Material and Method: In this study, we evaluated 81 synovial sarcoma cases referred to our tertiary tumor center during a period of 20 years. We applied bcl-2, c-myc and survivin immunohistochemically and investigated the relationship with prognosis for those 65 cases with follow-up. The relationship between the conventional morphological findings (mitosis, necrosis, grade) with prognosis was also investigated.
Results: Five-year disease free survival rate was 44% and ten-year progression free survival rate was 38%, reflecting the aggressive behavior of synovial sarcoma. Tumor grade (according to FNCLCC) was the most significant prognostic input in this study. We obtained a significant difference between grade II (40 cases) and grade III (24 cases) group regarding progression-free survival and overall survival (p<0.001 and p<0.001 respectively). Grade II was divided into two groups according to mitotic index and necrosis (grade IIa and IIb) and there was a significant difference between them regarding prognosis (p=0.013 for progression free survival, p=0.003 for overall survival). There was a significant relationship between bcl-2 negative plus focally weak positive cases (9 cases) and focally strong cases (21 cases) and diffuse strong cases (35 cases) (p=0.042 and p=0.016 respectively). There was a significant relation between c-myc negative cases (25 cases) and nuclear positive cases (17 cases) regarding overall survival (p=0.043) and between c-myc negative cases and cytoplasmic positive cases (23 cases) regarding progression free survival (p=0.05). The relation between survivin and prognosis was not significant.
Conclusion: Tumor grade was the most significant prognostic parameter in this study. The grade IIa group (with less than 10 mitoses in 10 HPF, without necrosis) had a better prognosis than both the grade IIb and III groups. The grade IIb group was closer to grade III regarding the prognosis. Bcl-2 and c-myc (nuclear and/or cytoplasmic) immunohistochemical positivity had prognostic value but this finding has to be confirmed by large series.
The prognosis of synovial sarcomas is generally poor and the 5- and 10-year survival rates have been reported as 36-76% and 20-63% respectively[1,6-11]. The factors associated with a good prognosis are younger age (younger than 15 or 20 years of age), small tumor size (smaller than 5 or 7 cm), distal extremity location, low tumor stage and appropriate excision of the tumor. Having less-differentiated areas in the tumor, presence of tumor necrosis, and high mitotic activity (≥ 10 mitoses/10 HPF) have been reported as negative morphological prognostic parameters[1,6-12].
The immune expressions of bcl-2, c-myc and survivin in different types of sarcoma and synovial sarcoma cases and their relationship with the prognosis have previously been investigated[13-17]. Our aim in this study was to immunohistochemically evaluate the relationship between bcl-2, c-myc, survivin expression and the prognosis of synovial sarcoma because literature findings on the relationship of bcl-2 and c-myc immune expression with the prognosis are not clear. In addition, the relationship between conventional morphological parameters and prognosis was investigated.
The general information, follow-up durations and the information regarding the disease outcomes (recurrence, metastasis, survival data, etc.) of the cases were obtained from the Orthopaedics and Traumatology Department records, Radiation Oncology Department records, hospital records, and Cancer Monitoring and Control Centre (KİDE M) records.
The WHO (for histological type) and FNLCC (French National Cancer Center) criteria were used as the basis for determining grade of the tumor (differentiation, mitotic index and necrosis)[18]. The histological type was evaluated in four groups as epithelial predominant, biphasic, monophasic fibrous and poorly differentiated (Figure 1,2). All cases received three points for tumor differentiation during the grading[1]. Mitoses were counted at 10 HPF for mitotic activity. The Nikon Eclipse 80i microscope was used. During scoring, 1 point was given for 0-9 mitoses, 2 points for 10-19 mitoses and 3 points for 20 or more mitoses. Cases without necrosis were given 0 points, cases with less than 50% necrosis 1 point and cases with more than 50% necrosis 2 points. Cases with a score of 4 points were evaluated as grade IIa, 5 points as grade IIb and 6 or more points as grade III.
