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Volumn 95, Issue 9, 2000, Pages 2937-2942

Loss of heterozygosity on 10q and microsatellite instability in advanced stages of primary cutaneous T-cell lymphoma and possible association with homozygous deletion of PTEN

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EID: 0034193127     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v95.9.2937.009k15_2937_2942     Document Type: Article
Times cited : (113)

References (37)
  • 1
    • 0030904865 scopus 로고    scopus 로고
    • Recurring structural chromosomal abnormalities in peripheral blood lymphocytes of patients with mycosis fungoides/Sezary syndrome
    • Thangavelu M, Finn WG, Yelavarthi KK, et al. Recurring structural chromosomal abnormalities in peripheral blood lymphocytes of patients with mycosis fungoides/Sezary syndrome. Blood 1997; 89:3371.
    • (1997) Blood , vol.89 , pp. 3371
    • Thangavelu, M.1    Finn, W.G.2    Yelavarthi, K.K.3
  • 2
    • 0031022652 scopus 로고    scopus 로고
    • Chromosomal abnormalities in cutaneous T-cell lymphoma and in its premalignant conditions as detected by G-banding and interphase cytogenetic methods
    • Karenko L, Hyytinen E, Sarna S, Ranki A. Chromosomal abnormalities in cutaneous T-cell lymphoma and in its premalignant conditions as detected by G-banding and interphase cytogenetic methods. J Invest Dermatol. 1997;108:22.
    • (1997) J Invest Dermatol. , vol.108 , pp. 22
    • Karenko, L.1    Hyytinen, E.2    Sarna, S.3    Ranki, A.4
  • 3
    • 0029154840 scopus 로고
    • Chromosome aberrations, spontaneous SCE and growth kinetics in PHA-stimulated lymphocytes in 5 cases of Sezary syndrome
    • Limon J. Nedoszytko B, Brozek I, et al. Chromosome aberrations, spontaneous SCE and growth kinetics in PHA-stimulated lymphocytes in 5 cases of Sezary syndrome. Cancer Genet Cytogenet. 1995;83:75.
    • (1995) Cancer Genet Cytogenet. , vol.83 , pp. 75
    • Limon, J.1    Nedoszytko, B.2    Brozek, I.3
  • 4
    • 0032978535 scopus 로고    scopus 로고
    • Notable losses at specific regions of chromosome 10q and 13q in the Sezary syndrome detected by comparative genomic hybridization
    • Karenko L, Kahkonen M, Hyytinen E, Lindlof M, Ranki A. Notable losses at specific regions of chromosome 10q and 13q in the Sezary syndrome detected by comparative genomic hybridization. J Invest Dermatol. 1999;112:392.
    • (1999) J Invest Dermatol. , vol.112 , pp. 392
    • Karenko, L.1    Kahkonen, M.2    Hyytinen, E.3    Lindlof, M.4    Ranki, A.5
  • 5
    • 0028176731 scopus 로고
    • Bcl-2 protein expression and correlation with the inter-chromosomal 14;18 translocation in cutaneous lymphoma and pseudolymphoma
    • Cerroni L, Volkenandt M, Reiger E, Soyer P, Kerl H. Bcl-2 protein expression and correlation with the inter-chromosomal 14;18 translocation in cutaneous lymphoma and pseudolymphoma. J Invest Dermatol. 1994;102:231.
    • (1994) J Invest Dermatol. , vol.102 , pp. 231
    • Cerroni, L.1    Volkenandt, M.2    Reiger, E.3    Soyer, P.4    Kerl, H.5
  • 6
    • 0029918674 scopus 로고    scopus 로고
    • The t(2;5) chromosomal translocation is not a common feature of primary cutaneous CD30 + lymphoproliferative disorders: Comparison with anaplastic large-cell lymphoma of nodal origin
    • DeCoteau JF, Butmarc JR, Kinney MC, Kadin ME. The t(2;5) chromosomal translocation is not a common feature of primary cutaneous CD30 + lymphoproliferative disorders: comparison with anaplastic large-cell lymphoma of nodal origin. Blood. 1996;87:3437.
