PEI-PEG-Coated Mesoporous Silica Nanoparticles Enhance the Antitumor Activity of Tanshinone IIA and Serve as a Gene Transfer Vector

Tanshinone IIA (TanIIA) and gene therapy both hold promising potentials in hepatocellular carcinoma (HCC) treatment. However, low solubility and poor bioavailability of TanIIA limit its clinical application. Similarly, gene therapy with GPC3-shRNA, a type of short hairpin RNAs (shRNAs) capable of silencing the glypican-3 (GPC3) expression, is seriously limited due to its susceptibility to nuclease degradation and high off-target effects. In the present study, polyethyleneimine (PEI)-polyethylene glycol (PEG)-coated mesoporous silica nanoparticles (MSN-PEG) were used as a drug carrier. By encapsulating TanIIA into MSN-PEG, we synthesized MSN-TanIIA-PEG nanoparticles and observed the involved characteristics. This was followed by exploration of antitumor activity on the HepG2 cell lines in vitro. Meanwhile, in order to construct GPC3-shRNA plasmids, a shRNA sequence targeting GPC3 was synthesized and cloned into the pSLenti-U6 vector. Accordingly, the performance of MSN-PEG as a gene transfer carrier for GPC3-shRNA gene therapy of HCC in vitro was evaluated, including transfection efficiency and DNA binding biological characteristics. The results indicated successful encapsulation of TanIIA in MSN-PEG, which had satisfactory efficacy, favorable dispersity, suitable particle size, and sustained release effect. The in vitro anti-HCC effects of nano-TanIIA were greatly improved, which outperformed free-TanIIA in terms of proliferation and invasion inhibition, as well as apoptosis induction of HCC cells. As expected, MSN-PEG possessed excellent gene delivery capacity with good binding, release, and protection from RNase digestion. Using MSN-PEG as a gene carrier, the plasmids were successfully transfected into HepG2 cells, and both the mRNA and protein expressions of GPC3 were significantly downregulated. It was thus concluded that a sustained release TanIIA delivery system for HCC treatment was synthesized and that MSN-PEG could also serve as a gene transfer carrier for gene therapy. More interestingly, MSN-PEG may be a potential delivery platform that combines TanIIA and GPC3-shRNA together to enhance their synergistic effect.


Introduction
Hepatocellular carcinoma (HCC), as a malignancy characterized by high incidence and mortality, harms people's life and health in a tremendous manner. Seriously, its mortality and morbidity have been steadily increasing over the last few decades [1]. To date, chemotherapy remains the most common treatment for all stages of carcinoma patients. However, several potential chemotherapeutics that can treat HCC still show limitations such as severe adverse reactions and drug resistance [2]. Moreover, the intricacy of the molecular pathogenesis poses great difficulties on seeking cure. Enormous endeavors have thus been made to develop high-efficacy multitarget antineoplastics with less adverse effects.
Several effective plant constituents, which are used in traditional Chinese medicine with insignificant adverse actions, have aroused a wide range of interest as an adjuvant therapy [3]. Among them, TanIIA, an effective component extracted from the Salvia miltiorrhiza roots, features high efficacy, natural source, and low toxicity [4]. Based on the existing studies on TanIIA, it exerts a broad spectrum of antitumor activities in a variety of human carcinoma cells by suppressing proliferation and migration, triggering autophagy and apoptosis, and reversing the multidrug resistance [5]. Additionally, TanIIA has a synergistic effect in combination with other chemotherapeutics commonly used in clinics, which makes its application in the cancer and adjuvant therapies promising and offers a new insight into diverse cancer treatments as well [6].
Unsatisfactorily, being a lipophilic constituent, TanIIA is poorly bioavailable, which limits its further application [7]. Due to poor water solubility, it exhibits robust hepatic elimination after oral medication and can be easily eliminated from the circulatory system after intravenous medication [8,9]. Hence, diverse delivery systems (nanoscale) have been proposed for controlled release of TanIIA, in order to overcome its disadvantages and to elevate its bioavailability [2,9].
Amongst various nano-based drug delivery platforms developed, mesoporous silica nanoparticles (MSNs) have attracted a considerable attention owing to their good biocompatibility, monodispersity, feeble toxicity, tunable pore size, and large pore volumes, among other characteristics [10]. Despite being in part a potential solution to the foregoing problems with TanIIA, it still cannot escape the influence of the reticuloendothelial system (RES). Rapid elimination by the RES will inevitably hamper the nanosized drugs' absorption efficiency in tumor regions, leading to reduced bioavailability [11]. Being highly hydrophilic and positively charged, PEG is commonly used to decorate nanoparticles [12], which has been proven as one of the most effective methods to improve nanoparticle biodistribution and reduce opsonization by the RES [11].
Studies over the last decades have demonstrated that GPC3 is highly and specifically expressed in HCC, revealing its potential from an encouraging biomarker for the early HCC detection to an effective epitope for targeted HCC treatment. Past several years have witnessed the exploration of the GPC3-targeting gene therapies [13,14]. As promising as it looks, their applications are severely limited because of the physicochemical traits of nucleotide drugs, including high molecular weight, susceptibility to nuclease degradation, easy missing of target, and anionic charge [15]. is has necessitated carrier design as the gene therapy advances in order to achieve highly efficient drug delivery to the target cells. ShRNAs, the small molecules of RNA, have specific function of gene silencing, which can be delivered to the targets via the support of nanoparticles [16]. Recently, nanostructured carriers such as PEG and PEI or inorganic nanoparticles have shown multiple advantages concerning RNA interference (RNAi) delivery [17]. PEI, as one of the most classic nonviral vectors, is the most broadly applied polycation transfection reagent owing to its high stability and transfection performance, while PEI-25k has been considered the gold standard for nonviral vectors [18,19]. Moreover, PEI combined with PEG could improve the systemic circulation and prolong the treatment time [19,20].
Based on the aforementioned theory, this study aims to construct an intelligent nanoplatform to improve the water solubility and bioavailability of TanIIA, which also serves as a vehicle of GPC3-shRNA. Herein, we propose a facile method, where TanIIA was physically adsorbed by mesoporous silica and then surface-modified with PEI-PEG to make it positively charged. In this way, the stability of the complex can be improved, which is conducive to loading GPC3-shRNA plasmids. e physicochemical property elucidation of the complex was accomplished, in vitro antitumor activities were investigated, and the feasibility of MSN-PEG as a GPC3-shRNA carrier was explored. Finally, we found that this novel drug delivery system is promising for HCC treatment. Figure 1 is a schematic illustration of the preparation of MSN-PEG nanoparticles and their delivery.

