key: cord-1025451-2vso98ry
authors: Chen, Yeng; Azman, Siti Nuraishah; Kerishnan, Jesinda P.; Zain, Rosnah Binti; Chen, Yu Nieng; Wong, Yin-Ling; Gopinath, Subash C. B.
title: Identification of Host-Immune Response Protein Candidates in the Sera of Human Oral Squamous Cell Carcinoma Patients
date: 2014-10-01
journal: PLoS One
DOI: 10.1371/journal.pone.0109012
sha: 865949791a49615aa67ae0444e5987348c82ba65
doc_id: 1025451
cord_uid: 2vso98ry

One of the most common cancers worldwide is oral squamous cell carcinoma (OSCC), which is associated with a significant death rate and has been linked to several risk factors. Notably, failure to detect these neoplasms at an early stage represents a fundamental barrier to improving the survival and quality of life of OSCC patients. In the present study, serum samples from OSCC patients (n = 25) and healthy controls (n = 25) were subjected to two-dimensional gel electrophoresis (2-DE) and silver staining in order to identify biomarkers that might allow early diagnosis. In this regard, 2-DE spots corresponding to various up- and down-regulated proteins were sequenced via high-resolution MALDI-TOF mass spectrometry and analyzed using the MASCOT database. We identified the following differentially expressed host-specific proteins within sera from OSCC patients: leucine-rich α2-glycoprotein (LRG), alpha-1-B-glycoprotein (ABG), clusterin (CLU), PRO2044, haptoglobin (HAP), complement C3c (C3), proapolipoprotein A1 (proapo-A1), and retinol-binding protein 4 precursor (RBP4). Moreover, five non-host factors were detected, including bacterial antigens from Acinetobacter lwoffii, Burkholderia multivorans, Myxococcus xanthus, Laribacter hongkongensis, and Streptococcus salivarius. Subsequently, we analyzed the immunogenicity of these proteins using pooled sera from OSCC patients. In this regard, five of these candidate biomarkers were found to be immunoreactive: CLU, HAP, C3, proapo-A1 and RBP4. Taken together, our immunoproteomics approach has identified various serum biomarkers that could facilitate the development of early diagnostic tools for OSCC.

Oral cancer represents the sixth most prevalent cancer in the world. Among the different types of oral cancer, oral squamous cell carcinoma (OSCC) arising from the oral mucosa accounts for more than 90% of these malignancies. Thus, OSCC is the most common malignancy affecting the head and neck region. Notably, there are nearly 300,000 new cases of oral cancer reported annually [1, 2] , and it was estimated that approximately 128,000 oral cancer patients died worldwide in 2008 [3] . Therefore, despite recent advances in the diagnosis and treatment of oral cancer (e.g., chemotherapy, radiotherapy, and surgical therapy) the survival rate of OSCC patients has remained less than 60% [4, 5] . A fundamental barrier in improving the survival of OSCC patients is the fact that these malignancies often remain undetected until the later stages. In this regard, it was reported that a severalmonth delay in diagnosis could reduce the chance of survival from 80% to 40% [6] . Thus, in order to prevent the high OSCC-related mortality rate, recent attention has been focused on identifying potential diagnostic molecular markers (e.g., cell cycle regulators) that might represent biological predictors of oral cancer [7] . Moreover, OSCC has been linked to several risk factors, including various bacterial pathogens [8] , which might be useful for detecting OSCC.

Recent studies have indicated that early diagnosis, lifestyle modification, and effective treatment can prevent more than twothirds of OSCC-related mortalities. However, currently available diagnostic methods do not allow for the detection of oral cancer in the early stages. To visualize malignant lesions in the oral cavity, different microscopic methods are available, which make use of various techniques, including autofluorescence, chemiluminescence, or dye-based tissue staining. However, due to the low sensitivity and specificity of these diagnostic strategies, clinicians generally use biopsies to detect OSCC [9] . Nevertheless, successful diagnosis through tissue biopsy is highly dependent on acquiring whole and complete tissue samples from patients for examination. In this regard, biopsies harvested from oral cancer patients are often associated with the soft tissues that surround the cancer tissue. In addition, oral cancer frequently involves the development of multiple primary tumors. Indeed, the occurrence of a second primary tumor is 3-7% higher per year in oral cancer when compared to other malignancies [10] . Therefore, the identification of suitable and reliable OSCC biomarkers is essential for achieving early detection and treatment, which can reduce mortality rates in OSCC patients. In this respect, antibody-based diagnostic tests that recognize specific tumor-associated antigens in cancer sera might represent a valid methodology [11] .

