Weichselbaum R R, Tomkinson K, Little J B
Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Apr;47(4):445-56.
We examined X-ray induced potentially lethal damage repair (PLDR) in density inhibited plateau phase cultures of six fibroblast strains derived from patients with hereditary retinoblastoma and two patients with D-deletion retinoblastoma and compared them to three normal controls. PLD was measured in hereditary retinoblastoma (7 Gy exposure) and normal cells (7 and 9 Gy exposure) after 24 h repair time. PLD survival curves were performed at 2-9 Gy on six retinoblastoma and three normal control cell strains. Thus, PLDR was compared at equitoxic survival levels as well as after exposure to equal doses of radiation. Some retinoblastoma strains showed normal PLDR whereas others were possibly deficient. Implications of PLDR for susceptibility to radiation-induced and spontaneous tumours in hereditary retinoblastoma patients are discussed.
我们检测了来自遗传性视网膜母细胞瘤患者的6种成纤维细胞系以及2例D缺失性视网膜母细胞瘤患者的处于密度抑制平台期培养物中的X射线诱导的潜在致死性损伤修复(PLDR),并将其与3个正常对照进行比较。在24小时修复时间后,对遗传性视网膜母细胞瘤(7 Gy照射)和正常细胞(7和9 Gy照射)测量PLD。在6种视网膜母细胞瘤和3种正常对照细胞系上,于2 - 9 Gy进行PLD存活曲线测定。因此,在等毒性存活水平以及暴露于等量辐射后比较PLDR。一些视网膜母细胞瘤细胞系显示出正常的PLDR,而其他细胞系可能存在缺陷。本文讨论了PLDR对遗传性视网膜母细胞瘤患者辐射诱导和自发性肿瘤易感性的影响。