Preparation of the Nanoparticles.
e MSN-TanIIA-PEG was prepared according to a film dispersion-ultrasonic method in the published articles [9,21]. e first step was preparation of TanIIA-loaded MSNs. 5 mg MSN (25 mg/mL) and 500 μg TanIIA (10 mg/mL) were mixed evenly in ethanol, and then 100 μL of water was added slowly into the above solution under ultrasonic condition followed by 2-h incubation in a 37°C shaker. Finally, centrifugation was carried out at 10,000 rpm for 15 min to remove the residual solvent, so as to obtain the required sample (denoted as MSN-TanIIA), which was dried in a 45°C vacuum for 12 h and then stored at 4°C. e next step was coating of the prepared MSN-TanIIA with PEI-PEG. In a nutshell, 5 mg MSN-TanIIA (10 mg/mL) was dripped into 20 mg (50 mg/mL) PEI-PEG followed by probe sonication for 20 min. After removing extra PEI-PEG and free-TanIIA in the solution via 10-min centrifugation (10,000 rpm), the remaining was washed three times in 2 mL of saline via 5-min centrifugation (10,000 rpm) to get TanIIA-loaded PEI-PEG-coated MSNs, denoted as MSN-TanIIA-PEG. Meanwhile, MSN-PEG was also prepared by the same method. e entrapped TanIIA in the obtained sample solution was quantified by HPLC. e drug loading capacity (DL, %) and encapsulation efficiency (EE, %) were calculated by the following equations:  [22], the high-performance liquid chromatography (HPLC) system (LC-15C; Shimadzu, Japan) with a WondaSil C18 column (4.6 × 250 mm, 5 μm) was used for determination of TanIIA in MSN-TanIIA and MSN-TanIIA-PEG. In addition, the mobile phase of the HPLC system consisted of 70% acetonitrile (A) and 30% ultrapure water (B) at a flow rate of 1 mL/min, column temperature was kept at 30°C, and the detection wavelength was 268 nm.

Standard Solution and Sample Preparation.
TanIIA standard solutions (1 mg/mL) were prepared in acetonitrile and stored at −20°C until use. Mobile phase was used to dilute standard solutions to the concentrations of 6.25, 12.5, 25, 50, and 100 μg/mL. Acetonitrile was used to break down the internal structure of the samples, thereby extracting the TanIIA before detecting [23,24].

