Abstract
We have examined the genetic aberrations in two near-diploid glioblastoma multiforme cell lines that appear to have arisen from different glial lineages. One cell line, Hu-O-2A/Gb1, expresses antigens and metabolic profiles characteristic of the oligodendrocyte-type-2 astrocyte (0-2A) lineage of the rat central nervous system. This line generates, in vitro, cells with characteristics of 0-2A progenitor cells, oligodendrocytes and astrocytes. The second cell line, IN1434, is derived from an astrocyte or a precursor cell restricted to astrocytic differentiation. In Hu-O-2A/Gb1 the sole homologue of chromosome 10 is disrupted at band 10p11–12.1 by translocation with chromosomes X and 15. The translocation breakpoint is localized between genetic markers D10S2103 and [D10S637, D10S1962, D10S355]. Other aberrations include a 5;14 translocation, deletion of the long and short arms of chromosome 16 and loss of one copy of the CDKN2 gene. IN1434 cells share some cytogenetic abnormalities with Hu-O-2A/Gb1 cells, despite their apparent derivation from a different biological origin, but also have translocations involving the long and short arms of chromosome 1 and the long arm of chromosome 7, and deletion of chromosome 13 at bands 13q12–21. © 1999 Cancer Research Campaign
Keywords: cytogenetics, FISH, molecular genetics, glioblastoma multiforme
Full Text
The Full Text of this article is available as a PDF (1.5 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Amariglio N., Friedman E., Mor O., Stiebel H., Phelan C., Collins P., Nordenskjold M., Brok-Simoni F., Rechavi G. Analysis of microsatellite repeats in pediatric brain tumors. Cancer Genet Cytogenet. 1995 Oct 1;84(1):56–59. doi: 10.1016/0165-4608(95)00085-2. [DOI] [PubMed] [Google Scholar]
- Barnett S. C., Hutchins A. M., Noble M. Purification of olfactory nerve ensheathing cells from the olfactory bulb. Dev Biol. 1993 Feb;155(2):337–350. doi: 10.1006/dbio.1993.1033. [DOI] [PubMed] [Google Scholar]
- Bignami A., Eng L. F., Dahl D., Uyeda C. T. Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. Brain Res. 1972 Aug 25;43(2):429–435. doi: 10.1016/0006-8993(72)90398-8. [DOI] [PubMed] [Google Scholar]
- Bottenstein J. E., Sato G. H. Growth of a rat neuroblastoma cell line in serum-free supplemented medium. Proc Natl Acad Sci U S A. 1979 Jan;76(1):514–517. doi: 10.1073/pnas.76.1.514. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chaplin T., Ayton P., Bernard O. A., Saha V., Della Valle V., Hillion J., Gregorini A., Lillington D., Berger R., Young B. D. A novel class of zinc finger/leucine zipper genes identified from the molecular cloning of the t(10;11) translocation in acute leukemia. Blood. 1995 Mar 15;85(6):1435–1441. [PubMed] [Google Scholar]
- Debiec-Rychter M., Alwasiak J., Liberski P. P., Nedoszytko B., Babińska M., Mrózek K., Imieliński B., Borowska-Lehman J., Limon J. Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases. Cancer Genet Cytogenet. 1995 Nov;85(1):61–67. doi: 10.1016/0165-4608(95)00129-8. [DOI] [PubMed] [Google Scholar]
- Eisenbarth G. S., Walsh F. S., Nirenberg M. Monoclonal antibody to a plasma membrane antigen of neurons. Proc Natl Acad Sci U S A. 1979 Oct;76(10):4913–4917. doi: 10.1073/pnas.76.10.4913. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Furnari F. B., Huang H. J., Cavenee W. K. Genetics and malignant progression of human brain tumours. Cancer Surv. 1995;25:233–275. [PubMed] [Google Scholar]
- Gillaspy G. E., Miller R. H., Samols D., Goldthwait D. A. Antigenic and differentiative heterogeneity among human glioblastomas. Cancer Lett. 1993 Feb;68(2-3):215–224. doi: 10.1016/0304-3835(93)90149-4. [DOI] [PubMed] [Google Scholar]
- Gyapay G., Morissette J., Vignal A., Dib C., Fizames C., Millasseau P., Marc S., Bernardi G., Lathrop M., Weissenbach J. The 1993-94 Généthon human genetic linkage map. Nat Genet. 1994 Jun;7(2 Spec No):246–339. doi: 10.1038/ng0694supp-246. [DOI] [PubMed] [Google Scholar]
