Cytogenetics of pediatric central nervous system tumors

Cancer Genetics and Cytogenetics

Volumn 91, Issue 1, 1996, Pages 13-27

  Sainati, Laura ^a,d   Bolcato, S ^b   Montaldi, A ^b   Celli, P ^b   Stella, M ^b   Leszl, A ^a   Silvestro, L ^c   Perilongo, G ^a   Di Montezemolo, L Cordero ^c   Basso, G ^c  

^a UNIVERSITY OF PADOVA   (Italy)

^b SAN BORTOLO HOSPITAL   (Italy)

^c UNIVERSITY OF TURIN   (Italy)

^d Dipartimento di Pediatria   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CENTRAL NERVOUS SYSTEM TUMOR; CHILDHOOD CANCER; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME ABERRATION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; KARYOTYPE; PEDIATRICS; PRIORITY JOURNAL;

ADOLESCENT; ASTROCYTOMA; BRAIN NEOPLASMS; CARCINOMA, EMBRYONAL; CEREBELLAR NEOPLASMS; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; EPENDYMOMA; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; MEDULLOBLASTOMA; PLOIDIES;

EID: 0030273566     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00036-2     Document Type: Article

References (67)

1. 1. Novakovic B (1994): U.S. Childhood Cancer survival, 1973-1987. Med Pediatr Oncol 23;480-486.
2. 2. Gilles FH (1985): Classifications of Childhood Brain Tumors. Cancer 56:1850-1857.
3. 3. Rorke LB, Gilles FH, Richard LD, Becker LE (1985): Revision of the World Health Organization Classification of Brain Tumors for Childhood Brain Tumors. Cancer 56:1869-1886.
4. 4. Seidal T, Mark J, Hagmar B, Angervall L (1982): Alveolar rhabdomyosarcoma: A cytogenetic and correlated cytological and histological study. Acta Pathol Microbiol Immunol Scand (A)90:345-354.
5. 5. Gilbert F, Feder M, Balaban G, Brangman D, Lurie DK, Podolosky R, Rinald V, Vinikoor N, Weisband J (1984): Human neuroblastomas and abnormalities of chromosomes 1 and 17. Cancer Res 44:5444-5449.
6. 6. Whang-Peng J, Triche TJ, Knutsen T, Miser J, Douglass EC, Israel MA (1984): Chromosome translocation in peripheral neuroepithelioma. N Eng J Med 311:584-585.
7. 7. Douglass EC, Valentine M, Ectubanas E, Parham D, Webber BL, Houghton PJ, Green AA (1987): A specific chromosomal abnormality in rhabdomyosarcoma. Cytogenetic Cell Genet 45:148-155.
8. 8. Turc-Carel C, Aurias A, Mugneret F, Lizard S, Sidaner I, Volk C, Thiery JP, Olshwang S, Philip I, Berger MP, Philip T, Lenoir GM, Mazabraud A (1988): Chromosomes in Ewing's sarcoma. An evaluation of 85 cases, remarkable consistency of t(11;22)(q24;q12). Cancer Genet Cytogenet 32(2):229-238.
9. 9. Sainati L, Stella M, Montaldi A, Bolcato S, Guercini N, Bonan F, Ninfo V, Zanesco L, Basso G (1992): Value of cytogenetics in the differential diagnosis of the small round cell tumors of childhood. Med Pediatr Oncol 20:130-135.
10. 10. Teyssier JR (1989): The chromosomal analysis of human solid tumors. Cancer Genet Cytogenet 37:103-125.
11. 11. Xiao-nan L, Qiang H, Zi-wei D (1992): Methodologic study of direct preparation for chromosome analysis of human solid brain tumors. Cancer Genet Cytogenet 58:160-164.
12. 12. Kleihues P, Burger PC, Scheithauer BW (1993): Histological typing of tumours of the central nervous system. World Health Organization. Berlin: Springer-Verlag.
