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Comparative proteomics analysis of oral cancer cell lines: identification of cancer associated proteins

Proteome Science volume 12, Article number: 3 (2014) Cite this article

Abstract

Background

A limiting factor in performing proteomics analysis on cancerous cells is the difficulty in obtaining sufficient amounts of starting material. Cell lines can be used as a simplified model system for studying changes that accompany tumorigenesis. This study used two-dimensional gel electrophoresis (2DE) to compare the whole cell proteome of oral cancer cell lines vs normal cells in an attempt to identify cancer associated proteins.

Results

Three primary cell cultures of normal cells with a limited lifespan without hTERT immortalization have been successfully established. 2DE was used to compare the whole cell proteome of these cells with that of three oral cancer cell lines. Twenty four protein spots were found to have changed in abundance. MALDI TOF/TOF was then used to determine the identity of these proteins. Identified proteins were classified into seven functional categories – structural proteins, enzymes, regulatory proteins, chaperones and others. IPA core analysis predicted that 18 proteins were related to cancer with involvements in hyperplasia, metastasis, invasion, growth and tumorigenesis. The mRNA expressions of two proteins – 14-3-3 protein sigma and Stress-induced-phosphoprotein 1 – were found to correlate with the corresponding proteins’ abundance.

Conclusions

The outcome of this analysis demonstrated that a comparative study of whole cell proteome of cancer versus normal cell lines can be used to identify cancer associated proteins.

Background

Oral cancer is a devastating disease that ranks as the fifth most common type of cancer affecting humans worldwide [1]. Incidence and mortality rates vary widely across the world. There are approximately 500,000 new oral and pharyngeal cancer cases diagnosed annually, with three quarters being registered in developing countries [2, 3]. The disease is highly associated with established cultural risk factors such as tobacco chewing/smoking, alcohol consumption and betel-quid chewing [4]. In western countries, cigarette smoking and alcohol drinking are the major risk factors while betel-quid chewing and smoking are the major risk factors that contribute to the development of oral cancer in South Asia, Southeast Asia and Taiwan [1]. Oral cancer appears as an abnormal growth within the mouth region and this include the buccal mucosa (cheek), tongue, floor of the mouth and lip. Oral squamous cell carcinoma (OSCC) represents the highest of all oral malignancy, accounting for more than 95% of total cases reported [1, 3].

There is a dearth of knowledge with regards to the development and progression of oral cancer. The exact molecular mechanisms remain unknown. However, it is known to involve the activation of oncogenes, change in expression of various proteins which would eventually lead to the development of cancer. Thus, a study of proteins that change in oral cancer will provide valuable information and add to our understanding of the disease. It may also identify candidate proteins that can potentially be utilized as biomarkers for early detection. The ability of proteomics to compare differences/changes in proteome profiles (including changes in post-translational modifications) which are related to tumor progression has been adapted in clinical research for the identification of biomarkers for disease such as cancer [5].

One of the main problems in performing proteomics analysis on cancerous cells is the difficulty in obtaining sufficient amounts of material to perform the analysis. The availability of cancer cell lines makes it possible to obtain an almost limitless amount of sample for proteomic analysis. Cultured cancer and normal cell lines can be used as a simplified model system for studying changes that accompany tumorigenesis. Thus, this study aims to utilize proteomics in identifying differences between proteome profiles of normal primary cultures vs oral cancer cell lines. Our results showed that such an analysis will identify cancer associated proteins.

Results and discussions

Identification of proteins with different abundance between normal primary cultures and cancer cell lines

More than 1000 individual protein spots were resolved and visualized on silver stained gels. A representative gel is shown in Figure 1. Image analysis identified 24 protein spots that exhibited significant difference in abundance (p < 0.05). All 24 were unambiguously identified by MALDI-TOF/TOF MS and their respective identities are shown in Table 1. The index numbers in Table 1 correspond to the numbers in Figure 1 and they indicate the location of the proteins on the 2DE gels. From this point forward, proteins will be referred to by their abbreviated names as shown in Table 1. Table 1 includes zoomed images for all protein spots. The identified proteins were classified into seven functional categories – structural proteins, enzymes, regulatory proteins, chaperones and others. For almost all identified proteins, the experimental and theoretical pI and molecular weights were matched.

Figure 1
figure 1

Representative 2DE gel of whole cell proteome of cell lines. The whole cell protein of normal primary cultures and cancer cell lines were resolved by 2DE pI 4–7, 11% second dimension polyacrylamide gel. Proteins with different abundance are shown as numbered spots. The numbers correspond to Spot Number in Table 1.

