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Volumn 81, Issue 961, 2008, Pages 51-58

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATAXIA TELANGIECTASIA; CELL CULTURE; COCKAYNE SYNDROME; CONTROLLED STUDY; DATA ANALYSIS; FIBROBLAST; HUMAN; HUMAN CELL; IONIZING RADIATION; PHENOTYPE; RADIOSENSITIVITY; SUN EXPOSURE; XERODERMA PIGMENTOSUM; CELL LINE; CELL SURVIVAL; DOSE RESPONSE; GAMMA RADIATION; PATHOLOGY; RADIATION DOSE; RADIATION EXPOSURE;

EID: 38449094426     PISSN: 00071285     EISSN: None     Source Type: Journal    
DOI: 10.1259/bjr/27072321     Document Type: Article
Times cited : (17)

References (50)
  • 1
    • 85057506870 scopus 로고    scopus 로고
    • Xeroderma pigmentosum, cockayne syndrome and trichothiodystrophy: Sun sensitivity, DNA repair defects and skin cancer
    • Eeles R, Ponder B, Easton DF, Horwich EA, editors, London, UK: Arnold;
    • Arlett CF, Lehmann AR. Xeroderma pigmentosum, cockayne syndrome and trichothiodystrophy: sun sensitivity, DNA repair defects and skin cancer. In Eeles R, Ponder B, Easton DF, Horwich EA, editors. Genetic predisposition to Cancer. London, UK: Arnold; 2004: 214-31.
    • (2004) Genetic predisposition to Cancer , pp. 214-231
    • Arlett, C.F.1    Lehmann, A.R.2
  • 2
    • 0034332704 scopus 로고    scopus 로고
    • Four radiation hypersensitivity cases and their implications for clinical radiotherapy
    • Rogers PB, Plowman PN, Harris SJ, Arlett CF. Four radiation hypersensitivity cases and their implications for clinical radiotherapy. Radiother Oncol 2000;57:143-54.
    • (2000) Radiother Oncol , vol.57 , pp. 143-154
    • Rogers, P.B.1    Plowman, P.N.2    Harris, S.J.3    Arlett, C.F.4
  • 4
    • 0042552984 scopus 로고
    • Defective repair of γ-irradiated DNA in a case of xeroderma pigmentosum
    • Mikhelson VM. Defective repair of γ-irradiated DNA in a case of xeroderma pigmentosum. Fort Onkol 1979;4:157-70.
    • (1979) Fort Onkol , vol.4 , pp. 157-170
    • Mikhelson, V.M.1
  • 5
    • 34347092151 scopus 로고
    • Uber Strahlenempfindlichkeit bei xeroderma pigmentosum (Untersuchungen an einem weiteren fall).
    • Martenstein H, Bobowitcz A. Uber Strahlenempfindlichkeit bei xeroderma pigmentosum (Untersuchungen an einem weiteren fall). Arch Dermatol Syph 1926;150:165-76.
    • (1926) Arch Dermatol Syph , vol.150 , pp. 165-176
    • Martenstein, H.1    Bobowitcz, A.2
  • 6
    • 38549142957 scopus 로고
    • a bor sugarerzekenysegehez xeroderma pigmentosum-nal.
    • Heiner L. Adatok a bor sugarerzekenysegehez xeroderma pigmentosum-nal. Orvosi Hetilap 1925;69:540-2.
    • (1925) Orvosi Hetilap , vol.69 , pp. 540-542
    • Adatok, H.L.1
  • 9
    • 0030768038 scopus 로고    scopus 로고
    • Nucleotide excision repair in mammalian cells
    • Wood RD. Nucleotide excision repair in mammalian cells. J Biol Chem 1997;272:23465-8.
    • (1997) J Biol Chem , vol.272 , pp. 23465-23468
    • Wood, R.D.1
  • 10
    • 0033578040 scopus 로고    scopus 로고
    • The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta
    • Masutani C, Kusumoto R, Yamada A, Dohmae N, Yokoi M, Yuasa M, et al. The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta. Nature 1999;399:700-4.
