Chromosome 22q allelic losses at microsatellite loci in human astrocytic tumors

Neurologia Medico-Chirurgica

Volumn 37, Issue 8, 1997, Pages 606-611

  Muhammad, A K M Ghulam ^a   Yoshimine, Toshiki ^a   Maruno, Motohiko ^a   Tokiyoshi, Koji ^a   Takemoto, Osamu ^a   Hayakawa, Toru ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

Astrocytic tumors; Chromosome 22q; Loss of alleles; Microsatellite loci; Patient survival

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; ASTROCYTOMA; CANCER GENETICS; CANCER SURGERY; CANCER SURVIVAL; CHROMOSOME 22Q; CLINICAL ARTICLE; DISEASE COURSE; FEMALE; GENE LOSS; GLIOBLASTOMA; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MALE; POLYMERASE CHAIN REACTION;

EID: 0030793876     PISSN: 03872572     EISSN: None     Source Type: Journal    
DOI: 10.2176/nmc.37.606     Document Type: Article

References (26)

1. Akagi K, Kurahashi H, Arita N, Hayakawa T, Monden M, Mori T, Takai S, Nishisho I: Deletion mapping of the long arm of chromosome 22 in human meningiomas. Int J Cancer 60: 178-182, 1995
2. Bentley DR, Dunham I: Mapping human chromosomes. Curr Opin Genet Dev 5: 328-334, 1995
3. Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS: A microsatellite-based multipoint index map of human chromosome 22. Genomics 18: 329-339, 1993
4. Collins VP, James CD: Gene and chromosomal alterations associated with the development of human gliomas. FASEB J 7: 926-930, 1993
5. De Vitis LR, Tedde A, Vitelli F, Ammannati F, Mennonna P, Bono P, Grammatico B, Grammatico P, Radice P, Bigozzi U, Montali E, Papi L: Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin. Hum Genet 97: 638-641, 1996
6. Diedrich U, Lucius J, Bittermann H-J, Schlosser M, Eckert B, Behnke J, Pabst B: Loss of alleles in brain tumours: Distribution and correlations with clinical course. J Neurol 242: 707-711, 1995
7. Ganju V, Jenkins RB, O'Fallon JR, Scheithauer BW, Ransom DT, Katzmann JA, Kimmel DW: Prognostic factors in gliomas. Cancer 74: 920-927, 1994
8. Harada T, Irving RM, Xuereb JH, Barton DE, Hardy DG, Moffat DA, Maher ER: Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma. J Neurosurg 84: 847-851, 1996
9. Hoang-Xuan K, Merel P, Vega F, Hugot J-P, Cornu P, Delattre J-Y, Poisson M, Thomas G, Delattre O: Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas. Int J Cancer 60: 478-481, 1995
10. James CD, He J, Carlbom E, Mikkelsen T, Ridderheim P-A, Cavenee WK, Collins VP: Loss of genetic information in central nervous system tumors common to children and young adults. Genes Chromosomes Cancer 2: 94-102, 1990
11. Kleihues P, Burger PC, Scheithauer BW: The new WHO classification of brain tumours. Brain Pathol 3: 255-268, 1993
12. Louis DN, Ramesh V, Gusella JF: Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors. Brain Pathol 5: 163-172, 1995
13. Maruno M, Yoshimine T, Muhammad AKMG, Tokiyoshi K, Hayakawa T: Loss of heterozygosity of microsatellite loci on chromosome 9p in astrocytic tumors and its prognostic implications. J Neurooncol 30: 19-24, 1996
14. Mehrabian M, Gitt MA, Sparkes RS, Leffler H, Barondes SH, Lusis AJ: Two members of the S-lac lectin gene family, LGALS1 and LGALS2, reside in close proximity on human chromosome 22q12-13. Genomics 15: 418-420, 1993
15. Raz A, Pazerini G, Carmi P: Identification of a metastasis-associated, galactoside-binding lectin as a chimeric gene product with homology to an IgE-binding protein. Cancer Res 49: 3489-3493, 1989
16. Key JA, Bello MJ, de Campos JM, Vaquero J, Kusak ME, Sarasa JL, Pestana A: Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches. Cancer Genet Cytogenet 66: 1-10, 1993
17. Key JA, Bello MJ, Jimenez-Lara AM, Vaquero J, Kusak ME, de Campos JM, Sarasa JL, Pestana A: Loss of heterozygosity for distal markers on 22q in human gliomas. Int J Cancer 51: 703-706, 1992
18. Seizinger BR, Klinger HP, Junien C, Nakamura Y, Beau ML, Cavenee W, Emanuel B, Ponder B, Naylor S, Mitelman F, Louis D, Menon A, Newsham I, Decker J, Kaelbling M, Henry I, von Deimling A: Report of the committee on chromosome and gene loss in human neoplasia. Cytogenet Cell Genet 58: 1080-1096, 1991
19. Thibodeau SN, Bren G, Schaid D: Microsatellite instability in cancer of the proximal colon. Science 260: 816-819, 1993
20. Thiel G, Losanowa T, Kintzel D, Nisch G, Martin H, Vorpahl K, Witkoski R: Karyotypes in 90 human gliomas. Cancer Genet Cytogenet 58: 109-120, 1992
21. Tokiyoshi K, Yoshimine T, Maruno M, Muhammad AKMG, Hayakawa T: Accumulation of allelic losses of chromosome 10 in human gliomas at recurrence. Clin Mol Pathol 49: M218-M222, 1996
22. Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM, Eldridge R, Kley N, Menon AG, Pulaski K, Haase VH, Ambrose CM, Munroe D, Bove C, Haines JL, Martuza RL, MacDonald ME, Seizinger BR, Short MP, Buckler AJ, Gusella JF: A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 72: 791-800, 1993
23. Vallada HP, Collins JE, Dunham I, Dawson E, Murray RM, Gill M, Collier DA: Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22. Hum Genet 93: 688-690, 1994
24. von Deimling A, Bender B, Jahnke R, Waha A, Kraus J, Albrecht S, Wellenreuther R, Fassbbender F, Nagel J, Menon AG, Louis DN, Lenartz D, Schramm J, Wiestler OD: Loci associated with malignant progression in astrocytomas: A candidate on chromosome 19q. Cancer Res 54: 1397-1401, 1994
25. von Deimling A, von Ammon K, Schoenfeld D, Wiestler OD, Seizinger BR, Louis DN: Subsets of glioblastoma multiforme defined by molecular genetic analysis. Brain Pathol 3: 19-26, 1993
26. Wells V, Mallucci L: Identification of an autocrine negative growth factor: Mouse β-galactoside-binding protein is a cytostatic factor and cell growth regulator. Cell 64: 91-97, 1991