miR‑21 inhibitor facilitates the anticancer activity of doxorubicin loaded nanometer in melanoma
- Authors:
- Published online on: May 22, 2019 https://doi.org/10.3892/or.2019.7167
- Pages: 414-424
Abstract
Introduction
Cancer is the second most common cause of mortality in the United States, and the incidence rate is still increasing (1). Chemotherapy is still the most common treatment among the four major cancer therapy types: Surgical treatment, radiotherapy, chemotherapy and biological therapy (2). The majority of the approaches currently used involve interference in nucleic acid metabolism and DNA repair (3). Currently, there are >70 types of anti-tumor drugs commonly used in the clinic, and >400 new anti-tumor drugs have entered clinical trials (4). However, the majority of drugs fail due to their lack of specificity for tumor cells.
Targeted therapy is a way of targeting tumor cells with drugs and other active substances that kill tumor cells without affecting the function of normal tissues and cells (5). Subsequently, the curative effect is improved and side effects are relatively reduced based upon the application of target therapy. The targeted drug delivery uses a novel nano drug delivery system, which increases the selectivity of the drug to the target focus, thus increasing the drug concentration in the tumor tissue (6,7). Current, the drug delivery systems mainlyact by targeting an antigen or antibody on the surface of tumor cells (8,9). Doxorubicin is one of the common chemotherapeutic agents used to treat liver cancer (10). However, it has dose limitations due to its poor bioavailability, hydrophobicity and cytotoxicity. The cyclin-(RGDyk)[c(RGDyK)] peptide functionalized nanomicellar system can overcome the drawbacks of low transport of chemotherapeutics across the blood-tumor barrier (BTB) in multidrug-resistant cancer cells (11). The anti-tumor efficacy of chemotherapeutic agents was significantly facilitated with the assistance of the c(RGDyK) drug delivery system (12,13). However, the therapeutic effects of doxorubicin assisted by c(RGDyK)-modified liposomes on melanoma growth and the underlying mechanisms are largely unknown.
MicroRNAs (miRs) can act as oncogenes or tumor suppressor genes during cancer development (14,15). miRs regulate multiple signaling pathways and change the expression of mRNAs (16,17). miR-21 was reported to be upregulated in the tissues and cells of various solid tumors, including glioma, colon cancer, gastric cancer and melanoma tissue (18). Overexpression of miR-21 in glioma cells can inhibit apoptosis and miR-21 may have an oncogenic function (19). miR-21 is a potential therapeutic target for various types of cancer, particularly melanoma (18). Therefore, a miR-21 inhibitor could potentially facilitate the antitumor effect of a targeted therapy. In this study, cellular and animal models were used to explore the effect of doxorubicin capsuled in 4c[RGDyk]-L-[CD] nanoparticle and miR-21 inhibitor on melanoma cells, and to assess its associated mechanisms. This study may provide an experimental basis for the treatment of melanoma.
Materials and methods
Preparation of doxorubicin-loaded nanometer
Doxorubicin was obtained from Beijing Huafeng United Technology Co., Ltd. (Beijing, China). c(RGDyK) (molecular weight, 619.51) was synthesized by GL Biochem Ltd. (Shanghai, China). Liposomes loaded with doxorubicin and c(RGDyK)-L-[CD] were prepared in our lab using the method described previously (20). Doxorubicin (1 ml) diluted in PBS was added into a dialysis bag. After 48 h, the dialysis bag was cut and 2 ml 10% Triton X-100 was added to destroy all the liposomes. The final concentration of doxorubicin was 20 mg/ml.
Cell culture
Melanoma cell line B16F10 was purchased from Shanghai Cell Bank of Chinese Academy of Sciences and cultured in Dulbecco's modified Eagles medium (DMEM; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; HyClone; GE Healthcare Life Sciences, Logan, UT, USA) and 100 U/ml penicillin-streptomycin (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) in 5% CO2 at 37°C. When the cell confluence reached 90%, the culture medium was discarded and cells were washed twice with PBS and passaged following trypsin digestion.
miR-21 inhibitor transfection
At a density of 50–70 %, B16F10 cells (3×103 cells) were transfected with vector (miR-21 scrambled control) or inhibitor (1 µl) using Lipofectamine™ 2000 (Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions for 6 h. The miR-21 inhibitor and miR-21 negative control (NC) inhibitor were synthesized by Sangon Biotech Co., Ltd. (Shanghai, China). Cells were then cultured in DMEM containing 10% FBS for another 72 h. The sequences of miR-21 inhibitor and vector were 5′-UCAACAUCAGUCUGAUAAGCUA-3′ and 5′-UCUACUCUUUCUAGGAGGUUGUGA-3′.
