Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas

Clinical Cancer Research

Volumn 5, Issue 11, 1999, Pages 3569-3577

  Müller, Patrick ^b   Henn, Wolfram ^b   Niedermayer, Isolde ^b   Ketter, Ralf ^b   Feiden, Wolfgang ^b   Steudel, Wolf Ingo ^b   Zang, Klaus D ^b   Steilen Gimbel, Heike ^a,b  

^a SAARLAND UNIVERSITY   (Germany)

^b Department of Human Genetics ^*  (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 1P; CHROMOSOME ABERRATION; DISEASE COURSE; GENETIC ASSOCIATION; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MAJOR CLINICAL STUDY; MENINGIOMA; PRIORITY JOURNAL;

ALKALINE PHOSPHATASE; BIOPSY; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DISEASE PROGRESSION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MENINGEAL NEOPLASMS; MENINGIOMA; MONOSOMY; TRISOMY;

EID: 0345045573     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. Kujas, M. Meningioma. Curr. Opin. Neurol. Neurosurg., 6: 882-887, 1993.
2. Kleihues, P., Burger, P. C., and Scheithauer, B. W. Histological Typing of Tumors of the Central Nervous System, 2nd ed. Geneva: WHO, 1993.
3. McCutcheon, I. E. The biology of meningiomas. J. Neuro-Oncol., 29: 207-216, 1996.
4. Langford, A. L. Pathology of meningiomas. J. Neuro-Oncol., 29: 217-221, 1996.
5. Zang, K. D., and Singer, H. Chromosomal constitution of meningiomas. Nature (Lond.), 216: 84-85, 1967.
6. Zang, K. D. Cytological and cytogenetical studies on human meningioma. Cancer Genet. Cytogenet, 6: 249-274, 1982.
7. Bello, M. J., de Campos, J. M., Kusak, M. E., Vaquero, J., Sarasa, J. L., Pestana, A., and Rey. Allelic loss of 1p is associated with tumor progression of meningiomas. Genes Chromosomes Cancer, 9: 296-298, 1994.
8. Lekanne-Deprez, R. H., Riegmann, P. H., van Drunen, E., Warringa, U. L., Groen, N. A., Stefanko, S. Z., Koper, J. W., Avezaat, C. J. J., Mulder, P. G. H., Zwarthoff, E. C., and Hagemeijer, A. Cytogenetic, molecular genetic and pathological analyses in 126 meningiomas. J. Neuropathol. Exp. Neurol., 54: 224-235, 1995.
9. Kolles, H., Niedermayer, I., Schmitt, C., Henn, W., Feld, R., Steudel, W. I., Zang, K. D., and Feiden, W. Triple approach for diagnosis and grading of meningiomas: histology, morphometry of Ki-67/Feulgen stainings and cytogenetics. Acta Neurochir. (Wien), 137: 174-181, 1995.
10. Perry, A., Jenkins, R. B., Dahl, R. J., Moertel, C. A., and Scheithauer, B. W. Cytogenetic analysis of aggressive meningiomas. Cancer (Phila.), 77: 2567-2573, 1996.
11. Simon, M., von Deimling, A., Larson, J. J., Wellenreuther, R., Kaskel, P., Waha, A., Warnick, R. E., Tew, J. M., Jr., and Menon, A. G. Allelic losses on chromosomes 14, 10 and 1 in atypical and malignant meningiomas: a genetic model of meningioma progression. Cancer Res., 55: 4696-4701, 1995.
12. Menon, A. G., Rutter, J. L., von Sattel, J. P., Synder, H., Murdoch, C., Blumenfeld, A., Martuza, R. L., von Deimling, A., Gusella, J. F., and Houseal, T. W. Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putitative "tumor progression" locus. Oncogene, 14: 611-616, 1997.
13. Maltby, E. L., Ironside, J. W., and Battersby, R. D. Cytogenetic studies in 50 meningiomas. Cancer Genet. Cytogenet., 31: 199-210, 1988.
14. Weber, R. G., Boström, J., Wolter, M., Baudis, M., Collins, P., Reifenberger, G., and Lichter, P. Analysis of genomic alteration in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression. Proc. Natl. Acad. Sci. USA, 94: 14719-14724, 1997.
15. Henn, W., Cremerius, U., Heide, G., Lippitz, B., Schröder, J. M., Gilsbach, J. M., Büll, U., and Zang, K. D. Monosomy 1p is correlated with enhanced in vivo glucose metabolism in meningiomas. Cancer Genet. Cytogenet., 79: 144-148, 1995.
16. Niedermayer, I., Feiden, W., Henn, W., Steilen-Gimbel, H., Steudel, W-I., and Zang, K. D. Loss of alkaline phosphatase activity in meningiomas: a rapid histochemical technique indicating progression-associated deletion of a putitative tumor suppressor gene on the distal part of the short arm of chromosome 1. J. Neuropathol. Exp. Neurol., 56: 879-886, 1997.
17. Russell, D. S., Krayenbuhl, H., and Cairns, H. The wet film technique in the histological diagnosis of intracranial tumours: a rapid method. J. Pathol., 45: 501-505, 1937.