Five micron thick serial sections were obtained from the paraffin-embedded blocks belonging to the selected suitable preparations fixed with formalin to study cytokeratin 7, bcl- 2, c-myc and survivin with the IHC method on positively charged slides and one for hematoxylin-eosin staining. The cytokeratin 7 (clone OVTL 12-30, Santa Cruz, 1:100 dilution), bcl-2 (clone 100, Santa Cruz, 1:50 dilution), c-myc (clone 9E10, Santa Cruz, 1: 25 dilution) and survivin (clone SPM331, Santa Cruz, 1:50 dilution) primary antibodies were investigated with IHC examination in the sections. The biotin-free, HRP multimer -based, hydrogen peroxide substrate and 3, 3’-diaminobenzidine tetrahydrochloride (DAB) chromogen containing ultraView™ Universal DAB Detection Kit (Catalog number 760–500, Ventana Medical Systems, Tucson, AZ) and a full automated immunohistochemistry staining device (Ventana BenchMark XT, Ventana Medical Systems, Tucson, AZ) were used as the IHC staining system.
Tissue profiles were taken on electrostatically charged slides (X-traTM, Surgipath Medical Industries, Richmond, Illinois, USA) and dried at 60 °C for at least two hours. The whole IHC staining process including deparaffinization and antigen revealing procedures were performed at the BenchMark XT and fully automated IHC staining device. Only the primary antibodies cytokeratin 7 (OVTL 12-30), bcl-2 (100), c-myc (9E10) and survivin (SPM331) were manually placed as drops and incubated at 37 °C for 32 minutes. The counter staining of the sections for which the counter staining was performed with hematoxylin and bluing solution in the device was followed by dehydration after which the sections were made transparent with xylene and the process was concluded with manual coverslip closure.
Cytoplasmic positivity as well as the diffuseness of the staining for bcl-2 were semi-quantitatively evaluated as diffuse (≥ 50%) or focal (less than 50) and the severity of the staining as 1 or 2 positive. Statistical evaluation was performed on three groups as negative focal faint positive, focal strong positive, and diffuse strong positive.
Cytoplasmic or nuclear positivity (more than 5% positivity) as well as the diffusion of c-myc were semi-quantitatively evaluated as diffuse (50% and over) or focal (less than 50%) and the severity of the staining as 1 or 2 positive. Statistical evaluation was performed on a total of three groups as a negative group, cytoplasmic positive group and nuclear positive group.
Cytoplasmic positivity and/or nuclear positivity (more than 5% positivity) as well as the diffuseness of the staining for survivin were semi-quantitatively evaluated as diffuse (50% and over) and focal (less than 50%) and the severity of the staining as 1 and 2 positive and the statistical evaluation was performed on a total of three groups as negative group, nuclear evident stained group and cytoplasmic evident stained group.
Statistical analysis was performed with the SPSS (Version 15.0) package software “Kaplan-Meier” survival analysis and “Cox Regression” analysis were used in the study. A p value below 0.05 was considered significant for the analyses.
Pancytokeratin or EMA positivity was present in all cases on immunohistochemical evaluation. A positive result was obtained in 54 cases and a negative result in 27 cases with cytokeratin 7.
Follow-up information was present in 65 (80.2%) of the 81 cases. No local recurrence or metastasis was found in 26 (40%) of these 65 patients. Nine (14%) had local recurrence but no metastasis. Five (8%) had local recurrence and metastasis. Twenty-five (38%) had recurrence and/or metastasis and died because of the tumor. The mean diseasefree survival duration was 34.2 ± 39.4 months in cases with local recurrence or metastasis and 89.5 ± 69.4 months in cases with no local recurrence or metastasis. The mean disease-free survival duration was 111.8 ± 16.1 months. The disease-free survival rate was 44% for five years and 38% for 10 years. The survival rate was 57% for five years and 48% for 10 years. The survival duration range in the 40 live cases among the 65 cases where follow-up could be found was 2 to 264 months and the mean survival duration was 82.9 ± 68.2 months. The survival duration range of the 25 cases who died was 12 to 132 months and the mean survival duration was 35.3 ± 25.8 months. The mean survival duration of all cases with follow up was 150.6 ± 16.8 months.
