spectrophotometer (Jasco V-570 UV/vis/NIR spectrophotometer, Shanghai, China). The Na, Cl, C, and O elements in the NaCl–DOX@PLGA nanoplatform were characterized using scanning electron microscopy (SEM) X-ray (energy-dispersive spectroscopy [EDS]). The progress of MW heating in vivo and in vitro was recorded by forward-looking infrared (FLIR) and thermal needle. An Olympus X71 optical microscope (Japan) was used to observe the fluorescence within stained paraffin sections. The in vitro MW heating effect of the NaCl–DOX@PLGA nanoplatforms was evaluated by measuring the temperature at different nanoparticle concentrations using less than 10 W for 1 min. Briefly, 2 mL NaCl–DOX@PLGA nanoparticles at high and low concentrations (11, 22 mg mL−1) were placed into a 12-well plate and irradiated with 10 W and 2450 MHz MW for 1 min. PLGA nanoparticles, deionized water, and saline solution (0.9%) were used as controls. The surrounding temperature away from the MW antenna was monitored using a thermal needle. The corresponding thermal progress imaging was recorded by FLIR.
The controlled-release of DOX from the NaCl–DOX@PLGA nanoplatform was investigated. NaCl–DOX@PLGA nanoparticles were dispersed in 0.1 M phosphate-buffered saline (PBS) (5 mg/mL) and placed onto a rotary platform at 37 °C for 48 h. The PBS solution used was pH 7, pH 5, and pH 7 in the MW-1, MW-2, and control groups, respectively. The nanoparticles in the MW-1 and MW-2 groups were irradiated by 2450 MHz MW and 5 W for 4 min, and the temperature increased to 55 °C. Subsequently, the solutions were continuously shaken by a shaking table to evenly mix the nanoparticles. A UV–vis spectrophotometer was used to examine the DOX concentration at 483 nm in the supernatant via centrifugation. The amount of DOX release over time was confirmed through a standard calibration curve.
mechanism study for the NaCl–DOX@PLGA nanoparticles sensitizing tumors to MW irradiation
Influence on intracellular Ca2+ concentration
We first tested the influence of free DOX with MW irradiation, and then the role of NaCl–DOX@PLGA nanoparticles combined with MW irradiation, on intracellular Ca2+ concentration. Tumor cells were plated into 6-well plates (2 × 105 per well) and cultured in a suitable environment for 24 h. The cells were divided into four groups: the control, free DOX, MW, and DOX + MW groups. Subsequently, 100 μL PBS and DOX (3 μmol/L) were incubated with the cells for 12 h. The cells were then washed twice with Hank's Balanced Salt Solution (HBSS, without Ca2+) to remove excess DOX. The washed cells were incubated with 5 μM Fluo-3/AM for 40 min at 37 °C. The cells in the MW and DOX + MW groups were irradiated with mild MW (4 W for 2 min) in the dark. The mean fluorescence intensity was analyzed using a flow cytometer (BD Bioscience) at 488 nm. DOX was then incorporated into the nanoparticles to reduce toxicity and increase the cellular accumulation. The experimental methods were similar with the abovementioned methods to illustrate the influence of NaCl–DOX@PLGA nanoparticles combined with MW irradiation on intracellular Ca2+ concentration. The only difference was the replacement of DOX with NaCl–DOX@PLGA nanoparticles (186 μg/mL).
