Background
Endometrial carcinoma (EC) is one of the most common gynecologic malignancies and it is totally classified into two subtypes referred to as type I and type II EC [
1]. Type I EC, occurring in ~85% of patients, often displays ER positive. Tumors with this type tend to be well differentiated, of low grade and good prognosis. In contrast, type II, consisting mostly of serous and clear cell carcinoma, typically arises in atrophic endometrium via a mechanism unrelated to estrogen exposure. This type is usually ER negative, and poorly differentiated, of high grade and poor prognosis. Although type II ECs account for approximately 15% of cases, they are responsible for about 50% of all relapses [
2]. Great progress was made in the therapies of type II EC, but its 5-year survival rate is still less than 15%. Molecular mechanisms explaining the development and progression of type II EC are still unknown.
MicroRNAs are ~22 nucleotide (nt) non-coding RNAs that function as sequence-specific regulators of gene expression through translational repression and/or transcript cleavage [
3‐
6]. Since the roles and functions of endogenously expressed microRNAs were first described in
C. elegans in 1993 [
7], more and more studies have shown that microRNAs play key roles in cellular processes of differentiation, proliferation, apoptosis and metabolic homeostasis. MicroRNAs profiles have shown that there was much microRNAs expression variation across the different subtypes and stages of carcinogenesis, with data indicating that they may play vital roles in the initiation and progression of human malignancies [
8,
9]. In cancer tissues, microRNAs appear to be dysregulated such that those with tumor-suppressor activity are abrogated, while those that are overexpressed may function as oncogenes promoting proliferation, migration and invasion, and repressing apoptosis respectively. Recent data showed that overexpression or lack of expression of certain specific microRNAs were correlated to metastatic and aggressive clinical phenotypes [
10‐
12]. It was demonstrated that miR-125b was dysregulated in many tumors such as prostate cancer [
13], leukemia [
14,
15] liver cancer [
16], and oligodendroglial tumors [
17]. In addition, miR-125b has been demonstrated to mediate the proliferative effects through down-regulating p53 [
18], pro-apoptotic Bcl-2 antagonist killer 1 (Bak1) [
19], and Bcl-2 modifying factor (Bmf) [
20]. It has also been proved to be one of etiologic factors of leukemia [
21]. Taken together, these observations suggest that miR-125b may play a vital role in the initiation and progression of cancers.
In our previous work, we chose well-differentiated EC cells (ishikawa, RL95-2) with ER positive and metastatic EC cells (KLE, AN3CA) with ER negative as models of type I and type II EC, respectively. Using microRNAs microarray, we found that miR-125b was significantly overexpressed in ER-negative cells, especially in AN3CA cells, when compared with ER-positive cells. Although recent studies have shown the important role of miR-125b in several tumors and overexpression of miR-125b in advanced ECs [
22], its function in this disease has not yet been defined. The findings promoted us to hypothesize that miR-125b may contribute to malignancy of type II EC. In the present study, we confirmed the result of microRNAs microarray, and further investigated the functions of miR-125b in EC and found new downstream targets of miR-125b.
Methods
Reagents
Four synthetic, chemically modified short single- or double-stranded RNA oligonucleotides: miR-125b mimics (miR-125bm), miR-125b mimics negative control (miR-125bm NC), miR-125b inhibitors (miR-125bi) and miR-125b inhibitors negative control (miR-125bi NC) were synthesized from Shanghai GenePharma Co., Ltd. Commercial miR-125b expression plasmid and control vector were purchased from Shanghai GeneChem Co., Ltd.
Cell culture and transfection
Ishikawa, RL95-2, KLE, and AN3CA cells were obtained from American Type Culture Collection (ATCC, Manassas, Va) and were maintained DMEM/F12 media (11030; Gibco, Auckland, NZ) supplemented with 10% FBS (S1810; Biowest, Nuaillé, France), 100 units/ml penicillin, and 100 μg/ml streptomycin. All cells were grown in sterile conditions at 37°C in a humidified atmosphere of 5% CO2 and 95% air. Before the experiment, the ER expressions of these cells were confirmed by immunocytochemistry. Cells were seeded in 6-well plates at 70-80% confluence and grown overnight before transfection. Transfection of AN3CA cells (or ishikawa cells) with miR-125bi (or miR-125bm) or counterpart negative control using the lipfectamine2000 transfection reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. The total experiments were classified into three groups, which were miR-125bm (or miR-125bi) group, miR-125bm NC (or miR-125bi NC) group, and untransfected group.