MTT assay
The effects of doxorubicin-loaded nanometer (DLN) on melanoma cell growth were evaluated by MTT assay. The cells were treated with different concentrations of DLN (0–20 µl) for 24–72 h. To investigate the anti-tumor effects of association application of DLN with miR-21 inhibitor, the experiments were divided into five groups: Control group, vector (miR-21 inhibitor NC) group, DLN group, miR-21 inhibitor group, and miR-21 inhibitor + DLN group. Following the indicated treatments, an MTT assay was applied to evaluate cell proliferation. DMSO (100 µl) was added to each well to dissolve the formazan. The optical density was determined via microplate reader (BioTek Instruments, Inc., Winooski, VT, USA) at 570 nm and represented cell viability.
Transwell assay
B16F10 cells in the logarithmic growth phase were cultured in serum-free medium for 24 h. The medium was discarded and the cells were digested using trypsin. The cells underwent washing, centrifugation and resuspension in a low serum DMEM medium (containing 0.2% FBS) to form a single cell suspension with a density of 5×105/ml. The cells in different groups were treated for 48 h. Subsequently, the cells were collected and suspended cells (100 µl; 1×106/ml) were added into each Transwell chamber. DMEM/F12 (600 µl) containing 10% FBS was added into each well in a 24-well plate. The prepared Transwell chambers were placed in the 24-well plate for 20 h at 37°C and 5% CO2. Cells in the lower chamber were fixed in 4% paraformaldehyde for 30 min at room temperature and stained with 3% crystal violet for 5 min at room temperature. Four fields in the upper and lower, left and right positions were selected for counting in each well. The experiment was repeated for three times and mean value was calculated.
Cell migration
B16F10 cells (3×105) were seeded in 6-well plates and treated with the indicated drugs for 72 h. After that, the cells were collected and suspended cells (100 µl; 1×106/ml) were incubated in the plates for 24 h. A line was drawn across the center of the wells. After incubation in CO2 incubator at 37°C, the images were captured under a light microscope. The migration speed was calculated based on the formula: Cell mobility (µm/h)=[width(1)-width(2)]/72 h. Width(1) and width(2) represented the width measured at 0 and 72 h, respectively.
Flow cytometry
B16F10 cells (3×105) were seeded in 6-well plates and treated with indicated drugs for 72 h. The cells were collected following trypsin digestion. The cells were incubated with Annexin V-fluorescein isothiocyanate (0.5 µl) and propidium iodide (PI; 0.5 µl; cat. no. C1062; Beyotime Institute of Biotechnology, Haimen, China) for 30 min in the dark. Subsequently, apoptosis was detected by flow cytometry (BD Biosciences, San Jose, CA, USA) and data were analyzed using FlowJo 10 (FlowJo LLC, Ashland, OR, USA). Following transfection for 72 h, the cells were collected for PI staining (0.5 µl/ml) and the cell cycle distribution was assessed by flow cytometry (BD Biosciences) within 1 h of staining.
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
B16F10 cells (3×105) were seeded in 6-well plates and treated with indicated drugs for 72 h. RNA in different groups was extracted using a TRIzol (Thermo Fisher Scientific, Inc.). Subsequently, RNA was transcribed into cDNA according to the instructions of a Reverse Transcription Kit (Takara Biotechnology Co., Ltd., Dalian, China). Fluorescence qPCR was utilized to detect the expression level of the target RNAs using cDNA as the template following the instruction of Platinum™ II Taq Hot-Start DNA Polymerase (cat. no. 14966005; Thermo Fisher Scientific, Inc.). SYBR-Green (cat. no. HY-K0501; MedChemExpress, Monmouth Junction, NJ, USA) was used as fluorophore and the thermocycling conditions were as follows: Initial denaturation at 95°C for 10 min, followed by 40 cycles of a two-step PCR at 95°C for 15 sec and 60°C for 1 min. The expression of miR-21 was normalized to U6. The expression of BCL-2, Bax and P53 was normalized to GAPDH. The primers are listed in Table I. The 2−ΔΔCq method was used to quantify the results as previously described (21).