13. 13. ISCN: An International System for Human Cytogenetic Nomenclature. Report of the standing committee on human cytogenetic nomenclature. Harnden DG, Klinger HP (eds). Basel, 1985.
14. 14. ISCN: Guidelines for cancer cytogenetics, supplement to an international system for human cytogenetic nomenclature. Mitelman F (eds):Basel, 1991.
15. 15. Pinkel D, Straume GJW (1986): Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 88:2934-2936.
16. 16. Babu VR, Wikton A (1991): A fluorescence in situ hybridization technique for retrospective cytogenetic analysis. Cytogenet Cell Genet 57:16-17.
17. 17. Giangaspero F, Rigobello L, Badiali M, Loda M, Andreini L, Basso G, Zorzi F, Montaldi A (1992): Large-cell medulloblastomas. A distinct variant with highly aggressive behavior. Am J Surg Pathol 16(7):687-693.
18. 18. Sainati L, Montaldi A, Putti MC, Giangaspero F, Rigobello L, Stella M, Zanesco L, Basso G (1992): Cytogenetic t(11;17) (q13;q21) in a pediatric ependymoma. Is 11q13 a recurring breakpoint in ependymomas? Cancer Genet Cytogenet 59:213-216.
19. 19. Farwell JR, Dohrmann GJ, Flannery JTN (1987): Central nervous system tumors in children. Cancer 40:3123-3132.
20. 20. Chatty EM, Earle KM (1971): Medulloblastoma: A report of 201 cases with emphasis on the relationship of histologic variants to survival. Cancer 28:977-983.
21. 21. Griffin CA, Hawkins AL, Packer RJ, Rorke LB, Emanuel BS (1988): Chromosome abnormalities in pediatric brain tumors. Cancer Res 48:175-180.
22. 22. Beigel JA, Rorke LB, Packer RJ, Emanuel BS (1989): Isochromosome 17q is the most common structural abnormality in primitive neuroectodermal tumors. Pediatr Neurosci 14:150-160.
23. 23. Karnes PS, Tran TN, Cui MY, Raffel C, Gilles FH, Barranger JA, Ying KL (1992): Cytogenetic analysis of 39 pediatric central nervous system tumors. Cancer Genet Cytogenet 59:12-19.
24. 24. Bigner SH, Mark J, Friedman HS, Biegel JA, Bigner DD (1988): Structural chromosomal abnormalities in human medulloblastoma. Cancer Genet Cytogenet 30:91-101.
25. 25. Gallen DF, Cirrocco L, Moore L (1989): A der(11)t(8;11) in two medulloblastomas. A possible non random cytogenetic abnormality. Cancer Genet Cytogenet 38:255-260.
26. 26. Bigner SH, Mark J, Bigner DD (1990: Cytogenetics of human brain tumors. Cancer Genet Cytogenet 47:141-154.
27. 27. McDonald JD, Daneshvar L, Willert JR, Metzger A, Mack E, Edwards MSB, Cogen PH (1993): Clinical and molecular genetic analysis of medulloblastoma. 5th International Symposium on Pediatric Neuro-Oncology: Medulloblastoma. Marseilles, June 12-15.
28. 28. Stratton MR, Darling J, Cooper CS, Reeves BR (1991): A case of cerebellar medulloblastoma with a single chromosome abnormality. Cancer Genet Cytogenet 53:101-103.
29. 29. Douglass EC, Green AA, Hayes FA, Ectubanas E, Horowitz M, Wilimas JA (1985): Chromosome 1 abnormalities: A common feature of pediatric solid tumors. JNCI 75:51-54.
30. 30. Kaneko Y, Kanda N, Maseki N, Sakurai M, Tsuchida Y, Takeda T, Okabe I, Sakurai M (1987): Different karyotypic patterns in early and advanced stage neuroblastomas. Cancer Res 47:311-318.
31. 31. Christiansen H, Lampert F (1988): Tumor karyotype discriminates between good and bad prognostic outcome in neuroblastoma. Br J Cancer 57:121-126.
