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An in vitro investigation of genetic susceptibility to cancer in diploid fibroblasts from retinoblastoma patients

Journal Article · · Teratog., Carcinog., Mutagen.; (United States)
OSTI ID:5335111
Thirty-two diploid fibroblast strains from individuals with the three forms of retinoblastoma were examined with an in vitro clonogenic survival assay to determine their sensitivity to killing by X rays. Strains from sporadic unilateral retinoblastoma patients and normal controls were indistinguishable from one another (group D0's . 147 +/- 15 rads and 146 +/- 5 rads, respectively) while the strains from patients with the hereditary form of the disease were significantly more X-ray sensitive (D0 . 111 +/- 12). Strains derived from individuals with the D-deletion form of the disease resembled the hereditary strains with respect to sensitivity and heterogeneity, suggesting a possible, common etiology for these two forms of the disease. A DNA-repair defect is hypothesized as reflected by the observed hypersensitivity to X-irradiation in these cells. We suggest that this defect may be associated with the enhanced frequency of spontaneous and radiation-induced second tumors seen in some retinoblastoma patients.
Research Organization:
Joint Center for Radiation Therapy, Harvard Medical School, Boston
OSTI ID:
5335111
Journal Information:
Teratog., Carcinog., Mutagen.; (United States), Journal Name: Teratog., Carcinog., Mutagen.; (United States) Vol. 1:2; ISSN TCMUD
Country of Publication:
United States
Language:
English