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Volume 2012 (2012), Article ID 425636, 15 pages
Discovery of Biomarkers for Osteosarcoma by Proteomics Approaches
1Department of Orthopedic Surgery, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan
2Division of Pharmacoproteomics, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan
3Department of Orthopedic Surgery, Tachikawa Memorial Hospital, 4-2-22 Nishikichou, Tachikawa, Tokyo 190-8531, Japan
4Division of Musculoskeletal Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan
Received 3 July 2012; Accepted 30 August 2012
Academic Editor: Norman Jaffe
Copyright © 2012 Yoshiyuki Suehara et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Osteosarcomas are the most common malignant bone tumors, and the identification of useful tumor biomarkers and target proteins is required to predict the clinical outcome of patients and therapeutic response as well as to develop novel therapeutic strategies. Global protein expression studies, namely, proteomic studies, can offer important clues to understanding the tumor biology that cannot be obtained by other approaches. These studies, such as two-dimensional gel electrophoresis and mass spectrometry, have provided protein expression profiles of osteosarcoma that can be used to develop novel diagnostic and therapeutic biomarkers, as well as to understand biology of tumor progression and malignancy. In this paper, a brief description of the methodology will be provided followed by a few examples of the recent proteomic studies that have generated new information regarding osteosarcomas.
Osteosarcoma is the most common, nonhematopoietic, primary malignant bone tumor and most frequently occurs in the second decade, with 60% of patients under the age of 25 years . After the initial diagnosis, patients usually receive multiagent preoperative chemotherapy and surgical resection of the tumor, followed by postoperative chemotherapy. Chemotherapy has improved the cure rate of patients with localized OS from 15%–20% achieved with surgery alone to approximately 70% [1, 2]. The response to preoperative chemotherapy is critical information for patients and the chemosensitive patients are divided into two groups based on the pathological features: the good responder (>90% tumor necrosis) and the poor responder (<90% tumor necrosis) [1, 2]. However, patients who have a poor response to chemotherapy often have a poor outcome and a high risk of developing metastasis compared to patients who have a good response to chemotherapy [1, 2]. Therefore, it is critical to identify proteins associated with chemoresistance as predictive biomarkers and novel theoretical targets in osteosarcomas. Additionally, despite significant progress regarding chemotherapy and improvements in the outcome for patients with localized osteosarcomas, patients who have metastases at diagnosis are not uncommon, and patients with metastases still have poor prognosis [1, 2]. Therefore, the development of a novel focus on the identification of prognostic indicators, and novel therapeutic targets that inhibit biological pathways known to contribute to osteosarcoma growth, are essential.
The use of high-throughput screening approaches, such as array-based comparative genomic hybridization analysis and cDNA microarray technology, allows for the screening of several thousand DNA and mRNA sequences and can identify the genes relevant to the diagnosis and clinical features of tumors [3–13]. These comprehensive studies have identified several genes that may be involved in the development or progression of osteosarcomas, and represent candidate biomarkers and/or drug targets [3–13]. However, in clinical applications, there are currently no specific markers available for predicting the prognosis and chemosensitivity of osteosarcomas. The identification of these factors could provide not only a new method for stratifying patients and selecting the treatment strategy, but could also provide novel therapeutic targets for osteosarcoma. Global protein expression studies, an approach known as “proteomics,” may also be more clinically relevant than genomic studies, since proteins directly regulate the aberrant tumor phenotypes. Moreover, DNA sequencing or measurement of mRNA expression cannot detect posttranslational modifications of proteins that affect their activity, such as phosphorylation, glycosylation, and acetylation, or differences in protein stability, and these factors play important roles in the malignant behavior of tumor cells [14–17]. Furthermore, many lines of evidence have indicated that there is discordance between the mRNA and protein expression [14–17]. Therefore, proteomic studies are becoming critical tools for understanding the biology of tumors, as well as for the identification of biomarkers for various cancers. In addition, the results obtained from proteomic studies are more easily applied to the clinical field, because of the potential use of specific antibodies.
Recent advances in proteomic technology have made it possible to identify disease-related proteins in clinical samples, and extensive efforts are now being made to identify biomarkers of specific cancers that can be used for diagnostic or therapeutic purposes [15, 16, 18–25]. The standard proteomic techniques, such as two-dimensional gel electrophoresis (2DE) and mass spectrometry (MS), have been developing over the past three decades. From the end of the 1990s, through the development of high-throughput platforms, proteomics has become able to allow the simultaneous measurement of multiple protein products and protein modifications. These newlydeveloped technologies provide ways to detect crucial protein expression patterns corresponding to disease progression or responses to treatment and are now considered vital research tools [15, 16, 18–34]. Therefore, proteomic studies can be particularly useful to identify novel biomarkers and therapeutic targets of sarcomas. Our studies have identified some candidate proteins associated with a differential diagnosis [15, 16, 20, 21], prognosis [18, 19, 25], and in predicting the response to chemotherapy [16, 23] in bone and soft-tissue sarcomas. The following section describes how proteomic approaches have been applied to osteosarcoma and reviews many of the articles regarding proteomic studies of osteosarcoma.
We identified approximately 30 papers about proteomic research on osteosarcoma during a search of PubMed (Table 1). In this paper, in order to discuss the contributions of proteomics to the identification of useful clinical biomarkers and targets for human osteosarcomas, we chose the articles that used actual patient samples, such as surgical materials and plasma, rather than information from human cell lines and animal studies (Table 1). In this paper, we briefly discuss the proteomic technologies, especially electrophoresis-based techniques, as well as the identification of biomarkers and novel targets for osteosarcoma identified by proteomic approaches.