Mitochondrial inner membrane potential
The lipophilic cation-staining agent 5,50,6,60-tetrachloro-1,10,3,30-tetraethylbenzimidazolylcarbocyanine iodide (JC-1) was selected to evaluate changes in the MMP. JC-1 emits a red fluorescence signal in the upper left quadrant of the fluorescence-activated cell-sorting (FACS) display (J-aggregate) when the membrane potential increases, and a green signal is emitted in the upper right and lower right quadrants of the FACS display when apoptosis occurs. Cells in a 12-well plate were cultured in a thermostat incubator at 37 °C in a humid atmosphere with 5% CO2. They were subsequently washed with PBS and divided into four groups: the control, positive, MW, and MW + NaCl–DOX@PLGA groups. The MW + NaCl–DOX@PLGA group had 1 mL NaCl–DOX@PLGA nanoparticles (186 μg/mL) added to the cell medium, and 1 mL DMEM was added to the other groups. All cells were cultured in a stable environment for 12 h. Subsequently, the cells in the MW and MW + NaCl–DOX@PLGA groups were treated with MW (4 W for 2 min) and were cultured for an additional 1 h. The cells in the positive group were incubated with CCCP (10 μmol/L) for 30 min. Subsequently, all cells were incubated at 37 °C for 20 min with 5 mg/mL JC-1. After two wash cycles with phosphate-buffered JC-1 solution, the green fluorescence of monomeric JC-1 and the red fluorescence of aggregate JC-1 were recorded as a function of time using a Fluostar Omega microplate reader. Excitation was fixed at 490 nm, and the emission was alternately collected at 530 and 590 nm. Data were expressed as ratio of red/green fluorescence after correction for DOX autofluorescence and/or energy transfer to JC-1.
The fluorescence intensity changes were also measured by flow cytometry to quantify changes in mitochondrial inner membrane potential caused by MW and the presence of nanoparticles. The experimental methods were similar with the JC-1staining methods as previously mentioned. The differences included cells were cultured in a 6-well, rather than a 12-well, plate at 37 °C, and the influence of MW, MW + DOX, and MW + NaCl–DOX@PLGA nanoparticles on mitochondrial inner membrane potential was evaluated. The fluorescence intensity of the cells was analyzed using a flow cytometer.
Cellular uptake and measurement of cellular viability
To study the cellular uptake of PLGA nanoparticles, HepG2 cells were seeded into 12-well plates and cultured in a suitable environment for 24 h. The medium was then replaced with 1 ml of fresh medium containing nanoparticles encapsulated with rhodamine 6G (30 μg/ml). All samples were rinsed three times with PBS after incubation with the cells for 8 h. Then the cells were further incubated for 10 min in the medium containing 4′,6-diamidino-2-phenylindole(DAPI). After being washed with PBS three times, the cells were observed using a fluorescence microscope (IX73IPF, Olympus Corporation, Japan).
HepG2 cells were seeded in 6-well plates. After 24 h incubation, the cells were divided into five groups, with three samples in each group. The cells in the MW + NaCl–DOX@PLGA and NaCl–DOX@PLGA groups were cultured with NaCl–DOX@PLGA nanoparticles (186 μmol/L) for 12 h. The cells in the MW + DOX group were cultured with free DOX (3 μmol/L) for 12 h. Twelve hours later, the cells in the MW, MW + DOX, and MW + NaCl–DOX@PLGA groups were irradiated with mild MW (4 W for 2 min) and were subsequently placed back in the thermostat incubator. The cells were harvested after 4 h and stained with the Annexin V-FITC/PI apoptosis detection kit, according to manufacturer's instructions. Apoptotic cells were detected and analyzed by flow cytometry.
Effect of EGTA, 2-APB, TMB-8, and thapsigargin on MW and nanoparticle-increased intracellular Ca2+ concentration
An increase in intracellular Ca2+ concentration primarily originates from an increased release of intracellular Ca2+ from the endoplasmic reticulum (ER) Ca2+ stores and plasmalemmal Ca2+ entry from store-operated Ca2+ entry in hepatocytes. We explored the Ca2+ pathway in response to MW and nanoparticles in HepG2 cells. Extracellular Ca2+ chelator, EGTA (0.5 mM), store-operated Ca2+ influx inhibitor, 2-aminoethoxydiphenyl borate (2-APB, 50 μM), ER Ca2+ release inhibitor, 3,4,5-trimethoxybenzoic acid 8-(diethylamino) octyl ester (TMB-8, 100 nM), and sarco/ER-Ca2+-ATPase inhibitor(SERCA) inhibitor thapsigargin (0.1 mM) were added to the cells to remove Ca2+. After 12 h culture, the cells were stained with Fluo-3 for 40 min and subsequently treated with mild MW irradiation (4 W for 2 min). The fluorescence intensity was measured with a FACSCalibur flow cytometer (Becton Dickinson). The results of 10,000 fluorescent events by CellQuest were analyzed with FCS Express 4.0 (De Novo Software) and expressed as the mean fluorescence intensity of 10,000 cells.
