In vitro effect of iASPP on cell growth of oral tongue squamous cell carcinoma

Yu Chen＊, Wangxiang Yan＊, Shuqi He, Jiechun Chen, Dan Chen, Zhaoqiang Zhang, Zhiguo Liu, Xueqiang Ding, Anxun Wang

1Department of Oral & Maxillofacial Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China,2Department of Stomatology, First Affliated Hospital of Jinan University, Guangzhou 510630, China;3Operation Room, First Affliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China;4Department of Stomatology, Sixth Affliated Hospital of Sun Yat-Sen University, Guangzhou 510655, China＊These authors contributed equally to this work.

Correspondence to: Anxun Wang. Department of Oral & Maxillofacial Surgery, First Affliated Hospital, Sun Yat-Sen University, #58Zhonshan RoadII, Guangzhou 510080, China. Email: anxunwang@yahoo.com.

In vitro effect of iASPP on cell growth of oral tongue squamous cell carcinoma

Yu Chen1＊, Wangxiang Yan1＊, Shuqi He2, Jiechun Chen3, Dan Chen1, Zhaoqiang Zhang4, Zhiguo Liu1, Xueqiang Ding1, Anxun Wang1

1Department of Oral & Maxillofacial Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China,2Department of Stomatology, First Affliated Hospital of Jinan University, Guangzhou 510630, China;3Operation Room, First Affliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China;4Department of Stomatology, Sixth Affliated Hospital of Sun Yat-Sen University, Guangzhou 510655, China＊These authors contributed equally to this work.

Correspondence to: Anxun Wang. Department of Oral & Maxillofacial Surgery, First Affliated Hospital, Sun Yat-Sen University, #58Zhonshan RoadII, Guangzhou 510080, China. Email: anxunwang@yahoo.com.

iASPP is an inhibitory member of the apoptosis-stimulating proteins of P53 (ASPP) family. iASPP is over expressed in several malignant tumors and potentially affects cancer progression. However, the expression and potential role of iASPP in oral tongue squamous cell carcinoma (OTSCC) have not been addressed. In our study, we detected iASPP expression in OTSCC by immunohistochemistry. iASPP expression is up-regulated in OTSCC tissues. Moreover, in clinical pathology specimens, we found that increased iASPP expression correlates with poor differentiation and lymph node metastasis. Using multicellular tumor spheroids (MTS) and flow cytometry, we demonstrated that iASPP down-regulation arrests OTSCC cells at the G0/G1 phase, induces OTSCC cell apoptosis and inhibits OTSCC cell proliferation. These results indicate that iASPP plays a signifcant role in the progression of OTSCC and may serve as a biomarker or therapeutic target for OTSCC patients.

iASPP; oral tongue squamous cell carcinoma (OTSCC); apoptosis; proliferation

View this article at:http://dx.doi.org/10.3978/j.issn.1000-9604.2014.07.05

Introduction

Oral tongue squamous cell carcinoma (OTSCC) is one of the most common head and neck squamous cell carcinomas. Each year, approximately 10,990 new cases of tongue cancer are diagnosed in the United States, accounting for approximately 30% of all oral cavity and pharynx cancers (1). Because of its specific histologic structure, the tongue is not equipped to protect itself from tumor invasion and metastasis (2).

The tumor suppressor p53 plays a central role in regulating cell cycle arrest, apoptosis, and DNA repair in a variety of cells (3). However, p53 is either absent or mutated in over half of human cancers. The discovery of the ASPP protein family as specific regulators of p53 provides a new mechanism by which the apoptotic function of p53 is regulated (4-6).

The ASPP family consists of three proteins, ASPP1, ASPP2 and iASPP, that interact with and/or modulate the behavior of p53 (5,7,8). ASPP1 and ASPP2 enhance the apoptotic function of p53, whereas iASPP inhibits p53-dependent apoptosis (9,10). Binding assays reveal differential binding of the C-terminal domains of iASPP and ASPP2 to the core domains of the p53 family members p53, p63, and p73 (11).