Western blot
B16F10 cells (3×105) were seeded in 6-well plates and treated with indicated drugs for 72 h. Protein was extracted from the treated cells using a protein isolation kit (cat. no. 28-9425-44, GE Healthcare Life Sciences). Protein levels were quantified with a bicinchoninic acid protein assay kit. Protein (25 µg/lane) was separated via SDS-PAGE on 12% gels and transferred onto nitrocellulose membranes. The membranes were blocked in 5% skim milk for 2 h at room temperature. The antibodies against BCL-2 (cat. no. ab32124; Abcam, Cambridge, MA, USA; 1:1,000), Bax (cat. no. ab32503; Abcam; 1:2,000), P53 (cat. no. A11212; ABclonal Biotech Co., Ltd., Woburn, MA, USA; 1:1,000) and GAPDH (cat. no. AC033; ABclonal Biotech Co., Ltd.; 1:1,000) were incubated overnight at 4°C. After washing, the membranes were incubated with the secondary antibody (horseradish peroxidase-labeled goat anti-rabbit IgG; 1:100; cat. no. ab131368; Abcam) for 2 h at room temperature. Enhanced chemiluminescence kit (cat. no. RPN2133; GE Healthcare Life Sciences) was added to the membrane and visualized using a gel imaging system (Bio-Rad Laboratories, Inc., Hercules, CA, USA).
Establishment of in vivo tumor model
All animal experiments were approved by the Ethics Committee of Jiangxi Tumor Hospital (approval no. 20170312). Female Balb/c nude mice (6-week old; 20 g) were purchased from Hunan SLAC Experimental Animal Co. Ltd. (SCXK2016-0002) and housed in a specific pathogen-free condition that was automatically maintained at a temperature of 23±2°C, a relative humidity of 45–65 %, and with a controlled 12 h light /dark cycle. The mice implanted with the tumor cell lines were randomly divided into six groups (n=5 in each group): Control group, doxorubicin group, DLN group, miR-21 inhibitor group, miR-21 inhibitor + doxorubicin group and miR-21 inhibitor + DLN group. B16F10 cells in the logarithmic growth phase (1×107) were diluted in 0.2 ml PBS and injected (subcutaneous injection) into the Balb/c nude mice. Doxorubicin, DLN and miR-21 inhibitor group were administered for 10 consecutive days, following attainment of a tumor size of 50 mm3. In the miR-21 group, each mouse received miR-21 inhibitor [intraperitoneal injection (i.p.), 20 µl]. In the miR-21 inhibitor + doxorubicin group, each mouse received 20 µl (1 µg/µl) miR-21 inhibitor (i.p.) and 20 µl doxorubicin (5 mg/kg). In the miR-21 inhibitor + DLN group, each mouse received 20 µl miR-21 inhibitor (i.p.) and 20 µl DLN (5 mg/kg). General conditions of the mice were monitored daily and the tumor size was measured every 2 days. Following 10 days of drug administration, the mice were anesthetized using isoflurane and decapitated, and the whole tumor was removed. The tumor specimens were fixed in 4% paraformaldehyde in PBS (pH 7.4) at 4°C overnight and then embedded in paraffin for tissue sectioning. The tissues were sectioned into 5 µm-thick sections. Subsequently, the slides were stained with hematoxylin (3%) and eosin (3%) for 5 min at room temperature. The images were captured under light microscopy.
Statistical analysis
The data were presented as the mean + standard deviation and analyzed using SPSS 17.0 (SPSS, Inc., Chicago, IL, USA). Statistical significance was determined by one-way analysis of variance with Newman-Keuls as the post-hoc test. P<0.05 was considered to indicate a statistically significant difference.
Results
DLN inhibits cell growth of B16F10 cells
Initially, we detected the effects of 5 µl DLN on cell growth of B16F10 cells. As shown in Fig. 1A, DLN inhibits the cell growth in a time-dependent manner (0–72 h). Significant difference was observed at the 48 and 72 h time points compared with the 0 h control (P<0.05). As shown in Fig. 1B, 5 µl DLN (5 mg/ml) the optimal effects on cell growth were observed after 72 h treatment. Therefore, 5 µl DLN was selected to treat the cells for 72 h in the subsequent experiments.
miR-21 inhibitor reduces miR-21 expression
miR-21 expression was confirmed by RT-qPCR. As shown in Fig. 2, miR-21 inhibitor significantly reduced miR-21 expression (P<0.05), while control miR-21 inhibitor NC did not affect miR-21 expression.
miR-21 inhibitor facilitates the anti-migration effect of DLN
As shown in Fig. 3, DLN significantly inhibited the migration of melanoma cells (P<0.05). miR-21 inhibitor also significantly inhibited cell migration compared with control (P<0.05). Combined application of DLN and miR-21 inhibitor further inhibited cell migration compared with single application of DLN and miR-21 inhibitor.
