Stability of microsatellites in myeloid neoplasias

Cancer Genetics and Cytogenetics

Volumn 106, Issue 1, 1998, Pages 54-61

  Boyer, Jayne C ^a   Risinger, John I ^b   Farber, Rosann A ^a,b  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BASE PAIRING; CANCER GENETICS; DNA DETERMINATION; GENE LOCUS; HUMAN; HUMAN CELL; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

CHROMOSOME ABERRATIONS; DNA REPAIR; HUMANS; LEUKEMIA, MYELOCYTIC, ACUTE; LOSS OF HETEROZYGOSITY; MICROSATELLITE REPEATS; MYELODYSPLASTIC SYNDROMES; POLYMERASE CHAIN REACTION;

EID: 0032192331     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00043-0     Document Type: Article

References (52)

1. 1. Eshleman JR, Markowitz SD (1995): Microsatellite instability in inherited and sporadic neoplasms. Curr Opin Oncol 7: 83-89.
2. 2. Boland M (1995): Hereditary nonpolyposis colorectal cancer: the syndrome, the genes and historical perspectives. J Natl Cancer Inst 87:1114-1125.
3. 3. Eshleman JR, Markowitz SD (1996): Mismatch repair defects in human carcinogenesis. Hum Mol Genet 5:1489-1494.
4. 4. Lothe RA (1977): Microsatellite instability in human solid tumors. Mol Med Today 3:61-68.
5. 5. Kolodner R (1996): Biochemistry and genetics of eukaryotic mismatch repair. Genes Dev 19:1433-1442.
6. 6. Baker SM, Bronner CE, Zhang L, Plug AW, Robatzek M, Warren G, Elliott EA, Yu J, Ashley T, Arnheim N, Flavell RA, Liskay M (1995): Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell 82:309-319.
7. 7. Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, Yao X, Christie D-M, Monell C, Arnheim N, Bradley A, Ashley T, Liskay M (1996): Involvement of mouse MIh1 in DNA mismatch repair and meiotic crossing over. Nat Genet 13:336-342.
8. 8. de Wind N, Dekker M, Berns A, Radman M, Riele H (1995): Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination and predisposition to cancer. Cell 82:321-330.
9. 9. Reitmair AH, Schmits R, Ewel A, Bapat B, Redston M, Mitri A, Waterhouse P, Mittrucker HW, Wakeham A, Liu B, Thomason A, Griesser H, Gallinger S, Ballhausen WG, Fishel R, Mak TW (1995): MSH2 deficient mice are viable and susceptible to lymphoid tumors. Nat Genet 11:64-70.
10. 10. Reitmair AH, Redston M, Cai JC, Chuang TCY, Bjerknew M, Cheng H, Hay K, Gallinger S, Bapat B, Mak TW (1996): Spontaneous intestinal carcinomas and skin neoplasms in msh2-deficient mice. Cancer Res 56:3842-3849.
11. 11. Lowsky R, DeCoteau JF, Reitmair AM, Ichinohasama R, Dong W-F, Xu Y, Mak TW, Kadin ME, Minden MD (1997): Defects of the mismatch repair gene MSH2 are implicated in the development of murine and human lymphoblastic lymphomas and are associated with the aberrant expression of rhombotin-2 (Lmo-2) and Tal-1 (SCL). Blood 89:2276-2282.
12. 12. Peng H, Chen G, Du M, Singh N, Isaacson PG, Pan L (1996): Replication error phenotype and p53 gene mutation in lymphomas of mucosa-associated lymphoid tissue. Am J Pathol 148:643-648.
13. 13. Ben-Yehuda D, Krichevsky S, Caspi O, Rund D, Polliack A, Abeliovich D, Zelig O, Yahalom V, Paltiel O, Or R, Peretz T, Ben-Neriah S, Yehuda O, Rachmilewitz EA (1996): Microsatellite instability and p53 mutations in therapy-related leukemia suggest mutator phenotype. Blood 88:4296-4303.
14. 14. Bedi G, Westra WH, Farzadegan H, Pitha PM, Sidransky D (1995): Microsatellite instability in primary neoplasms from HIV+ patients. Nat Med 1:65-68.