    • (1999) Nature , vol.399 , pp. 700-704
    • Masutani, C.1    Kusumoto, R.2    Yamada, A.3    Dohmae, N.4    Yokoi, M.5    Yuasa, M.6
  • 11
    • 14544287434 scopus 로고    scopus 로고
    • Replication of damaged DNA by translesion synthesis in human cells
    • Lehmann AR. Replication of damaged DNA by translesion synthesis in human cells. FEBS Lett 2005;579:873-6.
    • (2005) FEBS Lett , vol.579 , pp. 873-876
    • Lehmann, A.R.1
  • 12
    • 0019168178 scopus 로고
    • Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation
    • Arlett CF, Harcourt SA, Lehmann AR, Stevens S, Ferguson-Smith MA, Morley WN. Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation. Carcinogenesis 1980;1:745-51.
    • (1980) Carcinogenesis , vol.1 , pp. 745-751
    • Arlett, C.F.1    Harcourt, S.A.2    Lehmann, A.R.3    Stevens, S.4    Ferguson-Smith, M.A.5    Morley, W.N.6
  • 13
    • 0016024730 scopus 로고    scopus 로고
    • Mikhelson VM, Aikazian EV, Center EI, Pleskach NM. Increased sensitivity of human cells to ionizing radiation in one of the forms of the hereditary disease xeroderma pigmentosum (a study of single-stranded DNA breaks and chromosomal aberrations). Tsitologiia 1974;16:203-10.
    • Mikhelson VM, Aikazian EV, Center EI, Pleskach NM. Increased sensitivity of human cells to ionizing radiation in one of the forms of the hereditary disease xeroderma pigmentosum (a study of single-stranded DNA breaks and chromosomal aberrations). Tsitologiia 1974;16:203-10.
  • 14
    • 0022065327 scopus 로고
    • Occurrence and elimination of single- and double-strand DNA breaks in the fibroblasts of xeroderma pigmentosum patients exposed to gamma radiation
    • Mikhelson VM, Pleskach NM, Prokofeva VV. Occurrence and elimination of single- and double-strand DNA breaks in the fibroblasts of xeroderma pigmentosum patients exposed to gamma radiation. Tsitologiia 1985;27:592-8.
    • (1985) Tsitologiia , vol.27 , pp. 592-598
    • Mikhelson, V.M.1    Pleskach, N.M.2    Prokofeva, V.V.3
  • 15
    • 0026344254 scopus 로고
    • Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition
    • Price FM, Parshad R, Tarone RE, Sanford KK. Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition. Cancer Genet Cytogenet 1991;57:1-10.
    • (1991) Cancer Genet Cytogenet , vol.57 , pp. 1-10
    • Price, F.M.1    Parshad, R.2    Tarone, R.E.3    Sanford, K.K.4
  • 18
    • 0031751372 scopus 로고    scopus 로고
    • Xeroderma pigmentosum: Spinal cord astrocytoma with 9 year survival after radiation and isotretinoin therapy
    • Di Giovanna JJ, Patronas N, Katz D, Abangan D, Kraemer KH. Xeroderma pigmentosum: spinal cord astrocytoma with 9 year survival after radiation and isotretinoin therapy. J Cutan Med Surg 1998;2:153-8.
    • (1998) J Cutan Med Surg , vol.2 , pp. 153-158
    • Di Giovanna, J.J.1    Patronas, N.2    Katz, D.3    Abangan, D.4    Kraemer, K.H.5
  • 19
    • 0032957045 scopus 로고    scopus 로고
    • Molecular analysis of glioma and skin-tumour alterations in a xeroderma-pigmentsum child
    • Giglia G, Bouffet E, Jouvet A, Ohgaki H, Kleihues P, Sarasin A. Molecular analysis of glioma and skin-tumour alterations in a xeroderma-pigmentsum child. Int J Cancer 1999;81:345-50.
