Advances in cancer cytogenetics

As the end of the millenium approaches, recognition of the milestones achieved in the field of cancer cytogenetics is mandatory. With regard to cancer cytogenetics, the turning century can be divided in three main era: the pre‐banding period that has posed important hypothesis and technical premises, the fruitful banding era that led to the discovery of the critical chromosomal rearrangements and cloning of cancer genes and the more recent revolutionizing era of molecular cytogenetics where technological advances permit a global visualization and high‐level resolution of chromosomal alterations. J. Cell. Biochem. Suppls. 32/33:173–182, 1999. © 1999 Wiley‐Liss, Inc.

[1]  C. Bartoli,et al.  c-erbB2/neu gene and chromosome 17 analysis in breast cancer by FISH on archival cytological fine-needle aspirates , 1999, British Journal of Cancer.

[2]  E. Buchdunger,et al.  In vivo eradication of human BCR/ABL-positive leukemia cells with an ABL kinase inhibitor. , 1999, Journal of the National Cancer Institute.

[3]  F. Rilke,et al.  bcl‐2 expression in synovial sarcoma , 1998, The Journal of pathology.

[4]  M. Pierotti,et al.  Role of the TFG N-terminus and coiled-coil domain in the transforming activity of the thyroid TRK-T3 oncogene , 1998, Oncogene.

[5]  Peter Lichter,et al.  Minimal sizes of deletions detected by comparative genomic hybridization , 1998, Genes, chromosomes & cancer.

[6]  Thomas Ried,et al.  Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping , 1997, Nature Genetics.

[7]  H. Ito,et al.  CHROMOSOMAL REARRANGEMENT t(11;22) IN EXTRASKELETAL EWING'S SARCOMA AND PRIMITIVE NEUROECTODERMAL TUMOUR ANALYSED BY FLUORESCENCE IN SITU HYBRIDIZATION USING PARAFFIN‐EMBEDDED TISSUE , 1997, The Journal of pathology.

[8]  D. Ledbetter,et al.  Multicolor Spectral Karyotyping of Human Chromosomes , 1996, Science.

[9]  M. Borrello,et al.  Cytogenetics and molecular genetics of carcinomas arising from thyroid epithelial follicular cells , 1996, Genes, chromosomes & cancer.

[10]  G. Sozzi,et al.  Variant translocation t(6;10)(p21;q22) in pulmonary chondroid hamartoma , 1996, Genes, chromosomes & cancer.

[11]  M. Rugge,et al.  Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines. , 1996, Cancer research.

[12]  C. Croce,et al.  The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers , 1996, Cell.

[13]  B. Gusterson,et al.  REVIEW ARTICLE. THE MOLECULAR PATHOLOGY OF SMALL ROUND‐CELL TUMOURS—RELEVANCE TO DIAGNOSIS, PROGNOSIS, AND CLASSIFICATION , 1996, The Journal of pathology.

[14]  R. Hipskind,et al.  Interphase cytogenetic analysis of distinct X‐chromosomal translocation breakpoints in synovial sarcoma , 1995, The Journal of pathology.

[15]  T. Rabbitts,et al.  Chromosomal translocations in human cancer , 1994, Nature.

[16]  J Piper,et al.  Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors , 1994, Genes, chromosomes & cancer.

[17]  M. Caligiuri,et al.  ALL-1 partial duplication in acute leukemia. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[18]  W. Gerald,et al.  Fusion of the EWS and WT1 genes in the desmoplastic small round cell tumor. , 1994, Cancer research.

[19]  M. Borrello,et al.  A t( 10; 17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinoma , 1994, Genes, chromosomes & cancer.

[20]  S. Korsmeyer,et al.  Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programed cell death , 1993, Cell.

[21]  Myriam Alcalay,et al.  The acute promyelocytic leukemia-specific PML-RARα fusion protein inhibits differentiation and promotes survival of myeloid precursor cells , 1993, Cell.

[22]  M. Santoro,et al.  Characterization of an inversion on the long arm of chromosome 10 juxtaposing D10S170 and RET and creating the oncogenic sequence RET/PTC. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[23]  P. Nowell,et al.  Cloning of ALL-1, the locus involved in leukemias with the t(4;11)(q21;q23), t(9;11)(p22;q23), and t(11;19)(q23;p13) chromosome translocations. , 1991, Cancer research.

[24]  S. Korsmeyer,et al.  BCL2 protein is topographically restricted in tissues characterized by apoptotic cell death. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Christine Chomienne,et al.  The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus , 1990, Nature.

[26]  Stephen H. Friend,et al.  A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma , 1986, Nature.

[27]  C. Turc‐Carel,et al.  Consistent chromosomal translocation in alveolar rhabdomyosarcoma. , 1986, Cancer genetics and cytogenetics.

[28]  P. Nowell,et al.  Molecular cloning of the chromosomal breakpoint of B-cell lymphomas and leukemias with the t(11;14) chromosome translocation. , 1984, Science.

[29]  P. Nowell,et al.  Transcriptional activation of an unrearranged and untranslocated c-myc oncogene by translocation of a C lambda locus in Burkitt. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[30]  Meyerhoff Jo Exacerbation of psoriasis with meclofenamate. , 1983 .

[31]  C. Croce,et al.  Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[32]  J. Minna,et al.  A nonrandom chromosomal abnormality, del 3p(14-23), in human small cell lung cancer (SCLC). , 1982, Cancer genetics and cytogenetics.

[33]  J. Rowley,et al.  Further evidence for a non‐random chromosomal abnormality in acute promyelocytic leukemia , 1977, International journal of cancer.

[34]  J. Rowley A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining , 1973, Nature.

[35]  P. Nowell,et al.  Chromosome studies on normal and leukemic human leukocytes. , 1960, Journal of the National Cancer Institute.

[36]  Y. Pekarsky,et al.  Role of FHIT in human cancer. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[37]  J. Dumanski,et al.  Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma , 1997, Nature Genetics.

[38]  M. Caligiuri,et al.  Developments in cytogenetics and oncogenes in acute leukemia. , 1997, Current opinion in oncology.

[39]  Chromosomal translocations in Ewing's sarcoma. , 1983, The New England journal of medicine.

[40]  Th. Boveri,et al.  The origin of malignant tumors , 1929 .