- Hamilton S. R., Liu B., Parsons R. E., Papadopoulos N., Jen J., Powell S. M., Krush A. J., Berk T., Cohen Z., Tetu B. The molecular basis of Turcot's syndrome. N Engl J Med. 1995 Mar 30;332(13):839–847. doi: 10.1056/NEJM199503303321302. [DOI] [PubMed] [Google Scholar]
- Ichimura K., Schmidt E. E., Miyakawa A., Goike H. M., Collins V. P. Distinct patterns of deletion on 10p and 10q suggest involvement of multiple tumor suppressor genes in the development of astrocytic gliomas of different malignancy grades. Genes Chromosomes Cancer. 1998 May;22(1):9–15. doi: 10.1002/(sici)1098-2264(199805)22:1<9::aid-gcc2>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]
- Jennemann R., Rodden A., Bauer B. L., Mennel H. D., Wiegandt H. Glycosphingolipids of human gliomas. Cancer Res. 1990 Dec 1;50(23):7444–7449. [PubMed] [Google Scholar]
- Johansson B., Heim S., Mandahl N., Mertens F., Mitelman F. Trisomy 7 in nonneoplastic cells. Genes Chromosomes Cancer. 1993 Apr;6(4):199–205. doi: 10.1002/gcc.2870060402. [DOI] [PubMed] [Google Scholar]
- Kamb A., Gruis N. A., Weaver-Feldhaus J., Liu Q., Harshman K., Tavtigian S. V., Stockert E., Day R. S., 3rd, Johnson B. E., Skolnick M. H. A cell cycle regulator potentially involved in genesis of many tumor types. Science. 1994 Apr 15;264(5157):436–440. doi: 10.1126/science.8153634. [DOI] [PubMed] [Google Scholar]
- Karlbom A. E., James C. D., Boethius J., Cavenee W. K., Collins V. P., Nordenskjöld M., Larsson C. Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10. Hum Genet. 1993 Sep;92(2):169–174. doi: 10.1007/BF00219686. [DOI] [PubMed] [Google Scholar]
- Kashima T., Tiu S. N., Merrill J. E., Vinters H. V., Dawson G., Campagnoni A. T. Expression of oligodendrocyte-associated genes in cell lines derived from human gliomas and neuroblastomas. Cancer Res. 1993 Jan 1;53(1):170–175. [PubMed] [Google Scholar]
- Kim D. H., Mohapatra G., Bollen A., Waldman F. M., Feuerstein B. G. Chromosomal abnormalities in glioblastoma multiforme tumors and glioma cell lines detected by comparative genomic hybridization. Int J Cancer. 1995 Mar 16;60(6):812–819. doi: 10.1002/ijc.2910600615. [DOI] [PubMed] [Google Scholar]
- Kraus J. A., Koopmann J., Kaskel P., Maintz D., Brandner S., Schramm J., Louis D. N., Wiestler O. D., von Deimling A. Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma. J Neuropathol Exp Neurol. 1995 Jan;54(1):91–95. doi: 10.1097/00005072-199501000-00011. [DOI] [PubMed] [Google Scholar]
- Li J., Yen C., Liaw D., Podsypanina K., Bose S., Wang S. I., Puc J., Miliaresis C., Rodgers L., McCombie R. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science. 1997 Mar 28;275(5308):1943–1947. doi: 10.1126/science.275.5308.1943. [DOI] [PubMed] [Google Scholar]
- Liu B., Parsons R., Papadopoulos N., Nicolaides N. C., Lynch H. T., Watson P., Jass J. R., Dunlop M., Wyllie A., Peltomäki P. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med. 1996 Feb;2(2):169–174. doi: 10.1038/nm0296-169. [DOI] [PubMed] [Google Scholar]
- Ma N. S., Zheng C., Benchekroun Y., Deaven L. L., Longmire J. L., Moir D. T., Mao J. Characterization of a flow-sorted human chromosome 10 cosmid library by FISH. Cytogenet Cell Genet. 1996;74(4):266–271. doi: 10.1159/000134432. [DOI] [PubMed] [Google Scholar]
- Mao X., Jones T. A., Williamson J., Gutowski N. J., Pröschel C., Noble M., Sheer D. Assignment of the human and mouse LIM-kinase genes (LIMK1; Limk1) to chromosome bands 7q11.23 and 5G1, respectively, by in situ hybridization. Cytogenet Cell Genet. 1996;74(3):190–191. doi: 10.1159/000134411. [DOI] [PubMed] [Google Scholar]
- Mollenhauer J., Wiemann S., Scheurlen W., Korn B., Hayashi Y., Wilgenbus K. K., von Deimling A., Poustka A. DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours. Nat Genet. 1997 Sep;17(1):32–39. doi: 10.1038/ng0997-32. [DOI] [PubMed] [Google Scholar]
- Noble M., Fok-Seang J., Cohen J. Glia are a unique substrate for the in vitro growth of central nervous system neurons. J Neurosci. 1984 Jul;4(7):1892–1903. doi: 10.1523/JNEUROSCI.04-07-01892.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Noble M., Gutowski N., Bevan K., Engel U., Linskey M., Urenjak J., Bhakoo K., Williams S. From rodent glial precursor cell to human glial neoplasia in the oligodendrocyte-type-2 astrocyte lineage. Glia. 1995 Nov;15(3):222–230. doi: 10.1002/glia.440150304. [DOI] [PubMed] [Google Scholar]