18. Lutz, S., Welter, C., Zang, K. D., Seitz, G., Blin, N., and Urbschat, K. A two-colour technique for chromosome in situ hybridization in tissue sections. J. Pathol., 167: 279-282, 1992.
19. Steilen-Gimbel, H., Henn, W., Kolles, H., Moringlane, J. R., Feiden, W., Steudel, W. I., and Zang, K. D. Early proliferation enhancement by monosomy 10 and intratumor heterogeneity in malignant human gliomas as revealed by smear preparations from biopsies. Genes Chromosomes Cancer, 16: 180-184, 1996.
20. Buroker, N., Bestwick, R., Haight, G., Magenis, R. E., and Litt, M. A hypervariable repeated sequence on human chromosome 1p36. Hum. Genet., 77: 175-181, 1987.
21. Cooke, H. J., and Hindley, J. Cloning of human satellite III DNA: different components are on different chromosomes. Nucleic Acids Res., 6: 3177-3197, 1979.
22. Limon, J., Dal Cin, P., and Sandberg, A. A. Application of long-term collagenase disaggregation for the cytogenetic analysis of human solid tumors. Cancer Genet. Cytogenet., 23: 305-313, 1986.
23. ISCN. F. Mitelman (ed.). Guidelines for cancer cytogenetics. Supplement to an international system for cytogenetic nomenclature. Basel, Karger, 1995.
24. Louis, D. N., Budka, H., and von Deimling, A. Meningiomas. In: W. K. Cavenee and P. Kleihues Pathology & Genetics: Tumours of the Nervous System, pp. 134-141. Lyon, France: IARC, 1997.
25. Kahn, J., Parsa, N. Z., Harada, T., Meltzer, P. S., and Carter, N. P. Detection of gains and losses in 18 meningiomas by comparative genomic hybridization. Cancer Genet. Cytogenet., 103: 95-100, 1998.
26. Ishino, S., Hashimoto, N., Fushiki, S., Date, K., Mori, T., Fujimoto, M., Nakagawa, Y., Ueda, S., Abe, T., and Inazawa, J. Loss of material from chromosome arm 1p during malignant progression of meningioma revealed by fluorescent in situ hybridization. Cancer, 83: 360-366, 1998.
27. Schwab, M., Praml, C., and Amler, L. A. Genomic instability in 1p and human malignancies. Genes Chromosomes Cancer, 16: 211-229, 1996.
28. Hattinger, C. M., Rumpler, S., Stehl, S., Ambros, I. M., Zoubek, A., Potschger, U., Gadner, H., and Ambros, P. F. Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors. Genes Chromosomes Cancer, 24: 243-254, 1999.
29. Kuroki, T., Fujiwara, Y., Tsuchiya, E., Nakamori, S., Imaoka, S., Kanematsu, T., and Nakamura, Y. Accumulation of genetic changes during development and progression of hepatocellular carcinoma: loss of heterozygosity on chromosome arm 1p occurs at an early stage of hepato-carcinogenesis. Genes Chromosomes Cancer, 13: 163-167, 1995.
30. Weber, R. G., Sabel, M., Reifenberger, J., Sommer, C., Oberstrass, J., Reifenberger, G., Kiessling, M., and Cremer, T. Characterisation of genomic associated with glioma progression by comparative genomic hybridization. Oncogene, 13: 983-994, 1994.
31. Nienhaus, I., Urbschat, I., Romeike, B., Brunner, C., Jung, V., Henn, W., Feiden, W., and Zang, K. D. Genetic micro-heterogeneity of oligoastrocytomas and oligodendrogliomas. Cancer Genet. Cytogenet., 112: 89, 1999.
32. Kepes, J. J. Meningiomas: Biology, Pathology, and Differential Diagnosis. New York: Masson Publishing, 1982.
33. Böker, D. K., Meurer, H., and Gullotta, F. Recurring intracranial meningiomas. Evaluation of some factors predisposing for tumor recurrence. J. Neurosurg. Sci., 29: 11-17, 1985.
34. de la Monte, S. M., Flickinger, J., and Linggood, R. M. Histopathologic features predicting recurrence of meningiomas following subtotal resection. Am. J. Surg. Pathol., 10: 836-843, 1986.
35. Scheidthauer, B. W. Tumors of the meninges: proposed modifications of the World Health Organization classification. Acta. Neuropathol., 80: 343-354, 1990.
36. Brito-Babapulle, V., and Atkin, N. B. Break points in chromosome #1 abnormalities of 218 human neoplasms. Cancer Genet. Cytogenet., 4: 215-225, 1981.
37. Munn, K. E., Walker, R. A., and Varley, J. M. Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast. Oncogene, 10: 1653-1657, 1995.
38. Bostrom, J., Muhlbauer, A., and Reifenberger, G. Deletion mapping of the short arm of chromosome 1 identifies a common region of deletion distal to D1S496 in human meningiomas. Acta Neuropathol., 94: 479-485, 1997.