Microsatellite Markers in Leukaemia and Lymphoma: Comments on a Timely Topic

References

• Sutherland G. R., Richards R. I. DNA repeats ‐ a treasury of human variation. New England Journal of Medicine 1994; 331: 191–192
   PubMed Web of Science ®Google Scholar
• Miesfeld R., Krystal M., Arnheim N. A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human δ‐ and β‐globin genes. Nucleic Acids Research 1981; 9: 5931–5947
   PubMed Web of Science ®Google Scholar
• Hamada H., Petrino M. G., Kakunaga T. Molecular structure and evolutionary origin of the human cardiac muscle actin gene. Proceedings of the National Academy of Sciences USA 1982; 79: 5901–5905
   PubMed Web of Science ®Google Scholar
• Hamada H., Petrino M. G., Kakunaga T. A novel repeated element with Z‐DNA‐forming potential is widely found in evolutionarily diverse eukaryotic genomes. Proceedings of the National Academy of Sciences USA 1982; 79: 6465–6469
   PubMed Web of Science ®Google Scholar
• Shen L. P., Rutter W. J. Sequence of the human somatostatin I gene. Science 1984; 224: 168–171
   PubMed Web of Science ®Google Scholar
• Litt M., Luty J. A. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. American Journal of Human Genetics 1989; 44: 397–401
   PubMed Web of Science ®Google Scholar
• Weissenbach J., Gyapay G., Dib C., Vignal A., Morissette J., Millasseau P., Vaysseix G., Lathrop M. A second‐generation linkage map of the human genome. Nature 1992; 359: 794–801
   PubMed Web of Science ®Google Scholar
• Dib C., Fauré S., Fizames C., Samson D., Drouot N., Vignal A., Millasseau P., Marc S., Hazan J., Seboun E., Lathrop M., Gyapay G., Morissette J., Weissenbach J. A comprehensive genetic map of the human genome based on 5′264 microsatellites. Nature 1996; 380: 152–154
   PubMed Web of Science ®Google Scholar
• Loeb L. A. Microsatellite instability: marker of a mutator phenotype in cancer. Cancer Research 1994; 54: 5059–5063
   PubMed Web of Science ®Google Scholar
• Mao L., Lee D. J., Tockman M. S., Erozan Y. S., Askin F., Sidransky D. Microsatellite alterations as clonal markers for the detection of human cancer. Proceedings of the National Academy of Sciences USA 1994; 91: 9871–9875
   PubMed Web of Science ®Google Scholar
• Mao L., Schoenberg M. P., Scicchitano M., Erozyn Y. S., Merlo A., Schwab D., Sidransky D. Molecular detection of primary bladder cancer by microsatellite analysis. Science 1996; 271: 659–662
   PubMed Web of Science ®Google Scholar
• Nagel S., Borisch B., Thein S. L., Oestreicher M., Nöthiger F., Birrer S., Tobler A., Fey M. F. Somatic mutations detected by mini‐ and microsatellite DNA markers reveal clonal intratumor heterogeneity in gastrointestinal cancers. Cancer Research 1995; 55: 2866–2870
   PubMed Web of Science ®Google Scholar
• Fishel R., Ewel A., Lee S., Lescoe M. K., Griffith J. Binding of mismatched microsatellite DNA sequences by the human MSH2 protein. Science 1994; 266: 1403–1495
   PubMed Web of Science ®Google Scholar
• Gourdon G., Radvanyi F., Lia S. S., Duros C., Blanche M., Abitbol M., Junien C., Hofmann‐Radvanyi H. Moderate intergenerational and somatic instability of a 55‐CTG repeat in transgenic mice. Nature Genetics 1997; 15: 190–192
   PubMed Web of Science ®Google Scholar
• Rubinsztein D. C., Amos W., Leggo J., Goodburn S., Ramesar R. S., Old J., Bontrop R., McMahon R., Barton B. E., Ferguson‐Smith M. A. Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence. Nature Genetics 1994; 7: 525–530
