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Volumn 8, Issue 4, 2013, Pages

Spectrum and Risk of Neoplasia in Werner Syndrome: A Systematic Review

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGE DETERMINATION; AGE DISTRIBUTION; AGED; ARTICLE; BONE CANCER; BONE MARROW CANCER; CANCER CLASSIFICATION; CANCER INCIDENCE; CANCER LOCALIZATION; CANCER RISK; CONTROLLED STUDY; DISEASE ASSOCIATION; EPIDEMIOLOGICAL DATA; FEMALE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JAPAN; LEUKEMIA; MAJOR CLINICAL STUDY; MALE; MELANOMA; MENINGIOMA; PRELEUKEMIA; PRIMARY TUMOR; RISK ASSESSMENT; SENSITIVITY ANALYSIS; SOFT TISSUE SARCOMA; STANDARDIZED INCIDENCE RATIO; STANDARDIZED PROPORTIONATE INCIDENCE RATIO; SYSTEMATIC REVIEW; THYROID TUMOR; TISSUE CHARACTERIZATION; WERNER SYNDROME;

EID: 84875673276     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0059709     Document Type: Article
Times cited : (171)

References (35)
  • 1
    • 0013907774 scopus 로고
    • Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process
    • Epstein CJ, Martin GM, Schultz AL, Motulsky AG, (1966) Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine (Baltimore) 45: 177-221.
    • (1966) Medicine (Baltimore) , vol.45 , pp. 177-221
    • Epstein, C.J.1    Martin, G.M.2    Schultz, A.L.3    Motulsky, A.G.4
  • 2
    • 0030691121 scopus 로고    scopus 로고
    • Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing
    • Goto M, (1997) Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing. Mech Ageing Dev 98: 239-254.
    • (1997) Mech Ageing Dev , vol.98 , pp. 239-254
    • Goto, M.1
  • 3
    • 33744990645 scopus 로고    scopus 로고
    • The spectrum of WRN mutations in Werner syndrome patients
    • Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, et al. (2006) The spectrum of WRN mutations in Werner syndrome patients. Hum Mutat 27: 558-567.
    • (2006) Hum Mutat , vol.27 , pp. 558-567
    • Huang, S.1    Lee, L.2    Hanson, N.B.3    Lenaerts, C.4    Hoehn, H.5
  • 4
    • 0034798464 scopus 로고    scopus 로고
    • Cancer pathogenesis in the human RecQ helicase deficiency syndromes
    • Goto M, Miller RW, editors, Tokyo: Japan Scientific Societies Press
    • Monnat RJ Jr (2001) Cancer pathogenesis in the human RecQ helicase deficiency syndromes. In: Goto M, Miller RW, editors. From Premature Gray Hair to Helicase- Werner Syndrome: Implications for Aging and Cancer. Tokyo: Japan Scientific Societies Press. pp. 83-94.
    • (2001) From Premature Gray Hair to Helicase - Werner Syndrome: Implications for Aging and Cancer , pp. 83-94
    • Monnat Jr., R.J.1
  • 7
    • 79151482545 scopus 로고    scopus 로고
    • Volumes I to IX website. Lyon, France: International Agency for Research on Cancer. Available:. Accessed 2012 Jun 19., Available:. Accessed 2012 Jun 19
    • Ferlay J, Parkin DM, Curado MP, Bray F, Edwards B, et al. (2010) Cancer Incidence in Five Continents, Volumes I to IX website. Lyon, France: International Agency for Research on Cancer. Available: http://ci5.iarc.fr. Accessed 2012 Jun 19.
    • (2010) Cancer Incidence in Five Continents
    • Ferlay, J.1    Parkin, D.M.2    Curado, M.P.3    Bray, F.4    Edwards, B.5
  • 12
    • 0344867894 scopus 로고    scopus 로고
    • Prevalence of Werner's syndrome heterozygotes in Japan
    • Satoh M, Imai M, Sugimoto M, Goto M, Furuichi Y, (1999) Prevalence of Werner's syndrome heterozygotes in Japan. Lancet 353: 1766.
    • (1999) Lancet , vol.353 , pp. 1766
    • Satoh, M.1    Imai, M.2    Sugimoto, M.3    Goto, M.4    Furuichi, Y.5
  • 15
    • 0033566689 scopus 로고    scopus 로고
    • Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race
    • Monnat RJ Jr, (1999) Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race. Cancer 86: 728-729.
    • (1999) Cancer , vol.86 , pp. 728-729
    • Monnat Jr, R.J.1
  • 16
    • 78649467087 scopus 로고    scopus 로고
    • Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology
    • Monnat RJ Jr, (2010) Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology. Semin Cancer Biol 20: 329-339.
    • (2010) Semin Cancer Biol , vol.20 , pp. 329-339
    • Monnat Jr, R.J.1
  • 17
    • 0025169778 scopus 로고
    • Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients
    • Fukuchi K, Tanaka K, Kumahara Y, Marumo K, Pride MB, et al. (1990) Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients. Hum Genet 84: 249-252.
    • (1990) Hum Genet , vol.84 , pp. 249-252
    • Fukuchi, K.1    Tanaka, K.2    Kumahara, Y.3    Marumo, K.4    Pride, M.B.5
  • 19
    • 0034194139 scopus 로고    scopus 로고
    • Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes
    • Moser MJ, Bigbee WL, Grant SG, Emond MJ, Langlois RG, et al. (2000) Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes. Cancer Res 60: 2492-2496.