Proteomic analysis allows the identification and quantification of proteins and peptides in biological samples [12] . However, through this approach, numerous post-translational forms of protein regulation, including regulating enzymes and low abundance proteins may remain undetected. Thus, in the present investigation, we employed an immunoproteomic approach and pooled human antibodies to detect host-specific response proteins in OSCC patients. Specifically, we used a well-characterized analytical platform combining two-dimensional gel electrophoresis (2-DE) and mass spectrometry (MS) to identify biomarkers in unfractionated sera from OSCC patients and normal controls. This immunoproteomics approach can be used to identify antigens targeted by the immune system in sera during disease progression. In addition, the immune responses are known to be involved in the mechanism of carcinogenesis [13] . Therefore, our comparative analyses revealed distinct OSCC biomarkers that might promote the development of specific diagnostic tests for early detection of oral cancer. 3(09) ]) approve this consent procedure. We obtained the permission from the above committee and they have cleared all the approval and having the record. This study was also conducted in accordance with International Conference on Harmonisation-Good Clinical Practice (ICH-GCP) guidelines and the Declaration of Helsinki.

We performed 2-DE as previously described [14] . Briefly, unfractionated human serum samples (10 ml) were lysed, rehydrated in lysis buffer (2M thiourea, 8M urea, 4% CHAPS, 1% dithreitol, and 2% pharmalyte), and subjected to isoelectric focusing in 13-cm rehydrated precast immobilized dry strips (pH 4-7; GE Healthcare, Sweden). Sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE) was performed using 8-18% gradient polyacrylamide gels in the presence of SDS for the second dimension separation. Gel silver staining was performed as previously described [15] . Silver staining and Coomassie Brilliant Blue staining for MS were conducted using slightly modified published methods [16] .

The ImageScanner III (GE Healthcare, Sweden) was used to capture and store 2-DE gel images. PD-Quest 2-D gel analysis software (version 8.0.1, Bio-Rad) was employed to evaluate the differentially expressed protein spots. Identical spots were matched in the serial gels and normalized by correcting for spot quantification values and gel-to-gel variation unrelated to expression changes. For the normalization method, we used total densities from the gel images (i.e., raw quantity of each gel spot was divided by the total quantity of all spots within the gel). All protein concentration values are presented as means of percentage volume (% volume) 6 standard deviations (SD). The student's ttest and one-way analysis of variance (ANOVA) were used to analyze differences between patients and controls. P-values less than 0.05 (p,0.05) were considered as statistically significant.

Spots of interest were excised and subjected to in-gel tryptic digestion using a commercially available kit (Calbiochem, Germany). MS analysis and database searches were performed at the Proteomic Center within the Faculty of Biological Sciences at the National University of Singapore. Digested peptides were mixed with 1.2 ml of CHCA matrix solution (5 mg/ml of cyano-4hydroxy-cinnamic acid in 0.1% trifluoroacetic acid [TFA] and 50% acetonitrile [ACN]) and spotted onto MALDI target plates. An ABI 4800 Proteomics Analyzer MALDI-TOF/TOF Mass Spectrometer was used for spectra analysis (Applied Biosystems, USA), and the MASCOT search engine (version 2.1; Matrix Science, UK) was employed for database searches. In addition, GPS Explorer software (version 3.6; Applied Biosystems, USA) was utilized along with MASCOT to identify peptides and proteins. Search parameters allowed for N-terminal acetylation, C-terminal carbamidomethylation of cysteine (fixed modification), and methionine oxidation (variable modification). Peptide and fragment mass tolerance were set to 100 ppm and 60.2 Da, respectively. The peptide mass fingerprinting (PMF) parameters were set as follows: one missed cleavage allowed in trypsin digest; monoisotropic mass value; 60.1 Da peptide mass tolerance; and 1+ peptide charge state.