15. 15. Wada C, Shionoya S, Fujino Y, Tokuhiro H, Akahoshi T, Uchida T, Ohtani H (1994): Genomic instability of microsatellite repeats and its association with the evolution of chronic myelogenous leukemia. Blood 83:3449-3456.
16. 16. Larson RS, Scott M, McCurley TL, Vnencak-Jones CL (1996): Microsatellite analysis of posttransplant lymphoproliferative disorders: determination of donor/recipient origin and identification of putative lymphomagenic mechanism. Cancer Res 56:4378-4381.
17. 17. Kaneko H, Horike S, Inazawa J, Nakai H, Misawa S (1995): Microsatellite instability is an early event in myelodysplastic syndrome. Blood 86:1236-1237.
18. 18. Hatta Y, Yamada Y, Tomonaga M, Miyoshi I, Said JW, Koeffler HP (1997): Frequent microsatellite instability in acute adult T-cell leukemia (ATL). Proceedings of the American Association for Cancer Research 38: Abstract #1010.
19. 19. Kaneko H, Horiike S, Taniwake M, Misawa S (1996): Microsatellite instability is an early genetic event in myelodysplastic syndrome but is infrequent and not associated with TGF-B receptor type II gene mutation. Leukemia 10:1696-1699.
20. 20. Pabst T, Schwaller, J, Bellomo MJ, Oestreicher M, Muhlematter D, Tichelli A, Tobler A, Fey MF (1996): Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias. Blood 88:1026-1034.
21. 21. Cross NCP, Silly H, Goldman JM (1994): Microsatellite instability in myeloid leukemia. Blood 84:3236-3237.
22. 22. Gartenhaus R, Johns MM III, Wang P, Rai K, Sidransky D (1996): Mutator phenotype in a subset of chronic lymphocytic leukemia. Blood 87:38-41.
23. 23. Indraccolo S, Simon M, Hehlmann R, Erfle V, Chieco-Bianchi L, Leib-Moesch C (1995): Genetic instability of a dinucleotide repeat-rich region in three hematologic malignancies. Leukemia 9:1517-1522.
24. 24. Silly H, Chase A, Mills KI, Apfelbeck U, Sormann S, Goldman JM, Cross NCP (1994): No evidence for microsatellite instability or consistent loss of heterozygosity at selected loci in chronic myeloid leukemia blast crisis. Leukemia 8:1923-1928.
25. 25. Robledo M, Marinez B, Arranz E, Trujillo MJ, Ageitos AG, Rivas C, Benitez J (1995): Genetic instability of microsatellites in hematological neoplasms. Leukemia 9:960-964.
26. 26. Tasaka T, Lee S, Spira S, Takeuchi S, Hatta Y, Nagai M, Takahara J, Koeffler P (1996): Infrequence microsatellite instability during the evolution of the myelodysplastic syndrome to acute myelocytic leukemia. Leuk Res 20:113-117.
27. 27. Volpe F, Gamberi B, Pasture C, Roetto A, Pautasso M, Parvis G, Camaschella C, Mazza U, Saglio G, Gaidano G (1996): Analysis of microsatellite instability in chronic lymphoproliferative disorders. Ann Hematol 72:67-71.
28. 28. Sill H, Goldman JM, Cross NCP (1996): Rarity of microsatellite alterations in acute myeloid leukaemia. Br J Cancer 74:255-257.
29. 29. Gamberi B, Gaidano G, Parsa N, Carbone A, Roncella S, Knowles D, Louie DC, Shibata D, Changanti RSK, Dalla-Favera R (1997): Microsatellite instability is rare in B-cell non-Hodgkin's lymphomas. Blood 89:975-979.
30. 30. Mori N, Takeuchi S, Tasaka T, Lee S, Spira S, Ben-Yehuda D, Mizoguchi M, Schiller G, Koeffler HP (1997): Absence of microsatellite instability during the progression of chronic myelocytic leukemia. Leukemia 11:151-152.
31. 31. Hangaishi A, Ogawa S, Mitani K, Hosaya N, Chiba S, Yazaki Y, Hirai H (1997): Mutations and loss of expression of a mismatch repair gene, hMLH1, in leukemia and lymphoma cell lines. Blood 89:1740-1747.