The relationship of gender and age distribution parameters with disease-free survival or survival duration was not statistically significant.
The distribution of histological subtypes in the 81 cases was epithelial predominant in two (2.5%), biphasic in 15 (18.5%), monophasic fibrous in 60 (74.1%) and poorly differentiated in 4 (4.9%) cases. No local recurrence and/or metastasis was found in the two epithelial predominant cases and both were alive. Local recurrence and/or metastasis was present in 11 of 14 biphasic cases (78.6%) and absent in 3 (21.4%). Eight of fourteen biphasic type cases (57.1%) were alive while six (42.9%) had died. Local recurrence and/or metastasis was found in 24 of 45 monophasic fibrous type cases (53.3%) and was absent in 21 (46.7%). 29 of the monophasic fibrous type cases (64.4%) were alive and 16 (35.6%) had died. Local recurrence and/or metastasis was detected in all of the four poorly differentiated synovial sarcoma cases. One (25%) was alive and three (75%) had died. Although the disease-free survival and survival durations were shorter in the biphasic type synovial sarcoma cases compared to the monophasic fibrous type, this difference was not statistically significant.
The mean number of mitosis was 7.8 ± 7.8 in the 26 cases with no local recurrence or metastasis. The mean number of mitoses was 14 ± 9.4 in the 29 cases with local recurrence and/or metastasis. The relationship between mitosis and disease-free survival was statistically significant (p=0.01). The number of mitoses in the 40 cases who were alive was 8.9 ± 8.5. The number of mitoses in the 25 cases who died was 15.6 ± 9.2. The relationship between mitosis and survival was statistically significant (p=0.01).
Necrosis was evaluated in 64 (79%) of 81 cases. 17 (21%) cases were excluded from the evaluation as they contained post-treatment changes associated with neoadjuvant therapy. No necrosis was found in 39 (60.9%) of the 64 cases. Necrosis under 50% was observed in 25 (39.1%) cases. The mean survival duration was 217.3 ± 18.8 months and the mean disease-free survival duration 146.2 ± 22.1 months in the group without necrosis when evaluated in 50 of the 64 cases with follow-up. The mean survival duration was 60.4 ± 12.2 months and the mean disease-free survival duration 45 ± 10.5 months in the group with necrosis. The relationship of the necrosis status of the tumor with survival duration and disease-free survival duration was statistically significant (p<0.001 and p=0.0013 respectively).
Grading could be performed in 64 (79%) of 81 cases. 17 (21%) cases were excluded from the evaluation as they contained post-treatment changes associated with neoadjuvant therapy. Of the 64 cases, 40 (62.5%) were evaluated as grade II and 24 (37.5%) as grade III. The disease-free survival duration was 192 ± 24 months in the grade IIa group, 56 ± 13 months in the grade IIb group and 36 ± 9 months in grade III group at the evaluation performed on 50 patients with follow-up out of 64 patients. The relationship between grade IIa and grade IIb and between grade IIa and grade III was statistically significant in terms of disease-free survival (p = 0.013 and p < 0.001 respectively) (Figure 3).
Figure 3: Kaplan-Meier disease-free survival analysis in different tumor grades of synovial sarcoma.
While disease-free survival duration was 159 months in the grade II group (grade IIa + IIb) it was 36 months in the grade III group. The difference between grade II and III was significant in terms of disease-free survival (p<0.001). No statistically significant difference was found between grade IIb and grade III in terms of disease-free survival (p=0.13). A statistically significant difference was found between grade IIa and grade IIb and between grade IIa and grade III in terms of survival (p = 0.003 and p < 0.001 respectively) (Figure 4). The difference between grade II and III in terms of survival was significant (p<0.001). No significant difference was found between grade IIb and III regarding survival (p=0.15). The grade-related metastasis, recurrence, and survival information of the cases are presented in Table I.