Peptides were initially identified using the ProteinPilot proteomics software on the Mass Spectrometer (Applied Biosystems, USA). A score reflecting the relationship between theoretically and experimentally determined masses was calculated and assigned. Analyses were conducted using the International Protein Index (http://www.ebi.ac.uk/IPI) and NCBI Unigene human databases (version 3.38). A total of 100,907 entries were searched, and a score of .82 was considered as significant in the MASCOT NCBI database.

Our 2-DE gel immunoblotting protocol was organized into four categories: (1) normal sera probed with normal sera, (2) normal sera probed with OSCC sera, (3) OSCC sera probed with normal sera, and (4) OSCC sera probed with OSCC sera. After running the 2-DE gels, they were transferred onto nitrocellulose membranes using the Multiphor II Novablot semi-dry system (GE Healthcare, Sweden). Membranes were blocked with SuperBlock (Pierce, USA) and washed three times with Tris-buffered saline (TBS)-Tween-20. The membranes were subsequently incubated overnight (4uC) with pooled sera from patients or healthy subjects that contains the primary antibodies against various targets (1:200 dilution). Following washing, membranes were incubated for 1 hour at room temperature with horseradish peroxidase (HRP)linked monoclonal anti-human immunoglobulin M (IgM) (1:5000; Invitrogen, USA). The membranes were again washed and then visualized using chemiluminescence substrate (Pierce, USA) and 18 cm 6 24 cm films (Kodak, USA).

Functional annotation analysis was performed using DAVID v6.7 (Database for Annotation, Visualization, and Integrated Discovery), which provides a comprehensive set of functional annotation tools to understand the biological significance associated with large lists of genes or proteins [17] . This functional categorization is considered significant when a p-value of less than 0.05 (p,0.05) is obtained. STRING v9.1 (Search Tool for the Retrieval of Interacting Genes) was used to examine proteinprotein interaction networks [18] .

Image analysis of 2-DE serum protein profiles from healthy subjects and OSCC patients Unfractionated serum samples were separated via 2-DE to generate high-resolution proteome profiles for healthy subjects (Fig. 1a) and OSCC patients (Fig. 1b) . Protein spots in the 2-DE gels from OSCC patients (n = 25) and normal controls (n = 25) were analyzed using PDQuest 2-D gel analysis software. This comparative analysis revealed several up-and down-regulated proteins in the serum of OSCC patients ( Table 1) .

Following digestion of the differentially expressed spots, MS analysis allowed us to identify the following seven host-specific proteins: leucine-rich a2-glycoprotein (LRG), alpha-1-B-glycoprotein (ABG), clusterin (CLU), PRO2044, haptoglobin (HAP), proapolipoprotein A1 (proapo-A1) and retinol-binding protein 4 precursor (RBP4) ( Table 1) . Furthermore, MS analysis revealed complement C3c (C3) as additional host-specific protein, which found to be immunoreactive and also five non-host factors (A1, A2, A3, A4, and A5), which corresponded to antigens from Acinetobacter lwoffii, Burkholderia multivorans, Myxococcus xanthus, Laribacter hongkongensis, and Streptococcus salivarius. In total, we identified 13 host and non-host specific protein spots, which were subsequently subjected to MS analysis (MALDI-TOF/ TOF). Data regarding the identification (ID), MASCOT accession number, isoelectric point (pI), and molecular mass (Mr) for each protein are presented in Table 2 and 3 .

Comparing our candidate OSCC biomarkers to control samples, we found that LRG, ABG, CLU, and PRO2044 displayed 0.21-, 0.45-, 0.6-, and 0.63-fold down regulation, respectively (p,0.05). This indicated that CLU and PRO2044 represented the most significantly decreased protein spots. Notably, all of these down-regulated factors have been previously studied and could be important with regard to OSCC.