    • (1999) Int J Cancer , vol.81 , pp. 345-350
    • Giglia, G.1    Bouffet, E.2    Jouvet, A.3    Ohgaki, H.4    Kleihues, P.5    Sarasin, A.6
  • 20
    • 0021337531 scopus 로고
    • Abnormal sensitivity of some Cockayne's syndrome cell strains to UV- and gamma-rays. Association with a reduced ability to repair potentially lethal damage
    • Deschavanne PJ, Chavaudra N, Fertil B, Malaise EP. Abnormal sensitivity of some Cockayne's syndrome cell strains to UV- and gamma-rays. Association with a reduced ability to repair potentially lethal damage. Mutat Res 1984;131:61-70.
    • (1984) Mutat Res , vol.131 , pp. 61-70
    • Deschavanne, P.J.1    Chavaudra, N.2    Fertil, B.3    Malaise, E.P.4
  • 21
    • 0942268166 scopus 로고    scopus 로고
    • DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
    • Lehmann AR. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. Biochimie 2003;85:1101-11.
    • (2003) Biochimie , vol.85 , pp. 1101-1111
    • Lehmann, A.R.1
  • 23
    • 24044438505 scopus 로고    scopus 로고
    • Transcription-coupled repair: A complex affair
    • Mellon I. Transcription-coupled repair: A complex affair. Mutat Res 2005;577:155-61.
    • (2005) Mutat Res , vol.577 , pp. 155-161
    • Mellon, I.1
  • 25
    • 0035824601 scopus 로고    scopus 로고
    • The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA
    • Tuo J, Muftuoglu M, Chen C, Jaruga P, Selzer RR, Brosh RM, et al. The Cockayne Syndrome group B gene product is involved in general genome base excision repair of 8-hydroxyguanine in DNA. J Biol Chem 2001;276:45772-9.
    • (2001) J Biol Chem , vol.276 , pp. 45772-45779
    • Tuo, J.1    Muftuoglu, M.2    Chen, C.3    Jaruga, P.4    Selzer, R.R.5    Brosh, R.M.6
  • 26
  • 27
    • 0026079289 scopus 로고
    • Comparative human cellular radiosensitivity: III. Gamma-radiation survival of cultured skin fibroblasts and resting T-lymphocytes from the peripheral blood of the same individual
    • Green MHL, Arlett CF, Cole J, Harcourt SA, Priestley A, Waugh APW, et al. Comparative human cellular radiosensitivity: III. Gamma-radiation survival of cultured skin fibroblasts and resting T-lymphocytes from the peripheral blood of the same individual. Int J Radiat Biol 1991;59:749-65.
    • (1991) Int J Radiat Biol , vol.59 , pp. 749-765
    • Green, M.H.L.1    Arlett, C.F.2    Cole, J.3    Harcourt, S.A.4    Priestley, A.5    Waugh, A.P.W.6
  • 28
    • 0018837288 scopus 로고
    • Survey of radio -sensitivity in a variety of human cell strains
    • Arlett CF, Harcourt SA. Survey of radio -sensitivity in a variety of human cell strains. Cancer Res 1980;40:926-32.
    • (1980) Cancer Res , vol.40 , pp. 926-932
    • Arlett, C.F.1    Harcourt, S.A.2
  • 29
    • 0023757362 scopus 로고
    • Comparative human cellular radiosensitivity: I. The effect of SV40 immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotes
    • Arlett CF, Green MHL, Priestley A, Harcourt SA, Mayne LV. Comparative human cellular radiosensitivity: I. The effect of SV40 immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotes. Int J Radiat Biol 1988;54:911-28.