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Table 1 List of proteins with different abundance in cancer cell lines
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When proteins with different abundance in oral cancer were subjected to analysis using IPA, 18 were predicted to be related to cancer with involvements in hyperplasia, metastasis, invasion, growth and tumorigenesis. Table 2 shows a list of proteins known to have roles in various cancers based on IPA. Figure 2 shows a graphical representation of the predicted molecular relationships between these proteins. The predicted network involved interplay between the various proteins and suggested that changes in abundance of these proteins may influence the function of other proteins within the network. IPA also predicted that most of the proteins were of cytosolic origin.

Table 2 Proteins that are known to be cancer associated based on IPA
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Figure 2
figure 2

Top-scored molecular network with identified proteins implicated in cancer progression according to the IPA software. Proteins in the network are represented by their gene symbols. Green colored shapes denote proteins with lower abundance in oral cancer cell lines, while red colored shapes denote proteins with higher abundance in oral cancer cell lines A) molecule types, B) relationship types.

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Coordinate regulation of proteins with similar function

Two groups of proteins - detoxification enzymes and proteasome activator complex - appeared to show coordinate change in protein abundance in oral cancer.

Detoxification enzymes

Four enzymes involved in the protection of cells against oxidative stress - Lactoylglutathione lyase (LGUL), Peroxiredoxin-4 (PRDX4), Glutathione S-transferase P (GSTP1) and Superoxide dismutase (SODC) - were found to be in higher abundance in oral cancer. Malignant cells are in general under increased oxidative stress [6–8]. Thus, an increase of enzymes involved in protection against oxidative stress may be a mechanism to tolerate such stress.

LGUL Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione. Inhibitors of LGUL have been proposed as possible antitumor agents that function by inducing elevated levels of methylglyoxal in cancer cells. Methylglyoxal has been shown to inhibit the growth of human leukaemia 60 cells in culture [9]. It has also been shown that LGUL inhibitors may also be a drug resistance-reversing agent [10]. Increase of LGUL level has been found in drug-resistant tumor cells and in invasive ovarian cancer and breast cancer [11].

PRDX4 is involved in the redox regulation of the cell. The level of peroxiredoxins (in particular PRDX3, PRDX4 and PRDX5) has been shown to be increased in cancer, suggesting the induction of PRDX as a response to increased production of reactive oxygen species in carcinomatous tissue [12].

GSTP1 conjugates reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. It plays an important role in the protection of cells from the products of oxidative stress as well as from several environmental carcinogens. The GSTP1 gene has been shown to be overexpressed in many human tumors [13].

SODC destroys radicals which are normally produced within the cells and which are toxic to biological systems. The level of SODC has been shown to increase in a number of cancers [14–16].

Proteasome activator complex

Proteasome activator complex subunit 1 (PSME1) and proteasome activator complex subunit 2 (PSME2) are implicated in immunoproteasome assembly and is required for efficient antigen processing. IPA showed that both proteins also interact and influence the function of the 26 s and 20 s proteaseome. The proteasome is a multicatalytic proteinase complex that is responsible for the degradation of most intracellular proteins, including proteins that are crucial to cell cycle regulation and programmed cell death, or apoptosis. Targeting the proteasome is being investigated as a useful anticancer strategy [17]. PSME has also been proposed as a potential biomarker for ovarian cancer [18]. Interestingly, our proteomics analysis showed a decrease in abundance of these proteins, whereas the proteoasome activity is expected to increase in most cancers.

Proteins with higher abundance in oral cancer cell line

Structural protein

Stathmin (STMN1) is involved in the regulation of the microtubule filament system where it prevents the assembly and promotes disassembly of microtubules. It has been shown to be present at high levels in a variety of human cancers and has been proposed as a potential target in cancer therapies that disrupt the mitotic apparatus [19].

Enzymes

A number of enzymes were found to be in higher abundance in cancer cell lines. Triosephosphate isomerase (TPIS) is a glycolysis enzyme that catalyzes the reversible interconversion of triosephosphate isomers - dihydroxyacetone phosphate and D-glyceraldehyde 3-phosphate. TPIS may be associated with cancer metastasis [20].

Nucleoside diphosphate kinase A (NDKA) plays a major role in the synthesis of nucleoside triphosphates other than ATP. NDKA is involved in cell proliferation, differentiation and development, signal transduction, G protein-coupled receptor endocytosis, and gene expression. It has been shown to act as both a metastasis suppressor and promoter in different tumors [21].

Ubiquitin-conjugating enzyme E2 N (UBE2N) mediates the transcriptional activation of target genes. The increased abundance of UBE2N and other ubiquitin conjugating enzymes has been reported in various cancers [22–25].