2. Proteomic Technologies and Analyses in Sarcomas
Proteomics is the large-scale study of proteins, especially their structures and functions . Technologies used in proteomics research include electrophoresis, mass spectrometric technologies, protein labeling, protein arrays, antibody-based approaches, imaging, and bioinformatics technology. As a result of the recent advances in these technologies, proteomics may provide powerful information for improved biomarker and novel therapeutic target discovery in malignant tumors. In particular, mass spectrometry technologies are now high throughput, allowing for the rapid and accurate identification of thousands of proteins present within a complex tumor specimen. Furthermore, a differential protein expression analysis can be used to compare tumors with normal tissues, and is able to identify a range of protein markers potentially related to the malignant features of tumors [35–37]. Bone and soft tissue sarcomas are relatively rare compared with other malignancies. The development of diagnostic and prognostic modalities, identification of novel therapeutic targets, and understanding of the mechanisms of sarcomagenesis are currently the main research priorities. Therefore, various strategies are now being employed to identify tumor-specific proteins in sarcoma using proteomics technologies.
Based on a search of the PubMed database, electrophoresis, specifically 2D difference gel electrophoresis (2D-DIGE) [15, 16, 19–21, 25, 32, 34, 38] and mass spectrometry, especially matrix-assisted laser desorption ionization mass spectrometry (MALDI MS)  and surface-enhanced laser desorption/ionization (SELDI) [26, 33, 40], have mainly been used to obtain protein expression profiles of bone and soft-tissue sarcomas. We briefly summarized both the advantages and disadvantages of main platforms for performing a proteomic analysis (Table 2). In this article, we mainly discuss 2D-DIGE, because this technology is the most commonly used method for obtaining protein expression profiles in proteomic studies of bone and soft tissue tumors [15, 16, 18–21, 25, 26, 32–34, 38–40].
We routinely employ 2D-DIGE for biomarker identification [15, 16, 18–21, 25, 41, 42]. 2D-DIGE is an advanced variation of 2D-PAGE (two-dimensional polyacrylamide gel electrophoresis) and has the potential to solve many drawbacks of classical 2D-PAGE (Figure 1) [41, 42]. The standard 2D-PAGE technique employs isoelectric separation according to protein charge as a first dimension, coupled with MW resolution by polyacrylamide gel electrophoresis. Our 2D-DIGE method uses DIGE dyes which react with cysteine residues. There are only a few cysteines per protein and the cysteine-reactive dyes are highly soluble zwitterions. Therefore, these dyes are suitable for saturation labeling of all cysteine residues. As a result, the sensitivity for protein detection is improved and enables a successful 2D-PAGE analysis with of even low protein concentrations [41–43], and various studies have demonstrated the successful application of saturation labeling to detect protein differences in scarce samples derived from 1000 to 5000 protein spots. These two DIGE labeling options provide rapid methods for preparing differentially labeled samples for fluorescence-based proteome comparisons [41–43].
Using our 2D-DIGE method, proteins were extracted from surgical specimens, and all protein samples were labeled with different fluorescent dyes before gel electrophoresis (Figure 1) [15, 16, 18–21, 25, 41, 42]. We first created a common internal control sample, which was a mixture of a small portion of all individual samples, and labeled it with a fluorescent dye that is different from the one used to label the individual samples. These differentially labeled internal control and individual samples are then mixed together and separated by both their pH and molecular weight ranges by 2D-PAGE (Figure 1). Laser scanning can be used to obtain the gel images, because all proteins are labeled with fluorescent dye before the gel electrophoresis (Figure 1). By normalizing the 2D image of each individual sample with that of the common internal control sample in the same gels, there is compensation for gel-to-gel variations, and reproducible results can be obtained across multiple gel images. These gel images provide data about protein spots as protein expression profiles. In the data analysis, the protein spots whose intensities are significantly different between the groups examined are identified using the Wilcoxon test, Hierarchical clustering, a principle component analysis, correlation matrix studies, and a support vector analysis using a data-mining software program (Figure 1). Proteins corresponding to the spots of interest are identified by mass spectrometry. Protein identification and differential expression are confirmed by a western-blotting analysis and/or immunohistochemistry using specific antibodies. Finally, in order to identify useful biomarkers and to develop clinical applications, we usually try to verify the value of biomarkers or targets using a large scale validation set which consists of clinical samples by an immunohistochemical analysis (Figure 1).
3. The Identification of Tumor-Specific Biomarkers and Therapeutic Targets in Osteosarcoma
In osteosarcoma, the biology of malignant progression and tumorigenesis are still largely unknown. Therefore, protein and gene expression studies have mainly been used to provide a source of expression profiles and to obtain clues about the causes of osteosarcomas. The identification of tumor-specific biomarkers and therapeutic targets are the most important goals of global protein and gene expression studies. The current gene expression profiling technologies have been used to identify upregulated or downregulated genes associated with tumor progression, or that can be used to predict the malignant potential in osteosarcoma [3–6]. In this section, we mainly describe pertinent proteomic studies that have identified tumor-specific proteins corresponding to tumor progression and that can be used as prognostic biomarkers and therapeutic targets in osteosarcoma using patient materials. Two papers reported comparative proteomic studies using tissue samples; (i) osteosarcoma versus normal bone  and (ii) osteosarcoma samples versus benign tumors . Additionally, one paper described a plasma proteomic study comparing osteosarcoma patients’ plasma with plasma from patients with benign bone tumors (Table 1) .
Folio et al. carried out comparative proteomic studies using five paired samples of osteosarcomas and normal bone to identify the proteins involved in malignant transformation and that were tumor-specific (Table 1) . Additionally, the authors described that they could identify the proteins associated with metastasis and chemoresistance in their study. The five pairs of samples (tumor versus normal bone) were isolated form surgical tissue samples as cell lines. The study detected 56 differentially-expressed protein spots () and 16 proteins were identified as having differences in their relative abundance in osteosarcomas and paired normal bones by nanoliquid chromatography/electrospray ionization tandem mass spectrometry (Nano-LC-ESI-MS/MS). Both alpha-crystallin B chain (CRYAB) and ezrin (EZR) were confirmed to be differentially expressed using an immunohistochemical analysis and real-time PCR. The confirmation studies revealed that tumor tissues had higher protein expression levels of both CRYAB and EZR than normal tissues. This study also demonstrated that there were significant differences in the metastasis and recurrence rates between positive and negative samples in terms of both CRYAB and EZR.