Figure 4: Kaplan-Meier survival analysis in different tumor grades of synovial sarcoma.
Table I: Local recurrence, metastasis and survival information of tumor grades
Bcl-2 was negative or faint positive in 9, focal strong positive in 21 and diffuse strong positive in 35 of 65 patients with follow-up (Figure 5). The Bcl-2 positivity distribution and prognosis relationship is provided in Table II. The relationship between the bcl-2 negative and faint positive groups and between the focal strong positive and diffuse strong positive groups was statistically significant in terms of disease-free survival (p=0.042 and p=0.016 respectively) (Figure 6).
Figure 5: Cytoplasmic bcl-2 positivity in synovial sarcoma (bcl-2; x100).
C-myc was negative in 25, cytoplasmic positive in 23 and nuclear positive in 17 of 65 cases with follow-up (Figure 7). C-myc positivity distribution and the relationship with prognosis is provided in Table II. The relationship between c-myc negative and cytoplasmic positive cases in terms of disease-free survival and between c-myc negative and nuclear positive cases in terms of survival was statistically significant (p = 0.05 and p = 0.043 respectively) (Figure 8).
Figure 7: Nuclear c-myc positivity in synovial sarcoma (myc, x200).
Figure 8: Kaplan-Meier survival analysis with c-myc immunoexpression in synovial sarcoma.
Survivin was negative in 23, nuclear positive in 18 and cytoplasmic positive in 24 of 65 cases with follow-up (Figure 9). The relationship between survivin expression and prognosis was not statistically significant (Table II).
Synovial sarcomas are usually aggressive tumors and the five-year survival rate has been reported as 36% to 76% and the 10-year survival rate as 20% to 63% in various studies[1,6-11]. The five-year survival rate was 57%, and the 10- year survival rate 48% in our study, confirming the literature information that synovial sarcomas are aggressive tumors.
Marked tumor necrosis in the synovial sarcoma and high mitotic activity (> 10 mitosis/10 HPF) have been reported as negative prognostic factors[15,16]. The mitotic index and the necrosis status of the tumor was associated with survival and disease-free survival and this relationship was statistically significant in our study. The relationship between the tumor grade (where necrosis and mitotic index are used as parameters) and the prognosis was markedly statistically significant. The relationship between the tumor grade and prognosis in synovial sarcoma cases has been reported in the literatüre[8,21]. The differences in prognosis between grade II and III cases are a well-known finding. We divided grade II cases into two groups as IIa and IIb according to the mitosis and necrosis status and found no statistically significant difference between them in terms of prognosis. Grade IIb was found closer to grade III regarding prognosis.
Cytokeratin 7 is reported to react positively in synovial sarcoma cases[2]. One study evaluated synovial sarcoma cases containing all subtypes and reported the staining rates for cytokeratin 7 in the biphasic, monophasic fibrous and poorly differentiated types as 100%, 79% and 50% respectively[22]. Cases found to be positive for pancytokeratin or EMA were included in this study. Positivity with cytokeratin 7 was found in two of three cases.
The bcl-2 gene plays an important role in pathophysiological processes as a mechanism ensuring the elimination of unwanted apoptotic cells. The interruption of this function creates one of the tumor development mechanisms. The bcl-2 oncogene and the protein it encodes have been reported for the first time in follicular lymphoma cases[23]. The bcl-2 gene and the protein product prolong the life of the cell, and the correlation between the expression level and prognosis has been studied in various tumors. For example, a correlation has been found between bcl-2 expression and unfavorable histological parameters and clinical course in tumors such as neuroblastoma and Ewing sarcoma[24]. Bcl-2 positivity in synovial sarcoma (highly diffuse positive) is a well-known finding[6,25-27] but its relationship with prognosis is unclear[13]. A correlation has recently been found between the bcl-2 m-RNA level and immunohistochemical expression severity and diffuseness in 32 synovial sarcoma cases where the SS18/SSX1 or SS18/SSX2 fusion gene was detected on PCR. A higher metastasis rate and shorter life was found in cases with more bcl-2 immunohistochemical expression in the same study but this finding was not statistically significant[13]. The disease-free survival duration was significantly shorter in cases showing strong positively bcl-2 staining than in bcl-2 negative and focal faint positive cases in our study. Although bcl-2 staining is not specific for the diagnosis of synovial sarcoma it may be contribute to determining the diagnosis in addition it may have prognostic value. However, we believe this finding needs to be verified in larger series due to the low number of negative and focal faint positive cases compared in our study.
