Introduction
To date, pancreatic ductal adenocarcinoma (PDA) is the fourth most common cause of cancer-related deaths worldwide [
1]. A large part of PDAC patients can only be diagnosed at an advanced stage and have non-specific symptoms before clinical manifestations. PDA mortality is almost equal to its morbidity and it is a fatal disease [
2,
3]. After the intervention of surgery, chemotherapy and radiation therapy, the 5-year survival rate of pancreatic cancer is still less than 8% [
4]. Moreover, distant metastases occur in 60% of patients within 24 months of surgery [
5]. Albumin-bound paclitaxel (nab-paclitaxel) in combination with gemcitabine and fluorouracil is widely used as first-line treatment for metastatic PDA to improve survival and overall response rate [
6‐
8]. Unfortunately, with the emergence of gemcitabine and fluorouracil resistance, the therapeutic efficacy of GEM in pancreatic cancer is declining [
7,
8]. Recent research on PDA pointed out that the abnormal expression of genes or proteins plays an important role in the occurrence and development of this tumor [
9,
10]. In general, it is urgent to deepen the understanding of the molecular mechanism of PDA and find new therapeutic targets.
MEX3 has a conserved region of 65 to 70 amino acids, including two K homology domains and one human gene family homologous to MEX3, MEX3A-D [
11]. MEX3A is located in the paratope (156,072,013–156,081,998) and has 9986 base pairs [
11]. The RNA-binding protein of evolutionarily conserved MEX3 family are first characterized in heterogeneous ribonucleoproteins, as mediators of post-transcriptional regulation in different organisms, participating in different physiological environments [
12]. MEX3A has been identified to be associated with diseases, especially cancer, such as Wilms tumors [
13], gastric carcinomas [
14], colorectal carcinomas [
15]. It is important to determine their effects on cancer development and assess their potential of cancer progression or prognosis.
Materials and methods
Cell culture
The PDA cell lines PANC-1 and SW1990 were cultured in 6-well plates with 5% CO2 in 37 °C humid air and supplemented with DMEM containing 10% fetal bovine serum (FBS). The medium was changed every 72 h, and subculture was performed with 0.05% trypsin and 0.02% EDTA at a concentration of 80%. After 24 h in DMEM without FBS, followup experiments were performed.
Target gene RNA interferes with the preparation of lentiviral vector
MEX3A was used as a template to design multiple RNA interference target sequences, and the target sequence (5′-AGGCAAGGCTGCAAGATTAAG-3′) with the highest MEX3A knockdown efficiency was screened for downstream experiments. BRV-112 linear vector (Shanghai bioscienceres Co. Ltd., Shanghai, China) was obtained by restriction endonuclease Age I (NEB, # R3552L) and EcoR I (NEB, # R3101L) digestion. Construction of target gene RNA interference lentiviral vector. The products were transformed into the 100 µL TOP10 competent cells of Escherichia coli (TIANGEN, # CB104-03). After that, positive clones with correct sequencing were selected by PCR and then plasmids were extracted by using plasmid extraction kit (TIANGEN, # DP117). Virus packaging Helper plasmid (Helper 1.0, Helper 2.0) and the target plasmid were co-infected into 293T (lentivirus packaging cells). The supernatant of 293T cells was collected 48 h after infection for the quality test of lentivirus. Lentivirus vectors were labeled with fluorescence and observed under fluorescence microscope after infection 72 h (GFP, Cherry).
qRT-PCR
Total RNA extraction according to sigma Trizol instructions (Invitrogen, Carlsbad, CA, USA). RNA reverse transcription was used to obtain cDNA using vazyme Hiscript QRT super mix (gDNA wiper) (Vazyme, Nanjing, China). The qRT-PCR was performed by using AceQ qPCR SYBR Green Master Mix (Vazyme, Nanjing, China). GAPDH was used as a reference control.