Li et al. conducted a proteomic study of osteosarcoma to identify the specific protein markers of the disease and to improve the understanding of the tumorigenesis and progression of osteosarcoma (Table 1) . Protein samples were extracted from five osteosarcoma tissue samples and five benign bone tumor samples (two osteoblastoma, two chondroblastoma, and one giant cell tumor). The protein expression profiles were acquired by comparing the osteosarcoma profiles with those of benign tumors using 2DE analyses. A total of 30 protein spots () were detected as differentially expressed in this study, and 18 proteins were finally identified by mass spectrometry. These proteins included 12 upregulated proteins (VIM, TUBA1C, ZNF133, EZR, ACTG1, TF, etc.) and six downregulated proteins (ADCY1, ATP5B, TUBB, RCN3, ACTB, and YWHAZ). They confirmed the differences in the protein expression levels of TUBA1C and ZNF133 by the western-blotting and immunohistochemical analyses. The study concluded that these identified proteins might be potential biomarkers for osteosarcomagenesis and might represent novel therapeutic targets for the disease.
Both studies (Folis et al. and Li et al.) identified osteosarcoma-specific proteins, as well as proteins associated with malignant progression and tumorigenesis in bone tumors, especially osteosarcomas [32, 33]. EZR was a common protein identified by both studies (Tables 3(a) and 3(b)). In a cDNA microarray study of osteosarcoma, EZR was also identified as a highly expressed gene in osteosarcomas, and that study suggested that EZR may have an important role in metastasis .
EZR, an ezrin/radixin/moesin (ERM) family member, is evolutionarily conserved both structurally and functionally [44, 45]. By regulating membrane-cytoskeleton complexes, EZR has critical roles in normal cellular processes such as the maintenance of membrane dynamics, survival, adhesion, motility, cytokinesis, phagocytosis, and integration of membrane transport with signaling pathways [45, 46]. The activation of EZR is mediated by both exposure to PIP2 and phosphorylation of the C-terminal threonine (T567) [44, 47]. The deactivation of EZR is also important for physiologic functions, including the dynamics of actin-rich membrane projections. EZR has been implicated in various steps of the metastatic process, for example, as a conduit for signals between metastasis-associated cell surface molecules and signal transduction components .
In osteosarcoma studies, EZR was necessary for metastasis, and a high expression of ezrin was associated with the early development of metastasis . A relationship was also shown between high expression levels of EZR and a poor outcome in 19 pediatric osteosarcoma patients . In addition, two articles that compared the EZR expression in high- and low-grade human osteosarcoma tumor samples demonstrated a clear correlation between ezrin expression and survival [50, 51]. Furthermore, some studies suggested that EZR phosphorylation is not only present in the early stage of metastasis, but also late in tumor progression, at the leading edge of large metastatsic lesions. More importantly, using dominant-negative mutants, antisense RNA or RNA interference, these experiments demonstrated that EZR overexpression is not only sufficient for metastatic progression, but it is also necessary in these experimental systems [49, 52]. Finally, the suppression of EZR protein expression significantly reduced the metastatic behavior in two murine models and it was also associated with a decreased Akt and mitogen-activated protein kinase (MAPK) activity [49, 52, 53]. These findings suggest that targeting EZR might improve the treatment of osteosarcoma, especially in metastasis cases.
Li et al. conducted a proteomic study to identify a plasma protein signature that was tumor-specific or that corresponded to the malignancy of osteosarcoma using SELDI-MS (Table 1) . The study compared the plasma specimens between 29 patients with osteosarcomas and 20 with osteochondromas. They identified 19 ion peaks which had statistically significant differences in the protein expression levels between the osteosarcoma group and the benign bone tumor group ( and false discovery rate, 10%). The statistical analyses detected that there was a significant difference in the expression of one of the proteins (m/z 11 704) in the proteomic signature, which was found to be serum amyloid protein A by PMF. Serum amyloid protein A is highly expressed in the plasma samples of osteosarcoma patients. A Western blotting analysis also confirmed that there were high expression levels of serum amyloid protein A in the plasma of osteosarcoma patients compared to that of osteochondroma patients and normal subjects. That study concluded that the findings based on this plasma proteomic signature might be useful to differentiate malignant bone cancer from benign bone tumors, and also might contribute to early detection of a high-risk osteosarcoma group.
In summary, we believe that these proteins, which are tumor-specific and associated with the malignancy of osteosarcomas, may contribute to understanding the biology of the tumors and may be useful as biomarkers. An analysis of the functions of these proteins and their correlations with osteosarcoma would provide insight into the biology of osteosarcoma and improve the therapeutic management of osteosarcoma patients.
4. The Identification of Biomarkers of Chemosensitivity in Osteosarcoma
The major prognostic factor in patients with localized osteosarcoma is the development of resistance to preoperative chemotherapy. Therefore, the identification of biomarkers of chemosensitivity in osteosarcoma is critical. Some gene expression studies have been conducted to identify genes associated with the chemosensitivity in osteosarcoma [3–6]. In this section, we mainly introduce pertinent proteomic studies that have previously identified markers of the response to chemotherapy in osteosarcoma. We found only two papers, which are our own studies, that have conducted protein expression studies of potential biomarkers of chemosensitivity in osteosarcoma using tissue samples (Table 1) [16, 23]. Another paper described a chemosensitivity study of osteosarcoma using patient plasma samples (Table 1) .
In our study, we employed a proteomic approach to identify novel biomarkers of the chemosensitivity of osteosarcoma (Table 1) . We used 12 biopsy samples, including six osteosarcoma samples from patients who were good responders and six osteosarcoma patients who were poor responders, according to the Huvos grading system. The protein expression profiles obtained by 2D-DIGE consisted of 2250 protein spots. We identified 55 protein spots () whose intensity was significantly different between the two groups. Mass spectrometric protein identification demonstrated that these 55 spots corresponded to 38 distinct gene products, including peroxiredoxin 2 (PRDX2). The PRDX2 spots had higher intensity in the poor responder group, and we also confirmed the presence of an increased protein expression of PRDX2 in the poor responder group by a western blot analysis. In order to validate the prediction of chemosensitivity using the markers we identified, we performed a validation study using an additional four osteosarcoma samples, including two samples each from good responders and poor responders by a western blot analysis. The validation study demonstrated that the poor responders had higher PRDX2 expression levels compared to the good responders. We concluded that PRDX2 might be a candidate marker for chemosensitivity in osteosarcoma patients. In our other paper, by Kawai et al., we identified 10 protein spots which were found to be correlated with chemoresistance by 2D-DIGE, but the study did not identify the protein names associated with the spots, so we will not discuss the details of these findings here.
