Bangladesh J Pharmacol. 2014; 9: 533-538
Available Online: 25 October 2014; DOI: 10.3329/bjp.v9i4.20398
Wnt5a silencing inhibits the osteosarcoma migration by suppressing PI3K/AKT signaling pathway
Jun Chen, Ye Wang and Wei-Xin Shi
Department of Orthopedics, The Central Hospital of E-Zhou, Hubei 436000, China.
Osteosarcoma is one of the most common malignant bone tumors in children and adults. Till this date, molecular mechanism behind the growth and invasiveness of osteosarcoma is poorly understood. Wnt5a plays an important role in the oncogenesis and cancer metastasis. Results show that Wnt5a has a remarkable influence on the U2OS and SaOS-2 cancer cell migration. The cell migration was dependent on the concentration of Wnt5a with low concentration (25 ng/mL) has almost no effect on the cell migration while it has remarkable influence at 100 ng/mL. The results revealed that Wnt5a can control the osteosarcoma cell migration via PI3K/Akt signalling pathways. We showed that Wnt5a activated the PI3K (p-Tyr458) and Akt phosphorylation (p-Ser473) immediately after the ligand incubation. More importantly, we demonstrated that chemotherapeutic drug like doxorubicin can effectively suppress the activity of Wnt5a ligand and thereby can inhibit the osteosarcoma cell growth and tumorigenesis. This lay the foundation for therapeutic application of Wnt5a towards the treatment of osteosarcoma.
Keywords: Cell migration; Doxorubicin; Osteosarcoma; PI3K/AKT signaling; Wnt5a
In the aforementioned perspective, Wnt signalling plays an important role in the development of osteoblastogenesis and tumorigenesis (Nusse, 2005). Osteopro-genitor cell proliferation/progression has been reported to increase with the Wnt signalling along with the prevention of apoptosis in osteoblasts. It has been reported that Wnt ligands and Wnt receptors are overexpressed in osteosarcoma while at the same time Wnt inhibitor was found in lowest level in bone malignancies (Bodine and Komm, 2006). In Wnt/β-catenin signaling pathways, Wnt ligands binds with the Frizzled receptors and low-density lipoprotein receptor-related protein 5/6 (LRP5/6) coreceptors leading to the activation of disheveled (Dsh) that releases β-catenin from the axin-adenomatous polyposis coli (APC)-glycogen synthase kinase-3β(GSK-3β) complex (Bodine, 2008; Gaur et al., 2005). Wnt5a has been classified in a non-canonical Wnt group. Wnt signalling activates Ca2+ pathways leading to the ultimate activation of activate protein kinase C (PKC) and Ca2+/calmodulin kinase II. Besides, it can activate various intracellular proteins including c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase (ERK), and Akt (McQueen et al., 2011).
Earlier, it has been demonstrated that trimeric G protein activates the phospholipase C and phosphodiesterase which is in turn involved in the activation of Wnt-induced gene expression (Veeman et al., 2003). Recent-ly, it was showed that Phosphatidylinositol-3 kinases (PI3Ks) could be involved in the progression of cancers (Kuhl et al., 2000). PI3Ks are a group of enzyme family that are involved in the various intracellular functions such as cell proliferation, progression, differentiation, and cell survival which are important part of cancer developments. Moreover, serine/threonine kinase Akt influences the PI3K pathways along with polypeptide growth factors (Almeida et al., 2005; Yamanaka et al., 2002).
Doxorubicin (DOX), a topoisomerase II inhibitor, is a potent chemotherapeutic agent used in the treatment of wide variety of malignancies including lung, breast, ovarian, leukemia and osteosarcoma (Gabizon et al., 2003). This drug acts by the intercalation of DNA in the cancer cells resulting in the inhibition of macromolecular biosynthesis. Till date, none demonstrated its potential in osteosarcoma via inhibition of Wnt signalling pathways (Chamberlain et al., 2013).
Herein, the main aim of our study was to investigate the role of PI3K/Akt signaling pathway in Wnt-mediated osteosarcoma cell progression and study the effect of chemotherapeutic drug on the cell migration and bone cell apoptosis. U2OS and SaOS-2 osteosar-coma cells were selected to study the migration of OS cells. The effect of Wnt5a on PI3K activation of OS cells was investigated. The effect of Wnt5a on cell migration via AKT pathways was also demonstrated. Finally, influence of DOX on the cell apoptosis and cell migration was noted in U2OS cells.
Cell culture: U2OS and SaOS-2 human osteosarcoma cell lines were procured from American Tissue Culture Collection (ATCC), Rockville, MD. U2OS and SaOS-2 cells were cultured in McCoy’s 5A medium. Prior to that, growth medium was prepared by adding 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin in the rest of the media. The cells were maintained in a sophisticated incubator at ambient conditions (37°C and 5%CO2). The mouse anti-β-actin antibody was purchased from KangChen Biotech, Shanghai, China. The rabbit anti-Akt antibody, rabbit antiphospho-Akt (p-Ser473) antibody, rabbit anti-PI3K p85 antibody, rabbit anti-phospho-PI3K p85 (Tyr458) (Cell Signaling Technology, Danvers, MA), mouse anti-β-catenin antibody, rabbit anti-phospho-β-catenin (p-Ser33) antibody were purchased from Santa Cruz Biotechnology, Santa Cruz, CA.