MEX3A Primer-F | CGGAGTGGACTCTGGCTTTGAG |
MEX3A Primer-R | CAGAGGAGAAGAGCACGGAGGT |
GAPDH Primer-F | TGACTTCAACAGCGACACCCA |
GAPDH Primer-R | CACCCTGTTGCTGTAGCCAAA |
Western blot analysis
The PDA cell lines PANC-1 and SW1990 were collected and lysed with RIPA lysis buffer (Cell Signal Technology, Danvers, MA, USA) according to the instructions. Quantitative extraction of proteins with BCA Protein Assay Kit (HyClone-Pierce, Waltham, MA, USA, # 23225). Then western blot analysis was performed by SDS-PAGE (10%). The protein was transferred to polyvinylidene fluoride (PVDF) membrane and incubated with 5% BSA containing 0.5% Tween 20 for 60 min, then incubated overnight at 4 °C with the following primary antibodies (see primary antibody information table for western blot). After washing with TBST, the blot was incubated with horseradish peroxidase (HRP) labeled polyclonal secondary antibody (1:3000) (Beyotime, Beijing, China, # A0208) at room temperature for 1 h. ECL and plus TM western blot system kit (Amersham, Chalfont, UK, # RPN2232) were used for color development.
MEX3A | 54 | 1:1000 | Rabbit | Abcam | AB79046 |
N-cadherin | 125 | 1:1000 | Rabbit | Abcam | AB18203 |
Vimentin | 54 | 1:2000 | Rabbit | Abcam | AB92547 |
Snail | 29 | 1:1000 | Rabbit | Abcam | 3879S |
Akt | 60 | 1:1000 | Rabbit | CST | 4685 |
p-Akt | 60 | 1:1000 | Rabbit | Bioss | BS5193R |
CDK6 | 37 | 1:1000 | Rabbit | Abcam | AB15127 |
PIK3CA | 110 | 1:1000 | Rabbit | Abcam | AB40776 |
MAPK9 | 48 | 1:1000 | Rabbit | Abcam | AB76125 |
GAPDH | 37 | 1:3000 | Rabbit | Bioworld | AP0063 |
MTT assay
First, PANC-1 and SW1990 cells were trypsinized, completely suspended and counted. The cell density was 2000 cells/well and inoculated to 96-well plates (100 µL/well) (Corning, Corning, NT, USA, # 3599) overnight, and the cells were repeated 3–5 times in each group. 5 mg/mL MTT (5 mg/mL) (3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide) (Genview, Beijing, China; # JT343) 20 μL was added 4 h before the end of the culture from the day after the planking, without changing the fluid. After 4 h, the medium was completely removed, 100 µL DMSO was added. The oscillator was oscillated for 5 min, OD value was detected by the enzyme-connected immunodetector 490/570 nm and the data were recorded for analysis.
PANC-1 and SW1990 cells were trypsinized, and the culture medium was completely suspended to prepare a cell suspension. The cells cultured in the 6-well plate, 1000 cells/well were inoculated for 8 days, medium was changed every 3 days, and cell status was observed. Cell clones were photographed under fluorescence microscope before the termination of the experiment, and the cells were washed with PBS. 1 mL 4% paraformaldehyde was added to each well, the cells were fixed for 50 min and washed with PBS. After that, GIEMSA dye solution was added to each well for 20 min, dried them, cell clones were then photographed for counting.
Apoptotic assay
PANC-1 and SW1990 cells were cultured with 6-well plates, 2 ml/well, digested with trypsin, and then the cell suspension was suspended, centrifuged at 1300 rmp for 5 min, and supernatant was discarded. Cell precipitate was washed with 4 °C pre-cooled D-Hanks (pH = 7.2–7.4). The cells were washed with 1 × binding buffer for precipitation, and centrifuged at 1300 rmp for 3 min to collect the cells. 200 μL 1 × binding buffer was added to suspend cell precipitation, followed by 10 μL Annexin V-APC staining at room temperature and dark for 15 min. Finally, 1 × binding buffer 500 μL was added and tested on machine.
Transwell assay
100 μL serum-free medium was added and placed in the incubator for 1–2 h. PANC-1 and SW1990 cells were digested with trypsin, and the cell suspension was prepared by resuspension with low serum medium. Carefully removed the medium from the small chamber and added 600 μL containing 30% FBS to the lower chamber. The cells were inoculated in 24 well plates 100,000 cells/well, 100 μL/well in inner chamber and 600 μL/well in outer chamber for 24 h. Place the chamber upside down on the blotting paper to remove the medium and gently remove the metastatic cells using a cotton swab. Added 400 μL stain to the hole in the 24-well plate and soak the chamber in the staining solution for 20 min, dyed the cells on the lower surface of the membrane to transfer the cells. Soaked the chamber in a large water cup and rinsed it in the air after washing it several times. Microscope photo membrane dissolved at 10% acetic acid, detection of absorbent 0D540.