The c-myc protein functions as a transcription factor ensuring the regulation of critical cellular processes such as cell cycle regulation, cell differentiation, apoptosis, adhesion and migration[28,29]. Contrary to the regulated myc expression during normal cell proliferation, the expression of myc protein is commonly sustained and sometimes excessive in tumors. This can lead to continuous transcription of critical target genes and subsequently to neoplastic transformation. Oncogenic activation occurs through gene amplification and chromosomal translocation. C-myc expression has been reported to be associated with a poor prognosis in solid tumors such as synovial sarcoma, osteosarcoma, leiomyosarcoma, and liposarcoma[30]. C-myc overexpression has also been identified in high-grade liposarcoma, chondrosarcoma, and uterine leiomyosarcoma[31]. A study evaluated 28 cases that were histologically and immunohistochemically diagnosed with leiomyosarcoma. C-myc expression was found to be associated with survival and c-myc was identified as an independent prognostic factor in multivariate analysis[32]. The relationship between c-myc and prognosis was investigated in 27 synovial sarcoma cases with at least 24 months follow-up and c-myc nuclear positivity was reported to be a negative prognostic indicator[33]. Although c-myc is a marker expected to give a nuclear reaction, it can also show cytoplasmic staining[34]. There was a statistically significant relationship between c-myc negative cases and the cytoplasmic and/or nuclear positive cases in this study. Survival and disease-free survival duration was found to be longer in c-myc negative cases. We think that this finding should be verified with larger series as the statistical significance was low.
Survivin is a member of the apoptosis inhibitor family and shows its effect by inhibiting caspase activity. Survivin can be detected in the cytoplasm and/or nucleus of tumor cells. Cytoplasmic expression of survivin is reported to be associated with apoptosis inhibition and control of cell life and its nuclear expression with facilitating cell proliferation. Some studies report that nuclear positivity is associated with the prognosis while others report that both nuclear and cytoplasmic positivity is associated with the prognosis[16,35,36]. There are some studies indicating the survivin expression is associated with the prognosis in osteosarcoma, leiomyosarcoma and synovial sarcoma[16,35]. Survivin expression was linked to the prognosis in osteosarcomas and nuclear positivity was found to result in long-term survival[35]. Both nuclear and cytoplasmic immunohistochemical positivity of survivin have been reported to be independent prognostic factors for synovial sarcoma and leiomyosarcoma in 24 leiomyosarcoma and 26 synovial sarcoma cases[36]. The survival or disease-free survival durations in survivin-negative cases were longer than the survivin-positive cases in our study but this was not statistically significant.
In conclusion, necrosis and proliferative activity, and tumor grade (where directly associated with these two parameters) are important for predicting possible aggressive behavior. We divided grade II synovial sarcoma cases into two subgroups unlike the general approach reported in the literature and found significant difference between these two subgroups in terms of prognosis. Our results indicate that cases with 10 or more mitoses on 10 HPF or containing necrosis (grade IIb) show a relatively more aggressive course (prognosis closer to grade III) or in other words cases without necrosis and less than 10 mitoses per 10 HPF (grade IIa) have a relatively better prognosis. Furthermore, this finding highlights the importance of conventional parameters such as mitosis and necrosis. We determined that the immunohistochemical markers bcl-2 and c-myc may have prognostic significance in synovial sarcoma cases but the statistical value of the relationship between these findings and the prognosis was borderline and should be verified with larger series.