Characterization of the Nanoparticles.
e physical and chemical properties of MSN-TanIIA-PEG were characterized by transmission electron microscopy (TEM), zeta potential, and dynamic light scattering (DLS). e particle size (nm) and zeta potential (mV) of nanoparticles were evaluated by dynamic light scattering (DLS) at 25°C using the Zeta Plus Zetasizer (Brookhaven Instruments, USA). All the samples were dispersed in deionized water and sonicated before the analysis. e morphology of the uncoated and coated nanoparticles was observed by a JEM-2100 TEM instrument (JEOL, Japan).   For apoptosis detection, the cells were collected and PBSwashed followed by staining with Annexin V-Alexa Fluor 647 (5 μL) and PI (10 μL, 20 μg/mL) at room temperature protected from light for 15 min and a subsequent resuspension in 500 μL of binding buffer (10 mM HEPES/NaOH, pH 7.4, 140 mM NaCl, 2.5 mM CaCl 2 ). e stained cells were detected immediately using FACSCalibur (BD Biosciences, USA).
For the cell cycle assessment, the cells were harvested, PBS-washed, and fixed overnight at 4°C in cold 70% ethanol. After collecting and washing with PBS, the cells were stained using propidium iodide (PI) solution (100 μL; 20 μg/mL PI and 5 μg/mL RNase A in PBS) in the dark for 30 min at ambient temperature followed by FACSCalibur analysis.
Initially, 50 mg/L Matrigel (BD Biosciences, USA) was coated onto the transwell insert membrane at a 1 : 8 dilution at the apical side. After collection from every group, the cells were resuspended in a serum-free medium, and then 1 × 10 5 cells (200 μL) were transferred into the upper transwell chambers (8 μm; BD Biosciences, USA). e inferior chamber was filled with 500 μL of 10% FBS-containing DMEM. Following 24-h incubation at 37°C, the cells were subjected to twice PBS washing, 30-min fixation in 4% paraformaldehyde, and 20-min staining with crystal violet (0.1%) at room temperature. en, the cells were washed with water 3 times. After this, a cotton swab was used to remove the nontraveled cells from the upper filter surface in a gentle manner. Finally, the cell pictures were obtained under a microscope and the cell numbers were quantified with ImageJ software. e cell invasion inhibition rate was calculated following this formula: e cell invasion inhibition rate (%) � (cells' count of untreated group − cells' count of the treatment group)/cells' count of untreated group × 100.

Construction and Identification of the GPC3-shRNA
Plasmid.

MSN-PEG Transfection Efficiency Detection.
MSN-PEG and GPC3-shRNA-EGFP plasmids were individually dispersed in the DMEM culture medium. MSN-PEG and GPC3-shRNA-EGFP plasmids were incubated at a mass ratio of 20 : 1 for 30 min to make them mix sufficiently.
After HepG2 cells were cultured overnight, the medium was replaced with the above mixture. e culture medium was replaced by fresh DMEM after 5-h incubation. Additional 24-h incubation sustained before harvesting cells. Meanwhile, Lipofectamine 2000 transfection method, which conducted according to the instruction, served as comparison.

Western
Blotting. Total proteins from transfected and untransfected HepG2 cells were extracted using RIPA buffer (Vazyme Biotech, China). BCA assay (Beyotime, China) was conducted to quantify the extracted total proteins. For isolation of the protein samples, 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was carried out followed by transfer to polyvinylidene fluoride membranes (0.45 μm) with 300 mA current for 90 min. After transfer, the membranes were blocked in 5% BSA at ambient temperature for 1 h and then incubated overnight using rabbit antibodies against GPC3 (Abcam, USA; diluted 1 : 1000) and a rabbit antibody against GAPDH (Sangon Biotech, China; diluted 1 : 5000) as an internal standard at 4°C to normalize the protein expressions. On the next day, the membranes were further incubated using goat anti-rabbit IgG-HRP (Sangon Biotech, China; diluted 1 : 5000) for 1 h and then subjected to protein visualization using enhanced chemiluminescence (Vazyme Biotech, China). e G:BOX Chemi XX9 imaging system (Syngene, UK) was used for protein visualization.

Statistical Analysis.
Quantitative variables were represented as the mean ± standard deviation (x ± s). P < 0.05 was considered statistically significant. e data were Evidence-Based Complementary and Alternative Medicine determined by one-way ANOVA analysis using GraphPad Prism 8.0 software.