Gamma-glutamylcyclotransferase (GGCT) catalyzes the formation of 5-oxoproline from gamma-glutamyl dipeptides and may play a significant role in glutathione homeostasis. It induces the release of cytochrome c from the mitochondria resulting in the induction of apoptosis. GGCT may be associated in the induction of apoptosis in leukemia U937 cells [26].

Proteasome subunit beta type 4 (PSB4) belongs to the proteasome multicatalytic proteinase complex. This complex is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu adjacent to the leaving group at neutral or slightly basic pH.

Regulatory proteins

14-3-3 protein beta/alpha (1433B) is an adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. 1433B binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding will generally result in the modulation of the activity of the binding partner.

Prohibitin (PHB) has a role in regulating cell proliferation where it inhibits DNA synthesis. It has been shown to be involved in a number of different cancers [27–30].

Stress-induced-phosphoprotein 1 (STIP1) mediates the association of the molecular chaperones HSC70 and HSP90. STIP1 has been shown to be secreted by, and induces proliferation in glioma cells [31]. It has also been implicated in a number of other cancers [32–34].

Interleukin-1 receptor antagonist protein (IL1RA) inhibits the activity of IL-1 by binding to its receptor. The level of IL1RA has been shown to change in cancer [35–37].

Rho GDP-dissociation inhibitor 1 (GDIR) regulates the GDP/GTP exchange reaction of the Rho proteins by inhibiting the dissociation of GDP from them, and the subsequent binding of GTP to them. In cancer, GDIR has been implicated in metastasis, mediation of cancer cell motility and drug resistance [38–40].

Ran-specific GTPase-activating protein (RANG) inhibits GTP exchange on Ran and plays an essential role in nuclear transport by permitting RanGAP-mediated hydrolysis of GTP on Ran complexed to karyopherin b [41].

Chaperones

Heat-shock protein beta-1 (HSPB1) is involved in stress resistance and actin organization. Heat shock proteins (HSPs) are a large and heterogeneous group of chaperones whose synthesis can be induced by both physiological and pathological conditions, such as heat shock, oxidative stress, mitogenic signals, inflammation, infection and neoplastic transformation. Although a number of HSPs has been implicated with cancer, association of HSPB1has not been reported.

Proteins with lower abundance in oral cancer cell line

Structural proteins

Tropomyosin alpha-3 chain (TPM3) binds to actin filaments in muscle and non-muscle cells. In association with the troponin omplex, it plays a central role in the calcium dependent regulation of vertebrate striated muscle contraction.

Myosin regulatory light chain-2 (ML12A) is a myosin regulatory subunit that plays an important role in regulation of both smooth muscle and non-muscle cell contractile activity via its phosphorylation. ML12A has been implicated in cytokinesis, receptor capping, and cell locomotion. Phosphorylation of ML12A has been shown to be critical in the invasiveness of metastatic cancer cells [42].

Regulatory protein

14-3-3 protein sigma, also known as stratifin (1433S) is an adapter protein implicated in the regulation of a wide variety of both general and specialized signaling pathways. 1433S is a potential lymph node metastasis-related protein in lung squamous carcinoma [43].

Chaperones

T-complex protein 1 subunit zeta-2 (TCPW) is a molecular chaperon that assists in the folding of proteins upon ATP hydrolysis [44].

Others

Chloride intracellular channel protein 1 (CLIC1) is a protein that can insert into cellular membranes to form chloride ion channels. It has been shown that overexpression of CLIC1 promoted cell motility and invasion of low metastasic cell lines (GBC-SD18L) in vitro, while RNA interference of CLIC1 decreased cell motility and invasive potency of highly metastasic cell lines (GBC-SD18H) in vitro, suggesting that CLIC1 may play an important role in metastasis of gallbladder carcinoma [45]. CLIC1 has also been proposed as a potential biomarker [46, 47] and therapeutic target [48] for cancer.

Assessment of mRNA transcript

Quantitative real-time PCR was performed to assess the mRNA expression of four proteins - STMN1, 1433S, STIP1 and GSTP1. These proteins were selected due the marked difference in their abundance and/or possible involvement in cancer. They also represented proteins from various functional categories. The mRNA expression of all four genes was found to correlate with its corresponding protein abundance. However, only 1433S and STIP1 was found to be statistically significant (Figure 3). This suggested that these proteins may be regulated at the mRNA level.

