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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

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Summary

Chromosome aberrations in two glioma cell lines were analyzed using biotinylated DNA library probes that specifically decorate chromosomes 1, 4, 7, 18 and 22 from pter to qter. Numerical changes, deletions and rearrangements of these chromosomes were radily visualized in metaphase spreads, as well as in early prophase and interphase nuclei. Complete chromosomes, deleted chromosomes and segments of translocated chromosomes were rapidly delineated in very complex karyotypes. Simultaneous hybridizations with additional subregional probes were used to further define aberrant chromosomes. Digital image analysis was used to quantitate the total complement of specific chromosomal DNAs in individual metaphase and interphase cells of each cell line. In spite of the fact that both glioma lines have been passaged in vitro for many years, an under-representation of chromosome 22 and an over-representation of chromosome 7 (specifically 7p) were observed. These observations agree with previous studies on gliomas. In addition, sequences of chromosome 4 were also found to be under-represented, especially in TC 593. These analyses indicate the power of these methods for pinpointing chromosome segments that are altered in specific types of tumors.

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References

  • Al-Saadi A, Latimer F, Madercic M, Robbins T (1987) Cytogenetic studies of human brain tumors and their clinical significance. II. Meningioma. Cancer Genet Cytogenet 26:127–141

    Google Scholar 

  • Atkin NB (1986) Chromosome 1 aberrations in cancer. Cancer Genet Cytogenet 21:279–285

    Google Scholar 

  • Bigner SH, Mark J, Bullard DE, Mahaley MS Jr, Bigner DD (1986) Chromosomal evolution in malignant human gliomas starts with specific and usually numerical deviations. Cancer Genet Cytogenet 22:121–135

    Google Scholar 

  • Bigner SH, Wong AJ, Mark J, Muhlbaier LH, Kinzler KW, Vogelstein B, Bigner DD (1987) Relationship between gene amplification and chromosomal deviations in malignant gliomas. Cancer Genet Cytogenet 29:165–170

    Google Scholar 

  • Bigner SH, Burger PC, Wong AJ, Werner MH, Hamilton SR, Muhlbaier LH, Vogelstein B, Bigner DD (1988) Gene amplification in malignant human gliomas: clinical and histopathologic aspects. J Neuropathol Exp Neurol 47:191–205

    Google Scholar 

  • Bloomfield CD, Trent JM, Berghe H van den (1987) Report of the committee on structural chromosme changes in neoplasia. (9th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 46:344–366

    Google Scholar 

  • Boveri T (1914) Zur Frage der Entstehung maligner Tumoren. Fischer, Jena

    Google Scholar 

  • Brodeur GM, Green AA, Hayes FA, Williams KJ, Tsiafis HA (1981) Cytogenetic features of human neuroblastomas and cell lines. Cancer Res 41:4678–4686

    Google Scholar 

  • Burns J, Chan VTW, Jonasson JH, Fleming KA, Taylor S, McGee J O'D (1985) Sensitive system for visualizing biotinylated DNA probes hybridized in situ: rapid sex determination of intact cells. J Clin Pathol 38:1085–1092

    Google Scholar 

  • Cremer T, Landegent JE, Brückner H, Scholl HP, Schardin M, Hager HD, Devilee P, Pearson PL, Ploeg M van der (1986) Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84. Hum Genet 74:346–352

    Google Scholar 

  • Cremer T, Tesin D, Hopman AHN, Manuelidis L (1988) Rapid interphase and metaphase assessment of specific chromosomal changes in neuroectodermal tumor cells by in situ hybridization with chemically modified DNA probes. Exp Cell Res 176:199–220

    Google Scholar 

  • Hansen MF, Cavence WK (1987) Genetics of cancer predisposition. Cancer Res 47:5518–5527

    Google Scholar 

  • Harris H (1986) The genetic analysis of malignancy. J Cell Sci [Suppl] 4:431–444

    Google Scholar 

  • Henn W, Blin N, Zang KD (1986) Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines. Hum Genet 74:104–106

    Google Scholar 

  • Knudson AG (1986) Genetics of human cancer. Annu Rev Genet 20: 231–251

    Google Scholar 

  • Landegent JE, Jansen in de Wal N, Baan R, Hoeijmakers JHJ, Ploeg M van der (1984) 2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences. Exp Cell Res 153:61–72

