Background
Colon carcinoma is one of the commonly tumors that threaten human beings as its highly morbidity and mortality [
1,
2]. The development of colon carcinoma is a complex process that requires a series of integrated steps including cellular neoplastic transformation, unlimited growth, and the acquisition of invasive/metastatic properties, as well as immunologic escape [
3,
4]. Although extensive investigation explored some important factors of colon carcinoma, the effect of various treatment approaches including surgical operation, chemotherapy and immune cell based therapy remains limited because of the complex process of development of colon carcinoma [
5,
6]. Thus, new strategies are still required for achieving effective treatment of colon carcinoma, which might ultimately aid the clinical therapy for colon carcinoma patients.
MiRNA-21 is an important member of miRNAs, which located on chromosome 17q23-2 overlapping with the TMEM49 gene and is regulated through its promoter containing binding sites for AP-1 and PU.1 transcription factors [
7]. Numbers of researches have been reported on miRNA-21 play a critical role in the development of kinds of tumors via a variety of molecular mechanisms [
8,
9]. To colon carcinoma, recent evidences also suggested that miR-21 as an oncomiRNA molecule played an important regulator role in the development of colon carcinoma including the proliferation, invasion and metastatic potential of cancer cells. For instance, Drusco et al. reported that miRNA-21 might be a potential metastatic signature of colon cancer, and a useful marker distinguishing colon cancer recurrences to lymph nodes from liver, or colon cancer liver metastasis from primary hepatic tumor [
10]. Similarly, Roy et al. found that overexpression of miR-21 could enhance the growth of colon cancer cells in vivo through down-regulation of PTEN [
11]. Nangia-Makker et al. further reported that metformin combined with 5-fluorouracil and oxaliplatin in the treatment of colon carcinoma induced cell apoptosis in chemo-resistant HCT116 cells, which was associated with reduced expression of miRNA-21 [
12]. In addition, Li et al. showed that miRNA-21 might be a useful biological marker which was closely related to the diagnosis and prognosis of colon carcinoma [
7]. These researches indicated the important role of miR-21 in the development and the diagnosis, as well as prognosis of colon carcinoma. However, whether miR-21 may be used as a potential target in the biological therapy against colon carcinoma remains to be further elucidated.
To this aim, in present study, we constructed an eukaryotic expression vector encoding antisense oligonucleotides (ASOs) against miR-21 (termed as p-miR-21-ASO) and assessed its possible effect on the proliferation and migration capacity of human colon carcinoma cells and explored the related mechanism, which might be helpful for the development of miR-21-based therapeutic strategies against clinical colon carcinoma.
Discussion
In present study, we firstly showed that miR-21 ASO could reduce the expression of miR-21 in human colon carcinoma cells. Moreover, miR-21 ASO also could impair the proliferation and colony formation capacity, as well as metastatic potential, of human colon carcinoma cells, which was related to altered expression of PTEN and successive transduction of AKT and ERK pathway. These data suggested that miR-21 might be a potential target for the therapeutic strategy against clinical colon carcinoma.
Accumulating literatures suggested that miR-21 was a critical regulator in the development of a various type of cancers [
22‐
24]. Moreover, miR-21 was also reported as a potential biomarker for diagnosis and prognosis of clinical colon carcinoma [
25,
26]. Recent researches further suggested that antisense oligonucleotides (ASO) against specific miRNA molecules might be a useful strategy for the development of biological therapy in clinical diseases including cancers. Such as, our recent evidence showed that ASO against miR-155, which was highly expressed in lung tissues in acute lung injury (ALI), could enhance the recovery of ALI [
27]. To cancers, Li et al. reported that miR-150 ASO could inhibit proliferation of lung cancer cells by regulating miR-150 expression [
28]. Moreover, Qiang et al. demonstrated that ASO against miR-20a could inhibit the invasion and migration of prostate cancer cells [
29]. In present study, we found that miR-21 ASO could reduce the expression of miR-21 in human colon carcinoma cells. Moreover, the growth and colony formation capacity of colon carcinoma cells also were significantly impaired. Similarly, Li et al. reported that miR-21 ASO could abrogate the expression of miR-21 and reduce the growth of EGFR-TKI-sensitive human lung adenocarcinoma cells [
30]. These data suggested that miR-21 might be a useful target for the development of therapeutic strategy against colon carcinoma. Therefore, successive research work on the effect of miR-21 ASO in the growth of human colon carcinoma cells in vivo was much valuable for the validation of the development of miR-21 targeted based therapeutic strategy against colon carcinoma.
