Genetic changes in bone and soft tissue tumors

Acta Orthopaedica Scandinavica, Supplement

Volumn 70, Issue 285, 1999, Pages 30-40

  Mandahl, Nils ^a   Mertens, Fredrik ^a   Mitelman, Felix ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BCR ABL PROTEIN;

ADIPOSE TISSUE; BONE TUMOR; CHROMOSOME 22Q; CHROMOSOME 9Q; CHROMOSOME ABERRATION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; EWING SARCOMA; FIBROHISTIOCYTOMA; FIBROMA; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; MUSCLE TUMOR; PROGNOSIS; REVIEW; SOFT TISSUE TUMOR; SYNOVIAL SARCOMA; CHROMOSOME MAP; FACTUAL DATABASE; GENETIC SCREENING; KARYOTYPING; PATHOLOGY; REGISTER; SARCOMA; SCANDINAVIA;

BONE NEOPLASMS; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; DATABASES, FACTUAL; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PROGNOSIS; REGISTRIES; SARCOMA; SCANDINAVIA; SOFT TISSUE NEOPLASMS;

EID: 0032776560     PISSN: 03008827     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (60)

1. de Alava E, Kawai A, Healey J H, Fligman I, Meyers P A, Huvos A G, Gerald W L, Jhanwar S C, Argani P, Antonescu C R, Pardo-Mindan F J, Ginsberg J, Womer R, Lawlor E R, Wunder J, Andrulis I, Sorensen P H B, Barr F G, Ladanyi M. EWS-FLII fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma. J Clin Oncol 1998; 16: 1248-55.
2. Åman P, Ron D, Mandahl N, Fioretos T, Heim S, Arheden K, Willén H, Rydholm A, Mitelman F. Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11). Genes Chromosomes Cancer 1992; 5: 278-85.
3. Aurias A, Rimbaut C, Buffe D, Dubousset J, Mazabraud A. Translocations of chromosome 22 in Ewing's sarcoma. An analysis of 4 fresh tumors. N Engl J Med 1983; 309: 496-7.
4. Barr F G, Nauta L E, Davis R J, Schäfer B W, Nycum L M, Biegel J A. In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma. Hum Mol Genet 1996; 5: 15-21.
5. Caspersson T, Zech L, Johansson C. Differential binding of alkylating fluorochromes in human chromosomes. Exp Cell Res 1970; 60: 315-9.
6. Choong P F M, Mandahl N, Mertens F, Willén H, Alvegård T, Kreicbergs A, Mitelman F, Rydholm A. 19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma. Genes Chromosomes Cancer 1996; 16: 88-93.
7. Crozat A, Åman P, Mandahl N, Ron D. Fusion of CHOP to a novel RNA-binding protein in human liposarcoma. Nature 1993; 363: 640-4.
8. Delattre O, Zucman J, Plougastel B, Desmaze C, Melot T, Peter M, Kovar H, Joubert I, de Jong P, Rouleau G, Aurias A, Thomas G. Gene fusion with an ETS DNA - binding domain caused by chromosome translocation in human tumours. Nature 1992; 359: 162-5.
9. Driman D, Thorner P S, Greenberg M L, Chilton-MacNeill S, Squire J. MYCN gene amplification in rhabdomyosarcoma. Cancer 1994; 73: 2231-7.
10. El-Rifai W, Sarlomo-Rikala M, Knuutila S, Miettinen M. DNA copy number changes in development and progression in leiomyosarcomas of soft tissues. Am J Pathol 1998; 153: 985-90.
11. Fagnou C, Michon J, Peter M, Bernoux A, Oberlin O, Zucker J-M, Magdelenat H, Delattre O, for the Société Francaise d'Oncologie Pédiatrique. Presence of tumor cells in bone marrow but not in blood is associated with adverse prognosis in patients with Ewing's tumor. J Clin Oncol 1998; 16: 1707-11.
12. Ferguson-Smith M A. Genetic analysis by chromosome sorting and painting: Phylogenetic and diagnostic applications. Eur J Hum Genet 1997; 5: 253-65.
13. Fletcher J A, Naeem R, Xiao S, Corson J M. Chromosome aberrations in desmoid tumors. Trisomy 8 may be a predictor of recurrence. Cancer Genet Cytogenet 1995; 79: 139-43.
14. Fletcher C D M, Akerman M, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, van de Ven W, Vanni R, Willen H. Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the chromosomes and morphology (CHAMP) collaborative study group. Am J Pathol 1996; 148: 623-30.