ACKNOWLEDGMENTS
We thank Assistant Professor Dr. Timur Köse, a faculty
member in Ege University Department of Biostatistics and
Medical Informatics, for his assistance in the statistical
evaluation of this study.
CONFLICT of INTEREST
This study was supported by the Ege University Rectorate,
Commission of Scientific Research Projects (Project 2010
TIP 071).
1) Weiss SW, Golgblum JR. Synovial sarcoma. In: Enzinger FM,
Weiss SW, editors. Soft tissue tumors. 5th ed. St. Louis: CV
Mosby; 2008.1161-221.
2) Olsen SH, Thomas DG, Lucas DR. Cluster analysis of
immunohistochemical profiles in synovial sarcoma, malignant
peripheral nerve sheath tumor, and Ewing sarcoma. Mod Pathol.
2006;19:659-68.
3) Terry J, Saito T, Subramanian S, Ruttan C, Antonescu CR,
Goldblum JR, Downs-Kelly E, Corless CL, Rubin BP, van
de Rijn M, Ladanyi M, Nielsen TO . TLE1 as a diagnostic
immunohistochemical marker for synovial sarcoma emerging
from gene expression profiling studies. Am J Surg Pathol.
2007;31:240-6. [ Özet ]
4) Kosemehmetoglu K, Vrana JA, Folpe AL. TLE1 expression is not
specific for synovial sarcoma: A whole section study of 163 soft
tissue and bone neoplasms. Mod Pathol. 2009;22:872-8. [ Özet ]
5) Sandberg AA, Bridge JA. Updates on the cytogenetics and
molecular genetics of bone and soft tissue tumors. Synovial
sarcoma. Cancer Genet Cytogenet. 2002;133: 1-23. [ Özet ]
6) Spillane AJ, A’Hern R, Judson IR, Fisher C, Thomas JM. Synovial
sarcoma: A clinicopathologic, staging, and prognostic assessment.
J Clin Oncol. 2000;18:3794-803. [ Özet ]
7) Ladanyi M, Antonescu CR, Leung DH, Woodruff JM, Kawai A,
Healey JH, Brennan MF, Bridge JA, Neff JR, Barr FG, Goldsmith
JD, Brooks JS, Goldblum JR, Ali SZ, Shipley J, Cooper CS, Fisher
C, Skytting B, Larsson O. Impact of SYT-SSX fusion type on
the clinical behavior of synovial sarcoma: A multi-institutional
retrospective study of 243 patients. Cancer Res. 2002; 62:135-40. [ Özet ]
8) Brecht IB, Ferrari A, Int-Veen C, Schuck A, Mattke AC, Casanova
M, Bisogno G, Carli M, Koscielniak E, Treuner J. Grossly-resected
synovial sarcoma treated by the German and Italian Pediatric Soft
Tissue Sarcoma Cooperative Groups: Discussion on the role of
adjuvant therapies. Pediatr Blood Cancer. 2006; 46:11-7. [ Özet ] 9) T rassard M, Le Doussal V, Hacène K, Terrier P, Ranchère D,
Guillou L, Fiche M,Collin F, Vilain MO, Bertrand G, Jacquemier
J, Sastre-Garau X, Bui NB, Bonichon F, Coindre JM. Prognostic
factors in localized primary synovial sarcoma: A multicenter
study of 128 adult patients. J Clin Oncol. 2001;19:525-34. [ Özet ]
10) Spurrell EL, Fisher C, Thomas JM, Judson IR. Prognostic factors
in advanced synovial sarcoma: An analysis of 104 patients treated
at the Royal Marsden Hospital. Ann Oncol. 2005;16:437-44. [ Özet ] 11) Bergh P, Meis-Kindblom JM, Gherlinzoni F, Berlin O, Bacchini
P, Bertoni F, Gunterberg B, Kindblom LG. Synovial sarcoma:
Identification of low and high risk groups. Cancer. 1999;85:
2596-607. [ Özet ]
12) Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F (Eds):
Who Health Organization Classification of Tumors Pathology
and Genetics of Tumors of Soft Tissue and Bone. Lyon: IARC
Press; 2013. 213-5.