PTEN is a discovered well-known tumor suppressor gene and involved in the regulation of various type of cancers including colon carcinoma [
31‐
33]. For instance, Setia et al. reported that the expression of PTEN was significantly decreased in carcinogenic condition in colon cancer [
34]. Jaqan et al. further showed that overexpression of PTEN could abrogate the dissemination and growth of colon carcinoma cells [
35]. In this study, we found that miR-21 ASO could reverse the expression of PTEN, which was a target of miR-21, accompanied by reduced metastatic potential of colon carcinoma cells. Furthermore, the transduction of AKT and ERK pathway also were altered. Consistently, Setia et al. found that the transduction of AKT and ERK pathway was elevated in colon cancer [
36]. Auyeung et al. further showed that inhibition of AKT and ERK pathway transduction could induce the apoptosis of colon cancer cells [
37,
38]. Most recently, Sun et al. reported that PTEN could reduce the proliferation of colon carcinoma through regulating the transduction of AKT pathway [
39]. In addition, some studies reported that PTEN also could regulate the expression of VEGF, which was important for the carcinogenesis of cancers [
40,
41]. Such as, Tian et al. reported that PTEN could regulate the expression of VEGF through AKT pathway in human hepatoblastoma cells [
18]. Similarly, we also found that miR-21 ASO could reduce the expression of VEGF in colon carcinoma cells. Therefore, combing these data further highlighted the critical role of PTEN pathway in the development of colon carcinoma. Taken together, we presumed that miR-21 ASO could reverse the expression of PTEN and successively alter the transduction of AKT and ERK pathway, accompanied by reduced expression of VEGF. Finally, it should be pointed out that we did not exclude the potential contribution of other target molecules of miR-21, which did not been investigated in present study, to the effect of miR-21 ASO on the proliferation and migration capacity of colon carcinoma cells. In fact, successive research work on these target molecules including PDCD4 [
42], was also important for the elucidation of effect of miR-21 ASO on colon carcinoma cells.
In summary, our study showed miR-21 ASO could effectively reduce the expression of miR-21 and successively impair the proliferation and migration of human colon carcinoma cells, which was closely related to altered expression of PTEN and transduction of AKT and ERK pathway, indicating that miR-21 might be a potential target and be useful for the development of new therapeutic strategy against clinical colon carcinoma.
Methods
Materials
McCoy 5A was purchased from Sigma. T4 DNA ligase was purchased from Fermentas. The pcDNA™6.2-GM/EmGFP-miR, pcDNA™6.2-GM/EmGFP-miR-neg-control plasmid and Lipofectamine 2000 were purchased from Invitrogen. Trizol reagent was purchased from Takara. RevertAid First Strand cDNA Synthesis kits were purchased from Thermo. Antibodies against VEGF, PTEN, AKT, and phospho-AKT were purchased from Abcam. Antibodies against GAPDH, ERK1/2 and phospho-ERK1/2 were purchased from Cell Signaling Technology. Cell counting kit-8 reagent was purchased from Boster. Transwell chambers were purchased from Costar. SYBR® Premix Ex Taq™ II was purchased from Takara. C1000™Thermal Cycler and S1000™Thermal Cycler were purchased from BIO-RAD. Flow cytometry from Beckman Coulter.
Vector construction
Designed antisense oligonucleotides targeting mature miRNA-21 sequence (UAGCUUAUCAGACUGAUGUUGA), sense strand: 5′-TGCTTCAACATCAGTCTGATAAGCTATTTTTG-3′, antisense strand: 5′-CCTGCAAAAATAGCTTATCAGACTGATGTTGA-3′. The pcDNA-6.2-miRNA-21-ASO vector was constructed through annealing synthesized ds oligonucleotides connected to pcDNA™6.2-GM/EmGFP-miR. Plasmid sequences were confirmed by sequencing.
Cell culture and transient transfection
Human colon carcinoma cell lines HCT-116, HT29, SW620 and normal colonic cell line FHC were obtained from National Rodent Laboratory Animal Resource (Shanghai, China). All the cancer cells were cultured in McCoy 5A, RPMI-1640 or Leibovitz’s L-15 medium containing 100 IU/mL penicillin, 100 μg/mL streptomycin, 20 mM glutamine and 10% heat-inactivated fetal bovine serum (FBS). All cells were cultured in a humidified atmosphere of 5% CO2 at 37°C. For transfection, cells were seeded at 70% confluence and 12 h later, cells were transfected with pcDNA-6.2-miRNA-21-ASO vector or pcDNA6.2-miR-neg-control vector with Lipofectamine 2000 according to the manufacturer’s instruction. Cells were harvested after indicated time for following experiments.