In vitro cytotoxicity
The standard MTT assay was used in the HepG2 cells to estimate the biocompatibility of the NaCl–DOX@PLGA nanoparticles. The cell viability and morphology reflect the cytotoxicity of the NaCl–DOX@PLGA nanoparticles. The tumor cells were plated into 96-well plates (1 × 104 per well) and cultured in a suitable environment for 24 h. Subsequently, 100 μL PBS and NaCl–DOX@PLGA nanoparticles were added to the plates. Nanoparticles of different concentrations (25, 50, 75, 150, 300, 400, and 600 μg/mL) were incubated with the cells for different durations. Subsequently, the cells were incubated for 24 h, and the cell viability was represented as the absorbance of formazan at 490 nm. The control, PBS treated, cells were considered as 100% viable.
In vitro hemolysis test
The hemolysis test was performed using rabbit's heart blood to evaluate the cytotoxicity of NaCl–DOX@PLGA nanoparticles in vitro. Five milliliters of blood was obtained from the rabbit heart, and 0.2 mL anticoagulant agent was added. The blood samples were washed with PBS to remove external and lysed red blood cells. After removal of the supernatant, 1 mL blood was diluted to 50 mL with PBS. Subsequently, 0.5 mL cells were mixed with NaCl–DOX@PLGA nanoparticles (0.5 mL) diluted in PBS at concentrations of 25, 50, 75, 150, 300, 400, and 600 μg mL−1. The positive and negative control groups composed of mixtures of 0.5 mL cells and 0.5 mL deionized water and 0.5 mL cells and 0.5 mL PBS, respectively. Three parallel experiments were performed in duplicate for each group. The mixtures were centrifuged under room temperature for a 3 h incubation period. The absorbance of the supernatant was measured at 570 nm via UV–vis.
Safety injection dose evaluation in vivo
Twenty healthy female nude mice were randomly and equally divided into four groups to investigate the safety injection dose of NaCl–DOX@PLGA nanoparticles. The mice were injected with NaCl–DOX@PLGA nanoparticles at different doses of 20 to 110 mg kg−1 (20, 60, and 110 mg kg−1, dispersed in PBS) via the tail vein and killed after 14 days. PBS-treated mice were used as the control group. The blood was collected for blood biochemistry and blood routine examination. Major organs, including the heart, spleen, liver, lung, and kidney, were harvested for histological examination.
Antitumor efficacy evaluation of NaCl–DOX@PLGA in vivo under mild MW irradiation
We randomly divided 48 HepG2-tumor-bearing female nude mice into the following six groups: PBS, PBS + MW, DOX, NaCl–DOX@PLGA, NaCl–DOX@PLGA + MW, and NaCl@PLGA + MW groups. The injection dose was 110 mg kg−1 except for the DOX group, which was 10 mg kg−1, and the abovementioned materials were injected into the mice via the tail vein. The MW antenna was inserted into the center of the tumor under real-time ultrasound guidance (Additional file 1: Figure S1) in the MW groups (PBS + MW, NaCl–DOX@PLGA + MW, and NaCl@PLGA + MW) at 6 h post-injection. The power was 2450 MHz, and the output energy was set at 2 W for 1.5 min. The temperature changes during MW heating in vivo were recorded using FLIR imaging. During the investigation, body weight and tumor size were carefully observed for 2 or 3 days.