13) Krsková L, Kalinová M, Brízová H, Mrhalová M, Sumerauer D,
Kodet R. Molecular and immunohistochemical analyses of BCL2,
KI-67, and cyclin D1 expression in synovial sarcoma. Cancer
Genet Cytogenet. 2009;193:1-8. [ Özet ] 14) Tsiatis AC, Herceg ME, Keedy VL, Halpern JL, Holt GE, Schwartz
HS, Cates JM. Prognostic significance of c-Myc expression in soft
tissue leiomyosarcoma. Mod Pathol. 2009;22:1432-8. [ Özet ] 15) Shen J, Scotlandi K, Baldini N, Manara MC, Benini S, Cerisano V,
Picci P, Serra M. Prognostic significance of nuclear accumulation
of c-myc and mdm2 proteins in synovial sarcoma of the
extremities. Oncology. 2000;58:253-60. [ Özet ]
16) Kappler M, Kotzsch M, Bartel F, Füssel S, Lautenschläger C,
Schmidt U, Würl P, Bache M, Schmidt H, Taubert H, Meye
A. Elevated expression level of survivin protein in soft-tissue
sarcomas is a strong independent predictor of survival. Clin
Cancer Res. 2003;9:1098-104. [ Özet ]
17) Taubert H, Heidenreich C, Holzhausen HJ, Schulz A, Bache
M, Kappler M, Eckert AW, Würl P, Melcher I, Hauptmann K,
Hauptmann S, Schaser KD. Expression of survivin detected by
immunohistochemistry in the cytoplasm and in the nucleus
is associated with prognosis of leiomyosarcoma and synovial
sarcoma patients. BMC Cancer. 2010;10:65. [ Özet ] 18) Coindre JM, Trojani M, Contesso G, David M, Rouesse J, Bui
NB, Bodaert A, De Mascarel I, De Mascarel A, Goussot JF.
Reproducibility of a histopathologic grading system for adult soft
tissue sarcoma. Cancer. 1986;58:306-9. [ Özet ]
19) Kawai A, Woodruff J, Healey JH, Brennan MF, Antonescu CR,
Ladanyi M. SYT-SSX gene fusion as a determinant of morphology
and prognosis in synovial sarcoma. N Engl J Med. 1998;338:
153-60. [ Özet ]
20) Cagle LA, Mirra JM, Storm FK, Roe DJ, Eilber FR. Histologic
features relating to prognosis in synovial sarcoma. Cancer.
1987;59:1810-4. [ Özet ]
21) Guillou L, Benhattar J, Bonichon F, Gallagher G, Terrier P, Stauffer
E, Somerhausen Nde S, Michels JJ, Jundt G, Vince DR, Taylor S,
Genevay M, Collin F, Trassard M, Coindre JM. Histologic grade
but not SYT-SSX fusion type is an important prognostic factor
in patients with synovial sarcoma: A multicenter retrospective
analysis. J Clin Oncol. 2004;22: 4040-50. 22) Miettinen M, Limon J, Niezabitowski A, Lasota J. Patterns of
keratin polypeptides in 110 biphasic, monophasic, and poorly
differentiated synovial sarcomas. Virchows Arch. 2000;437:
275-83. [ Özet ]
23) Chen-Levy Z, Nourse J, Cleary ML. The bcl-2 candidate protooncogene
product is a 24-kilodalton integral-membrane protein
highly expressed in lymphoid cell lines and lymphomas carrying
the t(14;18) translocation. Mol Cell Biol. 1989;9:701-10. [ Özet ]
24) Castle VP, Heidelberger KP, Bromberg J, Ou X, Dole M, Nuñez
G. Expression of the apoptosis-suppressing protein bcl-2, in
neuroblastoma is associated with unfavorable histology and
N-myc amplification. Am J Pathol. 1993;143:1543-50. [ Özet ]
25) Hirakawa N, Naka T, Yamamoto I, Fukuda T, Tsuneyoshi
M. Overexpression of bcl-2 protein in synovial sarcoma: A
comparative study of other soft tissue spindle cell sarcomas and
an additional analysis by fluorescence in situ hybridization. Hum
Pathol. 1996;27:1060-5. [ Özet ]
26) Mancuso T, Mezzelani A, Riva C, Fabbri A, Dal Bo L, Sampietro
G, Perego P, Casali P, Zunino F, Sozzi G, Pierotti MA, Pilotti S.
