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  • 29.30.Kv  (1)
  • Fibroblast  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 124 (1998), S. 415-420 
    ISSN: 1432-1335
    Keywords: Key words Radiosensitivity ; SF2 ; Fibroblast
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The in vitro radiosensitivity of dermal fibroblasts has been found to vary between individuals, and a number of studies have also shown that this parameter correlates with radiation-induced late injuries in clinical radiotherapy. In addition, certain genetic disorders are known to effect radiosensitivity, e.g. normal tissues of patients homozygous or heterozygous for the ataxia teleangiectasia gene show unusual sensitivity to radiation both in vivo and in vitro. Thus, it has been assumed that there is a genetically determined component resulting in a certain intrinsic cellular radiation response in an individual. To study this possible relationship between different cells of a specific patient, we established eight pairs of dermal and tumor fibroblast cultures. The donor patients had either adenocarcinoma of the uterus or squamous cell carcinoma (SCC) of the head and neck. The radiosensitivity of these strains was determined by a 96-well plate clonogenic assay, previously used by us for radiosensitivity testing of cancer cells. From a paired comparison, the values for the cell fraction surviving 2.0 Gy (SF2), of both fibroblast strains, were found to be on the same level in five out of eight cases. In patient 6, the SF2 of tumor fibroblasts was significantly higher than that of dermal fibroblasts (P = 0.0014). In two additional cases the tendency was the same, but not statistically significant. As groups, the two types of fibroblasts did not differ from each other, mean SF2 values of 0.24 ± 0.07 and 0.21 ± 0.05, respectively. The SF2 of tumor fibroblasts from SCC patients proved to be significantly higher than that of the adenocarcinoma patients (P = 0.030). These preliminary results indicate that the in vitro radiosensitivity of tumor fibroblasts correlates with normal cell sensitivity in many cases, but not in all. The radiosensitivity of tumor fibroblasts also seems to follow the level of in vitro radiosensitivity determined for the corresponding histological type of tumor cells. Further studies are needed to determine more closely the relationship between the radiosensitivities of tumor cells and tumor fibroblasts, thus evaluating the possibility of testing radiosensitivity from tumor fibroblasts in order to estimate tumor response.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-601X
    Keywords: 23.40.Hc ; 21.10.Dr ; 21.10.Pc ; 27.60.+j ; 29.30.Kv
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Neutron-rich isotopes of palladium were produced via the fission of238U by 20 MeV protons. These isotopes were selected using the ion guide-fed on-line mass-separator facility IGISOL at Jyväskylä. Their decays were studied byβ-ray,γ-ray and conversion-electron spectroscopy. For114Pd and116Pd, the decay schemes established previously were confirmed; additionally multipolarities were determined for a few transitions. In the case of118Pd, only an approximate half-life was known from a previous radiochemical experiment. In the present study, 15 gamma transitions were observed, most of which were placed in a decay scheme. The half-life and the decay energy were found to beT 1/2=1.9±0.1 s andQ β=4.0±0.2 MeV. The decay schemes of114Pd,116Pd and118Pd include — respectively — two, two and four 0+→1+ Gamow-Teller beta transitions with logft values between 4.1 and 5.1. The strength of these transitions is discussed in terms of the extreme single particle shell model with pairing and the spherical proton-neutron quasiparticle random phase approximation. The possible role of deformation is considered using a shell correction method. Predictions for the decay properties of the as yet unobserved120Pd are given.
    Type of Medium: Electronic Resource
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