Figure 3
figure 3

Results of quantitative RT-PCR showing relative expressions of STMN1, 1433S, STIP1 and GSTP1. Total mRNA was extracted from normal and oral cancer cell lines. Quantitative RT-PCR was then performed as described. A: Relative expression of STMN1, B: Relative expression of 1433S, C: Relative expression of STIP1, D: Relative expression of GSTP1. Relative intensities of all genes of interest were determined by using β-actin as an internal standard. Results represent the mean ± SD for three experiments. *p < 0.05.

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Conclusions

We have showed that a comparative study of the oral cancer cell line proteome may identify cancer associated proteins. IPA predicted that at least 18 of these proteins were associated with cancer development and progression. At least two identified proteins (CLIC1 and PSME) have previously been proposed as potential biomarkers for cancer. Two groups of proteins (detoxification enzymes and proteasome activator complex) appeared to show coordinate change in protein abundance. Taken together, these results has demonstrated the potential of this type of study as an alternative to directly analyzing tissue samples in identifying cancer associated proteins. This study can be further extended by investigating the presence/absence of these proteins in tissue samples.

Methods

Establishment of cell cultures

This project was approved by the Medical Ethics Committee, Faculty of Dentistry, University of Malaya and endorsed by the Ministry of Health, Malaysia (DFOP1006/0041[P]). Normal tissues were derived from surgically resected tissue specimens from different impacted tooth patients. Cancerous tissues were derived from surgically resected tissue specimens from three different oral squamous cell carcinoma patients. Sample collection was performed at the Faculty of Dentistry and University Malaya Medical Centre, Kuala Lumpur Hospital and Tengku Ampuan Rahimah Hospital. All tissues were acquired after written informed consent was obtained from the patients. The oral cancer cell lines and primary cultures were derived from squamous cells and were originated from the same anatomic site (gum). Cell cultures were established as previously described [49, 50].

Sample preparation and protein extraction

Cells were grown to confluence. Following trypsinization, cells were pelleted and washed 3× with PBS. The cells were then lysed by repeated freeze thawing in extraction buffer (5 M Urea, 2 M Thiourea, 2% SB3-10 and 2% CHAPS). Protein concentration was determined by Bradford assay using Bovine Serum Albumin as standard according to the manufacturer’s instruction (Bio-Rad Laboratories).

Two-Dimensional Gel Electrophoresis (2DE)

For each cell line/primary culture, 2DE was performed in triplicate on protein samples extracted from three different passages of growth. Isoelectric focusing for 2DE was performed using an IPGphor system (Amersham Biosciences) according to the manufacturer’s protocol. Briefly, IPG strips (24 cm Immobiline IPG Drystrip pH 4–7) were rehydrated overnight using 450 μl/strip urea rehydration stock solution (8 M Urea, 2% w/v CHAPS, 0.5% v/v Pharmalyte/IPG Buffer pH3-10, 1% trace bromophenol blue) without containing the sample. Protein extracts were solubilized in 80 μl sample lysis buffer (8 M Urea, 4% w/v CHAPS, 40 mM Tris, 65 mM DTT, 1% trace bromophenol blue) and loaded into the loading cup just before running. A total of 80 μg protein was loaded for analytical gels and 160 μg loaded for preparative gels. Isoelectric focusing was performed for 60 kVh with running conditions as follows: 500 V: 1 hour, 1000 V: 1 hour, 1000 V: 3 hours and finally a constant 8000 V at 20°C.

For the second dimension, the IPG strips were first equilibrated in 10 ml of SDS equilibration buffer (6 M Urea, 75 mM Tris–HCl pH8.8, 87% w/w glycerol, 2% SDS, 1% trace bromophenol blue) containing 1% DTT for 10 minutes, followed by a second equilibration for 10 minutes in the same equlibration buffer containing 2.5% Iodoacetamide. Equilibrated strips were then placed on 11% SDS-Polyacrylamide gel and enclosed with 0.5% agarose gel. Second dimension electrophoresis of reduced and alkylated samples was carried out using an Ettan Dalt twelve system (GE Healthcare). Electrophoresis was initially performed at 2 W for 45 minutes, followed by 110 W until the bromophenol blue dye reached the bottom edge of the gel.

Protein spots were visualized using protocols described in the PlusOneâ„¢ Silver staining kit (GE Healthcare). The complete protocol was followed for analytical gels. For preparative gels, a modified protocol was used. Glutaraldehyde was omitted from the sensitization step and formaldehyde omitted from the silver reaction step [51].

Gel image analysis

Following 2DE and silver staining, gels were scanned (Image Scanner III, GE Healthcare) and protein profiles compared using the ImageMaster Platinum 7.0 software (GE Healthcare). Protein spots were normalized using percentage volume. Statistical analysis for the comparison of protein abundance between the groups was performed by Student’s t-test. Only protein spots with fold difference > 1.4 and p < 0.05 were considered to have significantly changed in abundance.