Particle Size, Zeta Potential, and Morphological
Features. It was reported that nanocarriers have high drug loading capacity, excellent tolerability, high stability, and low drug degradation, which achieve controlled release and sustained delivery of antineoplastics [26]. In this study, TanIIA-loaded MSN-PEG nanoparticles were prepared, as described previously. e DL and EE of MSN-TanIIA-PEG nanoparticles were 9.32% and 93.13%, respectively. imply the successful modification of nanoparticles. Moreover, the positive charges enabled formation of an electrostatic complex by the carrier with shRNA, thereby protecting it from nucleases and facilitating its cellular uptake [27].
TEM analysis was performed to elucidate the morphology of the nanoparticles. According to the TEM micrographs in Figures 2(i)-2(l), the majority of the nanoparticles, regardless of modified or not, was about 50 nm in particle size, which had a regular spherical shape, uniform particle size, and good monodispersity. e surfacemodified particles maintained the basic morphology. Additionally, it was obviously observed that the surface mesoporous pores became blurred, and there was a white halo on the nanoparticle periphery, which corresponded to the surface modification with the polymer layer. It has been reported that nanoparticles with a size of 100-200 nm can be quickly eliminated from the blood by macrophages in the RES after entering the circulation. In contrast, the nanoparticles 50-100 nm in size are capable of entering liver cells and target drugs to the liver [2]. According to the EPR effect, nanoparticles with particle size less than 100 nm can easily pass through the interstices of the tumor tissue and thus remain in the tumor tissue [28]. In the present study, the prepared nanoparticle size was about 50 nm, which is in accordance with the preparation requirements of particle size between 50 nm and 100 nm.

In Vitro Drug
Release. Some studies have demonstrated that the entrapped drug release from the nanoparticles in a sustained manner extended the plasma biological half-life for the natural compounds [29,30]. For effectiveness validation of the nanoparticles in drug delivery, the in vitro release of TanIIA from MSN-TanIIA and MSN-TanIIA-PEG was employed at various time intervals (1,2,4,6,8,12,18, and 24 h), and the curve of TanIIA release was plotted (Figure 2(m)). According to the in vitro TanIIA release curve, both MSN-TanIIA and MSN-TanIIA-PEG showed a typical pattern of two-phase release. e TanIIA from MSN-TanIIA and MSN-TanIIA-PEG was initially released at a rapid rate with 71.89% and 59.7% in the first 6 h, which was denoted as incubation period. From 7 to 24 h, the sustained release phase, the cumulative release of the drug gradually increased. After 12 h, the release gradually decreased, which was followed by the smooth release until 24 h. e sustained release reached 97.27% and 97.95% at 24 h for MSN-TanIIA and MSN-TanIIA-PEG, respectively. It was obviously seen that the percentage of TanIIA release in MSN-TanIIA was higher than that of MSN-TanIIA-PEG. e high burst release of MSN-TanIIA may prevent drugs from reaching to the target tissues or cells, thus making it less effective. On the contrary, the sustained release of MSN-TanIIA-PEG was more suitable for the drug release properties of nanoparticles [31].
e results revealed increases in the growth inhibition rates of HepG2 cells in a dose-dependent manner.
e IC 50 of free-TanIIA, MSN-TanIIA, and MSN-TanIIA-PEG were 14.842 μg/mL, 9.298 μg/mL, and 6.959 μg/mL, respectively (Figure 3(a)), while the blank nanoparticles (MSN-PEG) and DMSO had no significant effects on the cells' growth. Suggestively, the slower and sustained TanIIA release from the MSN-TanIIA-PEG led to reduced effective dose (IC 50 ) and obtained superior therapeutic efficacy in vitro to the free-TanIIA for HCC cells. Similar observations have also been reported by Yang et al. [12] and Sun et al. [21], where IC 50 of many nanoparticles of natural products was lower than that of the free products.