Analysis of SYT-SSX fusion transcripts and bcl-2 expression
and phosphorylation status in synovial sarcoma. Lab Invest.
2000;80:805-13. [ Özet ]
27) Kawauchi S, Fukuda T, Oda Y, Saito T, Oga A, Takeshita M,
Yokoyama K, Chuman H, Iwamoto Y, Sasaki K, Tsuneyoshi
M. Prognostic significance of apoptosis in synovial sarcoma:
Correlation with clinicopathologic parameters, cell proliferative
activity, and expression of apoptosis-related proteins. Mod
Pathol. 2000;13:755-65. [ Özet ]
28) Knoepfler PS. Myc goes global: New tricks for an old oncogene.
Cancer Res. 2007;67:5061-3. [ Özet ] 29) Pelengaris S, Khan M, Evan G. c-MYC: More than just a matter of
life and death. Nat Rev Cancer. 2002;2:764-76. 30) Scionti I, Michelacci F, Pasello M, Hattinger CM, Alberghini M,
Manara MC, Bacci G, Ferrari S, Scotlandi K, Picci P, Serra M.
Clinical impact of the methotrexate resistance-associated genes
C-MYC and dihydrofolate reductase (DHFR)in high-grade
osteosarcoma. Ann Oncol. 2008;19:1500-8. [ Özet ] 31) Barrios C, Castresana JS, Kreicbergs A. Clinicopathologic
correlations and short-term prognosis in musculoskeletal
sarcoma with c-myc oncogene amplification. Am J Clin Oncol.
1994;17:273-6. [ Özet ]
32) Tsiatis AC, Herceg ME, Keedy VL, Halpern JL, Holt GE, Schwartz
HS, Cates JM. Prognostic significance of c-myc expression in soft
tissue leiomyosarcoma. Mod Pathol. 2009;22:1432-8. [ Özet ] 33) Shen J, Scotlandi K, Baldini N, Manara MC, Benini S, Cerisano V,
Picci P, Serra M. Prognostic significance of nuclear accumulation
of c-myc and mdm2 proteins in synovial sarcoma of the
extremities. Oncology. 2000;58:253-60. [ Özet ]
34) Feller K, Yang S, Tung N, Lee J, Mahalingam M. c-myc in
Kaposi’s sarcoma: Analyses by fluorescent in situ hybridization
and immunohistochemistry. J Eur Acad Dermatol Venereol.
2014;28:120-4.
35) Trieb K, Lehner R, Stulnig T, Sulzbacher I, Shroyer KR. Survivin
expression in human osteosarcoma is a marker for survival. Eur J
Surg Oncol. 2003;29:379-82. [ Özet ] 36) Taubert H, Heidenreich C, Holzhausen HJ, Schulz A, Bache
M, Kappler M, Eckert AW, Würl P, Melcher I, Hauptmann K,
Hauptmann S, Schaser KD. Expression of survivin detected by
immunohistochemistry in the cytoplasm and in the nucleus
is associated with prognosis of leiomyosarcoma and synovial
sarcoma patients. BMC Cancer. 2010;10:65. [ Özet ]
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