LRG is a protein that has been observed in patients with bacterial infections [19] , severe acute respiratory syndrome [20] , as well as various malignancies, including pancreatic [21] , liver [22] , and lung [23] cancers. Moreover, LRG has been suggested to play an anti-apoptotic role during stress. Nevertheless, Weivoda et al. [24] has reported low levels of LRG in patients with inflammatory arthritis, in spite of the fact that LRG can be produced in response to inflammation. Overall, the relevance of LRG in distinct patient groups remains ill defined.

ABG is one of the eight host-specific proteins observed in this study. Interestingly, decreased ABG expression has also been observed in pancreatic cancer [25] . On the other hand, upregulated ABG was previously reported in bladder cancer [26] , non-small cell lung cancer [27] , and squamous cell carcinoma of the uterine cervix [28] .

With regard to CLU, differential expression has been linked to oncogenesis and tumor growth in bladder [29] , breast [30] , colorectal [31] , ovarian [14] , pancreatic [32] , and prostate [33] cancers. However, although many researchers have reported increased CLU expression during tumorigenesis, we have observed significantly down-regulated CLU levels in sera from OSCC patients. Nevertheless, other reports have also described a similar loss of CLU expression in various tumors, including prostate cancer [34] , pancreatic cancer [32] , esophageal squamous cell carcinoma [35] and neuroblastoma [36] . Notably, these discrepancies may stem from the fact that there are differentially expressed CLU isoforms in human tissues and fluids that may exhibit distinct functions in tumors [14, 37] . Even though it has been suggested that CLU down regulation could be associated with disease progression [32, 38] , this may depend on the type of cancer [39, 40] . Notably, the true function of CLU has remained elusive despite extensive investigation. So far, CLU has been proposed to participate in the immediate cellular response to stress, which regulates cell growth and survival [41] . In this regard, its function appears isoform dependent, with both proapoptotic and anti-apoptotic forms [34] .

Finally, our analysis revealed that PRO2044 (the C-terminal fragment of albumin, ALB) was the most down-regulated protein in the sera of OSCC patients. Interestingly, Kawakami et al. [22] observed that PRO2044 was also down regulated in hepatocellular carcinoma patients following curative radiofrequency ablation. In contrast, Jin et al. [42] reported that PRO2044 levels were increased in the cerebrospinal fluid of patients with Guillain-Barré syndrome, an acute inflammatory autoimmune disorder of the peripheral nervous system.

In addition to down-regulated proteins, up-regulated hostspecific antigens were also identified in OSCC patients, including HAP, proapo-A1, and RBP4. Compared to the control samples, these proteins displayed 1.47-, 1.82-, and 2.66-fold increases, respectively (p,0.05). RBP4 was found to be the most upregulated.

Notably, a correlation between HAP expression and malignancies has been reported [43, 44] . Indeed, similar to a previous study by Lai et al. [45] , we found that HAP levels were significantly increased in sera from OSCC patients. Furthermore, since HAP is primarily hepatocyte-produced, a rise in its levels may indicate the occurrence of an acute phase response in OSCC [44] . Moreover, HAP has also been reported to participate in cell migration, extracellular matrix degradation, and arterial restructuring, suggesting its possible role in cancer [46] . In addition, HAP might act as an angiogenic agent that contributes to endothelial cell growth and differentiation [47] .

With regard to proapo-A1 (or apo-A1), our findings are consistent with studies that have found elevated expression in various malignancies, including breast [48] , colorectal [49] , nonsmall cell lung [50] pancreatic [51] , and hepatocellular [52] cancers. It is possible that increases in proapo-A1 might stem from reduced activity of proapo-A1 cleaving enzyme or higher turnover of apo-A1 [50, 53] .

We also observed an elevation of RBP4 levels in OSCC. It has been suggested that RBP4 over expression in cancer cells could result from an inhibition of phosphatidylinositol-3 kinase (PI3K) activity [54, 55] . Moreover, RBP4 expression might be related to retinoid depletion, which is a common feature in cancer patients [56] [57] [58] . In addition, RBP4 levels can be influenced by transthyretin, which could reduce renal clearance of RBP4 [59] .