    • (1988) Int J Radiat Biol , vol.54 , pp. 911-928
    • Arlett, C.F.1    Green, M.H.L.2    Priestley, A.3    Harcourt, S.A.4    Mayne, L.V.5
  • 30
    • 17344362697 scopus 로고    scopus 로고
    • ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: Expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer
    • Stankovic T, Kidd AMJ, Sutcliffe A, McGuire GM, Robinson P, Weber P, et al. ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer. Am J Hum Genet 1998;62:334-45.
    • (1998) Am J Hum Genet , vol.62 , pp. 334-345
    • Stankovic, T.1    Kidd, A.M.J.2    Sutcliffe, A.3    McGuire, G.M.4    Robinson, P.5    Weber, P.6
  • 32
    • 0022470541 scopus 로고
    • Radioresistant DNA synthesis in cells of patients showing increased chromosomal sensitivity to ionizing radiation
    • Barenfeld LS, Pleskach NM, Bildin VN, Prokofjeva VV, Mikhelson VM. Radioresistant DNA synthesis in cells of patients showing increased chromosomal sensitivity to ionizing radiation. Mutat Res 1986;165:159-64.
    • (1986) Mutat Res , vol.165 , pp. 159-164
    • Barenfeld, L.S.1    Pleskach, N.M.2    Bildin, V.N.3    Prokofjeva, V.V.4    Mikhelson, V.M.5
  • 33
    • 0007483056 scopus 로고
    • Human cellular radiosensitivity - the search for the holy grail or a poisoned chalice
    • Arlett CF. Human cellular radiosensitivity - the search for the holy grail or a poisoned chalice. Adv Radiat Biol 1992;16:273-92.
    • (1992) Adv Radiat Biol , vol.16 , pp. 273-292
    • Arlett, C.F.1
  • 35
    • 0028085120 scopus 로고
    • Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3
    • Vermeulen W, Scott RJ, Rodgers S, Muller HJ, Cole J, Arlett CF, et al. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. Am J Hum Genet 1994;54:191-200.
    • (1994) Am J Hum Genet , vol.54 , pp. 191-200
    • Vermeulen, W.1    Scott, R.J.2    Rodgers, S.3    Muller, H.J.4    Cole, J.5    Arlett, C.F.6
  • 36
    • 0036180585 scopus 로고    scopus 로고
    • The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity
    • Lalle P, Nouspikel T, Constantinou A, Thorel F, Clarkson SG. The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity. J Invest Dermatol 2002;118:344-51.
    • (2002) J Invest Dermatol , vol.118 , pp. 344-351
    • Lalle, P.1    Nouspikel, T.2    Constantinou, A.3    Thorel, F.4    Clarkson, S.G.5
  • 37
    • 12644310290 scopus 로고    scopus 로고
    • Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene
    • Taylor EM, Broughton BC, Botta E, Stefanini M, Sarasin A, Jaspers NGJ, et al. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene. Proc Natl Acad Sci USA 1997;94:8658-63.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 8658-8663
    • Taylor, E.M.1    Broughton, B.C.2    Botta, E.3    Stefanini, M.4    Sarasin, A.5    Jaspers, N.G.J.6
  • 38
    • 0034027382 scopus 로고    scopus 로고
    • Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels
    • Chavanne F, Broughton BC, Pietra D, Nardo T, Browitt A, Lehmann AR, et al. Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels. Cancer Res 2000;60:1974-82.
    • (2000) Cancer Res , vol.60 , pp. 1974-1982
    • Chavanne, F.1    Broughton, B.C.2    Pietra, D.3    Nardo, T.4    Browitt, A.5    Lehmann, A.R.6
  • 39
    • 0028868125 scopus 로고
    • Molecular and cellular analysis of the DNA-repair defect in a patient in Xeroderma-pigmentosum complementation Group-D who has the clinical-features of Xeroderma-pigmentosum and Cockayne-syndrome
    • Broughton BC, Thompson AF, Harcourt SA, Vermeulen W, Hoeijmakers JHJ, Botta E, et al. Molecular and cellular analysis of the DNA-repair defect in a patient in Xeroderma-pigmentosum complementation Group-D who has the clinical-features of Xeroderma-pigmentosum and Cockayne-syndrome. Am J Hum Genet 1995;56:167-74.