iASPP is located at the chromosomal region 19q13.3, which is coded by the PPP1R13L gene in humans and the ape-1 gene in C. elegans (12). iASPP can specifcally inhibit p53-mediated cell death. iASPP’s regulatory function of p53 is conserved from worms to humans (13). In addition, iASPP is an oncoprotein that cooperates with Ras, E1A, and E7, but not mutant p53, to transform cells in vitro (13).iASPP was originally described as RelA-associated inhibitor (RAI), which binds to the NF-κB subunit p65(RelA) to inhibit its transcriptional activity (14-16). Overexpression of iASPP is observed in types of human cancers, such as breast carcinoma, acute leukemia, hepatocellular carcinoma, and lung cancer (17-21). However, no information is available in the literature regarding the role of iASPP expression in OTSCC. In the present study, we first detected iASPP expression in OTSCC tissues. Next, we used small interfering RNA (siRNA) to knockdown iASPP expression in OTSCC cell lines (SCC25 and UM1). We used this system to investigate the effects of iASPP decrease on cell proliferation, apoptosis and cell cycle progression as well as to probe the feasibility of gene therapy for OTSCC.

Ethics statement

This study was approved by the Ethics Committee of First Affliated Hospital of Sun Yat-Sen University.

Material and methods

Tissue collection

All archived formalin-fixed, paraffin-embedded tissue specimens from OTSCC, oral premalignant dysplasia (OPD) and normal tongue biopsies (NTB) were collected from the Department of Oral and Maxillofacial Surgery at the First Affliated Hospital of Sun Yat-sen University from 1998-2007. The samples were comprised of 71 OTSCC, 20 OPD and 16 NTB cases. NTB samples were used as normal controls and obtained from normal tongue tissue close to the OTSCC lesion in OTSCC patients. None of the OTSCC patients received any form of adjuvant therapy prior to surgery. The tumor extent and tumor grade was classifed according to the TNM system by UICC and the WHO classifcation of histological differentiation, respectively.

Immunohistochemistry analysis

Tissues sections (5-µm thick) were dewaxed, and rehydrated in descending alcohol dilutions. Heat-mediated antigen retrieval was performed in 0.01 M citrate buffer (pH6.0) in a water bath for 30 minutes. Endogenous peroxidase activity in the sections was inhibited by incubation in 0.3% hydrogen peroxide in methanol for 10 minutes at room temperature.

After treatment with 5% normal buffer serum for 10 minutes to block non-specifc sites, the sections were incubated with an anti-iASPP rabbit antibody (Abnova, Taipei, Taiwan) at a dilution of 1:1,000 overnight at 4 ℃. The sections were then incubated with a horse radish peroxidase-conjugated anti-rabbit antibody for 30 minutes at 37 ℃. Color was then developed by incubation with horseradish per oxidase substrate solution containing 3,3’-diaminobenzidine typo chromogen reagent. The sections were counterstained with hematoxylin and then mounted with neutralbalsam.

To determine iASPP immunoreactivity, each case was assessed in three different felds at 400× magnifcation, and cytosolic staining of yellowish or brownish granules was graded as follows: 0 for background staining, 1 for faintstaining, 2 for moderate staining and 3 for strong staining. In addition, the amount of positive staining areas from the entire tissue section was graded as follows: 1 for ＜1/3, 2 for 1/3-2/3, and 3 for ＞2/3. The results obtained were multiplied together, yielding a scale with the values of 0, 1, 2, 3, 4, 6 and 9. From this scale, 0-4 were considered lowstaining, and 6 or 9 were considered high-staining. This multiplied scale subclassification system was previously described by Waltregny et al. (22).

Cell culture and antibodies

OTSCC cell lines (SCC-25and UM1) were maintained in DMEM/F12 supplemented with 10% FBS, 100 IU/mL penicillin and 100 µg/mL streptomycin (Gibco, NY, USA). Cells were cultured overnight at 37 ℃ under humidifed conditions of 5% CO2and 95% air.

siRNA and transient transfection

Sense and antisense siRNA oligonucleotides corresponding to the target sequence for the human iASPP gene (GenBank NM_006663.3, Table 1) were designed and synthesized by RiboBio (RiboBio, Guangzhou, China). Non-targeting siRNA was used as a control for the off-target effectscaused by RNA interference (RNAi). Cells were plated to 30-50% confluence in DMEM containing 10% FBS without antibiotics. Transfections were performed 24 hours later. Lipofectamine 2000 (Invitrogen, CA, USA) was diluted in Opti-MEM (Gibco, NY, USA) and incubated for 5 minutes. The iASPP siRNAs were diluted in Opti-MEM to a concentration of 50 nM. The two dilutions were mixed and incubated for 20 minutes at room temperature before transfection. Cells were analyzed 72 hours after transient transfection, and the protein expression was determined by western blotting.