Three mice in every group were killed 3 days after ablation to obtain tumor tissues to analyze the therapeutic effect at an early stage. Histological analysis was performed to analyze coagulative necrosis. Cell apoptosis and proliferation in the peripheral ablation area was assessed by TUNEL and PCNA staining. The TUNEL assay and PCNA staining (Roche, Basel, Switzerland, and California, USA, respectively) were performed on the basis of manufacturer's instructions. The percentages of TUNEL-positive and PCNA-positive nuclei were calculated as follows: four randomly chosen fields per section corresponding to at least 50 cells were examined at high magnification (400 ×). The mice were killed and marked as state of “death” if the tumor size in any one direction reached 20 mm. The survival rates of mice were measured similarly. The tumors and major organs of the mice in each group were excised and stained with hematoxylin and eosin (H&E) for histopathological analysis.
Results and discussion
Synthesis and characterization of NaCl–DOX@PLGA nanoparticles
The successful synthesis of NaCl@PLGA was confirmed by measuring the hydrodynamic diameter and zeta potential of the nanoparticles (Additional file 1: Figure S2a, b). The confinement effect of the nanoparticles can be used to accelerate the movement of encapsulated ions or molecules under the MW field, producing more heat and significantly increasing the surrounding temperature. This effect has been used to enhance tumor ablation [7, 29]. NaCl, a known ideal MW-sensitive material, can be loaded into the PLGA nanoparticles by a simple microemulsion method. The MW heating effect of 22 mg mL−1 NaCl@PLGA nanoparticles was tested. Additional file 1: Figure S3 shows that the temperature in the NaCl@PLGA group showed a more rapid increase than that in the PLGA and NaCl solution groups. The largest temperature gap was approximately 8.3 °C between the NaCl@PLGA and NaCl groups. Those results indicated that the PLGA nanoparticles were suitable to load NaCl to enhance MW ablation.
The loading capacities of DOX and NaCl in the PLGA nanoparticles were 29.1% ± 2.03% (w/w) and 3.1%, respectively. The temperature of the nanoparticles obviously increased because the nanoparticles were irradiated by MW. PLGA-based drug delivery systems have several therapeutic applications due to its biodegradability, biocompatibility, and sustained-release properties [25, 30]. The following three groups were designed to examine the MW-stimulated release properties of DOX from the as-made nanoparticles. 1) The control group: 22 mg NaCl–DOX@PLGA nanoparticles was dispersed into 1 mL phosphate-buffered saline (PBS) (0.1 M, pH 7.2) solution, and the released amount of DOX under constant shaking for 1 h at 37 °C was tested. 2) MW (pH = 5.0) group: 22 mg NaCl–DOX@PLGA nanoparticles were dispersed into 1 mL PBS, the solution was placed into a water bath at 37 °C and shaken continuously, treated for 4 min by MW 30 min after shaking. The supernatant of the solution was collected after MW irradiation to measure the released amount of DOX. 3) The MW (pH = 7.2) group: 22 mg NaCl–DOX@PLGA nanoparticles were dispersed into 1 mL PBS (0.1 M, pH 7.2) solution, and the following methods and MW output energy were same with the MW (pH = 5.0) group. The nanoparticles showed good drug release properties. The release of DOX from the control group was initially slow and reached 55.48% at 72 h. After MW irradiation, the release of DOX showed a different increase rate, particularly in the acid condition. Figure 2b shows that the amount of DOX released in the MW (pH = 5.0) group reached 65.43% after 10 h. Subsequently, the release decreased, and the final amount released was approximately 75.78% after 72 h. The results showed that DOX could be effectively released from the NaCl–DOX@PLGA after MW irradiation after uptake by tumor cells.