Cell migration analysis: Boyden chamber was used to determine the cell migration. The Boyden chamber is consists of two chambers which are separated by a polycarbonate membrane. U2OS and SaOS-2 cells were seeded in tissue culture plates and allowed to reach 90% confleuncy. The cells were detached by means of trypsinization. The cells were then centrifuged and made into a cell suspension. The serum free media was used to make the cell suspension which contains 5 µg/mL of BSA. Approximately, 6×104 cells were placed on to the wells containing the membrane at the bottom. Now, Wnt5a is added to the compartments located up and downside of chamber. The cells were allowed to migrate for 24 hours at 37°C in the Boyden chamber. Followed by this, culture medium was removed along with the floating cells and membranes were detached from the chamber. The membranes were stained with 0.5% crystal violet. The extent of cell migration in the membrane was visualized using a light microscope. Number of cells migrated on to the membrane can also be counted.
Immunoblot analysis: The cells were seeded on to well plates and allowed to incubate for 24 hours. siRNA du-plexes which is particular for Akt were incubated with U2OS and SaOS-2 cancer cells in order to start transfection. Lipofectamine 2000 reagent was used in serum free media as per the manufacturer’s protocol. It was allowed to transfect for 48 hours, following which protein levels in each cell was evaluated using western blotting.
The transfected cells were washed two times with PBS and lysed using lysis buffer. The lysis buffer was maintained at pH 7.4 and consists of 50 mmol/L Tris, 150 mmol/L NaCl, 1%Triton X-100, 1%sodium deoxy-cholate, 0.1%SDS, 1 mmol/L sodium orthovanadate, 1 mmol/L sodium fluoride, 1 mmol/L EDTA, 1 mmol/L PMSF, and 1% cocktail of protease inhibitors. The cell lysates were collected and centrifuged at 10,000 rpm for 20 min at 4°C. The proteins were separated using electrophoresis technique in a 10% SDS-acrylamide gel phase. This was blotted on a nitrocellulose membrane. The membranes were then blocked overnight in Tris buffer containing 0.1% (v/v) Tween 20 and 5% (w/v) fat-free dry milk. This was incubated with primary anti-body which is followed by a secondary antibody. The antibodies used includes mouse anti-β-actin antibody, rabbit anti-Akt antibody, rabbit anti-phospho-Akt (p-Ser473) antibody, rabbit anti-PI3K p85 antibody, rabbit anti-phospho-PI3K p85 (Tyr458), mouse anti-β-catenin antibody, rabbit anti-phospho-β-catenin (p-Ser33) anti-body. The protein bands were determined by incubation with horseradish peroxidase-conjugated antibodies and images were captured using an X-ray film detector. The bands were analyzed using the software provided by the manufacturer.
BrdU incorporation assay: The cells were seeded in a well plate and allowed to attach and grow overnight. Cells were incubated with Wnt3a conditioned medium and followed by doxorubicin for a specified time. Cells were trypsinized and harvested and incubated with 10 µM of 5'-bromo-2-deoxy-uridine (BrdU) for 3 hours. The cells were fixed with cold ethanol/HCL and BrdU labelling/detection kit (Roche Diagnostics GmbH, Mannheim, Germany) was employed to determine BrdU as per the instruction of manufacturer’s.
Statistical analysis: For all analyses, p<0.05 was consider-ed statistically significant. Two-tailed, unpaired Stu-dent’s t-test was used to calculate statistical difference/analysis using Microsoft excel or graph pad prism. The data are expressed as mean± standard deviation (SD) and performed in triplicate.
Wnt5a signalling pathway activates a range of physiological and pharmacological activities including the cellular proliferation, migration, invasion, cell cycle disruption, and suppresses the cell apoptosis in multi-ple cancers which includes osteosarcoma (Logan and Nusse, 2004). Wnt5a is the main ligand that activates the Wnt signalling pathways. Specifically, animal with abnormal Wnt signalling pathways frequently develops facial abnormalities, dwarfism, dysmorphic ribs and shortened limbs/tails (Klaus and Birchmeier, 2008). It has also been reported that lack of Wnt pathways would also result in abnormal distal lung morphogenesis, dysmorphic vertebrae, and complete absence of genital tubercle. This indicates how important Wnt signalling in the development and growth of critical organs (Weeraratna et al., 2002). In addition, Wnt-mediated cell signalling plays a unique role in the cancer proliferation and cancer differentiation. It has been reported that that Wnt5a promotes the cancer metastasis and proliferation in various malignant tissues including breast, melanoma, gastric and liver cancer (Zhu et al., 2012). Keeping all this facts in mind, present study was designed to investigate the effect of Wnt on osteosarcoma cancer cells including U2OS and SaOS-2 cancer cells. In addition, role of PI3K/Akt signaling pathway in Wnt pathway has been investigated.