   PubMed Web of Science ®Google Scholar
• Bennett S. T., Lucassen A. M., Gough S. C. L., Powell E. E., Undlien D. E., Pritchard L. E., Merriman M. E., Kawaguchi Y., Dronsfield M. J., Pociot F., Nerup J., Bouzekri N., Cambon‐Thomsen A., Ronningen K. S., Barnett A. H., Bain S. C., Todd J. A. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene mini‐satellite locus. Nature Medicine 1995; 9: 284–291
   Web of Science ®Google Scholar
• Pabst T., Schwaller J., Tobler A., Fey M. F. Detection of microsatellite markers in leukaemia using DNA from archival bone marrow smears. British Journal of Haematology 1996; 95: 135–137
   PubMed Web of Science ®Google Scholar
• Mashal R. D., Lester S. C., Sklar J. Clonal analysis by study of X‐chromosome inactivation in formalin‐fixed paraffin‐embedded tissue. Cancer Research 1993; 53: 4676–4679
   PubMed Web of Science ®Google Scholar
• Kopp P., Jaggi R., Tobler A., Borisch B., Oestreicher M., Sabacan L., Jameson J. L., Fey M. F. Clonal X‐inactivation analysis of human tumours using the human androgen receptor gene (HI/MARA) polymorphism: a nonradioactive and semiquantitative strategy applicable to fresh and archival tissue. Molecular and Cellular Probes 1997, in the press
   PubMed Web of Science ®Google Scholar
• Gruis N. A., Abeln E. C. A., Bardoel A. F. J., Devilee P., Frants R. R., Cornelisse C. J. PCR‐based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. British Journal of Cancer 1993; 68: 308–313
   PubMed Web of Science ®Google Scholar
• Pilkington S. P., Summers C., Thein S. L., O'Connor N. T. J., Wainscoat J. S. Hair root DNA: a source of constitutional DNA in leukaemia. Lancet 1987; 1: 112
   PubMed Web of Science ®Google Scholar
• Pabst T., Schwaller J., Jotterand Bellomo M., Oestreicher M., Mühlematter D., Tichelli A., Tobler A., Fey M. F. Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias. Blood 1996; 88: 1026–1034
   PubMed Web of Science ®Google Scholar
• Weinberg R. A. Tumor suppressor genes. Science 1991; 254: 1138–1146
   PubMed Web of Science ®Google Scholar
• Koufos A., Hansen M. F., Copeland N. G., Jenkins N. A., Lampkin B. C., Cavenee W. K. Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism. Nature 1985; 316: 330–334
   PubMed Web of Science ®Google Scholar
• Ionov Y., Peinado M. A., Malkhosyan S., Shibata D., Perucho M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 1993; 363: 558–561
   PubMed Web of Science ®Google Scholar
• Peltomäki P., Aaltonen L. A., Sistonen P., Pylkkänen L., Mecklin J. P., Järvinen H., Green J. S., Jass J. R., Weber J. L., Leach F. S., Peterson G. M., Hamilton S. R., de la Chapelle A., Vogelstein B. Genetic mapping of a locus predisposing to human colorectal cancer. Science 1993; 260: 810–812
   PubMed Web of Science ®Google Scholar
• Bronner C. E., Baker S. M., Morrison P. T., Warren G., Smith L. G., Lescoe M. K., Kane M., Earabine C., Lipford J., Lindblom A., Tannergård P., Bollag R. J., Godwin A. R., Ward D. C., Nodenskjøld M., Fishel R., Kolodner R., Liskay R. M. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non‐polyposis colon cancer. Nature 1994; 368: 258–261
   PubMed Web of Science ®Google Scholar