Cellular uptake and in vitro cytotoxicity
The cellular uptake of nanoparticles was evaluated via in vivo fluorescence images. With 8 h of incubation of HepG2 cells with PLGA nanoparticles, nanoparticls were successfully transported into cells (Additional file 1: Figure S4). An MTT assay was used to investigate the cytotoxicity of NaCl–DOX@PLGA on HepG2 cells. In our previous work, NaCl@PLGA nanoparticles showed good biocompatibility, which was suitable for further experiments in vivo. After being loaded with DOX, the NaCl–DOX@PLGA nanoparticles displayed similar cytotoxicity with NaCl@PLGA. Figure 2c shows that the NaCl–DOX@PLGA nanoparticles exhibit a dose-dependent cytotoxicity towards HepG2 cells. The relative cell viability was > 80% in groups exposed to a concentration below 600 μg mL−1.
A hemolysis test was performed to further evaluate the potential cytotoxicity of NaCl–DOX@PLGA nanoparticles. Figure 2d shows the hemolysis ratio caused by different NaCl–DOX@PLGA nanoparticle concentrations. None of the hemolysis ratios in any experimental group exceeded 5%, and the mean value was only 2.44%, indicating that the NaCl–DOX@PLGA nanoparticles showed low toxicity. The inset in Fig. 2d shows the visual hemolysis in the presence of NaCl–DOX@PLGA nanoparticles. No obvious hemolysis was observed in any of the experimental or negative control groups, whereas the positive control group showed significant hemolysis. On the basis of these results, we conclude that NaCl–DOX@PLGA nanoparticles have low toxicity and good biocompatibility.
Effects of DOX and MW on intracellular Ca2+ concentration
Inspired by these results, we further loaded DOX into the PLGA nanoparticles to create the NaCl–DOX@PLGA nanoplatform. The creation of the nanoplatform provided an opportunity to eliminate the undesirable side effects and poor targeting of DOX and to greatly improve the therapeutic effect of this chemotherapeutic treatment. We assessed the effect of NaCl–DOX@PLGA nanoparticles on the concentration of intracellular Ca2+ after the release of DOX from the nanoparticles was confirmed. The HepG2 cells were incubated with NaCl–DOX@PLGA nanoparticles for 12 h to guarantee sufficient uptake. Afterwards, the cells were gently washed with PBS to remove the extracellular nanomaterials and were subsequently irradiated with mild MW (2 W for 2 min). Flow cytometry results showed that the concentration of intracellular Ca2+ treated with both nanoparticles and MW increased significantly compared with that in cells irradiated with the MW or nanoparticles alone (Fig. 3b, d). The mean fluorescence intensity was 99.7 ± 4.7, 123 ± 13.6, and 316 ± 8.2 in the control, nanoparticle, and combination groups, respectively. These results indicate that mild MW irradiation can increase the Ca2+ concentration in HepG2 cells pretreated with NaCl–DOX@PLGA nanoparticles.
MMP changes after pretreatment with nanoparticles and MW irradiation
Cellular viability evaluation after combined treatment
The relationship between cell apoptosis/death and Ca2+ concentration was initially analyzed. Evidence gathered from the past 10 years showed the importance of Ca2+ in the activation and execution of cell death [37, 38]. Intracellular Ca2+ increases have been shown to be required for apoptosis to occur . The mitochondria is central to cell death . The increases in intracellular Ca2+ concentration cause the activation of mitochondrial membrane permeabilization, interruption of respiratory chain functions, and loss of MMP, which will result in apoptosis and necrosis . Our results confirmed that the increase in intracellular Ca2+ concentration caused by combined treatment can lead to dissipation of MMP. More apoptosis and dead tumor cells were detected in groups with higher intracellular Ca2+ concentration and lower MMP. Tumor cells become more sensitive to MW treatment after pretreatment with DOX, and this may be attributed to the nonthermal effects of MW exposure. However, this possibility needs more evidence.