RNA isolation and qRT- PCR
Total RNA was isolated from cultured cells with Tri-reagent (TR118; Molecular Research Center, Cincinnati, OH, USA) according to manufacturer's instructions. QRT-PCR analyses for microRNAs were performed using TaqMan microRNA assays. In brief, all reagents and primers were obtained from Applied Biosystems. U6 snRNA served as an endogenous control for normalization. Reverse transcriptase reactions and real-time PCR were performed according to the manufacturer's protocols. CDNA was made from 50 ng total RNA from each sample using the microRNA TaqMan Reverse Transcription Kit and miR-125b specific reverse transcription primer. QRT-PCR reactions were performed in triplicate on a RealPlex4 real-time PCR detection system from Eppendorf Co. LTD (Germany), with cycle threshold values determined using the manufacturer's software. Relative expression of miR-125b, relative to U6 snRNA, was calculated using the 2-delta delta CT method.
Northern blotting analysis
All steps of Northern blotting were performed as previously described [
20]. For all groups, 20 μg of good quality total RNA was subjected to electrophoresis on a 15% Urea-PAGE gel, and transferred to a Hybond N+ nylonmembrane (Amersham, Freiburg, Germany). After being UV-cross-linked and baked at 50°C for 30 min, the membrane was prehybridized at 42°C for 4 h and then hybridized with the miR-125b anti-sense StarFire probe, 5'-TCACAAGTTAGGGTCTCAGGGA-3' (IDT, Coralville, IA), to detect the 22-nt miRNA-125b fragments according to the instruction of the manufacturer. After washing, membranes were exposed for 20 ~ 40 h to Kodak XAR-5 films (Sigma-Aldrich). As a positive control, all membranes were hybridized with a human U6 snRNA probe, 5'-GCAGGGGCCATGCTAATCTTCTCTGTATCG-3'. Exposure times for the U6 control probe varied from 15-30 min.
SiRNA targeting
To inhibit expression of endogenous TP53INP1, we designed and prepared HPLC- purified TP53INP1 siRNA (sense: 5'-TCAGCCTCTGGAACAT-3'; anti-sense: 5'-ATGTTCCAGAGGCTGA-3') and, a scrambled siRNA with no homology to any known human mRNA was used as negative control (sense: 5'-CTGTTAAAAATCCAGG-3'; anti-sense: 5'-CCTGGATTTTTAACAG-3') according to the sequence of the TP53INP1 gene. SiRNA oligonucleotide duplexes were synthesized by Genephama Biotech (Shanghai, China).
Cell proliferation assay
Cells at 12 h post-transfection were seeded in 96-well plates at 2500 cells/well. After that, cell proliferation was evaluated using the CCK8 (C0038, Beyotime Inst Biotech, China) according to manufacturer's instructions. Briefly, 10 μl of CCK8 solution was added to the culture medium, and incubated for additional 3 h. The absorbance was determined at 450 nm wavelength with a reference wavelength of 630 nm.
Wound healing assay
Cells (6 × 106 per well) at 12 h post-transfection were seeded in six-well plates and allowed to adhere for 24 h. Confluent monolayer cells were scratched by a 200 μl pipette tip and then washed three times with 1 × PBS to clear cell debris and suspension cells. Fresh serum-free medium was added, and the cells were allowed to close the wound for 48 h. Photographs were taken at 0, 24, and 48 h at the same position of the wound.
Transwell migration assay
Cells (2 × 105) were resuspended in 200 μl of serum-free medium and seeded on the top chamber of the 8 μm pore, 6.5 mm polycarbonate transwell filters (Corning). The full medium (600 μl) containing 10% FBS was added to the bottom chamber. The cells were allowed to migrate for 24 h at 37°C in a humidified incubator with 5% CO2. The cells attached to the lower surface of membrane were fixed in 4% paraformaldehyde at room temperature for 30 min and stained with 4,6-diamidino-2-phenylindole (DAPI) (C1002, Beyotime Inst Biotech, China), and the number of cells on the lower surface of the filters was counted under the microscope. A total of 5 fields were counted for each transwell filter.
Western blotting analysis
Total proteins extracts of each group cells were resolved by 10% SDS-PAGE and transferred on PVDF (Millipore) membranes. After blocking, the PVDF membranes were washed 4 times for 15 min with TBST at room temperature and incubated with primary antibody (rabbit anti-human TP53INP1 polyclonal antibody; 1:1000, ab9775, Abcam). Following extensive washing, membranes were incubated with secondary peroxidase-linked goat anti-rabbit IgG (1:1000, sc2030, Santa Cruz) for 1 h. After washing 4 times for 15 min with TBST at room temperature once more, the immunoreactivity was visualized by enhanced chemiluminescence (ECL kit, Pierce Biotechnology), and membranes were exposed to Kodak XAR-5 films (Sigma-Aldrich).
