- Research article
- Open Access
- Open Peer Review
YY1 overexpression is associated with poor prognosis and metastasis-free survival in patients suffering osteosarcoma
- Filomena de Nigris†1, 6Email author,
- Licciana Zanella†2,
- Francesco Cacciatore†3,
- Anna De Chiara4,
- Flavio Fazioli5,
- Gennaro Chiappetta4,
- Gaetano Apice5,
- Teresa Infante6,
- Mario Monaco4,
- Raffaele Rossiello8,
- Gaetano De Rosa7,
- Marco Alberghini2 and
- Claudio Napoli1, 6
© Nigris et al; licensee BioMed Central Ltd. 2011
- Received: 26 May 2011
- Accepted: 2 November 2011
- Published: 2 November 2011
The polycomb transcription factor Yin Yang 1 (YY1) overexpression can be causally implicated in experimental tumor growth and metastasization. To date, there is no clinical evidence of YY1 involvement in outcome of patients with osteosarcoma. Prognosis of osteosarcoma is still severe and only few patients survive beyond five years. We performed a prospective immunohistochemistry analysis to correlate YY1 immunostaining with metastatic development and survival in a selected homogeneous group of patients with osteosarcoma.
We studied 41 patients suffering from osteosarcoma (stage II-IVa). Multivariate analysis was performed using Cox proportional hazard regression to evaluate the correlation between YY1 expression and both metastasis development and mortality.
YY1 protein is not usually present in normal bone; in contrast, a high number of patients (61%) showed a high score of YY1 positive cells (51-100%) and 39% had a low score (10-50% positive cells). No statistical difference was found in histology, anatomic sites, or response to chemotherapy between the two degrees of YY1 expression. Cox regression analysis demonstrated that the highest score of YY1 expression was predictive of both low metastasis-free survival (HR = 4.690, 95%CI = 1.079-20.396; p = 0.039) and poor overall survival (HR = 8.353, 95%CI = 1.863-37.451 p = 0.006) regardless of the effects of covariates such as age, gender, histology and chemonecrosis.
Overexpression of YY1 in primary site of osteosarcoma is associated with the occurrence of metastasis and poor clinical outcome.
- Osteosarcoma Patient
- Primary Malignant Bone Tumor
- Common Primary Malignant Bone
- Tumor Necrosis Rate
Osteosarcoma is the most common primary malignant bone tumor in adolescents and children . It occurs frequently in long bones and metastasizes preferentially to the lung . Despite recent advances in chemotherapy, the 5-year event-free survival and overall survival rates, closely linked to grade of osteosarcoma, are around 50-60%. This is due to the development of resistance to multiple types of chemotherapy and radiotherapy [2–4]. Clinical stage of the disease and several clinical biomarkers have been correlated with the outcome [5–11]. Nonetheless, these prognostic factors have limited utility in terms of predicting survival .
The ubiquitous, conserved, multifunctional polycomb transcription factor Yin Yang 1 (YY1) plays a pivotal role in biological processes [13–15]. YY1 regulates embryonic blood formation and its downstream hox genes, X chromosome inactivation, differentiation, and cell cycle [13, 14]. The majority of the data are consistent with the hypothesis that YY1 overexpression and/or its activation is associated with unchecked cellular proliferation, resistance to apoptotic stimuli, tumorigenesis and metastatic potential. We studied the role of YY1 in osteosarcoma carcinogenesis and tumor progression. YY1 is overexpressed in osteosarcoma cells and bioptic specimens, and is correlated with a high degree of malignancy [16, 17]. Moreover, YY1 silencing has been shown to be sufficient to significantly reduce osteosarcoma metastatic growth and neoangiogenesis in a nude mice model [18–20]. To date, there is no evidence of correlation between YY1 overexpression and clinical outcome in osteosarcoma patients. Thus, we designed a prospective study to analyze whether YY1 expression in the primary tumor of osteosarcoma patients could predict metastasis-free and overall survival.
We enrolled 41 osteosarcoma patients (stage II-IVa UICC/AJCC classification) from the Department of Pathology of the Istituto Ortopedico Rizzoli (Bologna, Italy) and from the Division of Surgical Pathology, Istituto Nationale Tumori, Fondazione G. Pascale (Naples, Italy), under their Local Ethical Committee approval. We used the bioptic samples of primary tumor before any treatment (see below). Of the 41 patients, 14 had metastasis at the first visit (synchronous), 15 developed metastasis during follow-up (metachronous) and 12 were metastasis-free. Metastases were localized in lung and the primary sites were in extremity bones. Extraskeletal, periosteal, and paraosteal osteosarcomas were excluded from this study. All slides of the cases were reviewed by two pathologists to confirm diagnosis. Patients received preoperative, postoperative or no chemotherapy according to degree of tumor stage. Necrosis area was defined by using the Huvos grading system, as described in detail [21, 22]. Accordingly, we subdivided patients into two groups (<90%) and (≥90%) based on chemonecrosis area as indicated by the European Cooperative Osteosarcoma Study Group coordinated by the Istituto Ortopedico Rizzoli (COSS) [21, 22], a partner of the present study.