In addition to the above down-and up-regulated self-antigens, we also identified five non-host markers in the proteomic profiles of OSCC patients. These proteins were derived from various bacteria, including A. lwoffii, B. multivorans, M. xanthus, L. hongkogenisis, and S. salivarius. Although our detection of these factors could have resulted from nosocomial infections [60, 61] , heightened risk of malignancy has been linked to viruses, bacteria, and schistosomes [62, 63] . In fact, the relationship between bacterial infections and cancer has been discussed for decades [64, 65] . In this regard, there are several possible mechanisms by which bacteria could be oncogenic. For example, altered host responses during bacterial infection (e.g., chronic inflammation, antigen-driven lymphoproliferation, and hormone induction that promotes epithelial cell proliferation) have been suggested to influence oncogenesis [66] . Also, bacterial infection can lead to the production of toxin and/or carcinogenic metabolites that enhance oncogenesis [67] . In contrast, bacterial infections have also been suggested to play a protective role by altering host physiology and reducing cancer risk [68] .

Oral cancer is considered to be a multi-factorial disease, as it can stem from exposure to several types of carcinogens, including microbial factors [69] . Indeed, several pieces of evidence have supported the association of microbial infection with oncogenesis. For instance, Helicobacter pylori has been linked to gastric cancer [70] and categorized by the World Health Organization International Agency for Research on Cancer (IARC) as a carcinogenic factor in humans [71] [72] [73] . Similarly, Chlamydophila pneumoniae has been associated with malignant lymphoma and lung cancer in males [74, 75] , whereas Candida albicans and Streptococcus anginosus have been linked to oral carcinoma [70- 76] . It has also been demonstrated that OSCC patients possess significantly elevated concentrations of certain bacteria in their saliva. Thus, changes in salivary microflora could represent a noninvasive diagnostic tool for predicting oral cancer [70] .

Immunoglobulin M (IgM) antibodies are present in the circulation of normal humans and other mammalian species. IgM is initially secreted by B cells upon primary antigen stimulation [77, 78] and participates in natural defenses against foreign pathogens as well as neoplastic cells and tumors [79] . In fact, autoantibodies against specific cancer antigens have been identified for several types of tumors, including colon, breast, lung, ovary, prostate, and head and neck. These antibodies have been found to recognize several overexpressed (e.g., Her2), mutated (e.g., p53), or tissue-restricted (e.g., testis-cancer antigens) proteins, which are produced by cancer cells and elicit immune responses [6] . Therefore, detection of such autoantibodies in patient sera could be exploited as a means of cancer diagnosis. Indeed, the specificity and sensitivity of the antibody response to low antigen levels make it an ideal screening/diagnostic tool for early identification of cancer biomarkers in serum-based assays.

In order to extend the results obtained from our immunoproteomics analyses, we performed 2-DE immunoblots using OSCC patient and control sera (Table 4 ). In this regard, we performed immunoblots based on the following four conditions (i.e., categories 1-4): (1) normal pooled sera probed with normal pooled sera; (2) normal pooled sera probed with OSCC pooled sera; (3) OSCC pooled sera probed with normal pooled sera; and (4) OSCC pooled sera probed with OSCC pooled sera.

The use of normal pooled sera against normal and OSCC pooled sera was to prove that the reaction was restricted to the tumor specificity. Therefore, only few host-specific proteins could be detected in the normal controls. Based on our results, only proapo-A1 could be detected in category 1 (Fig. 2a) , while HAP showed immunogenicity in category 2 blots (Fig. 2b) . The detection of HAP in category 2 blot reveals the supportive role of the natural immunity against cancer cells apart from its involvement in the defense system against pathogens [79] .

Based on the analysis in category 3 (Fig. 2C) , our results show that the healthy control serums have the autoantibodies against OSCC serum antigens, CLU, C3, proapo-A1, and RBP4, which are the host-specific proteins that showed the most immunoreactivity in the immunoblot. These aberrant host-specific proteins were found to be more immunoreactive in the OSCC sera compared to the normal sera. In addition, other antigenic protein spots (A1, A2, A3, A4, and A5) were also detected in the category 3.