15. Flrenes V A, Maelandsmo G M, Forus A, Andreassen A, Myklebost O, Fodstad. MDM2 gene amplification and transcript levels in human sarcomas: Relationship to TP53 gene status. J Natl Cancer Inst 1994; 86: 1297-1302.
16. Gibas L M, Gibas Z, Sandberg A A. Technical aspects of cytogenetic analysis of human solid tumors. Karyogram 1984; 10: 25-7.
17. Gray J W, Pinkel D. Molecular cytogenetics in human cancer diagnosis. Cancer 1992; 69: 1536-42.
18. Heim S, Mandahl N, Kristoffersson U, Mitelman F, Rööser B, Rydholm A, Willén H. Reciprocal translocation t(3;12)(q27;q13) in lipoma. Cancer Genet Cytogenet 1986; 23: 301-4.
19. nd ed. Wiley-Liss, New York 1995.
20. Hsu T C. Longitudinal differentiation of chromosomes. Ann Rev Genet 1973; 7:153-76.
21. Kallioniemi A, Kallioniemi O-P, Sudar D, Rutovitz D, Gray J W, Waldman F, Pinkel D. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992; 258: 818-21.
22. Kawai A, Woodruff J, Healey J H, Brennan M F, Antonescu C R, Ladanyi M. SYT-SSX gene fusion as a determinant of morphology and prognosis in synovial sarcoma. N Engl J Med 1998; 338: 153-60.
23. Knezevich S R, McFadden D E, Tao W, Lim J F, Sorensen P H B. A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma. Nat Genet 1998; 18: 184-7.
24. Ladanyi M. The emerging molecular genetics of sarcoma translocations. Diagn Mol Pathol 1995; 4: 162-73.
25. Larramendy M L, Tarkkanen M, Blomqvist C, Virolainen M, Wiklund T, Asko-Seljavaara S, Elomaa I, Knuutila S. Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker. Am J Pathol 1997; 151: 1153-61.
26. Limon J, Dal Cin P, Sandberg A A. Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors. Cancer Genet Cytogenet 1986a; 23: 305-13.
27. Limon J, Turc-Carel C, Dal Cin P, Rao U, Sandberg A A. Recurrent chromosome translocations in liposarcoma. Cancer Genet Cytogenet 1986b; 22: 93-4.
28. Mandahl N. Cytogenetics and molecular genetics of bone and soft tissue tumors. Adv Cancer Res 1996; 69: 63-99.
29. Mandahl N, Heim S, Johansson B, Bennet K, Mertens F, Olsson G, Rööser B, Rydholm A, Willén H, Mitelman F. Lipomas have characteristic structural chromosomal rearrangements of 12q13-q14. Int J Cancer 1987; 39: 685-8.
30. Mandahl N, Höglund M, Mertens F, Rydholm A, Willén H, Brosjö O, Mitelman F. Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors. Genes Chromosomes Cancer 1994; 9: 207-15.
31. Mark J. Chromosomal abnormalities and their specificity in human neoplasm. An assessment of recent observations by banding techniques. Adv Cancer Res 1977; 24: 165-222.
32. Mark J, Dahlenfors R, Ekedahl C, Stenman G. The mixed salivary gland tumor - A normally benign human neoplasm frequently showing specific chromosomal abnormalities. Cancer Genet Cytogenet 1980; 2: 231-41.
33. Mitelman F. Catalogue of Chromosome Aberrations in Cancer. Cytogenet Cell Genet 1983; 36: 1-515.
34. th ed. Wiley-Liss, New York 1998.
35. Mitelman F, Johansson B, Mandahl N, Mertens F. Clinical significance of cytogenetic findings in solid tumors. Cancer Genet Cytogenet 1997a; 95: 1-8.
36. Mitelman F, Mertens F, Johansson B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 1997b; 15: 417-74.
37. Nowell P C, Hungerford D A. A minute chromosome in human chronic granulocytic leukemia. Science 1960; 132: 1497.
38. Panagopoulos T, Åman P, Mertens F, Mandahl N, Rydholm A, Bauer HFC, Mitelman F. Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma. Genes Chromosomes Cancer 1996; 17: 102-7.
39. Rabbitts T H, Forster A, Larson R, Nathan P. Fusion of the dominant negative transcription regulator CHOP with a novel gene FUS by translocation t(12;16) in malignant liposarcoma. Nat Genet 1993; 4: 175-80.
40. Rowley J D. A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature 1973; 243: 290-3.
41. Sandberg A A, Bridge J A. The Cytogenetics of Bone and Soft Tissue Tumors, R G Landes Company, Austin 1994.
42. Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith M A, Ning Y, Ledbetter D H, Bar-Am I, Soenksen D, Garini Y, Ried T. Multicolor spectral karyotyping of human chromosomes. Science 1996; 273: 494-7.
43. Seidal T, Mark J, Hagmar B, Angervall L. Alveolar rhabdomyosarcoma: A cytogenetic and correlated cytological and histological study. Acta Pathol Microbiol Immunol Scand Sect A 1982; 90: 345-54.
44. Smith S, Reeves B R, Wong L. A consistent chromosome translocation in synovial sarcoma. Cancer Genet Cytogenet 1987; 26: 179-80.
45. Speicher M R, Ballard S G, Ward D C. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 1996; 12: 368-75.
46. Sreekantaiah C. The cytogenetic and molecular characterization of benign and malignant soft tissue tumors. Cytogenet Cell Genet 1998; 82: 13-29.
47. Sreekantaiah C, Leong S P L, Karakousis C P, McGee D L, Rappaport W D, Villar H V, Neal D, Fleming S, Wankel A, Herrington P N, Carmona R, Sandberg A A. Cytogenetic profile of 109 lipomas. Cancer Res 1991; 51: 422-33.
48. Stam K, Heisterkamp N, Grosveld V, de Klein A, Verma R S, Coleman M, Dosik H, Groffen J. Evidence of a new bcr / c-abl mRNA in patients with chronic myelocytic leukemia and the Philadelphia chromosome. New Engl J Med 1985; 313: 1429-33.
49. Szymanska J, Serra M, Skytting B, Larsson O, Virolainen M, Akerman M, Tarkkanen M, Huuhtanen R, Picco P, Bacchini P, Asko-Seljavaara S, Elomaa I, Knuutila S. Genetic imbalances in 67 synovial sarcomas evaluated by comparative genomic hybridization. Genes Chromosomes Cancer 1998; 23: 213-9.
50. Tarkkanen M, Karhu R, Kallioniemi A, Elomaa I, Kivioja A H, Nevalainen J, Böhling T, Karaharju E, Hyytinen E, Knuutila S, Kallioniemi O-P. Gains and losses of DNA sequences in osteosarcomas by comparative genomic hybridization. Cancer Res 1995; 55: 1334-8.
51. Turc-Carel C, Philip I, Berger MP, Philip T, Lenoir G M. Translocation (11;22)(q24;q12) in Ewing's sarcoma cell lines. N Engl J Med 1983; 309: 497-8.
52. Turc-Carel C, Dal Cin P, Limon J, Li F, Sandberg A A. Translocalion X;18 in synovial sarcoma. Cancer Genet Cytogenet 1986a; 23: 93.
53. Turc-Carel C, Lizard-Nacol S, Justrabo E, Favrot M, Philip T, Tabone E. Consistent chromosomal translocation in alveolar rhabdomyosarcoma. Cancer Genet Cytogenet 1986b; 19: 361-2.
54. Turc-Carel C, Dal Cin P, Rao U, Karakousis C, Sandberg A A. Cytogenetic studies of adipose tissue tumors. I. A benign lipoma with reciprocal translocation t(3;12) (q28;q14). Cancer Genet Cytogenet 1986c; 23: 283-9.
55. Weber-Hall S, Anderson J, McManus A, Abe S, Nojima T, Pinkerton R, Pritchard-Jones K, Shipley J. Gains, losses, and amplification of genomic material in rhabdomyosarcoma analyzed by comparative genomic hybridization. Cancer Res 1996; 56: 3220-4.
56. West D C, Grier H E, Swallow M M, Demetri G D, Granowetter L, Sklar J. Detection of circulating tumor cells in patients with Ewing's sarcoma and peripheral primitive neuroectodermal tumors. J Clin Oncol 1997; 15: 583-8.
57. Zang K D. Cytological and cytogenetical studies on human meningioma. Cancer Genet Cytogenet 1982; 6: 249-74.
58. Zoubek A, Dockhorn-Dworniczak B, Delattre O, Christiansen H, Niggli F, Gatterer-Menz I, Smith T L, Jürgens H, Gadner H, Kovar H. Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients? J Clin Oncol 1996; 14: 1245-51.
59. Zoubek A, Ladenstein R, Windhager R, Amann G, Fischmeister G, Kager L, Jugovic D, Ambros P F, Gadner H, Kovar H. Predictive potential of testing for bone marrow involvement in Ewing tumor patients by RT-PCR: A preliminary evaluation. Int J Cancer 1998; 79: 56-60.
60. Zucman J, Delattre O, Desmaze C, Plougastel B, Joubert I, Melot T, Peter M, De Jong P, Rouleau G, Aurias A, Thomas G. Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints. Genes Chromosomes Cancer 1992; 5: 271-7.