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Volumn 14, Issue 5, 2000, Pages 805-810

Allelotype analysis of the myelodysplastic syndrome

Author keywords

Allelotype; Genetic instability; LOH; MDS; Tumor suppressor gene

Indexed keywords

MICROSATELLITE DNA;

EID: 0034051860     PISSN: 08876924     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.leu.2401717     Document Type: Article
Times cited : (13)

References (45)
  • 1
    • 0022791937 scopus 로고
    • Myelodysplastic syndromes (preleukemia)
    • Koeffler HP. Myelodysplastic syndromes (preleukemia). Semin Hematol 1986; 23: 284-299.
    • (1986) Semin Hematol , vol.23 , pp. 284-299
    • Koeffler, H.P.1
  • 4
    • 0026059515 scopus 로고
    • Tumor suppressor genes
    • Marshall CJ. Tumor suppressor genes. Cell 1991; 64: 313-326.
    • (1991) Cell , vol.64 , pp. 313-326
    • Marshall, C.J.1
  • 5
    • 0027225286 scopus 로고
    • Genetic aspects of cancer
    • Plenum Press: New York
    • Goddard AD, Solomon E. Genetic aspects of cancer. In: Advances in Human Genetics. Plenum Press: New York 1993, pp 321-326.
    • (1993) Advances in Human Genetics , pp. 321-326
    • Goddard, A.D.1    Solomon, E.2
  • 6
    • 0029796608 scopus 로고    scopus 로고
    • Polymerase chain reaction-based diagnosis of del 5q in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval
    • Horrigan SK, Westbrook CA, Kim AH, Banerjee M, Stock W, Larson RA. Polymerase chain reaction-based diagnosis of del 5q in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval. Blood 1996; 88: 2665-2670.
    • (1996) Blood , vol.88 , pp. 2665-2670
    • Horrigan, S.K.1    Westbrook, C.A.2    Kim, A.H.3    Banerjee, M.4    Stock, W.5    Larson, R.A.6
  • 9
    • 0028945753 scopus 로고
    • Chromosomal deletions in myelodysplasia
    • Boultwood J, Fidler C. Chromosomal deletions in myelodysplasia. Leuk Lymphoma 1995; 17: 71-78.
    • (1995) Leuk Lymphoma , vol.17 , pp. 71-78
    • Boultwood, J.1    Fidler, C.2
  • 11
    • 0030927835 scopus 로고    scopus 로고
    • Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map
    • Zhao N, Stoffel A, Wang PW, Eisenbart JD, Espinosa R, Larson RA, LeBeau MM. Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map. Proc Natl Acad Sci USA 1997; 94: 6948-6953.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 6948-6953
    • Zhao, N.1    Stoffel, A.2    Wang, P.W.3    Eisenbart, J.D.4    Espinosa, R.5    Larson, R.A.6    Lebeau, M.M.7
  • 12
    • 0026751502 scopus 로고
    • Allelotype of non-small cell lung cacinoma-comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma
    • Tsuchiya E, Nakamura Y, Weng SY, Nakagawa K, Tsuchiya S, Sugano H, Kitagawa T. Allelotype of non-small cell lung cacinoma-comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma. Cancer Res 1992; 52: 2478-2481.
    • (1992) Cancer Res , vol.52 , pp. 2478-2481
    • Tsuchiya, E.1    Nakamura, Y.2    Weng, S.Y.3    Nakagawa, K.4    Tsuchiya, S.5    Sugano, H.6    Kitagawa, T.7
  • 13
    • 0031958714 scopus 로고    scopus 로고
    • Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormality
    • Sankar M, Tanaka K, Kumaravel TS, Arif M, Shintai T, Yagi S, Kyo T, Dohy H, Kamada N. Identification of a commonly deleted region at 17p13.3 in leukemia and lymphoma associated with 17p abnormality. Leukemia 1998; 12: 510-516.
    • (1998) Leukemia , vol.12 , pp. 510-516