Finally, four reactive protein spots were observed in category 4, corresponding to C3, HAP, proapo-A1, and RBP4 (Fig. 2d) . Therefore, the identified proteins are uniquely produced by the innate immune response of cancer cells. Altogether, five hostspecific proteins were found to be immunoreactive in OSCC patients: CLU, C3, HAP, proapo-A1 and RBP4. Based on these analyses, our data support the rationale of using host-specific proteins as cancer biomarkers panel for early detection and diagnosis of OSCC [11] .

Functional annotation analysis was performed for our eight candidate host-specific biomarkers using DAVID v6.7 (http:// david.abcc.ncifcrf.gov/) ( Table 5 ). An analysis of biological processes revealed that HAP, apo-A1, and RBP4 are involved in homeostasis. Indeed, cancer-related inflammation is considered to be an essential hallmark of cancer due to the tumor-promoting consequences of inflammatory responses [80] . Thus, the study of aberrant homeostatic mechanisms has indicated that there exists an interaction between cancer cells and host immune cells during carcinogenesis.

In addition, functional annotation analyses revealed that all of the host-specific proteins were located within the extracellular region and indicating that these proteins mediate immunogenic reactions against cancer cells. Therefore, this finding shows that these proteins could play an important role in the immunogenicity of carcinogenesis. Moreover, CLU, HAP, and apo-A1 were found to be associated with protein-lipid complexes that are responsible Table 4 . Host-and non-host specific proteins on the 2-DE immunoblots.

Antigenic Proteins Category

1) Host specific proteins:

2) Non-host specific proteins: for cholesterol and lipid transportation. In this regard, cholesterol acts as a key contributor to carcinogenesis by promoting cell migration and mediating inflammatory processes. Indeed, lipoproteins may be the major suppliers of cholesterol to cancer cells via receptor-mediated mechanisms [81] . Therefore, alterations in these proteins could alter lipid metabolism, increasing the risk of cancer development and progression. A protein interaction network was generated using the STRING v9.1 (http://string-db.org/) database to identify potential binding partners for our host-specific biomarkers (Fig. 3) . Interestingly, most of the host-specific proteins could be linked to ten predicted functional partners (ABCA1, apo-A2, apo-B, apo-C3, CFH, CFI, CR2, FN1, LCAT, and TTR). Moreover, when KEGG pathway analysis was performed using DAVID v6.7, complement and coagulation cascades as well as the peroxisome proliferator-activated receptor (PPAR) signaling pathway could be linked to our identified host-specific proteins. Notably, these two pathways have been predicted to play important roles in cancer biology [82] . There were a total of four proteins (C3, CFH, CFI, and CR2) found to be involved in complement and coagulation cascades (p = 1.9610 24 ). These pathways may participate in homeostatic processes that influence the host defense response. Indeed, the complement cascade is activated early in the immune response and might be important in cancer immunotherapy, as evidence has suggested that activation of complement regulators can promote tumor growth [83] . Activation of the coagulation cascade during cancer highlights how altered homeostasis can contribute to tumorigenesis. Indeed, it was reported that coagulation pathways could induce angiogenesis to facilitate tumor growth and metastasis [84] . As stated in the table 5 based on DAVID functional annotation analysis, ''homeostasis'' could be correlated with the proteins ApoA1, HAP and RBP4. However, it was reported that ApoA1, HAP have the possibility to relate with the process ''hemostasis'' [85, 86] .

Furthermore, apo-A1, apo-A2, and apo-C3 were found to be associated with the PPAR signaling pathway (p = 6.1610 24 ). PPARs are members of the nuclear hormone superfamily, which can be activated by fatty acids and their derivatives. The PPAR signaling pathway regulates lipid metabolism, cell proliferation, and cell differentiation. It has also been reported to be involved in the regulation of cancer cell apoptosis, proliferation, and differentiation. PPAR signaling is proposed to modify tumor growth by affecting angiogenesis, inflammation, and immune cell functions in the tumor cell environment [87] . Thus, targeting the PPAR signaling pathway could represent a potential strategy for cancer therapy.