Li et al. conducted a plasma proteomic study to identify proteins that could be used to distinguish good from poor responders in osteosarcoma patients prior to the start of treatment (Table 1) . Their study used two sets of 54 plasma samples that were collected from 27 prechemotherapy osteosarcoma patients and 27 postchemotherapy patients. The pre-chemotherapy samples included 14 good responders and 13 poor responders, and the postchemotherapy samples included 12 good responders and 15 poor responders. The analyses divided the subjects into two classes (consisting of good and poor responders) in both sets of plasma samples. In the post-treatment plasma set, 65 protein peaks were identified as the signature of the chemotherapeutic response. The levels of 29 protein peaks were higher and those of 36 protein peaks were lower in the plasma of poor responders. In the pretreatment plasma set, 56 protein peaks were identified, and the pre-treatment signature demonstrated that 32 and 24 protein peaks in the plasma of the poor responders were expressed at higher and lower levels, respectively, compared to good responders. These studies identified two plasma proteins, serum amyloid protein A and transthyretin, that appear to be especially sensitive markers. The expression of serum amyloid protein A was significantly higher in the plasma of the good responders, while transthyretin was more highly expressed in poor responders. These protein expression differences were confirmed by a western blot analysis. Both of these proteins are involved in innate immunity based on a protein database search. The authors concluded that the study might lead to the development of a simple blood test that can predict the response to chemotherapy in osteosarcoma patients and suggested that their findings might be corroborated by the notion that boosting the innate immunity in conjunction with chemotherapy leads to better anti-tumor activity, thus improving the overall survival of osteosarcoma patients.
Several reports have described that the histological response to preoperative chemotherapy has provided the most consistent and reliable prognostic indicator [1, 2, 5, 54]. The patients with localized disease whose tumors have undergone more than 90% necrosis have a 5-year survival of approximately 70%, while for those in whom the response falls short of 90%, survival rarely exceeds 40–50% [5, 54]. Furthermore, in comparison studies of osteosarcomas, the sample sets for chemosensitivity (poor responder versus good responder) were strongly correlated with the sets for prognosis (good outcome patients versus poor outcome patients). Therefore, we believe that the identified proteins associated with malignancy are also related to the chemosensitivity of the tumors.
Moreover, in a previous study, we have already discussed a comparison of the protein lists reported in Folio’s and Li’s studies (see above), with the Folio study examining tumor-specific and/or malignancy-related proteins (osteosarcoma versus normal tissue samples) and the Li study examining tumor malignancy (osteosarcoma versus benign bone tumor) (Table 3(a)). As noted above, we identified that EZR was a common protein identified in both studies (Table 3(b)). In this section, we also reviewed and organized the proteins lists from three papers: (i) Folio et al. reported tumor-specific and/or tumor malignancy-associated proteins (osteosarcoma versus normal tissue), (ii) Li et al. reported tumor malignancy-associated proteins (osteosarcoma versus benign bone tumors) and (iii) Kikuta et al. reported chemosensitivity- and/or tumor malignancy-related proteins (poor responder versus good responder) (Table 3(a)). During a further review of these studies, we found that not only EZR, but also the PRDX family were common proteins in the lists (Table 3(b)), with the study by Kikuta having identified PRDX2 and the Folio study having identified PRDX6 (Table 3(b)).
The PRDX family of proteins show peroxidase activities that degrade hydrogen peroxide (), as well as serving as alkyl hydroperoxides. In human tissues, six members of the family (PRDX1-6) have been identified so far . Several papers have reported that PRDX proteins act as cytoprotective antioxidant enzymes, while PRDX expression was shown to enhance oxidative damage in some cells and tissues [55–60]. Recently, PRDX proteins have received increasing attention in the field of cancer biology. The analyses of cancer samples obtained from patients have revealed that there is increased expression of PRDX in malignancies of various organs and tissues [61–66]. In addition, the upregulation of PRDX proteins (specifically, 1, 2, 4, 5, and 6) may contribute to the resistance of tumors to chemotherapy and radiotherapy [67–73]. In addition, some papers have demonstrated in functional studies of PRDX proteins that they appear to influence the efficacy of cancer therapy not only by supporting the resistance of cancer cells, but also by promoting their invasiveness and metastasis [62, 74]. Therefore, the mechanism(s) underlying these functions of PRDX and information about their expression patterns may be essential for obtaining a better understanding of tumor biology and the development of new treatment strategies for osteosarcoma.
In summary, based on the previous proteomic studies, there are several common proteins that have been identified as corresponding to chemoresistance and/or malignancy. Moreover, these proteins have been reported to be involved in malignancy and/or chemoresistance in other cancers [62, 67–74]. Therefore, these proteins should be major targets for development as diagnostic or prognostic biomarkers, and may also be useful for targeted therapy.
5. Our Experiences with Proteomic Studies of Osteosarcoma
Before the publication of Kikuta’s paper, we conducted the 2D-DIGE analyses using 16 OS tissue samples to identify proteins corresponding to chemoresistance (Table 4). We compared nine osteosarcoma samples from good responders with seven osteosarcoma samples from poor responders. However, the sample set included osteosarcoma samples that were collected from elderly patients and from a trunk origin (pelvis), while typical osteosarcomas occur in young patients (<30 years) and in the extremities (Table 4). More importantly, the sample set was mixed, because several chemotherapy protocols, such as HD-MTX and HD-IFM, had been used (Table 4). Although this study identified 41 (of 1465) protein spots that were differentially expressed (), there were no statistically significant differences between the two groups of patients (good/poor responders) (Figure 2). On the other hand, Kikuta’s study successfully identified 55 of 2250 protein spots () which had statistically significant differences when the good responders and poor responders were compared. One of the keys to the success of the latter study was that Kituta’s analyses used typical osteosarcoma samples, which were obtained only from tumors with an origin in an extremity and that were only obtained from young subjects. In addition, this study employed patient samples from only subjects who were treated with HD-IFM-based protocols. We think that the modified study design likely contributed to the successful identification of candidate proteins corresponding to chemosensitivity.