Chemotherapy protocols included methotrexate (12 g/m2) with leucovorin rescue, cisplatin (90-150 mg/m2), doxorubicin (60-90 mg/m2), and ifosfamide (6-10 g/m2). The scheduled duration of chemotherapy ranged from 24 to 38 weeks. For chemotherapy patients, surgery was scheduled to take place between weeks 9 and 11 and radiotherapy was not used. We collected clinical data from all patients including age, sex, tumor site, necrosis area after chemotherapy and surgical stage.
Biopsies before chemotherapy were fixed and paraffin embedded. Conventional immunohistochemical studies were performed on 5-6 μm section, as previously described in detail [16, 22]. Briefly, slides were immersed in a water bath (W-cap Bioptica) and incubated for 30 minutes at 95°C, then cooled for 20 minutes at room temperature. Sections were then incubated for 10 minutes in 3% hydrogen peroxide in distilled water, and washed in PBS for 5 minutes. Slides were incubated with the primary antibody (mouse-monoclonal YY1 diluted 1:100 sc7341 Santa Cruz) for 30 minutes in a Dako Autostainer device. The signal was then visualized with streptavidina-biotina Dako REAL Detection System Peroxidase/DAB, Rabbit/Mouse Dako Autostainer. Slides were counterstained with hematoxylin. Washing steps were included after each incubation. All samples were stained with vimentin as tissue quality controls while positive and negative conventional controls were used to test antibody as already reported . All controls gave satisfactory and reproducible results. Digital photos were obtained with Olympus Vanox AHBS3. The staining of tumor cells for evaluation of YY1 was scored from 0 to 4 (0=no staining; 1=weak 1-25% positive cells; 2= moderate 26%-50% positive cells; 3= strong 51%-75% positive cells; 4= very strong 76%-100% positive cells. This score was checked by two independent observers blinded for clinical outcome or other biological tumor features. Discrepant cases were decided on consensus.
Data were analyzed with SPSS 13.0 software. Results are reported as mean ± SD. YY1 was considered as a discrete variable and the patients were stratified into two classes: high score as 3-4, (>51-100% positive cells) and low score as 0-2, (0-<50% positive cells) of YY1. ANOVA was used to assess difference for continuous variables (age and mean follow-up) while Pearson chi square test was used to examine differences between YY1 expression and each clinical variable: gender, tumor site, histotype, chemonecrosis, presence of metastasis at diagnosis and occurrence of metastasis at follow-up (n = 41). Survival periods were counted in months from the date of first visit to date of death or last follow-up before study closure. Follow-up data started at time of diagnosis allowing a minimum of 3.8 months (mean 47.0 ± 25.3 month range, 3.8-95 months). Mean age of the sample was 19.4 ± 15.5 with a range from 4 to 76 years. Metastasis-free period was counted in months from the date of surgery to date of detection of first metastasis, since no local relapses occurred. We used life-table method to estimate the metastasis-free survival and overall survival for low and high levels of YY1 expression. Multivariate Cox regression analysis was used to evaluate the effect of YY1 expression on metastasis occurrence and survival independently of age, gender, histotype and chemonecrosis. A p value <0.05 was considered as statistically significant.
YY1 overexpression in osteosarcoma tissues
YY1 scoring as continuous variable
YY1 - 0
YY1 - 1
YY1 - 2
YY1 - 3
YY1 - 4
16.3 ± 7.4
30.1 ± 23.9
13.0 ± 2.2
12.3 ± 8.9
19.7 ± 13.4
Chemonecrosis ≥ 90%
Metachronous metastasis (%)*
Mean follow -up
50.3 ± 31.6
39.7 ± 21.0
62.0 ± 37.3
43.6 ± 23.0
48.5 ± 25.6
Univariate analysis of YY1 expression and clinical pathological characteristics of patients
Number of cases 41
YY1(low) (0-50% positive cells) 16 cases (39.0%)
YY1 (strong) (51%-100% positive cells) 25 cases (61.0%)
19.4 ± 15.6
24.4 ± 19.1
16.2 ± 12.0
Chemonecrosis ≥ 90%
Synchronous metastasis (%)
Metachronous metastasis (%) *
Mean time to metastasis (range 3-76 months)
29.4 ± 19.2
37.6 ± 22.9
22.9 ± 13.1
Mean follow-up (range 3-95 months)
47.0 ± 25.3
49.8 ± 27.5
45.2 ± 24.2
Multivariate Cox regression analysis on incidence of metachronous metastasis
Metachronous metastasis (95.0% CI)
Chemonecrosis ≥ 90%
YY1 in primary site (strong vs low)
Association between YY1 overexpression and probability of survival and median survival
Years after the first visit
% of survival patients 41 cases
% of survival patients per year stratified for YY1
YY1 Low (16 cases)
YY1 strong (25 cases)
Multivariate Cox regression analysis of clinical variables on overall survival
Chemonecrosis ≥ 90%
YY1 in primary site (strong vs low)
The present study demonstrates that a high level of YY1 protein expression increases the risk of metastasis (4.69-fold) and poor survival (8.35-fold) in osteosarcoma patients independently of covariates such as age, gender, histotype, and chemonecrosis. We report that the highest range of YY1 expression is a statistically significant prognostic factor setting the 5-year survival rate to 34% in patients with osteosarcoma. These results are in line with literature data and with the tumor necrosis rate which is currently the strongest clinical prognostic factor after chemotherapy [2, 23, 24].