Construction of reporter plasmids and luciferase assay
To construct a reporter plasmid containing the 3'UTR of TP53INP1, 480 bp DNA fragment of partial 3'UTR of TP53INP1 containing the wild-type 3'UTR of TP53INP1 or mutant 3'UTR of TP53INP1 was chemically synthesized and cloned into the pMIR-REPORT luciferase vector (Ambion) downstream of the luciferase gene and named pMIR-TP53INP1-3'UTR-WT and pMIR-TP53INP1-3'UTR-MT, respectively. The nucleotide sequences of the constructed plasmids were confirmed by DNA sequencing analysis. All steps of luciferase reporter assay were according to the previously described [
13,
23]. NIH-3T3 cells(1 × 10
5) were seeded into 24-well plates, and each was transfected with 0.5 μg of either pMIR-TP53INP1-3'UTR-WT vector or pMIR-TP53INP1-3'UTR-MT vector containing Firefly luciferase, together with 0.2 μg of the pRL-TK vector (Promega) containing Renilla luciferase and 50nM miR-125bm, miR-125bm NC or none using the Lipofectamine2000 transfection reagent according to the manufacturer's protocol. After 48 h transfection, luciferase activity was measured using the dual luciferase reporter assay system (Promega). The results were expressed as relative luciferase activity (Firely LUC/Renilla LUC).
Tumorigenicity assays in nude mice
All experimental protocols were approved by the Ethic Committee for Animal Experimentation of Shanghai Jiaotong University. A total of 5 × 106 cells suspended in 100 μl 1× PBS were injected into the bilateral hind leg subcutaneous tissue of four-week old female BALB/C athymic nude mice. Three groups of mice (n = 12) were tested. MiR-125b plasmid group was injected with ishikawa cells transfected with miR-125b expression plasmid. Control vector group was injected with ishikawa cells transfected with negative control plasmid. During a five-week follow-up period, the sizes of tumors were measured weekly. Mice were sacrificed at 42 days post-injection. Tumors were excised and measured. The short and long diameters of the tumors were measured using a caliper and tumor volumes (cm3) were calculated by using the following standard formula: tumor volumes (cm3) = (the longest diameter) × ( the shortest diameter)2 × 0.5.
Immunohistochemistry
Tissues were fixed in 4% paraformaldehyde and embedded in paraffin blocks. Sections (4 μm) were used for immunohistochemical examination. Ki67 protein expression of tumor tissues were detected using standard avidin-biotin immunohistochemical techniques with use of an anti-ki67 antibody (1:100, lab vision, Fremont, USA) according to the manufacturer's instructions. The labeled cell nuclei in tumor sections were regarded as positive. Proliferative tumor cells were counted in 10 randomly different microscopic fields respectively. The proliferative index was calculated as follows: (number of positive tumor cells/number of total tumor cells) × 100%.
Statistical analysis
Each experiment was performed as least three times, and data are shown as the mean ± SD where applicable, and differences were evaluated using one-way ANOVA for 3-group comparisons and t tests for 2-group comparisons. All statistical analyses were performed using SPSS 13.0 software package. The probability of P < 0.05 was considered to be statistically significant.
Discussion
Overexpression of miR-125b has been observed in many cancers such as prostate cancer [
13], pancreatic cancer [
24], and oligodendroglial tumors [
17]. Furthermore, miR-125b plays a vital role in promoting the development of precursor B-cell acute lymphoblastic leukemia and prostate cancer [
13,
25]. These reports suggested that miR-125b might be associated with tumorigenesis of other types of human tumors. Consistent with these published findings, our results support the concept that miR-125b may act as an oncogene in type II EC. One recent publication was about a comprehensive analysis of the miRNA profile of surgically staged early and advanced endometrial cancer using archival primary ECs tissue samples, and found that expression of miR-125b-1 and miR-125b-2 in stages III and IV ECs was 3.655 and 3.89 fold of stage I endometrioid ECs, respectively[
22]. Stages III and IV ECs mostly consist of type II endometrial carcinomas including papillary serous carcinoma and clear cell carcinomas. Previous profiles of microRNAs were totally obtained from microRNAs microarray of archived EC tissue samples, and there was a disadvantage that the findings might be interfered with mesenchymal cells and other non EC components. To solve the problem, we are first, to our knowledge, to choose well-differentiated EC cells with ER positive and metastatic EC cells with ER negative as models of type I and type II EC, respectively. Using microRNAs microarray, we found that miR-125b was significantly overexpressed in type II EC cells with ER negative. Moreover, qRT-PCR was further performed to demonstrate the results of microRNAs microarray. Besides, in our preresearches, we detected endogenous TP53INP1 expression on the archival paraffin-embedded EC specimens of between type I (endometrioid) and type II (papillary serous) patients (each 10 cases) by immunohistochemistry and found that TP53INP1 was expressed in 8/10 type I EC and 1/10 type II EC (unpublished data). Meanwhile, we selected significantly up-regulated miRNAs (n = 6, miR-125b, miR-196b, miR-625, miR-196a*, miR-29a, and miR-140-5P) in our microRNAs microarray (unpublished data) and validated their expression in type I and type II (each 10 cases) EC samples by qRT-PCR. We found that endogenous miR-125b expression was the most significantly up-regulated in type II EC samples compared with type I (additional file
2). These results suggested that the expression level of miR-125b was inversely to endogenous TP53INP1 expression in EC I vs. EC II primary tissues, although the number of the samples is too small to reach a solid conclusion. Our findings were consistent with a previous observation that miR-125b was overexpressed in stages III and IV ECs compared with stage I [
22]. MiR-125b is dysregulated in various human cancers but its underlying mechanisms of action are poorly understood.