32. 32. Brodeur GM, Seeger RC, Schwab M, Varmus HE, Bishop JM (1984): Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage. Science 224:1121-1124.
33. 33. Heim S, Mitelman F (1986): Secondary chromosomes aberrations in the acute leukemias. Cancer Genet Cytogenet 22: 331-338.
34. 34. Thiel CJ, McKeon C, Triche TJ, Ross RA, Reynolds P, Israel MA (1987): Differential proto-oncogene expression characterizes histopathologically indistinguishable tumors of the peripheral nervous system. J Clin Invest 80:804-811.
35. 35. Brodeur GM, Green AA, Haves FA, Williams DL, Tsiatis AA (1981): Cytogenetic features of human neuroblastomas and cell lines. Cancer Research 41:4678-4686.
36. 36. Franke F, Rudolph B, Christiansen H, Harbott J, Lampert F (1986): Tumor karyotype may be important in the prognosis of human neuroblastoma. J Cancer Res Clin Oncol 11:266-272.
37. 37. Kindblom LG, Lodding P, Hagmar B, Stenman G (1986): Metastasizing myxopapillary ependymoma of the sacrococcygeal region: A clinico-pathologic, light and electron microscopic, immunohistochemical, tissue culture, and cytogenetic analysis of a case. Acta Pathol Microbiol Immunol Scand 94:79-90.
38. 38. Horowitz ME, Parham DM, Kun LE, Houghton JA, Houghton PJ (1987): Development and characterization of human ependymoma xenograft HxBr5. Cancer Res 47:499-504.
39. 39. Rey JA, Bello MJ, de Campos JM, Kusak ME, Moreno S (1987): Chromosomal composition of a series of 22 human low grade gliomas. Cancer Genet Cytogenet 29:223-237.
40. 40. Dal Cin P, Sandberg AA (1988): Cytogenetic findings in a supratentorial ependymoma. Cancer Genet Cytogenet 30: 289-293.
41. 41. Jenkins RB, Kimmel DW, Moertel CA, Schultz CG, Scheithauer BW, Kelly PJ, Dewald GW (1989): A cytogenetic study of 53 human gliomas. Cancer Genet Cytogenet 39:253-279.
42. 42. Stratton MR, Darling J, Lantos PL, Cooper CS, Reeves BR (1989): Cytogenetic abnormalities in human ependymomas. Int J Cancer 44:479-581.
43. 43. Sawyer JR, Crowson ML, Roloson GJ, Chadduck WM (1991): Involvement of the short arm of chromosome 1 in a myxopapillary ependymoma. Cancer Genet Cytogenet 54:55-60.
44. 44. Weremowicz S, Kupsky WJ, Morton CC, Fletcher JA (1992): Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma. Cancer Genet Cytogenet 61:193-196.
45. 45. Thiel G, Losanowa T, Kintzel D, Nisch G, Martin H, Vorpahl K, Witkowski R (1992): Karyotypes in 90 human gliomas. Cancer Genet Cytogenet 58:109-120.
46. 46. Rogatto SR, Casartelli C, Rainho CA, Barbieri-Neto J (1993): Chromosomes in the genesis and progression of ependymomas. Cancer Genet Cytogenet 69:146-152.
47. 47. Neumann E, Kalousek DK, Norman MG, Steinbok P, Cochrane DD, Goddard K (1993): Cytogenetic analysis of 109 pediatric central nervous system tumors. Cancer Genet Cytogenet 71:40-49.
48. 48. Bown NP, Pearson ADJ, Davison EV, Gardner-Medwin D, Crawford P, Perry R (1988): Multiple chromosome rearrangements in childhood ependymoma. Cancer Genet Cytogenet 36:25-30.
49. 49. Theillet C, Adnane J, Szepetowki P, Simon MP, Jeanteur P, Birnbaun D, Gaudray P (1990): BCL-1 participates in the 11q13 amplification found in breast cancer. Oncogene 5:147-149.