Oteosarcoma is a heterogeneous tumor, the etiology of which is still largely unknown. Three global gene expression studies using cDNA microarrays were conducted to determine genes that were differentially expressed with regard to the response to chemotherapy using osteosarcoma tissue samples. Ochi et al. identified a 60-gene signature predicting the treatment response on the basis of the 23000 cDNA microarray analyses and biopsy samples from 13 osteosarcoma patients. Mintz et al. reported a 104-gene signature associated with histologically evident responses to chemotherapy in osteosarcoma using an Affymetrix chip analysis of 30 pretreatment biopsy specimens. Man et al. described a 45-gene signature using the 9000 cDNA microarray analyses and 20 definitive surgical excision samples of osteosarcoma. However, these gene expression profiles lacked overlapping genes. Some reviews have suggested that the heterogeneity of osteosarcomas might be one of the reasons for the non-overlap .
We conducted several proteomic studies using several kinds of surgical tissue samples and were able to identify candidate proteins associated with the prognosis of bone and soft tissue sarcomas, especially GISTs, Ewing sarcomas and synovial sarcomas [18, 19, 25]. Therefore, in our study that was not published, we conducted a proteomic approach to develop prognostic biomarkers for osteosarcoma using 2D-DIGE. In this trial, we used 17 surgical samples and divided the patients into two groups based on their prognosis ((i) the good prognosis group; five osteosarcoma patients who had not developed metastasis over a 3-year period and (ii) a poor prognosis group; 12 osteosarcoma patients who had developed metastasis within 2 years of the initial treatment) (Table 5). We compared the protein expression profiles between the two groups and identified that 72 of 1457 protein spots were differentially expressed (). However, these protein spots were not statistically different between the good and poor responder groups (Figure 3). As described above, we hypothesize that the heterogeneity of these osteosarcomas may have been one of the causes of the failure observed in this study.
The three types of tumors examined in our initial sarcoma studies; GISTs, Ewing sarcomas and synovial sarcomas, for which prognostic proteins could be identified in our studies, are associated with translocations or oncoproteins [18, 19, 25]. A general observation of both cDNA microarray- and proteomic-based expression profiling studies of sarcomas is that translocation-associated sarcomas are tightly clustered, whereas complex karyotype sarcomas tend to be less tightly clustered [15, 16, 75–79]. These findings and many reports indicate that translocation or oncoprotein-associated tumors are usually homogeneous tumors. On the other hand, complex karyotype sarcomas are usually heterogeneous tumors [15, 16, 75–79]. Therefore, based on our experiences with sarcoma proteomics, it likely to be more difficult to identify genes or proteins associated with the prognosis and chemosensitivity in heterogeneous tumors, like osteosarcoma, compared to homogenous tumors. Based on our experiences, we believe that it is vitally important to have a good study design which minimizes the noise by avoiding the inclusion of unsuitable samples. This will help to identify real and useful candidate proteins and will facilitate studies of highly heterogeneous tumors, such as osteosarcomas.
Several proteomic studies have identified candidate biomarkers relevant to a diagnosis of osteosarcoma, as well as for predicting its level of malignancy and chemosensitivity.
We believe that these proteins are potentially useful biomarkers which may be useful for various clinical applications. However, such proteomic studies have not verified the value of biomarkers in a large validation set by immunohistochemistry or another reliable method. DNA sequencing or measurement of mRNA expression cannot predict the posttranslational modifications of proteins, but proteomic analyses are more directly linked to aberrant tumor phenotypes, and can more accurately reflect the status of tumors. However, compared with cDNA microarray analyses (50,000 probe sets), the sensitivity of the current 2D-DIGE analysis (5000 spots) is still unsatisfactory. In addition, whole-genome sequence tautologies have been developed. Because osteosarcomas are heterogeneous tumors, it is necessary to employ these technologies, such as CGH arrays, cDNA microarrays, whole-genome sequences and 2D-DIGE in combination, so that their individual disadvantages can be overcome, and to identify the most promising and useful biomarkers and molecular targets. These hybrid comprehensive studies consisting of genomics, transcriptomics, and proteomics experiments may provide important, novel clues for understanding the biology of tumors and for revealing biomarkers and therapeutic targets for osteosarcoma.
Conflict of Interests
The corresponding author declares that there is no conflict of interest.
This work was supported by a grant from the Japan Society for the Promotion of Science (JSPS), science Grant-in-Aid for Young Scientists B, no. 22791405.
- C. D. M. Fletcher, K. K. Unni, and F. Mertens, World health organization classification of tumours, pathology and genetics, tumours of soft tissue and bone, 2002.
- A. J. Provisor, L. J. Ettinger, J. B. Nachman et al., “Treatment of nonmetastatic osteosarcoma of the extremity with preoperative and postoperative chemotherapy: a report from the children's cancer group,” Journal of Clinical Oncology, vol. 15, no. 1, pp. 76–84, 1997.
- K. Ochi, Y. Daigo, T. Katagiri et al., “Prediction of response to neoadjuvant chemotherapy for osteosarcoma by gene-expression profiles,” International Journal of Oncology, vol. 24, no. 3, pp. 647–655, 2004.
- M. B. Mintz, R. Sowers, K. M. Brown et al., “An expression signature classifies chemotherapy-resistant pediatric osteosarcoma,” Cancer Research, vol. 65, no. 5, pp. 1748–1754, 2005.
- P. Leonard, T. Sharp, S. Henderson et al., “Gene expression array profile of human osteosarcoma,” British Journal of Cancer, vol. 89, no. 12, pp. 2284–2288, 2003.
- T. K. Man, X. Y. Lu, K. Jaeweon et al., “Genome-wide array comparative genomic hybridization analysis reveals distinct amplifications in osteosarcoma,” BMC Cancer, vol. 4, article 45, 2004.