Tryptic digestion

Protein spots were excised and in-gel digested with trypsin (Promega) for mass spectrometric identification according to published protocols [52–54].

MALDI-TOF/TOF mass spectrometry analysis and database searching

Protein identification was performed as previously described using a MALDI-TOF mass spectrometer (ABI 4800 Plus, Applied Biosystems) [55, 56].

Bioinformatics

Categorization of protein function was determined based on Swiss-Prot/TrEMBL database search. Ingenuity Pathway Analysis (IPA, http://www.ingenuity.com) was used to determine the localization of identified proteins and their participation in molecular networks involved in carcinogenesis according to the well-established Ingenuity Knowledge Base. Details regarding proteins that were different in abundance were exported to the IPA software. Each protein identifier was then mapped to its corresponding protein object and was overlaid onto a global molecular network developed from information contained in the Ingenuity Knowledge Base. Protein networks were then algorithmically generated based on their connectivity. A Right-tailed Fischer’s exact test was used to calculate a p-value indicating the probability that each biological function assigned to the network is not due to chance alone.

Real-time PCR (RTPCR)

All experiments were performed according to manufacturers’ instructions. Total mRNA was extracted from cell pellets using RNAqueous®-4PCR Kit (Ambion). High Capacity cDNA Reverse Transcription kit (Applied Biosystems) was used to reverse transcribe total mRNA into cDNA templates. RTPCR was performed by either Taqman® Gene Expression Assay or Fast Sybr Green (Applied Biosystems).

Primers were either designed using the Primer3 software or were based on literature and PrimerBank [57, 58]. The specificity of primers was examined using NCBI primer-Blast (http://www.ncbi.nlm.nih.gov/tools/primer-blast/). All PCR reactions were performed using the StepOnePlus Real-Time PCR instrument (Applied Biosystems). PCR conditions were defined according to the manufacturer’s recommended parameters. Gene expression levels were comparatively analyzed using StepOne software v2.2. Raw data from the experiments were recalculated as a mean expression level of cancer and normal groups to generalize the results of comparisons between the two groups. Student’s unpaired t-test was then performed to determine the significance of the results.

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Acknowledgements

This project was funded by University of Malaya IPPP grant PS276/2010B and eScienceFund grant SF007-2013. This research had been facilitated by access to the University of Malaya Centre for Proteomics Research (UMCPR) and Medical Biotechnology Laboratory, Faculty of Medicine, University of Malaya. We gratefully acknowledge the staff of Oral Cancer Research & Coordinating Center (OCRCC), University of Malaya for assistance in normal tissues collection and Cancer Research Initiatives Foundation (CARIF) for providing cell culture facilities and other necessary equipments.

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Authors and Affiliations

  1. Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia

    Saiful Anuar Karsani & Nor Afiza Saihen

  2. Oral Cancer Research and Co-ordinating Centre & Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia

    Rosnah Binti Zain

  3. Oral Cancer Research Team, 2nd Floor Outpatient Centre, Sime Darby Medical Centre, Cancer Research Initiatives Foundation (CARIF), 47500 Subang Jaya, Selangor, Malaysia

    Sok-Ching Cheong

  4. Department of Clinical Oral Biology, Faculty of Dentistry, Universiti Kebangsaan Malaysia, 50300, Kuala Lumpur, Malaysia

    Mariati Abdul Rahman

  5. Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia

    Sok-Ching Cheong

  6. University of Malaya Centre for Proteomics Research (UMCPR), University of Malaya, 50603, Kuala Lumpur, Malaysia

    Saiful Anuar Karsani

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  1. Saiful Anuar Karsani
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  2. Nor Afiza Saihen
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  4. Sok-Ching Cheong
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  5. Mariati Abdul Rahman
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Correspondence to Saiful Anuar Karsani.

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The authors declare that they have no competing interests.

Authors’ contributions

SAK - principal investigator, designed and conceived the experiments, performed all MALDI-TOF/TOF analysis and prepared the manuscript. NAS - performed the experiments. RBZ - provided tissue samples from which cell lines were derived. SCC - established the cell cultures. MAR – designed and conceived the experiments and prepared the manuscript. All authors read and approved the final manuscript.

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Karsani, S.A., Saihen, N.A., Zain, R.B. et al. Comparative proteomics analysis of oral cancer cell lines: identification of cancer associated proteins. Proteome Sci 12, 3 (2014). https://doi.org/10.1186/1477-5956-12-3

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Keywords

Proteome Science

ISSN: 1477-5956