    • Sankar, M.1    Tanaka, K.2    Kumaravel, T.S.3    Arif, M.4    Shintai, T.5    Yagi, S.6    Kyo, T.7    Dohy, H.8    Kamada, N.9
  • 14
    • 0026525853 scopus 로고
    • Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders
    • Neuman WL, Rubin CM, Rios RB, Larson RA, Le Beau MM, Rowley JD, Vardiman JW, Schwartz JL, Farber RA. Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders. Blood 1992; 79: 1501-1510.
    • (1992) Blood , vol.79 , pp. 1501-1510
    • Neuman, W.L.1    Rubin, C.M.2    Rios, R.B.3    Larson, R.A.4    Le Beau, M.M.5    Rowley, J.D.6    Vardiman, J.W.7    Schwartz, J.L.8    Farber, R.A.9
  • 18
    • 0028788862 scopus 로고
    • Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer
    • Praml C, Finke LH, Herfarth C, Schlag P, Schwab M, Amler L. Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer. Oncogene 1995; 11: 1357-1362.
    • (1995) Oncogene , vol.11 , pp. 1357-1362
    • Praml, C.1    Finke, L.H.2    Herfarth, C.3    Schlag, P.4    Schwab, M.5    Amler, L.6
  • 19
    • 0028111570 scopus 로고
    • Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas
    • Yeh S-H, Chen P-J, Chen H-L, Lai M-Y, Wang C-C, Chen D-S. Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res 1994; 54: 4188-4192.
    • (1994) Cancer Res , vol.54 , pp. 4188-4192
    • Yeh, S.-H.1    Chen, P.-J.2    Chen, H.-L.3    Lai, M.-Y.4    Wang, C.-C.5    Chen, D.-S.6
  • 20
    • 0029825270 scopus 로고    scopus 로고
    • Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders
    • Asimakopoulos FA, Green AR. Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders. Br J Haematol 1996; 95: 219-226.
    • (1996) Br J Haematol , vol.95 , pp. 219-226
    • Asimakopoulos, F.A.1    Green, A.R.2
  • 21
    • 0028928283 scopus 로고
    • Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of P53 mutations
    • Lai JL, Preudhomme C, Zandecki M, Flactif M, Vanrumbeke M, Lepelley P, Wattel E, Fenaux P. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoiesis and a high incidence of P53 mutations. Leukemia 1995; 9: 370-381.
    • (1995) Leukemia , vol.9 , pp. 370-381
    • Lai, J.L.1    Preudhomme, C.2    Zandecki, M.3    Flactif, M.4    Vanrumbeke, M.5    Lepelley, P.6    Wattel, E.7    Fenaux, P.8
  • 23
    • 0032053793 scopus 로고    scopus 로고
    • Search from mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers
    • Nomoto S, Haruki N, Kondo M, Konishi H, Takahashi T, Takahashi I, Takahashi T. Search from mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers. Cancer Res 1998; 58: 1380-1383.
    • (1998) Cancer Res , vol.58 , pp. 1380-1383
    • Nomoto, S.1    Haruki, N.2    Kondo, M.3    Konishi, H.4    Takahashi, T.5    Takahashi, I.6    Takahashi, T.7
  • 24
    • 0025259643 scopus 로고
    • The locus of the polymorphic epithelial mucin (PEM) tumor antigen on chromosome 1q shows a high frequency of alteration in primary human breast tumors
    • Gedler SJ, Cohen EP, Craston A, Duhig T, Johnstone G, Barnes D. The locus of the polymorphic epithelial mucin (PEM) tumor antigen on chromosome 1q shows a high frequency of alteration in primary human breast tumors. Int J Cancer 1990; 43: 431-435.
    • (1990) Int J Cancer , vol.43 , pp. 431-435
    • Gedler, S.J.1    Cohen, E.P.2    Craston, A.3    Duhig, T.4    Johnstone, G.5    Barnes, D.6
  • 25
    • 0024447257 scopus 로고