    • (1995) Am J Hum Genet , vol.56 , pp. 167-174
    • Broughton, B.C.1    Thompson, A.F.2    Harcourt, S.A.3    Vermeulen, W.4    Hoeijmakers, J.H.J.5    Botta, E.6
  • 41
    • 0031802583 scopus 로고    scopus 로고
    • Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein
    • States JC, McDuffie ER, Myrand SP, McDowell M, Cleaver JE. Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein. Hum Mutat 1998;12:103-13.
    • (1998) Hum Mutat , vol.12 , pp. 103-113
    • States, J.C.1    McDuffie, E.R.2    Myrand, S.P.3    McDowell, M.4    Cleaver, J.E.5
  • 42
    • 0018650576 scopus 로고
    • Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum
    • Pawsey SA, Magnus IA, Ramsay CA, Benson PF, Giannelli F. Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum. Quart J Medicine 1979;190:179-210.
    • (1979) Quart J Medicine , vol.190 , pp. 179-210
    • Pawsey, S.A.1    Magnus, I.A.2    Ramsay, C.A.3    Benson, P.F.4    Giannelli, F.5
  • 43
    • 0028341685 scopus 로고
    • Mutations that disable the DNA-repair gene XPG in a Xeroderma-pigmentosum group-G patient
    • Nouspikel T, Clarkson SG. Mutations that disable the DNA-repair gene XPG in a Xeroderma-pigmentosum group-G patient. Hum Mol Genet 1994;3:963-7.
    • (1994) Hum Mol Genet , vol.3 , pp. 963-967
    • Nouspikel, T.1    Clarkson, S.G.2
  • 45
    • 0030990434 scopus 로고    scopus 로고
    • A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: Implications for a second XPG function
    • Nouspikel T, Lalle P, Leadon SA, Cooper PK, Clarkson SG. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. Proc Natl Acad Sci USA 1997;94:3116-21.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 3116-3121
    • Nouspikel, T.1    Lalle, P.2    Leadon, S.A.3    Cooper, P.K.4    Clarkson, S.G.5
  • 46
    • 0026465665 scopus 로고
    • ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
    • Troelstra C, van Gool A, de Wit J, Vermeulen W, Bootsma D, Hoeijmakers JHJ. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes. Cell 1992;71:939-53.
    • (1992) Cell , vol.71 , pp. 939-953
    • Troelstra, C.1    van Gool, A.2    de Wit, J.3    Vermeulen, W.4    Bootsma, D.5    Hoeijmakers, J.H.J.6
  • 47
    • 0020374786 scopus 로고
    • Three complementation groups in Cockayne syndrome
    • Lehmann AR. Three complementation groups in Cockayne syndrome. Mutat Res 1982;106:347-56.
    • (1982) Mutat Res , vol.106 , pp. 347-356
    • Lehmann, A.R.1
  • 49
    • 0020972378 scopus 로고
    • Limited and unlimited growth of SV40-transformed cells from human diploid MRC-5 fibroblasts
    • Huschtscha LI, Holliday R. Limited and unlimited growth of SV40-transformed cells from human diploid MRC-5 fibroblasts. J Cell Sci 1983;63:77-99.
    • (1983) J Cell Sci , vol.63 , pp. 77-99
    • Huschtscha, L.I.1    Holliday, R.2
  • 50
    • 0014941518 scopus 로고
    • Characteristics of a human diploid cell designated MRC-5
    • Jacobs JP, Jones CM, Baillie JP. Characteristics of a human diploid cell designated MRC-5. Nature 1970;227:168-70.
    • (1970) Nature , vol.227 , pp. 168-170
    • Jacobs, J.P.1    Jones, C.M.2    Baillie, J.P.3


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