Human apoptosis antibody array
The intracellular cell signaling pathway was examined using the Human Apoptosis Antibody Array Kit (# AB134001). All in all, the PANC-1 cells were collected after lentivirus infection for 3 days, washed with PBS, lysed with lysis buffer 2–8 °C for 30 min, and then gently shaken. The total extracted protein was diluted with the array diluent buffer kit to 0.5 mg/mL. Each array antibody membrane was blocked with blocking buffer for 30 min at room temperature, which incubated at 4 °C and gently shaken overnight. 1 × Biotin-conjugated Anti-cytokine was incubated overnight at 4 °C and gently shaken. HRP linked Streptavidin was added to the membranes. Protein was visualized using ChemiDoc XRS chemiluminescence detection and imaging system. The density of the spots was quantitated using Quantity One software and normalized to the α–tubulin levels.
Animal xenograft model
Animal research was approved by the ethics committee of West China Hospital, Sichuan University conducted in accordance with guidelines and protocols for animal care and protection. BALB/c female nude mice (4 weeks old) were purchased from Shanghai Jiesijie Experimental Animals Co., Ltd (Shanghai, China). PANC-1 cells with luciferase reporter tag infected with shMEX3A or shCtrl were subcutaneously injected into BALB female nude mice (5 × 106 cell per mouse). Data were collected (the weight and volume of the tumor) after 19 days of injection of PANC-1 cells, and then measured per week up to 45 days. Subsequently, D-luciferin (15 mg/mL) was injected into the mouse peritoneum at a dose of 10 μL/g, waiting for about 15 min, and then placing it in a dark room for bioluminescence imaging. The tumor load was evaluated weekly with bioluminescence imaging, and the IVIS spectral imaging system (emission wavelength 510 nm) analyzed. 10 min before in vivo imaging, anesthesia was performed by inhaling with 3% isoflurane. After 45 days, the mice were executed, injected with sodium pentobarbital, removed from the tumor and taken a photo, weighing.
Immunohistochemical staining
63 cases of survival-time PDA and matched normal adjacent cancer tissue were purchased from Shanghai Outdo Biotech Co., Ltd (Shanghai, China). The informed consents were collected from tissue donors (patients). Specimens were fixed in formalin and embedded in paraffin (FFPE). Xylene were used for paraffin section dewaxing 15 min per time and 100% alcohol for hydration 10 min. After repairing and blocking of the citrate antigen, the sample and MEX3A antibody (1: 1000, Abcam, USA, # AB79046) were incubated overnight in an incubator at 4 °C. After elution with PBS for 5 times, secondary antibody IgG (1: 400, Abcam, USA, # AB6721) was added, incubated at room temperature for 30 min, and washed with PBS for 3 times. Tissue slices were first stained with DAB, and then with hematoxylin. Finally, images were taken under a microscope and evaluated according to the German immune response score [
16]. In summary, the high or low expression level of MEX3A in PDA tissues is defined by the median based on total score of positive cells and total staining intensity.
Ki67 staining
Tumor tissue was sectioned from the sacrificed mice. After repairing and blocking of the citrate antigen, antibody Ki67 (1: 200, Abcam, USA, # AB16667) was added to the shMEX3A or shCtrl, respectively. After mixing, incubated overnight at 4 °C. PBS elution for several times, IgG (1: 400, Abcam, USA, # AB6721), secondary antibody was added and incubated at room temperature for 30 min. PBS was washed again. Tissue slices were first stained with DAB, and then with hematoxylin. Images were collected with a photomicroscope and analyzed.
Statistical analysis
The qRT-PCR was analyzed by 2 −∆∆CT method. T test were used to compare the difference. P values less than 0.05 were considered statistically significant. The data are expressed as mean ± SD (n ≥ 3) and analyzed using GraphPad Prism 6 software (GraphPad Software Inc., San Diego, CA, USA).
Discussion
MEX3A plays various roles in biological processes. Baumgart et al. pointed out that the expression of MEX3A is similar to that of mitotic markers of proliferating cell nuclear antigen [
17]. To date, few studies have evaluated the effects of MEX3A on tumor cells. For example, MEX3A overexpression is associated with the recurrence of Wilms tumors [
13]. In addition, Jiang et al. confirmed that abnormal activation of MEX3A in human gastric cancer cells promoted cell proliferation and migration [
14].