    • Loss of heterozygosity on chromosome 1q in human breast cancer
    • Chen LC, Dollbaum C, Smith HS. Loss of heterozygosity on chromosome 1q in human breast cancer. Proc Natl Acad Sci USA 1989; 86: 7204-7207.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 7204-7207
    • Chen, L.C.1    Dollbaum, C.2    Smith, H.S.3
  • 26
    • 0030776977 scopus 로고    scopus 로고
    • Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages
    • Johansson B, Brondum-Nielsen K, Billstrom R, Schiodt I, Mitelman F. Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages. Cancer Genet Cytogenet 1997; 99: 97-101.
    • (1997) Cancer Genet Cytogenet , vol.99 , pp. 97-101
    • Johansson, B.1    Brondum-Nielsen, K.2    Billstrom, R.3    Schiodt, I.4    Mitelman, F.5
  • 34
    • 0027314411 scopus 로고
    • Microsatellite instability in cancer of the proximal colon
    • Thibodeau SN, Bern G, Schaid D. Microsatellite instability in cancer of the proximal colon. Science 1993; 260: 816-819.
    • (1993) Science , vol.260 , pp. 816-819
    • Thibodeau, S.N.1    Bern, G.2    Schaid, D.3
  • 35
    • 0028029122 scopus 로고
    • Microsatellite instability occurs frequently in human gastric carcinoma
    • Rhyu MG, Park WS, Meltzer SJ. Microsatellite instability occurs frequently in human gastric carcinoma. Oncogene 1994; 9: 29-32.
    • (1994) Oncogene , vol.9 , pp. 29-32
    • Rhyu, M.G.1    Park, W.S.2    Meltzer, S.J.3
  • 38
    • 0033566355 scopus 로고    scopus 로고
    • Microsatellite instability and p53 mutations are associated with abnormal expression of the MSH2 gene in adult leukemia
    • Zhu YM, Das-Gupta EP, Russel NH. Microsatellite instability and p53 mutations are associated with abnormal expression of the MSH2 gene in adult leukemia. Blood 1999; 94: 733-740.
    • (1999) Blood , vol.94 , pp. 733-740
    • Zhu, Y.M.1    Das-Gupta, E.P.2    Russel, N.H.3
  • 39
    • 0029997507 scopus 로고    scopus 로고
    • Infrequent microsatellite instability during the evolution of myelodysplastic syndrome to acute myelocytic leukemia
    • Tasaka T, Lee S, Spira S, Takeuchi S, Hatta Y, Nagai M, Takahara J, Koeffler HP. Infrequent microsatellite instability during the evolution of myelodysplastic syndrome to acute myelocytic leukemia. Leukemia Res 1996; 20: 113-117.
    • (1996) Leukemia Res , vol.20 , pp. 113-117
    • Tasaka, T.1    Lee, S.2    Spira, S.3    Takeuchi, S.4    Hatta, Y.5    Nagai, M.6    Takahara, J.7    Koeffler, H.P.8
  • 40
    • 0029798825 scopus 로고    scopus 로고
    • Microsatellite instability is an early genetic event in myelodysplastic syndrome but is infrequent and not associated with TGF-beta receptor type II gene mutation
    • Kaneko H, Horiike S, Taniwaki M, Misawa S. Microsatellite instability is an early genetic event in myelodysplastic syndrome but is infrequent and not associated with TGF-beta receptor type II gene mutation. Leukemia 1996; 10: 1696-1699.
    • (1996) Leukemia , vol.10 , pp. 1696-1699
    • Kaneko, H.1    Horiike, S.2    Taniwaki, M.3    Misawa, S.4
  • 42
    • 0342384391 scopus 로고    scopus 로고
    • Microsatellite instability analysis in human leukemia
    • Ben-Yehuda D. Microsatellite instability analysis in human leukemia. Rev Clin Exp Hematol 1997; 3: 71-79.
    • (1997) Rev Clin Exp Hematol , vol.3 , pp. 71-79
    • Ben-Yehuda, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.