Recently, the role of the non-thermal effects of MW in the synthetic treatment of cancer has gained attention. Long et al.’s study have suggested that the nonthermal effects of MW irradiation can induce cellular uptake of therapeutic agents . Yu et al. have found that nonthermal effects of low-power microwave radiation can cause apoptosis in the epithelial cells of the lens , but no studies have illustrated the role of nonthermal MW on the intracellular Ca2+ concentration in tumor cells. MW irradiation may cause polarization and electronic vibrations of cellular membranes. This process might affect the function of the ER–mitochondrial interface and plasma membrane, which lies at the center of Ca2+ homeostasis . Coordinated reactive oxygen/nitrogen species (ROS/RNS) and Ca2+ surges are required for the initiation of apoptosis at the ER–mitochondrial interface . ROS is an important factor produced during photodynamic therapy and could induce cell death through apoptosis and/or necrosis pathways, tumor vasculature damages, Brandes et al. , Lismont et al. 44]. Mild MW irradiation may also have some influence on ROS production in tumor cells, but this needs further study.
Effect of EGTA, 2-APB, TMB-8, and thapsigargin on MW with nanoparticle-induced Ca2+ concentration in HepG2 cells
Increased intracellular Ca2+ concentration in non-excitable cells mainly originates from two pathways. These are Ca2+ release from the ER Ca2+ stores and plasmalemmal Ca2+ entry via store-operated Ca2+ entry. We investigated the possible mechanisms underlying the combined treatment-induced Ca2+ changes and related apoptosis by using the extracellular Ca2+ chelator EGTA, store-operated Ca2+ channel (SOC) inhibitor 2-APB, ER Ca2+-release-antagonist TMB-8, and sarco/ER-Ca2+-ATPase inhibitor thapsigargin. EGTA, 2-APB, TMB-8, and thapsigargin were cultured with cells before MW irradiation. TMB-8 significantly inhibited the increase in intracellular Ca2+ induced by MW irradiation (P < 0.05), whereas no significant inhibitions were found in cells cultured with EGTA, 2-APB, and thapsigargin (P > 0.05) (Fig. 5b). Different results were found in cells cultured with the abovementioned inhibitors and nanoparticles before MW irradiation. EGTA, 2-APB, and TMB-8 significantly decreased the concentration of intracellular Ca2+ after cells were cultured with nanoparticles and exposed to MW irradiation. No change was observed for thapsigargin (Fig. 5c). Our results showed that the increase in intracellular Ca2+ concentration caused by MW irradiation may be achieved by Ca2+ release from the ER. The increase in Ca2+ concentration induced by the combination of nanoparticles and MW irradiation was shown to be a more complicated pathway, including the release of Ca2+ from both external and internal sources.
Safety evaluation in vivo
In vivo antitumor efficacy evaluation of NaCl–DOX@PLGA combined with MW ablation
Additional file 1: Figure S7 shows that the body weight of nude mice increased during the experimental period, whereas the body weight in the MW, MW + NaCl@PLGA, and MW + NaCl–DOX@PLGA groups decreased 3 days after ablation and slowly increased afterwards. It was attributed to a compensative response of the body after tumor ablation. On days 18–21, the body weight had a tendency to decrease again. Local tumor progression was most frequently detected during this period. The increasing tumor burden may be the reason for the second decline in body weight. The DOX-loaded group (NaCl–DOX@PLGA with and without MW irradiation groups) did not indicate an obvious loss in body weight, which further validated the stability of DOX in the NaCl–DOX@PLGA platform and the good compatibility of the loaded nanoparticles.