32. 32. Baccichet A, Benachenhou N, Couture F, Lecler J-M, Sinnett D (1997): Microsatellite instability in childhood T cell acute lymphoblastic leukemia. Leukemia 11:797-802.
33. 33. Sanz GF, Sanz MA (1992): Prognostic factors in myelodysplastic syndromes. Leukemia Res 16:77-86.
34. 34. Hoang J-M, Cottu PH, Thuille B, Salmon RJ, Thomas G, Hamelin R (1997): BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines. Cancer Res 57:300-303.
35. 35. Risinger JI, Umar A, Barrett JC, Kunkel TA (1995): A hPMS2 mutant cell line is defective in strand-specific mismatch repair. J Biol Chem 270:18183-18186.
36. 36. Papadopoulos N, Nicolaides NC, Liu B, Parsons R, Lengauer C, Palombo F, D'Arrigo A, Markowitz S, Willson JWV, Kinzler KW, Jiricny J, Vogelstein B (1995): Mutations of GTBP in genetically unstable cells. Science 268:1915-1917.
37. 37. Risinger JI, Umar A, Boyd J, Berchuck A, Kunkel TA, Barrett JC (1996): Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair. Nat Genet 14:102-105.
38. 38. Rowley JD (1985): Chromosome abnormalities in human leukemia as indicators of mutagenic exposure. Carcinog Compr Surv 10:409-418.
39. 39. Le Beau MM, Albain KS, Larson RA, Vardiman JW, Davis EW, Blough RR, Golomb HM, Rowley JD (1986): Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. J Clin Oncol 4:325-345.
40. 40. Neuman WL, Rubin CM, Rios RB, Larson RA, Le Beau MM, Rowley JD, Vardiman JW, Schwartz JL, Farber RA (1992): Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders. Blood 79:1501-1510.
41. 41. Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, Fujiwars T, Jen J, Kinzler KW, Wyllie AH, Vogelstein B, Dunlop MG (1995): Genetic instability occurs in the majority of young patients with colorectal cancer. Nat Med 1:348-352.
42. 42. Risinger JI, Boyd J (1992): Dinucleotide repeat polymorphism in the human DCC gene at chromosome 18q21. Hum Mol Genet 1:657.
43. 43. Kimpton C, Walton A, Gill P (1992): A further tetranucleotide repeat polymorphism in the vWF gene. Hum Mol Genet 1:287.
44. 44. Rabbitts TH, Boehm T (1991): Structural and functional chimerism results from chromosomal translocation in lymphoid tumors. Adv Immunol 50:119-146.
45. 45. de Klein A, van Kessel AG, Grosveld G, Bartram CR, Hagemaijer A, Bootsma D, Spurr NK, Heisterkamp N, Groffen J, Stephenson JR (1982): A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukemia. Nature 300:765-767.
46. 46. Rabbitts RH (1994): Chromosomal translocations in human cancer. Nature 372:143-149.
47. 47. Marra G, Boland CR (1995): Hereditary nonpolyposis colorectal cancer: the syndrome, the genes and historical perspectives. J Natl Cancer Inst 87:1114-1125.
48. 48. Weber JL, Wong C (1993): Mutation of human short tandem repeats. Hum Mol Genet 2:1123-1128.
49. 49. Datta A, Adijiri A, New L, Crouse GF, Jinks-Robertson S (1996): Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccharomyces cerevisiae. Mol Cell Biol 16:1085-1093.
50. 50. Saparbaev M, Prakash L, Parakash S (1996): Requirement of mismatch repair genes MSH2 and MSH3 in the RAD1-RAD10 pathway of mitotic recombination in Saccharomyces cerevisiae. Genetics 142:727-736.
51. 51. Selva EM, New L, Crouse GF, Lahue RS (1995): Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae. Genetics 139:1175-1188.
52. 52. Inokuchi K, Ikejima M, Watanabe A, Nakajima E, Orimo H, Nomura T, Shimada T (1995): Loss of expression of the human MSH3 gene in hematologic malignancies. Biochem Biophys Res Comm 214:171-179.