- Noble M., Murray K. Purified astrocytes promote the in vitro division of a bipotential glial progenitor cell. EMBO J. 1984 Oct;3(10):2243–2247. doi: 10.1002/j.1460-2075.1984.tb02122.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nobori T., Miura K., Wu D. J., Lois A., Takabayashi K., Carson D. A. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature. 1994 Apr 21;368(6473):753–756. doi: 10.1038/368753a0. [DOI] [PubMed] [Google Scholar]
- Pröschel C., Blouin M. J., Gutowski N. J., Ludwig R., Noble M. Limk1 is predominantly expressed in neural tissues and phosphorylates serine, threonine and tyrosine residues in vitro. Oncogene. 1995 Oct 5;11(7):1271–1281. [PubMed] [Google Scholar]
- Raff M. C., Miller R. H., Noble M. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium. Nature. 1983 Jun 2;303(5916):390–396. doi: 10.1038/303390a0. [DOI] [PubMed] [Google Scholar]
- Ranscht B., Clapshaw P. A., Price J., Noble M., Seifert W. Development of oligodendrocytes and Schwann cells studied with a monoclonal antibody against galactocerebroside. Proc Natl Acad Sci U S A. 1982 Apr;79(8):2709–2713. doi: 10.1073/pnas.79.8.2709. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ritland S. R., Ganju V., Jenkins R. B. Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma. Genes Chromosomes Cancer. 1995 Apr;12(4):277–282. doi: 10.1002/gcc.2870120407. [DOI] [PubMed] [Google Scholar]
- Schröck E., Blume C., Meffert M. C., du Manoir S., Bersch W., Kiessling M., Lozanowa T., Thiel G., Witkowski R., Ried T. Recurrent gain of chromosome arm 7q in low-grade astrocytic tumors studied by comparative genomic hybridization. Genes Chromosomes Cancer. 1996 Apr;15(4):199–205. doi: 10.1002/(SICI)1098-2264(199604)15:4<199::AID-GCC1>3.0.CO;2-X. [DOI] [PubMed] [Google Scholar]
- Senger G., Ragoussis J., Trowsdale J., Sheer D. Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization. Cytogenet Cell Genet. 1993;64(1):49–53. doi: 10.1159/000133559. [DOI] [PubMed] [Google Scholar]
- Singh L. P., Pearl D. K., Franklin T. K., Spring P. M., Scheithauer B. W., Coons S. W., Johnson P. C., Pfeiffer S. E., Li J., Knott J. C. Neutral glycolipid composition of primary human brain tumors. Mol Chem Neuropathol. 1994 Feb-Apr;21(2-3):241–257. doi: 10.1007/BF02815353. [DOI] [PubMed] [Google Scholar]
- Sommer I., Schachner M. Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system. Dev Biol. 1981 Apr 30;83(2):311–327. doi: 10.1016/0012-1606(81)90477-2. [DOI] [PubMed] [Google Scholar]
- Steck P. A., Pershouse M. A., Jasser S. A., Yung W. K., Lin H., Ligon A. H., Langford L. A., Baumgard M. L., Hattier T., Davis T. Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet. 1997 Apr;15(4):356–362. doi: 10.1038/ng0497-356. [DOI] [PubMed] [Google Scholar]
- Steinkasserer A., Jones T., Sheer D., Koettnitz K., Hauber J., Bevec D. The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. Genomics. 1995 Feb 10;25(3):749–752. doi: 10.1016/0888-7543(95)80025-h. [DOI] [PubMed] [Google Scholar]
- Ueki K., Ono Y., Henson J. W., Efird J. T., von Deimling A., Louis D. N. CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated. Cancer Res. 1996 Jan 1;56(1):150–153. [PubMed] [Google Scholar]
- Zheng C. J., Ma N. S., Dorman T. E., Wang M. T., Braunschweiger K., Soares L., Schuster M. K., Rothschild C. B., Bowden D. W., Torrey D. Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10. Genomics. 1994 Jul 1;22(1):55–67. doi: 10.1006/geno.1994.1345. [DOI] [PubMed] [Google Scholar]
- van der Luijt R. B., Khan P. M., Vasen H. F., Tops C. M., van Leeuwen-Cornelisse I. S., Wijnen J. T., van der Klift H. M., Plug R. J., Griffioen G., Fodde R. Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis. Hum Mutat. 1997;9(1):7–16. doi: 10.1002/(SICI)1098-1004(1997)9:1<7::AID-HUMU2>3.0.CO;2-8. [DOI] [PubMed] [Google Scholar]