Cell Apoptosis Assays.
Hoechst 33342 is typically used for detecting cell apoptosis, and the principle is that it can permeate apoptotic cellular membranes freely, and that apoptotic cells can be identified by the bright blue-stained nuclei that are either condensed or scattered [32]. e apoptotic cell nuclei exhibit a high intensity of fluorescence, while weak fluorescence is noted in the nonapoptotic cells [33]. To evaluate the apoptosis of HepG2 cells induced by MSN-PEG, free-TanIIA, MSN-TanIIA, and MSN-TanIIA-PEG, the cellular nuclei were stained using Hoechst 33342 followed by fluorescence microscope evaluation. Compared with the intact control nuclei, the cells intervened with MSN-PEG showed little difference, while the cells intervened with free-TanIIA, MSN-TanIIA, and MSN-TanIIA-PEG all exhibited nucleus shrinkage and were stained bright blue or showed debris-like lobulation of nuclei (Figure 3(b)). However, within similar sized fields, there were more apoptotic cells in the MSN-TanIIA-PEG group than in the free-TanIIA and MSN-TanIIA groups. is observation is consistent with a previous finding that noisome-coated TanIIA could enhance the apoptosis of HepG2 cells [2].
Subsequently, HepG2 cells intervened with MSN and TanIIA were doubly stained with Annexin V-Alexa Fluor 647 plus PI, and then the cell apoptosis induced by intervention was determined by flow cytometry. As shown in Figure 3(c), the control cells exhibited an exceptionally low apoptosis rate, which was only 8.26 ± 2.83%. In contrast, the cell apoptosis induced by MSN-PEG, free-TanIIA, MSN-TanIIA, and MSN-TanIIA-PEG amounted to 12.81 ± 3.40%, 18.92 ± 3.55%, 30.63 ± 4.09%, and 38.68 ± 6.57%, respectively. Obviously, the cell apoptosis induced by MSN-TanIIA-PEG was far stronger than that induced by other methods (P < 0.05).
e finding was consistent with the result of Hoechst 33342 staining assay. Moreover, the apoptotic results coincided with the cell proliferation inhibition data as well.

Cell Cycle Assay.
Following the verification of cell apoptosis effect induced by MSN-TanIIA-PEG, flow cytometry was utilized to analyze the variation trends of HepG2 cell distribution by the MSN-PEG, free-TanIIA, MSN-TanIIA, and MSN-TanIIA-PEG over the cell cycle phases. According to Figure 3(d), the MSN-TanIIA-PEG intervention group showed an increased G0/G1 phase cell population compared with the control group, which was also more significant than the MSN-PEG, free-TanIIA, and MSN-TanIIA intervention groups. is finding suggested that nano-TanIIA intervention could affect the arrest of cell cycle at G0/G1, the phases of DNA replication [34]. In other words, MSN-TanIIA-PEG prevented the duplication of DNA, diminished the S phase cell proportion during DNA synthesis, and inhibited the G2/M phase accumulation of cells. As a result, HepG2 cells' growth and proliferation were effectively suppressed.     Evidence-Based Complementary and Alternative Medicine is finding is consistent with the previous research showing the ability of TanIIA to arrest cells at the G0/G1 checkpoint in a dose-related manner [35,36]. It also agreed with the finding of another study demonstrating a differing effect of the drug-entrapped nanoparticles on the distribution of cell cycle from the free-form drug [37]. However, the effect of TanIIA on the cell cycle distribution remains controversial. Some studies observed that TanIIA could arrest cells at the S/G2 phases [37,38]. After HepG2 cells were intervened with MSN-TanIIA-PEG, the G0/G1 phase cell distribution increased, while the proportion of S and G2/ M phase cells decreased, which remains to be further explored.

Cell Invasion Ability Assay.
To explore the role of TanIIA in the HCC development, the transwell experiment was employed to examine how TanIIA affected the HepG2 cell invasiveness. Similar to the above outcomes, TanIIA showed remarkable suppression of cell invasion. e cell invasion inhibition rate of the free-TanIIA group was 35.95 ± 8.98%, which was higher than MSN-PEG group's 20.17 ± 8.54% (Figure 3(e)). Compared with the free-TanIIA group, the cell invasion inhibition rate in nano-TanIIA groups (MSN-TanIIA: 59.66 ± 5.09% and MSN-TanIIA-PEG: 71.61 ± 2.58%) was significantly increased. As shown in Figure 3(e), HepG2 cells intervened with MSN-TanIIA-PEG exhibited higher cell invasion inhibition rates than other counterparts. ese results indicated that MSN-TanIIA-PEG has the strongest cell invasion inhibition effect on HepG2 cells.
Taken together, our findings suggested that MSN-TanIIA-PEG could suppress HCC cell growth and invasion and promote apoptosis, which may exert a crucial effect on the HCC progression. However, the specific mechanism still needs further verification by molecular biology experiments.

Identification of GPC3-shRNA Plasmid.
e presence of correct clones was identified by sequencing comparison, which implied that the GPC3-shRNA plasmids were constructed successfully (Figure 4(a)).