After 42 days of observation, the NaCl–DOX@PLGA group expressed a significant suppression in tumor growth than the other two groups among all nude mice treated with MW irradiation. Figure 7c shows that the mean tumor volume was 2351 and 760 mm3 in the MW and NaCl@PLGA + MW groups, respectively, whereas it reduced to 84 mm3 in the NaCl–DOX@PLGA + MW group. The mean tumor volume in nude mice without MW irradiation was approximately 3000 mm3, which indicated that NaCl–DOX@PLGA alone did not cause an obvious inhibitive effect on tumor growth. The tumor volume reached 760 mm3 in the NaCl@PLGA group versus 2351 mm3 in the MW alone group, which illustrated that NaCl@PLGA may help produce more energy to damage tumor cells under mild MW, but the effect was very limited. After loading DOX to the NaCl@PLGA nanoparticles, the DOX was not only used as a chemotherapeutic agent but also acted as a medium to enhance the nonthermal effect of MW ablation. DOX could sensitize tumor cells to MW irradiation and further induce more occurrences of tumor cell death, particularly for cells in the periphery of the ablation area. The representative photos of mice shown in Additional file 1: Figure S8 and Fig. 7d taken at different times, before and after, treatment illustrated the typical tumor development and were consistent with the results of tumor volume growth curves. A residual tumor was found in 60% of mice immediately after treatment in the MW group, and tumor progression was found in the rest of the mice on the 18th day after ablation. Obvious residual tumor in 80% of mice in the NaCl@PLGA + MW group was not found in the early period, whereas tumor progression was found between the 9th and 33rd days. In the NaCl–DOX@PLGA + MW group, all mice showed complete ablation in the early period of observation. Tumor progression was found in one mouse on the 24th day and one mouse on the 30th day. Obvious tumor progression was found later, but the speed of tumor growth in the NaCl–DOX@PLGA + MW group was slower than that in the two groups that received MW treatment.
At the end of observation, all nude mice died in the control and free DOX groups. In the NaCl–DOX@PLGA group, 40% of the mice were still alive, but the maximum tumor size was approximately 20 mm. Tumors harvested at the end of the experiment are shown in Fig. 6e. All nude mice were alive in groups that received MW treatment, and the final survival rate was 100% (Fig. 7f). H&E-stained images of the heart, liver, spleen, kidney, and lung harvested at the end (Additional file 1: Figure S9) illustrated good compatibility of the as-made nanoparticles. The outcomes demonstrated that combined chemotherapy and MW (nonthermal and thermal) therapies based on a NaCl–DOX@PLGA nanoplatform could significantly improve the survival rate of HepG2-tumor-bearing mice.
A biocompatible and biodegradable NaCl–DOX@PLGA nanoplatform was prepared with triple functions to realize the effective tumor killing under unlethal temperature. The as-made nanoplatform developed in this study was shown to significantly enlarge the ablation volume. The elevated intracellular Ca2+ caused by MW irradiation and DOX destroyed the homeostasis of tumor cells, inducing a decrease in MMP and massive apoptosis. This process can make tumor cells more sensitive to MW ablation and DOX chemotherapy, which could provide many clinical benefits by decreasing the output energy of MW and reducing the concentration of DOX used. The development of nano-scale microwave-sensitive agents to kill tumors in unlethal temperature reduced the dependence of ablation on high temperature and greatly improve the safety of ablation. The versatility of this unique nanoplatform provides promising biosafe therapeutic nanoagents for the non-invasive treatment of risk-location tumors in vivo.
DJP, WQ, FCH and ZDY prepared and performed the experiments. DJP, WQ and FCH analyzed the data and interpreted the results. LP, MXW and YJ conceived and supervised the study. The manuscript was written by DJP, FCH and YJ revised critically by LP and MXW. All authors read and approved the final manuscript.
This work was supported by the National Key R&D Program of China (No. 2017YFC0112000), National Natural Science Foundation (Project Nos. 81627803, 81622024 and 81801722).
Ethics approval and consent to participate
The protocols and the use of animals were approved by and in accordance with the animal welfare committee of Soochow University.
Consent for publication
All authors agree to be published.
The authors declare that they have no competing interests.
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