Recurrent chromosome aberrations in cancer

Mutation Research/Reviews in Mutation Research - Tập 462 Số 2-3 - Trang 247-253 - 2000
Felix Mitelman1
1Department of Clinical Genetics, University Hospital, SE-221 85 Lund, Sweden

Tóm tắt

Từ khóa


Tài liệu tham khảo

Hansemann, 1890, Ueber asymmetrische Zelltheilung in Epithelkrebsen und deren biologische Bedeutung, Virchows Arch. Anat., 119, 299, 10.1007/BF01882039

T. Boveri, Zur Frage der Entstehung maligner Tumoren, Gustav Fischer, Jena, 1914.

Nowell, 1960, A minute chromosome in human chronic granulocytic leukemia, Science, 132, 1497

Bayreuther, 1960, Chromosomes in primary neoplastic growth, Nature, 186, 6, 10.1038/186006a0

A.A. Sandberg, The Chromosomes in Human Cancer and Leukemia, Elsevier/North-Holland, New York, 1980.

Levan, 1966, Non-random representation of chromosome types in human tumor stemlines, Hereditas, 55, 28, 10.1111/j.1601-5223.1966.tb02032.x

van Steenis, 1966, Chromosomes and cancer, Nature, 209, 819, 10.1038/209819a0

F. Mitelman, The Rous sarcoma virus story: cytogenetics of tumors induced by RSV, in: J. German (Ed.), Chromosomes and Cancer, Wiley, New York, 1974, pp. 675–693.

Caspersson, 1970, Differential binding of alkylating fluorochromes in human chromosomes, Exp. Cell Res., 60, 315, 10.1016/0014-4827(70)90523-9

F. Mitelman, Catalog of Chromosome Aberrations in Cancer '98, CD-ROM, Version 1, Wiley-Liss, New York, 1998.

Cremer, 1988, Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes, Hum. Genet., 80, 235, 10.1007/BF01790091

Gray, 1992, Molecular cytogenetics in human cancer diagnosis, Cancer, 69, 1536, 10.1002/1097-0142(19920315)69:6+<1536::AID-CNCR2820691306>3.0.CO;2-J

Schröck, 1996, Multicolor spectral karyotyping of human chromosomes, Science, 273, 494, 10.1126/science.273.5274.494

Speicher, 1996, Karyotyping human chromosomes by combinatorial multi-fluor FISH, Nat. Genet., 12, 368, 10.1038/ng0496-368

F. Mitelman, F. Mertens, B. Johansson, Breakpoint map of recurrent cytogenetic aberrations in human neoplasia '99, NCI Cancer Genome Anatomy Project, http://www.ncbi.nlm.nih.gov/CGAP.

Gorunova, 1998, Cytogenetic analysis of pancreatic carcinomas: intratumor heterogeneity and nonrandom pattern of chromosome aberrations, Genes Chromosomes Cancer, 23, 81, 10.1002/(SICI)1098-2264(199810)23:2<81::AID-GCC1>3.0.CO;2-0

Gorunova, 1996, Massive cytogenetic heterogeneity in a pancreatic carcinoma — fifty-four karyotypically unrelated clones, Genes Chromosomes Cancer, 14, 259, 10.1002/gcc.2870140404

Johansson, 1996, Primary vs. secondary neoplasia-associated chromosomal abnormalities — balanced rearrangements vs. genomic imbalances?, Genes Chromosomes Cancer, 16, 155, 10.1002/(SICI)1098-2264(199607)16:3<155::AID-GCC1>3.0.CO;2-Y

Mitelman, 1997, A breakpoint map of recurrent chromosomal rearrangements in human neoplasia, Nat. Genet., 15, 417, 10.1038/ng0497supp-417

Kinzler, 1998, Landscaping the cancer terrain, Science, 280, 1036, 10.1126/science.280.5366.1036

S. Heim, F. Mitelman, Cancer Cytogenetics, 2nd edn., Wiley-Liss, New York, 1995.

Jin, 1997, Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa, Mutat. Res., 374, 63, 10.1016/S0027-5107(96)00219-9

Mitelman, 1997, Clinical significance of cytogenetic findings in solid tumors, Cancer Genet. Cytogenet., 95, 1, 10.1016/S0165-4608(96)00252-X