Western blot

Western blots were performed as described previously (23), using antibodies specifc to iASPP (Abnova, Taipei, Taiwan). Briefly, protein samples prepared from the cells were subjected to SDS-PAGE, transferred to PVDF membranes (Millipore, CA, USA) and detected using appropriate primary antibodies followed by horseradish peroxidaseconjugated goat, anti-rabbit IgG. The intensities of the western blot bands were quantifed by the image analysis software Quantity One (Bio-Rad, CA, USA).

Quantitative real-time PCR

Quantitative RT-PCR assays were used to detect iASPP expression as previously described by Chen et al. (21). Total RNA was extracted from the cells using the Trizol reagent (Invitrogen, CA, USA) and then reverse transcribed into cDNA using M-MLV-RTase (Promega, WI, USA). The resulting cDNA was used for PCR using the SYBR-Green Master PCR Mix in triplicate. The qRT-PCR primers are listed in Table 2. Melting curve analyses were performed to ensure the specifcity of the quantitative RT-PCR reactions. The relative quantification value for the iASPP gene compared with the target calibrator is expressed as 2–(Ct-Cc)(Ct and Cc are the mean threshold cycle differences after normalizing to GAPDH).

Cell proliferation assays

After transfection, the transfection medium in each well was replaced with 100 µL fresh serum-free medium with 10 µL MTS. After incubation at 37 ℃ for 4 hours, the absorbance was measured at 490 nm. Each assay was performed in triplicate. All tests were repeated three times.

Flow cytometry-based apoptosis and cell cycle analysis

Cells were grown in 6-well plates to approximately 30-50% confuence and transiently transfected with the desired iASPP siRNA. Flow cytometry-based apoptosis and cell cycle analyses were performed as described previously (24). For cell cycle analysis, the cells were harvested and resuspended in PBS, and the samples were then fxed in ethanol at –20 ℃ overnight. The cells were washed with PBS and resuspended in Staining Solution (50 µg/mL propidium iodide, 100 µg/mL RNase A, 0.2% Triton X-100 in PBS). The stained cells (1×105cells per well) were then analyzed with a fow cytometer (FACScan, Bectone Dickinson, CA, USA). For apoptosis measurement, the cells were harvested and washed twice in PBS. The cells were resuspended in 500 mL PBS plus AnnexinV-PE and 7-AAD (Annex-inVPE/7-AAD staining kit, BioVision, Mountain View, CA). The stained cells (1×105) were then analyzed with a fow cytometer (FACScan, Becton-Dickinson, CA, USA).

Statistical analysis

Statistical analysis was carried out using SPSS (version 16.0). Fisher’s Exact test was used to analyze the relationship between gene expression and the clinicopathologic features of OTSCC patients. One-way ANOVA was used to compare the differences between groups. For all statistical analyses, P＜0.05 was considered statistically signifcant.

Results

iASPP expression in OTSCC and OPD

Given that research regarding iASPP expression in human OTSCC tissues has not been reported to date, we performed immunohistochemical analysis to elucidate the expression of iASPP in OTSCC tissues. Representative immunohistochemical staining indicated that iASPP is primarily expressed in the cytoplasm with minimal staining in the nucleus. Compared with very low expression of iASPP in NTB (Figure 1A), it has more extensive and intense expressionin both cytoplasmic and nuclear compartments of OPD (Figure 1B) and OTSCC tissues (Figure 1C,D). iASPP expression was signifcantly increased in OTSCC cases compared with OPD and NTB, and iASPP expression is significantly higher in OTSCC compared to OPD tissues (P＜0.001, Table 3). These results indicate that iASPP is markedly upregulated in OTSCC tissues. The relationship between iASPP expression and clinicopathologic features of 71 OTSCC tissues is displayed in Table 4. iASPP expression is significantly associated with pathological stage and lymph node status (P＜0.05), and these characteristics have enhanced proliferative and metastatic potential. However, iASPP expression is not associated with patient age, gender, or T classifcation (P＞0.05).

Table 2 iASPP and GAPDH primers sequences for real-time PCR

Figure 1 analysis of iASPP expression in OTSCC tissues. The representative immunohistochemical staining shows that iASPP expression is primarily observed in the cytoplasm with minimal nuclear localization. Compared with very low expression of iASPP in NTB (A), it has more extensive and intense expression in both cytoplasmic and nuclear compartments of OPD (B) and OTSCC tissues (C,D). The magnifcation was 400×. OTSCC, oral tongue squamous cell carcinoma; OPD, premalignant dysplasia; NTB, normal tongue biopsies.