Binding, Release, and Digestion of MSN-PEG with GPC3-
shRNA Plasmids. Gene therapy targeting GPC3 holds a tremendous potential for HCC treatment, especially the RNAi therapy. e primary difficulty in its clinical application is still the safe and efficient design of delivery carriers. Inspiringly, PEG, a neutral and hydrophilic polymer, has been used widely, which helped lower the cytotoxicity and extend the circulation time. Moreover, there has also been a broad application of positively charged PEI owing to its high DNA condensing and transfection efficiencies [20,39]. e ability of plasmid binding onto MSN-PEG and the capacities

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(a)  of DNA digestion protection and release were identified by gel retardation assays. As seen from electrophoresis image, when plasmids were added at mass ratios (GPC3-shRNA to MSN-PEG) of 1 : 0, 1 : 5, and 1 : 10, a clear band was observable in the corresponding lane. When the mass ratio was 1 : 20, no band could be observed (Figure 4(b)), indicating that GPC3-shRNA plasmids could be completely loaded onto the nanoparticles, so that the optimal binding ratio was 1 : 20. Electrophoresis of release assay revealed that no DNA band was observed at 1, 4, 8, 12, or 24 h. Nevertheless, the brightness of the electrophoretic band increased within 48 and 72 h, and there was no significant difference between the 3rd and the 4th day, indicating that MSN-PEG was capable of protecting the pDNA from degradation and reasonably releasing pDNA under appropriate conditions (Figure 4(c)).
In order to observe the stability of the nanoparticle/ pDNA complex, the DNase-I digestion experiment was performed. After the complex of MSN-PEG/GPC3-shRNA was added with DNase-I enzyme, the brightness of the electrophoretic band remained stable in the first 1 h. On the contrary, after digestion with DNase-I enzyme, the naked pDNA was almost completely digested within 1 min, and no bands could be seen on the electrophoresis lane, verifying that nanoparticles could effectively protect the pDNA from nuclease digestion (Figure 4(d)).

Evaluation of MSN-PEG Gene Transfection Efficiency.
Using MSN-PEG as a carrier, the GPC3-shRNA-EGFP plasmids were transfected into HepG2 cells for the transfection efficiency observation of GPC3-shRNA plasmids under a fluorescence microscope. As the EGFP expression indicated, no obvious difference was observed in transfection efficiency between MSN-PEG and Lipo2000 in the HepG2 cells ( Figure 5(a)). Besides, the transfection efficiency of MSN-PEG was 34.37 ± 1.06% as analyzed by flow cytometry, with no significant difference from the liposome group's 31.78 ± 1.30% ( Figure 5(b)). As suggested by the foregoing findings, MSN-PEG has an encouraging potential as a gene-transferring carrier in gene therapy.
HepG2 cells were transfected with GPC3-shRNA via MSN-PEG for 24 h, and then GPC3 gene expression was examined by qRT-PCR combined with Western blotting. It was found that GPC3 mRNA expression in the untransfected (control) group differed indistinctly from that in the negative control (NC) group, although they were both higher than that in the GPC3-shRNA plasmid-transfected group ( Figure 5(c)). Correspondingly, the expression level of GPC3 protein was reduced after GPC3-shRNA plasmid transfection, as shown in Figure 5(d). is further confirms the successful establishment of GPC3-shRNA plasmids and the workability of using MSN-PEG to transfer target gene in gene therapy. In a word, it offered a new idea of using MSN-PEG as a vector to carry TanIIA and GPC3-shRNA for comprehensive treatment of HCC in clinics.

Conclusion
In this study, MSN-TanIIA-PEG with favorable dispersity and biological characteristics was successfully prepared. e antitumor efficacies of nano-TanIIA on HCC in vitro were greatly improved, which outperformed free-TanIIA in terms of proliferation and invasion inhibition, and apoptosis induction of HCC cells. Capable of releasing TanIIA into carcinoma cells in a sustained manner, this formulation may be an appropriate candidate for pharmacological application. Nonetheless, the specific mechanism still needs to be further explored, and its efficacy and safety deserve more in vivo investigations before clinical trials. Additionally, GPC3-shRNA plasmids were successfully constructed, and MSN-PEG showed an excellent gene transfection efficiency and may thus serve as a carrier for gene therapy. e findings of this study also offer a novel idea for HCC treatment, where MSN-PEG is used as a carrier to combine TanIIA together with GPC3-shRNA.
Data Availability e graphics and quantitative data used to support the findings of this study are included within the article.

Conflicts of Interest
e authors declare that they have no conflicts of interest.