Overall, the molecular complexity of osteosarcoma makes the known prognostic markers of limited utility [12, 25]. A multiple panel of biomarkers in addition to clinical parameters would be useful for predicting prognosis . In this setting, YY1 is the first osteosarcoma marker whose overexpression has been correlated with low metastasis-free and poor overall survival in a higher frequency of cases (61% in the present study) than reported in other studies leading us to set a higher cut-off value (YY1 > 50%) . In addition, low YY1 expression was correlated with best clinical prognosis and absence of metastasis during follow-up. One common limitation of immunohistochemical studies is both antibody sensitivity and specificity. To address these issues, we used an antibody previously tested by other groups [26, 27]. Immunohistochemistry was also performed in two different Institutions which studied different subgroups of patients [26, 27]. YY1 was localized in the nucleus irrespective of histologic subtype, patient age, or tumor site. Although this is a small study, there was no significant difference in YY1 scores between younger and older age groups suggesting its role in tumor development. The design of the present study stemmed from our previous in vitro observations demonstrating that YY1 was overexpressed in osteosarcoma cells and tissues with more aggressive phenotype [16–18]. This is in agreement with YY1 overexpression in prostate, gastrointestinal [26, 27] and other tumors . Moreover, in an in vivo mice model of osteosarcoma YY1 was also shown to play a key role in metastatic growth  by regulating vascular supply [20, 28].
Interestingly, the majority of patients analyzed revealed strong YY1 expression and showed poor response to chemotherapy based on Huvos grading system. Although the correlation between YY1 expression and prognosis may merely be a statistical association, the protein dosage points to a functional relationship between YY1 overexpression and a more aggressive tumor phenotype. Noteworthy, literature data from other tumoral and non-tumoral tissues provide at least some evidence for the proposed functional relationship. Resistance to Fas-mediated apoptosis of prostate cancer cells is linked to YY1 . A further potential link between YY1 overexpression and chemoresistance lies in the fact that YY1 regulates DR5 gene . We have recently demonstrated that YY1 is involved in CXCR4 and VEGF pathways [19, 20] which have both been genetically amplified and correlated with poor survival of soft-tissue sarcomas [8, 31, 32]. In addition, YY1 overexpression increases resistance to taxana treatment in epithelial ovarian cancer . Furthermore, in a meta-analysis, YY1 was scored as the most significant gene upregulated in metastatic breast cancer . Thus, YY1 screening may be useful in optimizing individual therapy management at the time of diagnosis in these patients.
In conclusion, we demonstrated for the first time that high YY1 expression in osteosarcoma is associated with metastasis development and mortality independently of age, gender, histotype and presence of metastasis at baseline. While other studies have analyzed larger cohorts of patients [34, 35], this is the first time a prognostic marker has demonstrated poor outcome by multivariate analysis. If data are confirmed in a larger cohort of patients, YY1 may become part of a multiple panel of biomarkers clinically useful for osteosarcoma prognosis.
Our study established that overexpression of YY1 in primary site of osteosarcoma is associated with the occurrence of metastasization and poor clinical prognosis. This may be a novel marker for patients with osteosarcoma.
We thank Sig. Concetta Aiello for her technical support. This work was supported by grant from the "Fondi di Ateneo 2008" to the Second University of Naples (F.DN. and C.N.) and from the "Progetto di Rilevante Interesse Nazionale Ministero Italiano Università e Ricerca" 2006 [Code 0622153_002 "Meccanismi fisiopatologici di danno vascolare/trombotico ed angiogenesi"] and 2008 [Code T85HLH_002 "Regolazione dell'espressione genica della via SIRT/Foxo1- dipendente in cellule endoteliali progenitrici nella nicchia vascolare] to the Second University of Naples (C.N.)
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