    • (1996) Blood , vol.87 , pp. 3437
    • DeCoteau, J.F.1    Butmarc, J.R.2    Kinney, M.C.3    Kadin, M.E.4
  • 9
    • 0033052124 scopus 로고    scopus 로고
    • Spectrum of p53 gene mutations suggests a possible role for ultraviolet radiation in the pathogenesis of advanced cutaneous lymphomas
    • McGregor JM, Crook T, Fraser-Andrews EA, Rozycka M, Crossland S, Whittaker SJ. Spectrum of p53 gene mutations suggests a possible role for ultraviolet radiation in the pathogenesis of advanced cutaneous lymphomas. J Invest Dermatol. 1999;112:317
    • (1999) J Invest Dermatol. , vol.112 , pp. 317
    • McGregor, J.M.1    Crook, T.2    Fraser-Andrews, E.A.3    Rozycka, M.4    Crossland, S.5    Whittaker, S.J.6
  • 10
    • 0030001775 scopus 로고    scopus 로고
    • Analysis of p53 and mdm-2 expression in 18 patients with Sezary syndrome
    • Marks DI, Vonderheid EC, Kurz BW, et al. Analysis of p53 and mdm-2 expression in 18 patients with Sezary syndrome. Br J Haematol 92:890, 1996.
    • (1996) Br J Haematol , vol.92 , pp. 890
    • Marks, D.I.1    Vonderheid, E.C.2    Kurz, B.W.3
  • 11
    • 0026551169 scopus 로고
    • A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T-cell acute lymphoblastic leukemia
    • Park JK, Le Beau MM, Shows TB, Rowley JD, Diaz MO. A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer. 1992;4:32.
    • (1992) Genes Chromosomes Cancer , vol.4 , pp. 32
    • Park, J.K.1    Le Beau, M.M.2    Shows, T.B.3    Rowley, J.D.4    Diaz, M.O.5
  • 13
    • 0032402201 scopus 로고    scopus 로고
    • Deletions in the long arm of chromosome 10 in lymphomas with t(14:18): A pathogenetic role of the tumour suppressor genes PTEN/MMAC1 and MXI1?
    • Siebert R, Gesk S, Harder S, et al. Deletions in the long arm of chromosome 10 in lymphomas with t(14:18): a pathogenetic role of the tumour suppressor genes PTEN/MMAC1 and MXI1? [letter] Blood. 1998;92:4487.
    • (1998) Blood , vol.92 , pp. 4487
    • Siebert, R.1    Gesk, S.2    Harder, S.3
  • 14
    • 0031004088 scopus 로고    scopus 로고
    • Germline mutations ol the PTEN gene in Cowden's disease, an inherited breast and thyroid cancer syndrome
    • Liaw D, Marsh DJ, Li J, et al. Germline mutations ol the PTEN gene in Cowden's disease, an inherited breast and thyroid cancer syndrome. Nat Genet. 1997;16:64.
    • (1997) Nat Genet. , vol.16 , pp. 64
    • Liaw, D.1    Marsh, D.J.2    Li, J.3
  • 15
    • 0030936323 scopus 로고    scopus 로고
    • PTEN, a putative protein tyrosine phosphatase mutated in human brain, breast and prostate cancer
    • Li J, Yen C, Liaw D, et al. PTEN, a putative protein tyrosine phosphatase mutated in human brain, breast and prostate cancer. Science. 1997; 275:1943.
    • (1997) Science , vol.275 , pp. 1943
    • Li, J.1    Yen, C.2    Liaw, D.3
  • 17
  • 19
    • 13144249184 scopus 로고    scopus 로고
    • High cancer susceptibility and embryonic lethality associated with mutation of the PTEN tumour suppressor gene in mice
    • Suzuki A, Pompa JL, Stambolic V, et al. High cancer susceptibility and embryonic lethality associated with mutation of the PTEN tumour suppressor gene in mice. Curr Biol. 1998;8:1169.