In current study, exogenous miR-125b expression stimulated the growth and mobility of ishikawa cells, whereas ablation of miR-125b inhibited the growth and mobility of AN3CA cells in vitro. In addition, in vivo xenograft experiment confirmed that forced miR-125b expression promoted proliferation potential of EC cells. We next asked how miR-125b might function inside cells accounting for the effect of miR-125b on biological behavior of EC cells. Using computational search, 148 potential targets of miR-125b were combinational predicted by TargetScan, Pictar-Vert, and Microrna.Org (additional file
3). Among 148 candidates, 4 are potential tumor suppressors including Bmf, adenomatous polyposis coli (APC), START domain containing 13 (STARD13), and TP53INP1. Bmf and STARD13 mRNA was not detectable in these EC cells. Aberrant APC expression, involving WNT signal pathway, was scarcely reported in publication about type II EC. Therefore, we focused on TP53INP1 involving p53 signal pathways.
The main pathway alterations in type II ECs involve p53 which, as a multifunctional transcription factor, plays a central role in cell cycle regulation and genetic stability. Over 90% type II ECs harbor mutant p53 with loss of function [
26,
27]. TP53INP1 is a proapoptotic stress-induced p53 target gene. It is a tumor suppressor gene with a known role in cellular homeostasis through its antiproliferative and proapoptotic activities via both p53-dependent and p53-independent means [
28,
29]. However, in the absence of wild type p53 in type II ECs, it may be more important for TP53INP1 to maintain cell homeostasis. There is still no research about TP53INP1 in ECs. However findings in recent years have shown a significant reduction or loss of TP53INP1 expression during the development of cancers of the breast [
30], stomach [
31], and pancreas [
32]. Besides TP53INP1 protein negativity was significantly associated with aggressive pathological phenotypes of gastric cancer; and TP53INP1-positive rate decreased with the progression of gastric cancer [
31]. These suggest that TP53INP1 play an important role in suppression of tumor progression [
31‐
34]. MicroRNAs are estimated to regulate the expression of over 30% genes and their functions [
35,
36], suggesting a possibility that some specific microRNAs might directly regulate TP53INP1. With respect to miRNAs which may regulate the expression of TP53INP1, several studies had reported that TP53INP1 was repressed by miR-155 in pancreatic cancer [
32] and miR-130b in hepatocelluar cancer [
37], respectively. However, miR-155 and 130b were not among differential expression miRNAs profiles in our studies. In present study, we newly identified miR-125b as the direct regulator of TP53INP1. MiR-125b can directly repress the TP53INP1 protein expression through its binding to the binding sites in 3'UTR of human TP53INP1 gene, thereby negatively regulating TP53INP1 functions. In addition to TP53INP1, three recent studies reported miR-125b can directly target p53 [
18], Bak1 [
19], and Bmf [
20] to enhance the initiation and progression of tumor. Thus, miR-125b might have many other targets that remain to be discovered in future.
The findings here show a regulatory interaction between miR-125b and the tumor suppressor protein, TP53INP1. The results agree with observations elsewhere that aberrant loss of TP53INP1 correlates with the proliferation and migration, but not metastasis [
37,
38]. This study not only will allow for better understanding of mechanisms which contributes to malignancy of type II ECs, but also will provided sight into the gradual importance of more effective cancer therapies against this disease.
Although some of the results presented here are novel, this study has some limitations. Firstly, the number of the cells line is too small to reach a solid conclusion. In addition, it is required further to evaluate the expression of TP53INP1 and miR-125b simultaneously in large type II EC tissue samples.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
FJ carried out the experimental studies and drafted and completed the manuscript. TL participated in the design of the study. YH and QY performed the tedious proofreading. HW participated in tumor pathological characterization. XC completed previous microRNAs microarray. XW conceived of the study and performed the statistical analysis. All authors read and approved the final manuscript.