Quantitative Real-time PCR for miRNA-21
Total RNA was extracted from cells with Trizol and reverse transcribed using RevertAid First Strand cDNA Synthesis kits according to the manufacturer’s instructions. The resulting complementary DNA (cDNA) was used for real-time PCR using the SYBR® Premix Ex Taq™ II with triplicates. Data collection was performed on the CFX96™ Real-Time System. All calculations were normalized to an endogenous control, GAPDH. The relative quantitation value for the target gene compared to its calibrator is expressed as 2−ΔΔCt. Aliquots of reaction mixture following conditions: initial denaturation at 95°C for 5 min followed by 40 cycles of 95°C for 15 s, 60°C for 30 s.
Cell counting kit-8 assay
HCT116 cells/SW620 cells were seeded in 96-well plates at 1 × 104/well with triplicate and infected with pcDNA-6.2-miRNA-21-ASO (p-miR-21-ASO) or pcDNA6.2-miR-Ctrl (p-Cont). At indicated time points, cells were detected using cell counting kit-8 (CCK-8) assay. 20 µL CCK-8 solution was added into each well. After 3 h of incubation at 37°C. The absorbance was measured with a spectrophotometer at 450 nm with 600 nm as a reference.
Collected infected 72 h HCT116 cells as above described. Cells were trypsinized to single cell suspension and seeded in 6-well plates at 1,000/well for clone forming experiment. Then, the cells were incubated in a humidified atmosphere of 5% CO2 at 37°C. The medium were renewed every 5 days. 13 days later, the colonies were stained with crystal violet and the colony diameter and number was statistically analyzed.
Cell invasion and migration assay
Cell invasion was performed by Matrigel invasion assay. 8-mm pore size-culture inserts were first coated with Matrigel (BD Bioscience). HCT116 cells transfected with p-miR-21-ASO or p-Cont for 48 h were harvested, suspended (5 × 104/well) in 200 µL serum-free medium and then seeded on the upper compartment of chamber. The lower chamber was added 500 µL McCoy 5A media with 10% FBS. After 48 h incubation, the cells in the bottom chamber that had invaded were stained with crystal violet and counted using fluorescence microscopy (100× magnification). In addition, Wound healing assay was also performed for analysis of cell migration in vitro. Cells were cultured as previously described. Then, a single scratch was made in the center of cell monolayer using a 1,000 tip. The scratch areas were visualized under fluorescence microscope with a magnification 100× and the migrated cells were counted. Three independent experiments were performed with triplicate wells.
Western blotting
Cells were lysed with RIPA lysis buffer [1 mM phenylmethylsulfonyl fluoride (PMSF), 1× Protease Inhibitors, 1× Phosphatase Inhibitors] on ice for 30 min. Total cellular proteins were assayed using Bio-Rad protein assay reagent. Equal amounts of protein were subjected to SDS-PAGE electrophoresis, then electrophoretic transfer to nitrocellulose membranes. Membranes were blocked with 5% nonfat dry milk in PBS with 0.1% Tween20 for 1 h at 37°C, Then incubated with antibodies VEGF, PTEN, phosphor-AKT, total AKT, phospho-ERK1/2, and total ERK1/2 at 4°C for overnight. Finally, incubated with horseradish peroxidase-conjugated secondary antibodies for 1 h. Results were analyzed by ECL detection system.
FACS analysis on PTEN expression
Collected infected 72 h HCT116 cells and then fixed with 4% paraformaldehyde for 10 min and then flushing with twice. Cells were blocked with 5% nonfat dry milk in PBS with 0.1% Tween 20, and incubated with antibodies against PTEN for 30 min at 22°C after flushing with twice. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H + L) at 1/500 dilution for 30 min at 22°C. Eventually the stained cells were analyzed by a flow cytometer.
Statistical analysis
All values were represented as the mean ± SD from at least three independent experiments. Student’s T-test for two groups or one-way analysis of variance (ANOVA) for three or more groups were performed to evaluate the statistical significance by using GraphPad Prism 5 software. P values less than 0.05 were considered statistically significant.
Authors’ contributions
LX and YT were participated in the overall study design and performed the experimental procedures and data analyses. YZ, WZ and JZ were contributions to experimental procedures. MG, YZ, NQ and JZ were contributions to data analyses and statistical analyses. YT participated in literature research and part manuscript editing, and LX finished the manuscript. LX served as the principal investigator. All authors read and approved the final manuscript.