• Liu B., Farrington S., Petersen G. M., Hamilton S. R., Parsons R., Papadopoulos N., Fujiwara T., Jen J., Kinzler K. W., Wyllie A. H., Vogelstein B., Dunlop M. G. Genetic instability occurs in the majority of young patients with colorectal cancer. Nature Medicine 1995; 1: 348–352
   PubMed Web of Science ®Google Scholar
• Liu B., Parsons R., Papadopulos N., Nicolaides N., Lynch H. T., Watson P., Jass J. R., Dunlop M. G., Wyllie A., Peltomäki P., de la Chapelle A., Hamilton S. R., Vogelstein B., Kinzler K. W. Analysis of mismatch repair genes in hereditary non‐polyposis colorectal cancer patients. Nature Medicine 1996; 2: 169–174
   PubMed Web of Science ®Google Scholar
• Marra G. C., Boland C. R. Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. Journal of the National Cancer Institute 1995; 87: 1114–1125
   PubMed Web of Science ®Google Scholar
• Nicolaides N., Papadopoulos N., Liu B., Wei Y. F., Carter K. C., Ruben S. M., Rosen C. A., Haseltine W. A., Fleischmann R. D., Fraser C. M., Adams M. A., Venter J. C., Dunlop M. G., Hamilton S. R., Petersen G. M., de la Chapelle A., Vogelstein B., Kinzler K. W. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature 1994; 371: 75–79
   PubMed Web of Science ®Google Scholar
• Mauillon J. L., Michel P., Limacher J. M., Latouche J. B., Dechelotte P., Charbonnier F., Martin C., Moreau V., Metayer J., Paillot B., Frebourg T. Identification of novel germline hMLH1 mutations including a 22 kb Alumediated deletion in patients with familial colorectal cancer. Cancer Research 1996; 56: 5728–5733
   PubMed Web of Science ®Google Scholar
• Parsons R., Li G. M., Longley M. J., Fang W., Papadopoulos N., Jen J., de la Chapelle A., Kinzler K. W., Vogelstein B., Modrich P. Hypermutability and mismatch repair deficiency in RER+ tumor cells. Cell 1993; 75: 1227–1236
   PubMed Web of Science ®Google Scholar
• Miozzo M., Sozzi G., Musso K., Piloti S., Incarbone M., Pastorino U., Pierotti M. A. Microsatellite alterations in bronchial and sputum specimens of lung cancer patients. Cancer Research 1996; 56: 2285–2288
   PubMed Web of Science ®Google Scholar
• Abrahamson G. M., Rack K., Oscier D. G., Fitchett M., Buckle V. J., Wainscoat J. S. Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders. American Journal of Hematology 1993; 42: 171–176
   PubMed Web of Science ®Google Scholar
• Vogelstein B., Fearon E. R., Kern S. E., Hamilton S. R., Presisinger A. C., Nakamura Y., White R. Allelotype of colorectal carcinomas. Science 1989; 244: 207–211
   PubMed Web of Science ®Google Scholar
• Takeuchi S., Bartram C. R., Wada M., Reiter A., Hatta Y., Seriu T., Lee E., Miller C. W., Miyoshi I., Koeffler H. P. Allelotype analysis of childhood acute lymphoblastic leukemia. Cancer Research 1995; 55: 5377–5382
   PubMed Web of Science ®Google Scholar
• Cavé H., Gérard B., Martin E., Guidal C., Devaux I., Weissenbach J., Elion J., Vilmer E., Grandchamp B. Loss of heterozygosity in the chromosomal region 12p 12–13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor‐suppressor gene distinct from p27KIPI. Blood 1995; 86: 3869–3875
   PubMed Web of Science ®Google Scholar
• Gartenhaus R. B. Allelic loss determination in chronic lymphocytic leukemia by immuno‐magnetic bead sorting and microsatellite analysis. Oncogene 1997; 14: 375–378
   PubMed Web of Science ®Google Scholar
• Silly H., Chase A., Mills K. I., Apfelbeck U., Sormann S., Goldman J. M., Cross N. C. P. No evidence for microsatellite instability or consistent loss of heterozygosity at selected loci in chronic myeloid leukemia blast crisis. Leukemia 1994; 8: 1923–928