    • (1998) Curr Biol. , vol.8 , pp. 1169
    • Suzuki, A.1    Pompa, J.L.2    Stambolic, V.3
  • 20
    • 0029916642 scopus 로고    scopus 로고
    • Genomic organization of human MXI1, a putative tumor suppressor gene
    • Wechsler DS, Shelly CA, Dang CV. Genomic organization of human MXI1, a putative tumor suppressor gene. Genomics. 1996;32:466.
    • (1996) Genomics , vol.32 , pp. 466
    • Wechsler, D.S.1    Shelly, C.A.2    Dang, C.V.3
  • 21
    • 0343989421 scopus 로고    scopus 로고
    • DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1
    • Mollenhauer J, Wiemann S, Scheurlen W, et al. DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1. Nat Genet. 1997; 15:356.
    • (1997) Nat Genet. , vol.15 , pp. 356
    • Mollenhauer, J.1    Wiemann, S.2    Scheurlen, W.3
  • 22
    • 0027158031 scopus 로고
    • Clues to the pathogenesis of familial colorectal cancer
    • Aaltonen LA, Peltomaki P, Leach FS, et al. Clues to the pathogenesis of familial colorectal cancer. Science. 1993;260:812.
    • (1993) Science , vol.260 , pp. 812
    • Aaltonen, L.A.1    Peltomaki, P.2    Leach, F.S.3
  • 23
    • 0028362315 scopus 로고
    • Instability of short tandem repeats (microsatellites) in human cancers
    • Wooster R, Cleton-Jansen A-M, Collins N, et al. Instability of short tandem repeats (microsatellites) in human cancers. Nat Genet. 1994;6:152.
    • (1994) Nat Genet. , vol.6 , pp. 152
    • Wooster, R.1    Cleton-Jansen, A.-M.2    Collins, N.3
  • 24
    • 0030041822 scopus 로고    scopus 로고
    • Replication error phenotype and p53 gene mutation in lymphomas of mucosa-associated lymphoid tissue
    • Peng H, Chen G, Du M, Singh N, Isaacson PG, Pan L. Replication error phenotype and p53 gene mutation in lymphomas of mucosa-associated lymphoid tissue. Am J Pathol. 1996;148: 643.
    • (1996) Am J Pathol. , vol.148 , pp. 643
    • Peng, H.1    Chen, G.2    Du, M.3    Singh, N.4    Isaacson, P.G.5    Pan, L.6
  • 26
    • 0030948472 scopus 로고    scopus 로고
    • Microsatellite instability is rare in B-cell non-Hodgkin's lymphomas
    • Gamberi B, Gaidano G, Parsa N, et al. Microsatellite instability is rare in B-cell non-Hodgkin's lymphomas. Blood. 1997;89:975.
    • (1997) Blood , vol.89 , pp. 975
    • Gamberi, B.1    Gaidano, G.2    Parsa, N.3
  • 27
    • 0033015405 scopus 로고    scopus 로고
    • Microsatellite instability as a potential marker for poor prognosis in adult T cell leukemia/lymphoma
    • Hayami Y, Komatsu H, Iida S, et al. Microsatellite instability as a potential marker for poor prognosis in adult T cell leukemia/lymphoma. Leuk Lymphoma. 1999;32:345.
    • (1999) Leuk Lymphoma , vol.32 , pp. 345
    • Hayami, Y.1    Komatsu, H.2    Iida, S.3
  • 28
    • 0026355129 scopus 로고
    • Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndrome
    • Whittaker SJ, Smith NP, Russell-Jones R, Luzzatlo L. Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndrome. Cancer. 1991;68:1572.
    • (1991) Cancer , vol.68 , pp. 1572
    • Whittaker, S.J.1    Smith, N.P.2    Russell-Jones, R.3    Luzzatlo, L.4
  • 29
    • 0029898239 scopus 로고    scopus 로고
    • T-cell receptor gene analysis in cutaneous T-cell lymphomas
    • Whittaker SJ. T-cell receptor gene analysis in cutaneous T-cell lymphomas. Clin Exp Dermatol. 1997;21:81.