- M. Zielenska, J. Bayani, A. Pandita et al., “Comparative genomic hybridization analysis identifies gains of 1p35~p36 and chromosome 19 in osteosarcoma,” Cancer Genetics and Cytogenetics, vol. 130, no. 1, pp. 14–21, 2001.
- S. dos Santos Aguiar, L. de Jesus Girotto Zambaldi, A. M. dos Santos, W. Pinto Jr., and S. R. Brandalise, “Comparative genomic hybridization analysis of abnormalities in chromosome 21 in childhood osteosarcoma,” Cancer Genetics and Cytogenetics, vol. 175, no. 1, pp. 35–40, 2007.
- C. C. Lau, C. P. Harris, X. Y. Lu et al., “Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma,” Genes Chromosomes and Cancer, vol. 39, no. 1, pp. 11–21, 2004.
- J. Atiye, M. Wolf, S. Kaur et al., “Gene amplifications in osteosarcoma—CGH microarray analysis,” Genes Chromosomes and Cancer, vol. 42, no. 2, pp. 158–163, 2005.
- C. M. Hattinger, G. Reverter-Branchat, D. Remondini et al., “Genomic imbalances associated with methotrexaate resistance in human osteosarcoma cell lines detected by comparative genomic hybridization-based techniques,” European Journal of Cell Biology, vol. 82, no. 9, pp. 483–493, 2003.
- J. A. Squire, J. Pei, P. Marrano et al., “High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays,” Genes Chromosomes and Cancer, vol. 38, no. 3, pp. 215–225, 2003.
- G. Lim, J. Karaskova, B. Beheshti et al., “An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma,” Genes Chromosomes and Cancer, vol. 42, no. 4, pp. 392–403, 2005.
- G. Chen, T. G. Gharib, C. C. Huang et al., “Discordant protein and mRNA expression in lung adenocarcinomas,” Molecular & Cellular Proteomics, vol. 1, no. 4, pp. 304–313, 2002.
- Y. Suehara, T. Kondo, K. Fujii et al., “Proteomic signatures corresponding to histological classification and grading of soft-tissue sarcomas,” Proteomics, vol. 6, no. 15, pp. 4402–4409, 2006.
- A. Kawai, T. Kondo, Y. Suehara, K. Kikuta, and S. Hirohashi, “Global protein-expression analysis of bone and soft tissue sarcomas,” Clinical Orthopaedics and Related Research, vol. 466, no. 9, pp. 2099–2106, 2008.
- S. P. Gygi, Y. Rochon, B. R. Franza, and R. Aebersold, “Correlation between protein and mRNA abundance in yeast,” Molecular and Cellular Biology, vol. 19, no. 3, pp. 1720–1730, 1999.
- Y. Suehara, N. Tochigi, D. Kubota et al., “Secernin-1 as a novel prognostic biomarker candidate of synovial sarcoma revealed by proteomics,” Journal of Proteomics, vol. 74, no. 6, pp. 829–842, 2011.
- Y. Suehara, T. Kondo, K. Seki et al., “Pfetin as a prognostic biomarker of gastrointestinal stromal tumors revealed by proteomics,” Clinical Cancer Research, vol. 14, no. 6, pp. 1707–1717, 2008.
- Y. Suehara, K. Kikuta, R. Nakayama et al., “GST-P1 as a histological biomarker of synovial sarcoma revealed by proteomics,” Proteomics—Clinical Applications, vol. 3, no. 5, pp. 623–634, 2009.
- Y. Suehara, K. Kikuta, R. Nakayama et al., “Anatomic site-specific proteomic signatures of gastrointestinal stromal tumors,” Proteomics—Clinical Applications, vol. 3, no. 5, pp. 584–596, 2009.
- Y. Suehara, “Proteomic analysis of soft tissue sarcoma,” International Journal of Clinical Oncology, vol. 16, no. 2, pp. 92–100, 2011.
- K. Kikuta, N. Tochigi, S. Saito et al., “Peroxiredoxin 2 as a chemotherapy responsiveness biomarker candidate in osteosarcoma revealed by proteomics,” Proteomics—Clinical Applications, vol. 4, no. 5, pp. 560–567, 2010.
- K. Kikuta, D. Kubota, T. Saito, et al., “Clinical proteomics identified ATP-dependent RNA helicase DDX39 as a novel biomarker to predict poor prognosis of patients with gastrointestinal stromal tumor,” Journal of Proteomics, vol. 75, no. 4, pp. 1089–1098.
- K. Kikuta, N. Tochigi, T. Shimoda et al., “Nucleophosmin as a candidate prognostic biomarker of ewing's sarcoma revealed by proteomics,” Clinical Cancer Research, vol. 15, no. 8, pp. 2885–2894, 2009.
- Y. Li, T. A. Dang, J. Shen et al., “Plasma proteome predicts chemotherapy response in osteosarcoma patients,” Oncology Reports, vol. 25, no. 2, pp. 303–314, 2011.
- K. Yanagisawa, Y. Shyr, B. J. Xu et al., “Proteomic patterns of tumour subsets in non-small-cell lung cancer,” The Lancet, vol. 362, no. 9382, pp. 433–439, 2003.
- A. A. Alaiya, B. Franzén, A. Hagman et al., “Molecular classification of borderline ovarian tumors using hierarchical cluster analysis of protein expression profiles,” International Journal of Cancer, vol. 98, no. 6, pp. 895–899, 2002.
- M. L. Reyzer, R. L. Caldwell, T. C. Dugger et al., “Early changes in protein expression detected by mass spectrometry predict tumor response to molecular therapeutics,” Cancer Research, vol. 64, no. 24, pp. 9093–9100, 2004.
- J. W. Cui, J. Wang, K. He et al., “Proteomic analysis of human acute leukemia cells: insight into their classification,” Clinical Cancer Research, vol. 10, no. 20, pp. 6887–6896, 2004.
- S. Varambally, J. Yu, B. Laxman et al., “Integrative genomic and proteomic analysis of prostate cancer reveals signatures of metastatic progression,” Cancer Cell, vol. 8, no. 5, pp. 393–406, 2005.