    • (2000) Cancer Res , vol.60 , pp. 2492-2496
    • Moser, M.J.1    Bigbee, W.L.2    Grant, S.G.3    Emond, M.J.4    Langlois, R.G.5
  • 20
    • 78649475037 scopus 로고    scopus 로고
    • Werner syndrome as a model of human aging
    • Conn PM, editor, Amsterdam: Elsevier Academic Press
    • Monnat RJ Jr (2006) Werner syndrome as a model of human aging. In: Conn PM, editor. Handbook of Models for Human Aging. Amsterdam: Elsevier Academic Press. pp. 961-976.
    • (2006) Handbook of Models for Human Aging , pp. 961-976
    • Monnat Jr., R.J.1
  • 21
    • 22144495071 scopus 로고    scopus 로고
    • Severe toxicity following induction chemotherapy for acute myelogenous leukemia in a patient with Werner's syndrome
    • Seiter K, Qureshi A, Liu D, Galvin-Parton P, Arshad M, et al. (2005) Severe toxicity following induction chemotherapy for acute myelogenous leukemia in a patient with Werner's syndrome. Leuk Lymphoma 46: 1091-1095.
    • (2005) Leuk Lymphoma , vol.46 , pp. 1091-1095
    • Seiter, K.1    Qureshi, A.2    Liu, D.3    Galvin-Parton, P.4    Arshad, M.5
  • 22
    • 0019950535 scopus 로고
    • Organ site specificity for cancer in chromosomal instability disorders
    • Feinberg AP, Coffey DS, (1982) Organ site specificity for cancer in chromosomal instability disorders. Cancer Res 42: 3252-3254.
    • (1982) Cancer Res , vol.42 , pp. 3252-3254
    • Feinberg, A.P.1    Coffey, D.S.2
  • 23
    • 0031052108 scopus 로고    scopus 로고
    • Bloom's syndrome: XX. The first 100 cancers
    • German J, (1997) Bloom's syndrome: XX. The first 100 cancers. Cytogenet Cell Genet 93: 100-106.
    • (1997) Cytogenet Cell Genet , vol.93 , pp. 100-106
    • German, J.1
  • 24
    • 0038288850 scopus 로고    scopus 로고
    • Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome
    • Wang LL, Gannavarapu A, Kozinetz CA, Levy ML, Lewis RA, et al. (2003) Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. J Natl Cancer Inst 95: 669-674.
    • (2003) J Natl Cancer Inst , vol.95 , pp. 669-674
    • Wang, L.L.1    Gannavarapu, A.2    Kozinetz, C.A.3    Levy, M.L.4    Lewis, R.A.5
  • 26
    • 0032480248 scopus 로고    scopus 로고
    • Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome
    • Birch JM, Blair V, Kelsey AM, Evans DG, Harris M, et al. (1998) Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome. Oncogene 17: 1061-1068.
    • (1998) Oncogene , vol.17 , pp. 1061-1068
    • Birch, J.M.1    Blair, V.2    Kelsey, A.M.3    Evans, D.G.4    Harris, M.5
  • 27
    • 0035797528 scopus 로고    scopus 로고
    • Relative frequency and morphology of cancers in carriers of germline TP53 mutations
    • Birch JM, Alston RD, McNally RJ, Evans DG, Kelsey AM, et al. (2001) Relative frequency and morphology of cancers in carriers of germline TP53 mutations. Oncogene 20: 4621-4628.
    • (2001) Oncogene , vol.20 , pp. 4621-4628
    • Birch, J.M.1    Alston, R.D.2    McNally, R.J.3    Evans, D.G.4    Kelsey, A.M.5
  • 28
    • 0037439356 scopus 로고    scopus 로고
    • Cancer in Fanconi anemia, 1927-2001
    • Alter BP, (2003) Cancer in Fanconi anemia, 1927-2001. Cancer 97: 425-440.
    • (2003) Cancer , vol.97 , pp. 425-440
    • Alter, B.P.1
  • 29
    • 0037306904 scopus 로고    scopus 로고
    • Cancer incidence in persons with Fanconi anemia
    • Rosenberg PS, Greene MH, Alter BP, (2003) Cancer incidence in persons with Fanconi anemia. Blood 101: 822-826.
    • (2003) Blood , vol.101 , pp. 822-826
    • Rosenberg, P.S.1    Greene, M.H.2    Alter, B.P.3
  • 31
    • 84860338982 scopus 로고    scopus 로고
    • Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry
    • Vlachos A, Rosenberg PS, Atsidaftos E, Alter BP, Lipton JM, (2012) Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry. Blood 119: 3815-3819.
    • (2012) Blood , vol.119 , pp. 3815-3819
    • Vlachos, A.1    Rosenberg, P.S.2    Atsidaftos, E.3    Alter, B.P.4    Lipton, J.M.5
  • 32
    • 59049102893 scopus 로고    scopus 로고
    • Shwachman-Diamond syndrome: implications for understanding the molecular basis of leukaemia
    • Dror Y, (2008) Shwachman-Diamond syndrome: implications for understanding the molecular basis of leukaemia. Expert Rev Mol Med 10: e38.
    • (2008) Expert Rev Mol Med , vol.10
    • Dror, Y.1
  • 33
    • 79851504903 scopus 로고    scopus 로고
    • Clinical spectrum and molecular pathophysiology of Shwachman-Diamond syndrome
    • Huang J, Shimamura A, (2011) Clinical spectrum and molecular pathophysiology of Shwachman-Diamond syndrome. Curr Opin Hematol 18: 30-35.
    • (2011) Curr Opin Hematol , vol.18 , pp. 30-35
    • Huang, J.1    Shimamura, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.