    • (1997) Clin Exp Dermatol. , vol.21 , pp. 81
    • Whittaker, S.J.1
  • 30
    • 0028231090 scopus 로고
    • The 1993-4 genethon human genetic linkage map
    • Gyapay G, Morissette J, Vignal A, et al. The 1993-4 Genethon Human Genetic Linkage Map. Nat Genet. 1994;7:246.
    • (1994) Nat Genet. , vol.7 , pp. 246
    • Gyapay, G.1    Morissette, J.2    Vignal, A.3
  • 31
    • 0032534069 scopus 로고    scopus 로고
    • A national cancer institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
    • Boland CR, Thibodeau SN, Hamilton SR, et al. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res. 1998;58: 5248.
    • (1998) Cancer Res. , vol.58 , pp. 5248
    • Boland, C.R.1    Thibodeau, S.N.2    Hamilton, S.R.3
  • 32
    • 15444349266 scopus 로고    scopus 로고
    • Frequent Inactivation of PTEN/MMAC1 in primary prostate cancer
    • Cairns P, Okami K, Halachmi S, et al. Frequent Inactivation of PTEN/MMAC1 in primary prostate cancer. Cancer Res. 1997;57:4997.
    • (1997) Cancer Res. , vol.57 , pp. 4997
    • Cairns, P.1    Okami, K.2    Halachmi, S.3
  • 33
    • 0029091503 scopus 로고
    • Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
    • Cairns P, Polascik TJ, Eby Y, et al. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet. 1995;11:210.
    • (1995) Nat Genet. , vol.11 , pp. 210
    • Cairns, P.1    Polascik, T.J.2    Eby, Y.3
  • 34
    • 0032800305 scopus 로고    scopus 로고
    • TCR gene analysis in the diagnosis of Sézary syndrome
    • Russell-Jones R, Whittaker SJ. TCR gene analysis in the diagnosis of Sézary syndrome. J Am Acad Dermatol. 1999;41:254.
    • (1999) J Am Acad Dermatol. , vol.41 , pp. 254
    • Russell-Jones, R.1    Whittaker, S.J.2
  • 35
    • 8544237725 scopus 로고    scopus 로고
    • Frequent loss of heterozygosity on chromosome 10q in muscle-invasive transitional cell carcinomas
    • Cappellen D, Medina S, Chopin D, Thiery JP, Radvanyi F. Frequent loss of heterozygosity on chromosome 10q in muscle-invasive transitional cell carcinomas. Oncogens. 1997;14: 3059.
    • (1997) Oncogens , vol.14 , pp. 3059
    • Cappellen, D.1    Medina, S.2    Chopin, D.3    Thiery, J.P.4    Radvanyi, F.5
  • 36
    • 0031964326 scopus 로고    scopus 로고
    • Allelic loss on chromosome 1 p is associated with progression and lymph node metastasis of primary breast carcinoma
    • Tsukamoto K, Noriko I, Yoshimoto M, et al. Allelic loss on chromosome 1 p is associated with progression and lymph node metastasis of primary breast carcinoma. Cancer. 1998;82: 317.
    • (1998) Cancer , vol.82 , pp. 317
    • Tsukamoto, K.1    Noriko, I.2    Yoshimoto, M.3
  • 37
    • 9844228503 scopus 로고    scopus 로고
    • Identification of allelic losses in benign, borderline, and invasive epilhelial ovarian tumors and correlation with clinical outcome
    • Saretzki G, Hoffmann U, Rohlke P, et al. Identification of allelic losses in benign, borderline, and invasive epilhelial ovarian tumors and correlation with clinical outcome. Cancer. 1997;80: 1241.
    • (1997) Cancer , vol.80 , pp. 1241
    • Saretzki, G.1    Hoffmann, U.2    Rohlke, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.