- C. Folio, M. I. Mora, M. Zalacain et al., “Proteomic analysis of chemonaïve pediatric osteosarcomas and corresponding normal bone reveals multiple altered molecular targets,” Journal of Proteome Research, vol. 8, no. 8, pp. 3882–3888, 2009.
- Y. Li, T. A. Dang, J. Shen et al., “Identification of a plasma proteomic signature to distinguish pediatric osteosarcoma from benign osteochondroma,” Proteomics, vol. 6, no. 11, pp. 3426–3435, 2006.
- Y. Li, Q. Liang, Y. Q. Wen et al., “Comparative proteomics analysis of human osteosarcomas and benign tumor of bone,” Cancer Genetics and Cytogenetics, vol. 198, no. 2, pp. 97–106, 2010.
- D. H. Conrad, J. Goyette, and P. S. Thomas, “Proteomics as a method for early detection of cancer: a review of proteomics, exhaled breath condensate, and lung cancer screening,” Journal of General Internal Medicine, vol. 23, supplement 1, pp. 78–84, 2008.
- C. A. Granville and P. A. Dennis, “An overview of lung cancer genomics and proteomics,” American Journal of Respiratory Cell and Molecular Biology, vol. 32, no. 3, pp. 169–176, 2005.
- R. Alessandro, S. Fontana, E. Kohn, and G. de Leo, “Proteomic strategies and their application in cancer research,” Tumori, vol. 91, no. 6, pp. 447–455, 2005.
- T. Takahashi, T. Naka, M. Fujimoto et al., “Aberrant expression of glycosylation in juvenile gastrointestinal stromal tumors,” Proteomics—Clinical Applications, vol. 2, no. 9, pp. 1246–1254, 2008.
- G. E. Holt, H. S. Schwartz, and R. L. Caldwell, “Proteomic profiling in musculoskeletal oncology by MALDI mass spectrometry,” Clinical Orthopaedics and Related Research, no. 450, pp. 105–110, 2006.
- P. A. Fetsch, N. L. Simone, P. K. Bryant-Greenwood et al., “Proteomic evaluation of archival cytologic material using SELDI affinity mass spectrometry: potential for diagnostic applications,” American Journal of Clinical Pathology, vol. 118, no. 6, pp. 870–876, 2002.
- T. Kondo and S. Hirohashi, “Application of highly sensitive fluorescent dyes (CyDye DIGE Fluor saturation dyes) to laser microdissection and two-dimensional difference gel electrophoresis (2D-DIGE) for cancer proteomics,” Nature Protocols, vol. 1, no. 6, pp. 2940–2956, 2006.
- T. Kondo and S. Hirohashi, “Application of 2D-DIGE in cancer proteomics toward personalized medicine,” Methods in Molecular Biology, vol. 577, pp. 135–154, 2009.
- J. S. Minden, S. R. Dowd, H. E. Meyer, and K. Stühler, “Difference gel electrophoresis,” Electrophoresis, vol. 30, supplement 1, pp. S156–S161, 2009.
- B. Fiévet, D. Louvard, and M. Arpin, “ERM proteins in epithelial cell organization and functions,” Biochimica et Biophysica Acta, vol. 1773, no. 5, pp. 653–660, 2007.
- G. Bulut, S. H. Hong, K. Chen et al., “Small molecule inhibitors of ezrin inhibit the invasive phenotype of osteosarcoma cells,” Oncogene, vol. 31, pp. 269–281, 2012.
- A. Bretscher, K. Edwards, and R. G. Fehon, “ERM proteins and merlin: integrators at the cell cortex,” Nature Reviews Molecular Cell Biology, vol. 3, no. 8, pp. 586–599, 2002.
- L. Ren, S. H. Hong, Q. R. Chen, et al., “Dysregulation of ezrin phosphorylation prevents metastasis and alters cellular metabolism in osteosarcoma,” Cancer Research, vol. 72, no. 4, pp. 1001–1012.
- S. Tsukita, S. Yonemura, and S. Tsukita, “ERM (ezrin/radixin/moesin) family: from cytoskeleton to signal transduction,” Current Opinion in Cell Biology, vol. 9, no. 1, pp. 70–75, 1997.
- C. Khanna, X. Wan, S. Bose et al., “The membrane-cytoskeleton linker ezrin is necessary for osteosarcoma metastasis,” Nature Medicine, vol. 10, no. 2, pp. 182–186, 2004.
- H. R. Park, R. L. Cabrini, E. S. Araujo, M. L. Paparella, D. Brandizzi, and Y. K. Park, “Expression of ezrin and metastatic tumor antigen in osteosarcomas of the jaw,” Tumori, vol. 95, no. 1, pp. 81–86, 2009.
- H. R. Park, W. W. Jung, P. Bacchini, F. Bertoni, Y. W. Kim, and Y. K. Park, “Ezrin in osteosarcoma: comparison between conventional high-grade and central low-grade osteosarcoma,” Pathology Research and Practice, vol. 202, no. 7, pp. 509–515, 2006.
- C. Di Cristofano, M. Leopizzi, A. Miraglia et al., “Phosphorylated ezrin is located in the nucleus of the osteosarcoma cell,” Modern Pathology, vol. 23, no. 7, pp. 1012–1020, 2010.
- Y. Yu, J. Khan, C. Khanna, L. Helman, P. S. Meltzer, and G. Merlino, “Expression profiling identifies the cytoskeletal organizer ezrin and the developmental homeoprotein Six-1 as key metastatic regulators,” Nature Medicine, vol. 10, no. 2, pp. 175–181, 2004.
- A. M. Davis, R. S. Bell, and P. J. Goodwin, “Prognostic factors in osteosarcoma: a critical review,” Journal of Clinical Oncology, vol. 12, no. 2, pp. 423–431, 1994.
- S. B. Lee, J. N. Ho, S. H. Yoon, G. Y. Kang, S. G. Hwang, and H. D. Um, “Peroxiredoxin 6 promotes lung cancer cell invasion by inducing urokinase-type plasminogen activator via p38 kinase, phosphoinositide 3-kinase, and Akt,” Molecules and Cells, vol. 28, no. 6, pp. 583–588, 2009.