Chiaravalli et al. suggested that a decrease in Mex3A expression may result in more pronounced inhibition of bladder cancer cell growth [
18]. Interestingly, Adiseshaiah et al. found that MEX3A expression was not a poor prognostic factor for bladder urothelial carcinoma [
19]. Importantly, MEX3A expression is involved in the regeneration of all intestinal epithelial cells with slow kinetics, helping to maintain cell renewal during chemotherapy and radiation therapy [
20]. Based on this, we are urged to explore the regulation mechanism of MEX3A in PDA and provide feasible treatment strategies for PDA.
In this study, it was found that MEX3A is not only highly expressed in tumor tissues and human cultured cells of PDA, but also significantly correlated with patients’ prognosis. In addition, MEX3A knockdown inhibits PDA cell proliferation, migration, promotes apoptosis, and disrupts the cell cycle. Specifically, in vivo studies demonstrated that decreased tumorigenicity after knockdown of MEX3A, which is consistent with in vitro studies.
Escape from apoptosis is the basis of cancer pathogenesis [
21]. Apoptosis involves a series of biochemical events, which are mediated by a variety of cellular signals. Moreover, MEX3A knockdown promotes PDA cell apoptosis through a series of apoptosis-related proteins, such as upregulating pro-apoptotic proteins, including Caspase3, Caspase8, and TNF-α; while downregulating anti-apoptotic proteins, such as Bcl-2, Bcl-w, HSP27, IGF-II, Survivin, sTNF-R1 and XIAP. It has been known previously that binding of TNF to TNF-R1 initiates the Caspase activation pathway through the intermediate membrane protein TNF receptor-related death domain (TRADD) and death domain protein (FADD) [
22]. The Bcl-2 family is a key regulator for supporting and resisting apoptosis, and perturbations may indicate cell-to-cell death or irreversibility [
23]. Furthermore, Schafer et al. proposed that HSP27 is involved in the regulation of PDA apoptosis pathway [
24]. Recently, Momeny et al. clarified that Cediranib inhibits the proliferation of PDAC cells by inhibiting the anti-apoptotic proteins Survivin and XIAP and induces apoptosis [
25]. In view of the above, it can be presented that MEX3A knockdown to promote PDA cell apoptosis is a complex process of apoptotic protein regulation.
This study found that MEX3A knockdown inhibited PDA cell migration while down-regulating EMT markers such as N-cadherin, Snail and Vimentin. EMT is a developmental process in which cells acquire the ability to migrate [
26]. EMT is essential for the vigorous movement of cells during embryogenesis, and tumor cells can reactivate the EMT program and increase their aggressiveness [
26]. David et al. Point out that carcinogenicity associated with EMT is a feature that must be selected during cancer progression [
27]. Momeny et al. found that cediranib can attenuate the migration and invasion of PDA cells by reducing the expression of EMT markers ZEB1, N-cadherin and Snail [
25]. The vitamin D analog MART-10 inhibits metastatic potential by downregulating EMT in PDA cells [
28]. Accordingly, it is possible to support PDA cell migration through EMT.
Furthermore, the knockdown of MEX3A affects various activities of PDA cells and involves the expression of downstream signal pathways Akt, p-Akt, PIK3CA, CDK6 and MAPK9. It has been reported that PI3K/Akt/NF-κB/mTOR is the main signal transduction axis that controls cell proliferation, survival, apoptosis and malignant transformation [
29]. PIK3CA mutations can cause pancreatic tumorigenesis and can be targeted by PI3K inhibitors proposed by Payne et al. [
30]. Deeb et al. demonstrated that inhibiting survival (anti-apoptosis) Akt/NF-κB/mTOR signal transduction affects PDA cell proliferation, cycle arrest and apoptosis [
31]. In addition, Liu et al. proposed that anti-CDK4/6 treatment can induce EMT and enhance PDA cell invasion by activating SMAD-dependent TGF-b signaling [
32]. Moreover, a large amount of evidence showed that MAPK9 signaling is related to lung cancer, breast cancer, colon cancer, and ovarian cancer, mainly to adenocarcinoma cells [
33]. From these reports, it is inferred that the occurrence of various activities of PDA cells is jointly regulated by a complex network system.
All in all, it was concluded that MEX3A was involved in the development and progression of PDA and that it could be potential prognosis indicator and therapeutic target. However, this study still has shortcomings. For example, the number of specimens included in this study is limited, and the underlying mechanism of MEX3A-mediated PDA regulation remains unclear. Therefore, in the future work, we will further deepen the understanding of the molecular mechanism of PDA related to MEX3A.
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