50. 50. Sawyer JR, Swanson CM, Chadduck WM, Roloson GJ (1991): Evolution of tumor chromosome abnormalities after therapy in a pediatric astrocytoma. Cancer Genet Cytogenet 53:119-123.
51. 51. Kovacs G (1985): Premature chromosome condensation: evidence of in vivo cell fusion in human malignant tumors. Int J Cancer 36:637-641.
52. 52. Sawyer JR, Roloson GJ, Hobson EA, Goosen LS, Chadduck WM (1990): Trisomy for chromosome 1q in a pontine astrocytoma. Cancer Genet Cytogenet 47:101-106.
53. 53. Sawyer JR, Swanson CM, Roloson GJ, Longee DC, Chadduck WM (1992): Cytogenetic findings in a case of pediatric glioblastoma. Cancer Genet Cytogenet 64:75-79.
54. 54. Rueda-Pedraza ME, Heifetz SA, Sesterhenn IA, Clark GB (1987): Primary intracranial germ cell tumors in the first two decades of life. A clinical, light-microscopic, and immunohistochemical analysis of 54 cases. Perspect Pediatr Pathol 10:160-207.
55. 55. Oosterhuis JW, Looijenga LHJ, van Kessel AG, de Jong B (1993): A cytogenetic classification of germ cell tumors, and its biological relevance. Eur Urol 23(2):6-8.
56. 56. Saul RA (1982): Prenatal documentation of craniofacial teratomas. Proc Greenwood Genet Center 1:34:35.
57. 57. Rostad S, Kleinschmidt D, Manchester DK (1985): Two massive congenital intracranial immature teratomas with neck extension. Teratology 32:163-169.
58. 58. Hecht F, Grix A, Hecht B, Berger C, Bixemann H, Szucs S, O'Keeffe D, Finberg HJ (1984): Direct prenatal chromosome diagnosis of a malignancy. Cancer Genet Cytogenet 11:107-111.
59. 59. Shen V, Chaparro M, Choi BH, Young R, Bernstein R (1990): Absence of isochromosome 12p in a pineal region malignant germ cell tumor. Cancer Genet Cytogenet 50:153-160.
60. 60. Heimdal K, Evensen S, Fossa S, Hirschberg H, Langhalm R, Broger A, Moller P (1991): Karyotyping of hematologic neoplasia developing shortly after treatment for cerebral extragonadal germ cell tumor. Cancer Genet Cytogenet 57:41-46.
61. 61. Albrecht S, Armstrong DL, Mahoney DH, Cheek WR, Cooley LD (1993): Cytogenetic demonstration of gene amplification in a primary intracranial germ cell tumor. Genes Chromosomes Cancer 6:61-63.
62. 62. Casalone R, Righi R, Granata P, Portentoso P, Minelli E, Meroni E, Solero CL, Allegranza A (1994): Cerebral germ cell tumor and XXY karyotype. Cancer Genet Cytogenet 74:25-29.
63. 63. Vagner-Capodano AM, Zattara-Cannoni H, Cambarelli D, Gentet JC, Genitori L, Lena G, Graziani N, Raybaud C, Choux M, Grisou F (1994): Detection of i(17q) chromosome by in situ hybridization (FISH) with interphase nuclei in medulloblastoma. Cancer Genetic Cytogenet 78(1):1-6.
64. 64. Zang KD (1982): Cytological and cytogenetical studies on human meningiomas. Cancer Genetic Cytogenet. 6:249-274.
65. 65. Seizinger BR, Martuza RL, Gusella JF (1986): Loss of genes on chromosomes 22 in tumorigenesis of human acoustic neuroma. Nature 322:644-647.
66. 66. Rey JA, Bello MJ, de Campos JM, Vaquero J, Kusak ME, Saims JC, and Pestana A (1993): Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches. Cancer Genet Cytogenet 66:1-10.
67. 67. Henn W, Cremerius U, Heide G, Lippitz B, Schroder JM, Gilsbach JM, Bull U, Zang KD (1995): Monosomy 1p is correlated with in vivo glucose metabolism in meningiomas. Cancer Genet Cytogenet 79:144-148.