Cell migration is a clear indication of the ligands influence on the cell proliferation and differentiation. The effect of Wnt5a on U2OS and SaOS-2 osteosarcoma cancer cells has been carried out after treating the individual cells with recombinant Wnt5a. The cell migration was evaluated using Boyden chamber assay. It can be clearly seen that Wnt5a has a remarkable influence on the U2OS cell migration. The concentration of Wnt was varied from 25 ng/mL to 100 ng/mL to observe the concentration dependent effect on the cell migration capacity. As can be seen (Figure 1), low con-centration (25 ng/mL) has almost no effect on the cell migration capacity while when the concentration of Wnt increased up to 50 ng/mL, the cell migration significantly inhibited. Specifically, appreciable cell migration inhibition was observed at around 75-100 ng/mL. Similar trend was observed in SaOS-2 cancer cells although the level of migration was different between both the cell lines. Followed by, number of cells per field was calculated and as expected the trend was similar to that of migration rate (Figure 1). The number of cells was almost equal to control at lowest concentration however it increased for the increase in the concentration of the Wnt. This result clearly indicates that Wnt5a is an effective stimulator of osteosarcoma cells.
Phosphatidylinositol-3 kinases (PI3Ks) enzyme family is involved in the vital cellular functions of the body including cell growth proliferation, differentiation, cell survival and intracellular trafficking. These pharmacological activities have been important for the development of cancers. Therefore in the present study, molecular mechanisms behind the role of Wnt on cancer growth have been investigated. The downstream signalling pathway in U2OS and SaOS-2 cells has been studied in detail (Figure 2). Firstly, PI3K activation state has been studied. Phosphorylated-PI3K p85 is considered as the important biomarker of PI3K activation state. For this, cells were starved from serum for 24 hours then treated with highest concentration of Wnt5a at which it showed the maximum cell migratory ability. The cells were collected at a specified time interval of 15, 30, and 60 min and SDS-PAGE and western blot experiments were conducted. The results clearly showed that basal phosphorylation has been increased at increasing the incubation time. Specifically, basal phos-phorylation was elevated after 15 min of Wnt5a stimulation, while it increased for 30 min incubation and decreased thereafter in both the cancer cell lines (Almeida et al., 2005).
Moreover, it is well known that PI3K is the important activator of Akt in the physiological systems (Kawasaki et al., 2007). Therefore we have next investigated the response of Akt for the Wnt incubation (Figure 3). For this, cells were starved from serum for 24 hours then treated with highest concentration of Wnt5a at which it showed the maximum cell migratory ability. phosphorylated-Akt (p-Ser473) is considered as the important biomarker of Akt activation state. Consistent with the PI3K results, basal phosphorylation has been increased at increasing the incubation time. Specifically, basal phosphorylation was elevated after 15 min of Wnt5a stimulation, while it increased for 30 min incubation and decreased thereafter in both the cancer cell lines.
It is well known that Wnt5a activates protein kinase C (PKC) and affect the tumor progression process in the cancer cells. It has been reported that Wnt5a inhibits the cell apoptosis by activating Akt and ERK pathways (Ko et al., 2014). We showed that Wnt5a activated the PI3K (p-Tyr458) and Akt phosphorylation (p-Ser473) immediately after the ligand incubation. Therefore it can be expected that by blocking Akt or PI3K will actively control the osteosarcoma cell proliferation.
We next investigated the effect of DOX on the proliferation of osteosarcoma cells. For this, we have treated the cells with both Wnt5a ligand as well as chemotherapeutic drug. As can be seen (Figure 4a,b), Wnt5a has a remarkable influence on the U2OS and SaOS-2 cell proliferation. Wnt5a remarkably increased the cell proliferation comparing to that control or untreated cells. Importantly, when DOX was exposed to the same cells, it resulted in decrease in the basal conditions. The results clearly indicate that DOX abolished the stimulatory effect of Wnt5a ligand in the cells.
The cell migration is an important factor in the development of osteosarcoma tumorigenesis and metastasis. Therefore, we have investigated the effect of DOX on the cell migration in an identical condition. As seen clearly (Figure 4c), comparing to control cells (untreated), DOX markedly inhibited the cell migration potential of cells.
Overall, our results show that PI3K/Akt signaling plays a central role in cell viability-promoting phenotypes such as inhibition of cell death and cell cycle progression. We showed that Wnt5a could influence U2OS and SaOS-2 cell progression and proliferation by activating PI3K/Akt pathways. This PI3K/Akt-dependent activation of cell cycle progression plays an important role in the osteosarcoma proliferation in the body (Kawasaki et al., 2007; Ko et al., 2014). We have further showed the influence of chemotherapeutic agent on the cell proliferation and Wnt5a therapeutic action. Results revealed that DOX remarkably halted the stimulatory effects of Wnt ligands. Consistently, it remarkably suppressed the migration of both the osteosarcoma cell lines.
The work was supported by the University Research Grant provided to the graduate student. One of the authors would like to thank Dr. Bao for his immense help.
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