miR-21 inhibitor facilitates the anti-invasion effect of DLN
As shown in Fig. 4, DLN significantly inhibited invasion of melanoma cells at the concentration of 5 µl (P<0.05). miR-21 inhibitor also significantly inhibited cell invasion (P<0.05). Results demonstrated that DLN and miR-21 inhibitor combination further inhibited cell invasion compared with DLN or miR-21 inhibitor alone.
miR-21 inhibitor promotes cell cycle arrest following DLN treatment
As shown in Fig. 5, miR-21 inhibitor and DLN increased the number of cells at G1 phase, and decreased the number of cells at S phase (P<0.05). miR-21 inhibitor further increased cell cycle arrest ability of DLN when combined treatment was performed.
miR-21 inhibitor facilitates the apoptosis induced by DLN
As shown in Fig. 6, DLN induced apoptosis of melanoma cells at a concentration of 5 µl (P<0.05). miR-21 inhibitor also induced apoptosis of melanoma cells (P<0.05). The co-application of miR-21 inhibitor and DLN produced a further increase in apoptosis compared with single application of DLN and miR-21 inhibitor.
miR-21 inhibitor promotes the effects of DLN on BCL-2, P53 and Bax
miR-21 and apoptosis-related gene expression were also detected. As shown in Fig. 7A, miR-21 expression in miR-21 inhibitor group and miR-21 inhibitor + DLN group was significantly reduced compared with control (P<0.05). By contrast, DLN treatment alone did not affect miR-21 expression. BCL-2 mRNA expression was downregulated by miR-21 inhibitor or DLN treatment (P<0.05). Additionally, the associated application of miR-21 inhibitor with DLN further reduced BCL-2 expression. Bax mRNA expression was upregulated by miR-21 inhibitor or DLN treatment (P<0.05). Furthermore, the associated application of miR-21 inhibitor with DLN further promoted Bax expression. P53 mRNA expression was upregulated by miR-21 inhibitor or DLN treatment (P<0.05), and the combined application of miR-21 inhibitor with DLN further promoted P53 expression. The protein expression of BCL-2, Bax and P53 was confirmed by western blotting, with a similar trend observed in different groups as the mRNA expression (Fig. 7B and C).
miR-21 inhibitor facilitates the anti-tumor effects of DLN in vivo
Mouse body temperature and behaviors were monitored each day. In the present study, the mice displayed normal wellbeing and all animals presented with a single subcutaneous tumor in the forelimb armpit and the longest diameter was <10 mm. Furthermore, no ulceration or abrasion of tumor surface was observed. The maximum tumor burden was observed in the control group (~8% of the body weight). As shown in Fig. 8, tumor weight in the doxorubicin, DLN, miR-21 inhibitor groups were significantly reduced compared with control (P<0.05). The combined treatment of miR-21 inhibitor with DLN further inhibited tumor growth compared with individual of miR-21 inhibitor or DLN treatment. As shown in Fig. 9, the tumor tissue in control group was rich in blood vessels. The tumor cells were arranged closely and the size was relatively consistent. Tumor cells in the doxorubicin group were loosely arranged, and tumor cells in the DLN group were significantly enlarged. Tumor cells in miR-21 inhibitor group exhibited vacuoles and necrosis. More tumor cells in miR-21 inhibitor + doxorubicin group exhibited necrosis. In addition, tumor cells in miR-21 inhibitor + DLN group were loosely arranged.
Discussion
In this study, in vitro cellular and animal models were used to explore the effect of DLN combined with miR-21 inhibitor on melanoma tumor cells. Our data revealed that DLN had stronger anticancer effects compared with direct application of doxorubicin. From a mechanistic perspective, DLN did not affect miR-21 expression to exert its antitumor effects, which was facilitated by miR-21 inhibitor. These data provided novel idea for the application of DLN in melanoma treatment.
Melanoma is a skin cancer caused by the dedifferentiation of melanocytes (22). Melanoma is characterized by strong immune escape ability (23). Currently, the treatment of melanoma is typically early surgery, followed by chemotherapy combined with biological therapy. As malignant tumor is caused by unlimited proliferation and abnormal differentiation (24), the available treatments involve stimulating differentiation and apoptosis. However, traditional chemotherapeutic drugs still have various problems. The most prominent is that chemotherapy drugs not only kill tumor cells, but also selectively damage normal cells, particularly hematopoietic tissue and cells (25). The C[RGDyk]-modified liposome targeted delivery system is one of the common active tumor-targeting drug delivery systems (26). This system improves therapeutic efficacy in bone metastasis from breast cancer (27) and glioblastoma (28). In this study, the anticancer effect of DLN in melanoma was investigated.