   PubMed Web of Science ®Google Scholar
• Jen J., Kim H., Piantadosi S., Liu Z. F., Levit R. C., Sistonen P., Kinzler K. W., Vogelstein B., Hamilton S. R. Allelic loss of chromosome 18q and prognosis in colorectal cancer. New England Journal of Medicine 1994; 331: 213–221
   PubMed Web of Science ®Google Scholar
• Wada C., Shionoya S., Fujino Y., Tokuhiro H., Akahoshi T., Uchida T., Ohtani H. Genomic instability of microsatellite repeats and its association with the evolution of chronic myelogenous leukemia. Blood 1994; 83: 3449–3456
   PubMed Web of Science ®Google Scholar
• Cross N. C. P., Silly H., Goldman J. M. Microsatellite instability in myeloid leukemias. Blood 1994; 84: 3236–3246
   PubMed Web of Science ®Google Scholar
• Indraccolo S., Simon M., Erfle V., Chieco‐Bianchi L., Leib‐Moesch C. Genetic instability of a dinucleotide repeat‐rich region in three hematologic malignancies. Leukemia 1995; 9: 1517–1522
   PubMed Web of Science ®Google Scholar
• Randerson J., Cawkwell L., Jack A., Child J. A., Lewis F., Hall N., Johnson P., Evans P., Barrans S., Morgan G. J. Microsatellite instability in follicle centre cell lymphoma. British Journal of Haematology 1996; 93: 160–162
   PubMed Web of Science ®Google Scholar
• Peng H., Chen G., Du M., Singh N., Isaacson P., Pan L. Replication error phenotype and p53 gene mutation in lymphomas of mucosa‐associated lymphoid tissue. American Journal of Pathology 1996; 148: 643–648
   PubMed Web of Science ®Google Scholar
• Bedi G. C., Westra W. H., Farzadegan H., Pitha P. M., Sidransky D. Microsatellite instability in primary neoplasms from HIV+ patients. Nature Medicine 1995; 1: 65–68
   PubMed Web of Science ®Google Scholar
• Larson R. S., Manning S., Macon W. R., Vnencak‐Jones C. Microsatellite instability in natural‐killer cell‐like T‐cell lymphomas in immunocompromised and immunocompetent individuals. Blood 1997; 89: 1114–1115
   PubMed Web of Science ®Google Scholar
• Larson R. S., Scott M. A., McCurley T. L., Vnencak‐Jones C. L. Microsatellite analysis of posttransplant lymphoproliferative disorders: determination of donor/recipient origin and identification of putative lymphomagenic mechanism. Cancer Research 1996; 56: 4378–4381
   PubMed Web of Science ®Google Scholar
• Gamberi B., Gaidano G. L., Parsa N., Carbone A., Roncella S., Knowles D. M., Louie D. C., Shibata D., Chaganti R. S. K., Dalla‐Favera R. Microsatellite instability is rare in B‐cell Non‐Hodgkin's lymphomas. Blood 1997; 89: 975–979
   PubMed Web of Science ®Google Scholar
• Reitmair A. H., Schnmits R., Ewel A., Bapat B., Redston M., Mitri A., Waterhouse P., Mirrücker H. W., Wakeham A., Liu B., Thomason A., Griesser H., Gallinger S., Ballhausen W. G., Fishel R., Mak T. W. MSH2 deficient mice are viable and susceptible to lymphoid tumours. Nature Medicine 1995; 11: 64–69
   Web of Science ®Google Scholar
• Hangaishi A., Ogawa S., Mitani K., Hosoya N., Chiba S., Yazaki Y., Hirai H. Mutations and loss of expression of a mismatch repair gene, hMLH1, in leukemia and lymphoma cell lines. Blood 1997; 89: 1740–1747
   PubMed Web of Science ®Google Scholar
• Robledo M., Martinez B., Arranz E., Trujillo M. J., Gonzalez Ageitos A., Rivas C., Benitez J. Genetic instability of microsatellites in haematological neoplasms. Leukemia 1995; 9: 960–964