    Google Scholar 

  • Larizza L, Schirrmacher V (1984) Somatic cell fusion as a source of genetic rearrangement leading to metastatic variants. Cancer Metastasis Rev 3:193–222

    Google Scholar 

  • Libermann TA, Nusbaum HR, Razon N, Kris R, Lax I, Soreq H, Whittle N, Waterfield MD, Ullrich A, Schlessinger J (1985) Amplification, enhanced expression and possible rearrangement of EFG receptor gene in primary human brain tumors of glial origin. Nature 313:144–147

    Google Scholar 

  • Lichter P, Cremer T, Borden J, Manuelidis L, Ward DC (1988) Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 80:224–234

    Google Scholar 

  • Manuelidis L (1985) Individual interphase domains revealed by in situ hybridization. Hum Genet 71:288–293

    Google Scholar 

  • Manuelidis L, Borden J (1988) Reproducible compartmentalization of indivudual chromosome domains in human CNS cells revealed by in situ hybridization and three dimensional reconstruction. Chromosoma 96:397–410

    Google Scholar 

  • Manuelidis L, Manuelidis EE (1979) Surface growth characteristics of defined normal and neoplastic neuroectodermal cells in vitro. In: Zimmermann HM (ed) Progress in neuropathology, vol 4. Raven Press, New York, pp 235–266

    Google Scholar 

  • McDermid HE, Duncan AMV, Higgins MJ, Hamerton JL, Rector E, Brasch KR, White BN (1986) Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. Chromosoma 94:228–234

    Google Scholar 

  • Merlino GT, Ishii S, Whang-Peng J, Knutsen T, Xu Y-H, Clark AJL, Stratton RH, Wilson RK, Ma DP, Roe BA, Hunts JH, Shimizu N, Pastan I (1985) Structure and localization of genes encoding aberrant and normal epidermal growth factor receptor RNAs from A431 human carcinoma cells. Mol Cell Biol 5:1722–1734

    Google Scholar 

  • Mitelman F (1985) Catalogue of chromosome aberrations in cancer, 2nd edn. Liss, New York

    Google Scholar 

  • Pinkel D, Straume T, Gray JW (1986) Cytogenetic analysis using quantitative, high sensitive, fluorescence hybridization. Proc Natl Acad Sci USA 83:2934–2938

    Google Scholar 

  • Rappold G, Cremer T, Hager HD, Davies KE, Müller CR, Yang T (1984) Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probes. Hum Genet 67:317–325

    Google Scholar 

  • Rey JA, Bello JM, Campos JM de, Kusak ME, Moreno S (1987) On trisomy of chromosome 7 in human gliomas. Cancer Genet Cytogenet 29:323–326

    Google Scholar 

  • Schardin M, Cremer T, Hager HD, Lang M (1985) Specific staining of human chromosomes in Chinese hamster x man hybrid cell lines demonstrates interphase chromosome territories. Hum Genet 71: 281–287

    Google Scholar 

  • Shapiro JR (1986) Biology of gliomas: heterogeneity, oncogenes, growth factors. Semin Oncol 13:4–15

    Google Scholar 

  • Showe LC, Croce CM (1987) The role of chromosomal translocations in B- and T-cell neoplasia. Annu Rev Immunol 5:253–277

    Google Scholar 

  • Trask B, Engh G van den, Pinkel D, Mullikin J, Waldman F, Dekken H van, Gray J (1988) Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization. Hum Genet 78:251–259

    Google Scholar 

  • Waye JS, England SB, Willard HF (1987) Genomic organization of chromosome-specific alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome. Mol Cell Biol 7:349–356

    Google Scholar 

  • Yamazaki H, Fukui Y, Ueyama Y, Tamaoki N, Kawamoto T, Taniguchi S, Shibuya M (1988) Amplification of the structurally and functionally altered epidermal growth factor receptor gene (cerbB) in human brain tumors. Mol Cell Biol 8:1816–1820

    Google Scholar 

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Cremer, T., Lichter, P., Borden, J. et al. Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum Genet 80, 235–246 (1988). https://doi.org/10.1007/BF01790091

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  • DOI: https://doi.org/10.1007/BF01790091

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