MTT assay was used to determine the appropriate concentration and appropriate time for the administration of the drug delivery system, which provided the basis for the following experiments. Based upon the data, 5 µl DLN (5 mg/ml) was selected and the cells were treated for 72 h. In the current study, the effect of 10 µl DLN on cell proliferation was not observable. Although the reasons were not identified, high concentrations of C[RGDyk]-modified liposome may affect the bioavailability of doxorubicin. These data receive more attention in a future study. miR-21 is a potential therapeutic target in melanoma (18,29,30). In this present study, miR-21 inhibitor was applied in melanoma cells. The results confirmed that the miR-21 inhibitor significantly reduced the expression of miR-21 in melanoma cells. More importantly, miR-21 inhibitor further promoted the anti-tumor effects of DLN, including inhibiting cell proliferation, invasion and migration, and promoting apoptosis of melanoma cells. In this study, the reduced proliferation following treatment with DLN may affect the cell invasion and migration results. Therefore, we resuspended the cells after treatments and similar numbers of cells in different groups were used in the analysis of cell migration and invasion, which may alleviate the bias of migration and invasion caused by reduced cell proliferation.
Invasive melanomas are characterized by the growth of melanocyte nests, which are surrounded by interstitial matrix and various types of stromal and immune cells. The surrounding tissue is typically matrix rich (31). Integrins are heterodimeric, transmembrane receptors that function as mechanosensors, adhesion molecules and signal transduction platforms in a multitude of biological processes, particularly in tumorigenesis (32). Self-aggregated pegylated poly-nanoparticles were tagged with c(RGDyK) peptide for targeted doxorubicin delivery to integrin-rich tumors (33). This may relieve the side effects of chemotherapeutics on normal organs. Although the cytotoxicity of DLN was not investigated in the current study, several studies have already verified the safety of DLN (34,35).
The data of the current study demonstrated that DLN may promote melanoma cell apoptosis and affect cell cycle, thus arresting cells at G1 phase and affecting cell proliferation. Although miR-21 inhibitor also demonstrated anti-cancer effect in melanoma, the co-application of DLN may further promote the effect. miR-21 can regulate multiple signaling pathways and change the expression of tumor-associated protein-coding mRNAs (36). Notably, DLN treatment did not cause a reduction of miR-21, which indicated that the effect of DLN was independent of miR-21. However, additional miR-21 inhibition promoted the anti-cancer effect of DLN.
BCL-2 is a cell-survival factor, while Bax is the most important apoptosis-associated factor. Bax protein can form heteromeric two polymers with BCL-2 (37). The ratio of Bax/BCL-2 is the key factor determining apoptosis (38). P53 can increase the expression of Bax and downregulate the expression of BCL-2 to promote apoptosis (39). P53 can also modulate apoptosis through the death receptor pathway (40). The current study demonstrated that miR-21 inhibitor aggravated the effect of DLN on the expression of BCL-2, Bax and P53. These results suggest that the induced apoptosis may be associated changes in the expression of these genes.
In order to further investigate the effect of DLN and miR-21 inhibitor on tumor growth, a tumor formation assay in nude mice was performed. The results revealed that DLN was more effective in inhibiting tumor development than doxorubicin. Based on previous publications (12,41,42), DLN may have high bioavailability, hydrophobicity and cytotoxicity in tumor cells. miR-21 inhibitor facilitates the anti-cancer activity of DLN in melanoma in vivo as demonstrated by the reduced tumor growth and the morphological changes. However, further experiments are essential for the verification of the mechanisms in vivo.
There were other limitations in this study. The mechanisms associated with the anti-tumor effects of miR-21 inhibitor and DLN require further investigation, although apoptosis may partially explain the effects. Additionally, only one dose of DLN was used in the study. More doses of DLN combined with miR-21 inhibitor should be delivered to further clarify the efficacy. For potential future clinical use, the toxicity of combination of DLN with miR-21 inhibitor in normal cells should also be evaluated.
In conclusion, miR-21 inhibitor promoted the anti-cancer effects of DLN in melanoma cells. Furthermore, the data revealed that the anti-cancer effect of DLN is miR-21-independent, and involves BCL-2, Bax and P53 expression. This study may provide an alternative treatment for melanoma.
Acknowledgements
Not applicable.
Funding
This research was supported by the Key R&D project in Jiangxi Province (grant no. 20161ACG70016).
Availability of data and materials
The datasets used during the present study are available from the corresponding author upon reasonable request.
Author's contributions
XW and CZ conceived and designed the experiments; XW, XY and JZ performed the experiments and analyzed the data; XW and CZ wrote the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All experimental protocols were approved by the Ethics Committee of Ethics Committee of Jiangxi Tumor Hospital (no. 20170312).
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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