   PubMed Web of Science ®Google Scholar
• Wainscoat J. S., Fey M. F. Assessment of clonality in human tumors: a review. Cancer Research 1990; 50: 1355–1360
   PubMed Web of Science ®Google Scholar
• Allen R. C., Zoghbi H. Y., Moseley A. B., Rosenblatt H. M., Belmont J. W. Methylation of HpaI1 and HhaI sites near the polymorphic CAG repeat in the human androgen‐receptor gene correlates with X‐chromosome inactivation. American Journal of Human Genetics 1992; 51: 1229–1239
   PubMed Web of Science ®Google Scholar
• Busque L., Mio R., Mattioli J., Brais E., Blais N., Lalonde Y., Maragh M., Gilliland D. G. Nonrandom X‐inactivation patterns in normal females: Iyonization ratios vary with age. Blood 1996; 88: 59–65
   PubMed Web of Science ®Google Scholar
• Willman C. L., Busque L., Griffith B. B., Favara B. E., McClain K. L., Duncan M., Gilliland G. Langerhans' cell histiocytosis (histiocytosis X) ‐ a clonal proliferative disease. New England Journal of Medicine 1994; 331: 154–160
   PubMed Web of Science ®Google Scholar
• Anan K., Ito M., Misawa M., Ohe Y., Kai S., Kohsaki M., Hara H. Clonal analysis of peripheral blood and haemopoietic colonies in patients with aplastic anaemia and refractory anaemia using the polymorphic short tandem‐repeat on the human androgen‐receptor (HUMARA) gene. British Journal of Haematology 1995; 89: 838–844
   PubMed Web of Science ®Google Scholar
• Fey M. F., Liechti‐Gallati S., von Rohr A., Borisch B., Theilkäs L., Schneider V., Oestreicher M., Nagel S., Ziemiecki A., Tobler A. Clonality and X‐inactivation patterns in hematopoietic cell populations detected by the highly informative M27β DNA probe. Blood 1994; 83: 931–938
   PubMed Web of Science ®Google Scholar
• Gale R. E., Wheadon H., Linch D. C. Assessment of X‐chromosome inactivation patterns using the hyper‐variable probe M27β in normal hemopoietic cells and acute myeloid leukemic blasts. Leukemia 1992; 6: 649–655
   PubMed Web of Science ®Google Scholar
• Gale R. E., Wheadon H., Boulos P., Linch D. C. Tissue specificity of X‐chromosome inactivation patterns. Blood 1994; 83: 2899–2905
   PubMed Web of Science ®Google Scholar
• Lawler M., Humphries P., McCann S. R. Evaluation of mixed chimerism by in vitro amplification of dinucleotide repeat sequences using the polymerase chain reaction. Blood 1991; å: 2504–2514
   Google Scholar
• Lo Y. M., Noakes L., Roux E., Jeannet M., Chapius B., Fleming K. A., Wainscoat J. S. Application of a polymorphic Y microsatellite to the detection of post bone marrow transplantation chimaerism. British Journal of Haematology 1996; 89: 645–649
   Web of Science ®Google Scholar
• Oberkirchner A. R., Strout M. P., Herzig G. P., Fritz P. D., Caliguri M. A. Description of an efficient and highly informative method for the evaluation of hematopoietic chimerism following allogeneic bone marrow transplantation. Bone Marrow Transplantation 1995; 16: 695–702
   PubMed Web of Science ®Google Scholar
• Gartenhaus R., Johns M. M., III, Wang P., Rai K., Sidransky D. Mutator phenotype in a subset of chronic lymphocytic leukemia. Blood 1996; 87: 38–41
   PubMed Web of Science ®Google Scholar
• Kaneko H., Horiike S., Inazawa J., Nakai H., Misawa S. Microsatellite instability is an early genetic event in myelodysplastic syndromes. Blood 1995; 86: 1236–1237
   PubMed Web of Science ®Google Scholar