Table 3 iASPP expression in various tongue tissues

Silencing of the expression of iASPP in OTSCC cells

To further examine the role of iASPP in OTSCC, iASPP was silenced by RNAi in the OTSCC cell line SCC25. Cells were divided into three groups as follows: non-infected cells (CON), non-silenced control cells (NC) and siRNA-infected cells. We selected three siRNA sequences from the iASPP region for evaluation. The siRNAs were transfected into SCC25 cells. Figure 2A,B showed that si-iASPP-3 had the highest interference effciency among the three siRNAs 72 hours after transfection; thus, si-iASPP-3 was chosen for use in the following experiments (P＜0.05). To further determine the effect of RNAi on iASPP expression in SCC25 and UM1 OTSCC cells, iASPP mRNA (3 days post transduction) and protein levels (3 days post transduction) were analyzed. The si-iASPP-3 group showed lower expression of iASPP mRNA and protein than the CON or NC groups (Figure 2C-E; P＜0.05).

Table 4 Correlations between iASPP expression and clinicopathologic features of OTSCC patients

However, no signifcant difference in iASPP protein expression was observed between the CON and NC groups. These results indicate that iASPP expression could be signifcantly reduced by si-iASPP-3 in SCC25 and UM1 cells.

Down-regulation of iASPP expression inhibits OTSCC cell proliferation

To investigate whether iASPP RNAi affects OTSCC cell proliferation, the MTS cell proliferation assay was used. As shown in Figure 3, the growth pattern was altered from the second to the third day in OTSCC cells, and the proliferation rate in the si-iASPP-3 group decreased by 22.3% in SCC25 and 18.7% in UM1 72 hours after transduction. In addition, the si-iASPP-3 group growth rate was signifcantly reduced compared with the CON or NC groups (P＜0.05). These results revealed that knockdown of iASPP expression by si-iASPP-3 siRNA in OTSCC cells inhibited OTSCC cells growth and proliferation.

Down-regulation of iASPP expression induces cell cycle arrest in OTSCC cells

Figure 2 iASPP siRNA leads to down-regulation of iASPP in OTSCC cells. Cells were divided into three groups as follows: non-infected cells (CON), non-silenced control cells (NC) and siRNA-infected cells. Three siRNAs were transfected into SCC25 cells. (A,B) show that si-iASPP-3 has the highest interference effciency among the three siRNAs 72 hours after transfection. si-iASPP-3 was chosen for use in the following experiments (P＜0.05). In UM1 and SCC25 cells (C-E; P＜0.05), the si-iASPP-3 group displayed reduced expression of iASPP mRNA and protein compared with the CON or NC groups. However, no signifcant difference in iASPP protein expression was observed between the CON and NC group.

Figure 3 iASPP RNAi affects OTSCC cell proliferation as assessed by the MTS cell proliferation assay. The si-iASPP-3 group showed a signifcantly reduced growth rate compared with the CON or NC groups 2 days post transduction (P＜0.05). RNAi, RNA interference; OTSCC, oral tongue squamous cell carcinoma; CON, non-infected cells; NC, non-silenced control cells; MTS, multicellular tumor spheroids.

Figure 4 Down-regulation of iASPP expression induces cell cycle arrest in OTSCC cells. The si-iASPP-3 group had signifcantly more cells in the G1/G0 phase and less cells in the G2/M phase compared with the CON or NC group (P＜0.05). OTSCC, oral tongue squamous cell carcinoma; CON, non-infected cells; NC, non-silenced control cells.

We performed fow cytometry to detect whether si-iASPP-3 affects OTSCC cell cycle 48 hours after transduction. These results showed that the proportion of OTSCC cells significantly increased in the G1/G0 phase and decreased in the G2/M phase of the si-iASPP-3 group compared with the CON or NC group (Figure 4; P＜0.01). Thus, our results suggest that knockdown of iASPP expression by si-iASPP-3 siRNA in OTSCC cells inhibits OTSCC cell proliferation through inhibition of the cell cycle.