- C. A. Neumann, D. S. Krause, C. V. Carman et al., “Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression,” Nature, vol. 424, no. 6948, pp. 561–565, 2003.
- T. H. Lee, S. U. Kim, S. L. Yu et al., “Peroxiredoxin II is essential for sustaining life span of erythrocytes in mice,” Blood, vol. 101, no. 12, pp. 5033–5038, 2003.
- X. Wang, S. A. Phelan, K. Forsman-Semb et al., “Mice with targeted mutation of peroxiredoxin 6 develop normally but are susceptible to oxidative stress,” The Journal of Biological Chemistry, vol. 278, no. 27, pp. 25179–25190, 2003.
- Y. Wang, S. I. Feinstein, and A. B. Fisher, “Peroxiredoxin 6 as an antioxidant enzyme: protection of lung alveolar epithelial type II cells from H2O2-induced oxidative stress,” Journal of Cellular Biochemistry, vol. 104, no. 4, pp. 1274–1285, 2008.
- Y. Wang, S. I. Feinstein, Y. Manevich, Y. S. Ho, and A. B. Fisher, “Peroxiredoxin 6 gene-targeted mice show increased lung injury with paraquat-induced oxidative stress,” Antioxidants and Redox Signaling, vol. 8, no. 1-2, pp. 229–237, 2006.
- S. T. Lehtonen, A. M. Svensk, Y. Soini et al., “Peroxiredoxins, a novel protein family in lung cancer,” International Journal of Cancer, vol. 111, no. 4, pp. 514–521, 2004.
- D. Q. Li, L. Wang, F. Fei et al., “Identification of breast cancer metastasis-associated proteins in an isogenic tumor metastasis model using two-dimensional gel electrophoresis and liquid chromatography-ion trap-mass spectrometry,” Proteomics, vol. 6, no. 11, pp. 3352–3368, 2006.
- P. Karihtala, A. Mäntyniemi, S. W. Kang, V. L. Kinnula, and Y. Soini, “Peroxiredoxins in breast carcinoma,” Clinical Cancer Research, vol. 9, no. 9, pp. 3418–3424, 2003.
- J. B. Lee, S. J. Yun, H. Z. Chae, Y. H. Won, Y. P. Kim, and S. C. Lee, “Expression of peroxiredoxin and thioredoxin in dermatological disorders,” British Journal of Dermatology, vol. 146, no. 4, pp. 710–712, 2002.
- V. L. Kinnula, S. Lehtonen, R. Sormunen et al., “Overexpression of peroxiredoxins I, II, III, V, and VI in malignant mesothelioma,” Journal of Pathology, vol. 196, no. 3, pp. 316–323, 2002.
- T. Yanagawa, T. Ishikawa, T. Ishii et al., “Peroxiredoxin I expression in human thyroid tumors,” Cancer Letters, vol. 145, no. 1-2, pp. 127–132, 1999.
- W. C. Chen, W. H. McBride, K. S. Iwamoto et al., “Induction of radioprotective peroxiredoxin-I by ionizing irradiation,” Journal of Neuroscience Research, vol. 70, no. 6, pp. 794–798, 2002.
- J. H. Kim, P. N. Bogner, N. Ramnath, Y. Park, J. Yu, and Y. M. Park, “Elevated peroxiredoxin 1, but not NF-E2-related factor 2, is an independent prognostic factor for disease recurrence and reduced survival in stage I non-small cell lung cancer,” Clinical Cancer Research, vol. 13, no. 13, pp. 3875–3882, 2007.
- Y. M. Chung, Y. D. Yoo, J. K. Park, Y. T. Kim, and H. J. Kim, “Increased expression of peroxiredoxin II confers resistance to cisplatin,” Anticancer Research, vol. 21, no. 2, pp. 1129–1133, 2001.
- S. H. Park, Y. M. Chung, Y. S. Lee et al., “Antisense of human peroxiredoxin II enhances radiation-induced cell death,” Clinical Cancer Research, vol. 6, no. 12, pp. 4915–4920, 2000.
- L. Smith, K. J. Welham, M. B. Watson, P. J. Drew, M. J. Lind, and L. Cawkwell, “The proteomic analysis of cisplatin resistance in breast cancer cells,” Oncology Research, vol. 16, no. 11, pp. 497–506, 2007.
- A. Kropotov, V. Gogvadze, O. Shupliakov et al., “Peroxiredoxin V is essential for protection against apoptosis in human lung carcinoma cells,” Experimental Cell Research, vol. 312, no. 15, pp. 2806–2815, 2006.
- A. Castagna, P. Antonioli, H. Astner et al., “A proteomic approach to cisplatin resistance in the cervix squamous cell carcinoma cell line A431,” Proteomics, vol. 4, no. 10, pp. 3246–3267, 2004.
- X. Z. Chang, D. Q. Li, Y. F. Hou et al., “Identification of the functional role of peroxiredoxin 6 in the progression of breast cancer,” Breast Cancer Research, vol. 9, no. 6, article R76, 2007.
- T. O. Nielsen, “Microarray analysis of sarcomas,” Advances in Anatomic Pathology, vol. 13, no. 4, pp. 166–173, 2006.
- K. Tschoep, A. Kohlmann, M. Schlemmer, T. Haferlach, and R. D. Issels, “Gene expression profiling in sarcomas,” Critical Reviews in Oncology/Hematology, vol. 63, no. 2, pp. 111–124, 2007.
- T. O. Nielsen, R. B. West, S. C. Linn et al., “Molecular characterisation of soft tissue tumours: a gene expression study,” The Lancet, vol. 359, no. 9314, pp. 1301–1307, 2002.
- C. R. Antonescu, “Molecular profiling in the diagnosis and treatment of high grade sarcomas,” Ultrastructural Pathology, vol. 32, no. 2, pp. 37–42, 2008.
- R. Nakayama, T. Nemoto, H. Takahashi et al., “Gene expression analysis of soft tissue sarcomas: characterization and reclassification of malignant fibrous histiocytoma,” Modern Pathology, vol. 20, no. 7, pp. 749–759, 2007.