Using proteomic profiling, we were able to identify several differentially expressed host-specific proteins in the sera of OSCC patients, including LRG, ABG, CLU, PRO2044, HAP, proapo-A1, and RBP4. The immunogenicity of five of these proteins was further confirmed by western blot analyses (CLU, C3, HAP, proapo-A1 and RBP4). In addition, five non-host factors were detected, including proteins from A. lwoffii, B. multivorans, M. xanthus, L. hongkogenisis, and S. salivarius. As previously suggested [88] , combined proteomic and serological approaches, such as the one used in the present study, can reflect numerous events occurring in vivo simultaneously due to the fact that patient serum is complex and consists of many proteins. Our data indicate that immunoproteomics approach could be a promising application for biomarker discovery and disease progression. Our study could be used as a landmark in a more comprehensive study and can be applied to individual patient serums or to a larger sample size. Using these methods, we have identified distinct serum biomarkers that might facilitate the development of early diagnostic tools for OSCC and promote further understanding the 'host responses' that occur in OSCC patients.

Global cancer statistics

Identification of tetranectin as a potential biomarker for metastatic oral cancer

Global cancer statistics

Oral cancer and precancerous lesions

Concurrent chemotherapy and radiotherapy for organ preservation in advanced laryngeal cancer

Autoantibody approach for serum-based detection of head and neck cancer

Advances and applications of oral cancer basic research

Oral bacteria and cancer

Critical evaluation of diagnostic aids for the detection of oral cancer

Second primary tumors in patients with oral cancer

Immunoproteomics to identify tumor-associated antigens eliciting humoral response

Proteomic profiling of cancer-opportunities, challenges, and context

Host immune response to infection and cancer: unexpected commonalities

Profiling of serum and tissue high abundance acute-phase proteins of patients with epithelial and germ line ovarian carcinoma

Improved silver staining procedure for fast staining in PhastSystem Development Unit. I. Staining of sodium dodecyl sulfate gels

Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

STRING v9.1: protein-protein interaction networks, with increased coverage and integration

Two-dimensional electrophoretic patterns of acute-phase human serum proteins in the course of bacterial and viral diseases

Plasma proteome of severe acute respiratory syndrome analyzed by two-dimensional gel electrophoresis and mass spectrometry

Plasma proteomics of pancreatic cancer patients by multi-dimensional liquid chromatography and two-dimensional difference gel electrophoresis (2D-DIGE): upregulation of leucine-rich alpha-2-glycoprotein in pancreatic cancer

Proteomic analysis of sera from hepatocellular carcinoma patients after radiofrequency ablation treatment

Plasma proteomics of lung cancer by a linkage of multi-dimensional liquid chromatography and two-dimensional difference gel electrophoresis

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A multiplexed bead assay for profiling glycosylation patterns on serum protein biomarkers of pancreatic cancer

Bladder cancer associated glycoprotein signatures revealed by urinary proteomic profiling

Integrative proteomics and tissue microarray profiling indicate the association between overexpressed serum proteins and non-small cell lung cancer

Plasma proteomic analysis of patients with squamous cell carcinoma of the uterine cervix

Evaluation of serum and urine clusterin as a potential tumor marker for urinary bladder cancer

Overexpression of clusterin in human breast carcinoma

Differential expression of serum clusterin isoforms in colorectal cancer

Expression of clusterin in human pancreatic cancer

Enhanced radiation sensitivity in prostate cancer by inhibition of the cell survival protein clusterin

Clusterin (SGP-2, ApoJ) expression is downregulated in low-and high-grade human prostate cancer

Loss of clusterin both in serum and tissue correlates with the tumorigenesis of esophageal squamous cell carcinoma via proteomics approaches

Essential requirement of apolipoprotein J (clusterin) signaling for IkappaB expression and regulation of NF-kappaB activity

Roles of clusterin in progression, chemoresistance and metastasis of human ovarian cancer

Altered expression of sialylated glycoproteins in ovarian cancer sera using lectin-based ELISA assay and quantitative glycoproteomics analysis

Development of resistance to chemotherapeutic drugs in human osteosarcoma cell lines largely depends on up-regulation of

Clusterin expression is associated with decreased disease-free survival of patients with colorectal carcinomas

Differential effects of clusterin/apolipoprotein J on cellular growth and survival