Down-regulation of iASPP promotes apoptosis of OTSCC cells

Further investigations of apoptosis elucidated a strong role for iASPP in cell apoptosis or survival. Apoptotic analysis by fow cytometry showed an increased apoptotic rate in the si-iASPP-3 group compared with NC or CON group (Figure 5; P＜0.01). These results suggested that iASPP expression in OTSCC may inhibit cellular apoptosis.

Discussion

Figure 5 Down-regulation of iASPP promotes apoptosis in OTSCC cells. Apoptotic analysis by fow cytometry showed that the apoptotic rate of the si-iASPP-3 group increased signifcantly compared with the NC or CON group (P＜0.05). OTSCC, oral tongue squamous cell carcinoma; NC, non-silenced control cells; CON, non-infected cells.

To the best of our knowledge, our present study is the first report on the expression and role of iASPP in OTSCC. iASPP expression could reflect the degree of OTSCC malignancy because iASPP expression increases with pathological grade. In addition, the relationship between iASPP expression and lymph node metastasis indicates that iASPP might serve as a potential target for OTSCC treatment. Consistent with previous studies, our investigations indicate that iASPP is localized to the cytoplasm and nucleus of epithelial cells (12,25,26). However, in other malignancies, such as hepatocellular carcinoma (20), non-small cell lung cancer (21), and prostate cancer (27), iASPP expression is exclusively localized to the cytoplasm. Liu et al. attributed these fnding to the different specifcity of the anti-iASPP antibodies. Liu et al. also found that ASPP expression is elevated in head and neck squamous cell carcinoma tissues and cell lines and serves as a novel prognostic marker and a potential therapeutic target in HNSCC (28). Furthermore, Jiang et al. found that increased iASPP expression is significantly associated with reduced disease-free survival of ovarian cancer patients and that iASPP expression is an independent prognostic factor (26). All these fndings indicate that iASPP plays an important role in mediating the malignant progression of OTSCC and may serve as a prognostic marker predictive of OTSCC clinical outcome.

In the present study, we demonstrate that inhibition of iASPP expression in UM1 and SCC25 cell lines induces G0/G1 arrest and cell apoptosis as well as reduces cell proliferation. Recent reports have indicated that iASPP down-regulation inhibits proliferation and induces cell apoptosis (4,18,21,29,30). Therefore, it is speculated that iASPP contributes to tumorigenesis. Over-expression of iASPP may be involved in tumor establishment and progression, whereas iASPP down-regulation may inhibit tumor development.

As a negative regulator of p53-activating apoptosis, iASPP may serve as a good candidate for targeted cancer therapy (31). UM1 and SCC25 cells express wildtype p53, and the effect of iASPP on apoptosis may be dependent on p53. In addition to its involvement with p53, iASPP participates in the p63-mediated epithelial integrity program by regulating the expression of genes essential for cell adhesion, thereby suggesting that iASPP is a key regulator of epithelial homeostasis (32). In addition, Chikh et al. found that the p53-related protein p73 has similar functions but is rarely lost or mutated in cancer (32). Other reports suggested that iASPP might promote carcinogenesis by other mechanisms in addition to p53 inhibition (19,33). iASPP may act as a novel NF-κB-binding protein, repressing transcriptional activity and preventing the survival of pre-cancerous cells (34). However, further studies are needed to dissect the pro apoptotic function and mechanism of iASPP knockdown in OTSCC cells.

In summary, we described the expression pattern of iASPP in OTSCC. iASPP overexpression correlates with malignant tumor progression. siRNA-mediated iASPP down-regulation inhibits proliferation and induces G0/G1 cell cycle arrest and cell apoptosis. Thus, our results suggest a critical role for iASPP in OTSCC tumorigenesis. iASPPmay serve as a novel therapeutic target for OTSCC.

Acknowledgements

This work was supported by grants from the Science and Technology Planning Project of Guangdong (2009B060700037, 2009B080701009, 2011B080701014).

Disclosure: The authors declare no confict of interest.

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Cite this article as:Chen Y, Yan W, He S, Chen J, Chen D, Zhang Z, Liu Z, Ding X, Wang A. In vitro effect of iASPP on cell growth of oral tongue squamous cell carcinoma. Chin J Cancer Res 2014;26(4):382-390. doi: 10.3978/ j.issn.1000-9604.2014.07.05

10.3978/j.issn.1000-9604.2014.07.05

Submitted May 18, 2014.Accepted for publication Jul 24, 2014.