Comparative proteomics analysis of oral cancer cell lines: identification of cancer associated proteins
© Karsani et al.; licensee BioMed Central Ltd. 2014
Received: 10 July 2013
Accepted: 7 January 2014
Published: 15 January 2014
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.
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.
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.
Oral cancer is a devastating disease that ranks as the fifth most common type of cancer affecting humans worldwide . 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 . 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 . 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 .
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
List of proteins with different abundance in cancer cell lines
Ascension number (Swissprot)/matched 2D coordinates
Peptides (% cov)
Relative change vs normal
Zoomed in gel image showing representative spots
Stathmin (Phosphoprotein p19)
P16949 /SPOT 2D-001YH8
Tropomyosin alpha-3 chain (Tropomyosin-3)
Myosin regulatory light chain-2
Lactoylglutathione lyase (Glyoxalase I). (EC 184.108.40.206)
Triosephosphate isomerase (EC 220.127.116.11)
Nucleoside diphosphate kinase A (EC 18.104.22.168)
Ubiquitin-conjugating enzyme E2 N (EC 22.214.171.124)
Gamma-glutamylcyclotransferase (EC 126.96.36.199)
Peroxiredoxin-4 (EC 188.8.131.52)
Superoxide dismutase [Cu-Zn] (EC 184.108.40.206)
Glutathione S-transferase P (GST class-pi). (EC 220.127.116.11)
Proteasome subunit beta type 4 precursor. (EC 18.104.22.168)
14-3-3 protein beta/alpha
Proteasome activator complex subunit 1
Proteasome activator complex subunit 2
14-3-3 protein sigma (Stratifin)
Interleukin-1 receptor antagonist protein precursor
Rho GDP-dissociation inhibitor 1
Ran-specific GTPase-activating protein
Heat-shock protein beta-1
T-complex protein 1 subunit zeta-2
Chloride intracellular channel protein 1 (membrane associated)
Proteins that are known to be cancer associated based on IPA
# of molecules
GSTP1, HSPB1, PHB, TPM3
GGCT, GLO1, GSTP1, NME1, PHB, RANBP1, SOD1, TPI1
Nodular hyperplasia of liver
CCT6B, GSTP1, NME1, PSME1, STIP1, STMN1
CCT6B, GSTP1, NME1, PSME1, STIP1, STMN1
GSTP1, HSPB1, TPM3
Multiplicity of benign tumor
Metastasis of melanoma
GSTP1, IL1RN, PHB
Digestive organ tumor
GSTP1, IL1RN, NME1, PHB, SFN, SOD1, STIP1, TPI1
Invasion of trophoblast
Urothelial bladder carcinoma
Non-small cell lung cancer
GSTP1, MYL12A, STMN1
CCT6B, GGCT, GLO1, GSTP1, HSPB1, IL1RN, MYL12A, NME1, PHB, PSME1, RANBP1, SFN, SOD1, STIP1, STMN1, TPI1, TPM3
GSTP1, NME1, SOD1, TPI1
Immortalization of keratinocytes
Invasion of extracellular matrix
Neoplasia of cells
NME1, PHB, SFN
GSTP1, NME1, PSME1, STIP1
Hereditary diffuse gastric cancer
Growth of secondary tumor
Incidence of hepatocellular carcinoma
Quantity of papilloma
Metastasis of cells
NME1, SOD1, TPI1
Acute myeloid leukemia
Tumorigenesis of colon cancer cell lines
Metastasis of cancer cells
Infection of cervical cancer cell lines
PSME2, RANBP1, STIP1
Growth of melanoma
Metastasis of melanoma cell lines
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.
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 . It has also been shown that LGUL inhibitors may also be a drug resistance-reversing agent . Increase of LGUL level has been found in drug-resistant tumor cells and in invasive ovarian cancer and breast cancer .
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 .
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 .
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 . PSME has also been proposed as a potential biomarker for ovarian cancer . 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
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 .
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 .
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 .
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 .
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.
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.
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 . It has also been implicated in a number of other cancers [32–34].
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 .
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
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 .
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 .
T-complex protein 1 subunit zeta-2 (TCPW) is a molecular chaperon that assists in the folding of proteins upon ATP hydrolysis .
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 . CLIC1 has also been proposed as a potential biomarker [46, 47] and therapeutic target  for cancer.
Assessment of mRNA transcript
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.
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 PlusOne™ 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 .
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.
MALDI-TOF/TOF mass spectrometry analysis and database searching
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.
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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