Proteomic identification of potential protein markers in cerebrospinal fluid of GBS patients

Expression of haptoglobinrelated protein and its potential role as a tumor antigen

Proteomicbased identification of haptoglobin-1 precursor as a novel circulating biomarker of ovarian cancer

Proteomics-based identification of haptoglobin as a novel plasma biomarker in oral squamous cell carcinoma

Circulating haptoglobin is an independent prognostic factor in the sera of patients with epithelial ovarian cancer

Haptoglobinalpha subunit as potential serum biomarker in ovarian cancer: identification and characterization using proteomic profiling and mass spectrometry

Biomarker discovery in breast cancer serum using 2-D differential gel electrophoresis/MALDI-TOF/TOF and data validation by routine clinical assays

Comparative study of proteome between primary cancer and hepatic metastatic tumor in colorectal cancer

Proteomicsbased identification of secreted protein dihydrodiol dehydrogenase as a novel serum markers of non-small cell lung cancer

Expression of glycolytic enzymes is increased in pancreatic cancerous tissues as evidenced by proteomic profiling by two-dimensional electrophoresis and liquid chromatography-mass spectrometry/mass spectrometry

Laser capture microdissection in comparative proteomic analysis of hepatocellular carcinoma

Exploration of Potential Tumor Markers for Lung Adenocarcinomas by Two-Dimensional Gel Electrophoresis Coupled with Nano-LC/MS/MS

CRBP suppresses breast cancer cell survival and anchorage-independent growth

Cellular retinol-binding protein-I inhibits PI3K/Akt signaling through a retinoic acid receptor-dependent mechanism that regulates p85-p110 heterodimerization

Cellular retinol-binding protein expression and breast cancer

Retinoid therapy of high-risk neuroblastoma

Decreased concentrations of retinol-binding protein 4 in sera of epithelial ovarian cancer patients: a potential biomarker identified by proteomics

RBP4: a controversial adipokine

Acinetobacter species as nosocomial pathogens

Bloodstream infection surveillance in a cancer centre: a prospective look at clinical microbiology aspects

Cancer and infection: estimates of the attributable fraction in 1990

Global burden of cancers attributable to infections in 2008: a review and synthetic analysis

Bacterial infection as a cause of cancer

Recovery of uncommon bacteria from blood: association with neoplastic disease

Role of bacteria in oncogenesis

Bacteria and cancer: cause, coincidence or cure? A review

The association of gastric leptin with oesophageal inflammation and metaplasia

Overview of Oral Cancer

Exploring the link between microorganisms and oral cancer: a systematic review of the literature

Helicobacter pylori: resurrection of the cancer link

Helicobacter pylori and gastrointestinal tract adenocarcinomas

Serological evidence of an association between chlamydial infections and malignant lymphomas

Chronic Chlamydophila pneumoniae infection in lung cancer, a risk factor: a case-control study

Streptococcus anginosus infection in oral cancer and its infection route

High level expression of functional human IgMs in human PER

Natural IgM antibodies and immunosurveillance mechanisms against epithelial cancer cells in humans

Hallmarks of cancer: the next generation

The role of cholesterol metabolism and cholesterol transport in carcinogenesis: a review of scientific findings, relevant to future cancer therapeutics

The functional cancer map: a systems-level synopsis of genetic deregulation in cancer

Complement in cancer and cancer immunotherapy

Tissue factor, thrombin, and cancer

Identification of fibrin clot-bound plasma proteins

Inhibition of arterial thrombus formation by ApoA1 Milano

PPARs Mediate Lipid Signaling in Inflammation and Cancer

Detection of immunogenic parasite and host-specific proteins in the sera of active and chronic individuals infected with Toxoplasma gondii

The authors acknowledged the Oral Cancer Research and Coordinating Centre (OCRCC), University of Malaya (UM) for providing serum samples.

Conceived and designed the experiments: YC SNA. Performed the experiments: YC SNA JPK. Analyzed the data: YC RBZ YNC YLW SCBG. Contributed reagents/materials/analysis tools: YC. Contributed to the writing of the manuscript: YC SNA JPK YLW SCBG.