Wang Y, Parks W C, Wigle J C, Maher V M, McCormick J J
Mutat Res. 1986 Oct;175(2):107-14. doi: 10.1016/0165-7992(86)90133-8.
Retinoblastoma (RB) is a cancer of the retina which characteristically occurs in early childhood. Bilateral RB is an inherited form of this disease. Such patients are at greatly increased risk of subsequently developing second tumors in mesenchymal tissue, especially in areas exposed to ionizing radiation therapy. Fibroblasts from bilateral RB patients have been reported to be more sensitive than normal fibroblasts to the cytotoxic effects of ionizing radiation. Because xeroderma pigmentosum patients have a hereditary predisposition to UV-induced cancer and the cells of such patients are abnormally sensitive to the cytotoxic and mutagenic effects of UV radiation, we compared fibroblasts from 6 bilateral RB patients and 3 normal individuals for their sensitivity to the mutagenic effects of cobalt 60, using resistance to 6-thioguanine (TG) as the genetic marker. The results showed no statistically significant difference between the two types of cell lines. The slope of the weighted least squares line representing the frequency of TG-resistant cells induced in the RB populations as a function of dose was 17 +/- 6 (S.E.)/10(6) cells/Gy with an intercept of 0.09 Gy; that for the normal cells was 17 +/- 7/10(6) cells/Gy with an intercept of 0.14 Gy. We also compared 8 bilateral RB cell lines and 9 age-matched normal cell lines for their sensitivity to the cytotoxic effect of 60Co, using survival of colony-forming ability. The cloning efficiency of the unirradiated RB cell lines ranged from 22% to 76% with an average of 52%; that of the normal cell lines from 21% to 89% with an average of 64%. The results showed the RB cells were somewhat more sensitive than the normal cells. The mean D0 for the RB cell lines ranged from 0.99 +/- 0.01 (S.E.) to 1.69 +/- 0.04 Gy with a weighted average of 1.44 +/- 0.08 Gy; that of the normal cell lines ranged from 1.42 +/- 0.17 to 2.24 +/- 0.10 Gy, with a weighted average of 1.79 +/- 0.11 Gy. The difference in means was estimated to be 0.34 +/- 0.14. The mean for the RB cell lines is statistically significantly lower than the mean for the normal cell lines, at a significance level ca. 1%.
视网膜母细胞瘤(RB)是一种视网膜癌症,典型地发生于儿童早期。双侧RB是这种疾病的一种遗传形式。这类患者随后在间充质组织中发生第二种肿瘤的风险大大增加,尤其是在接受电离辐射治疗的部位。据报道,双侧RB患者的成纤维细胞比正常成纤维细胞对电离辐射的细胞毒性作用更敏感。由于着色性干皮病患者有遗传性的紫外线诱导癌症易感性,且这类患者的细胞对紫外线辐射的细胞毒性和诱变作用异常敏感,我们以对6-硫鸟嘌呤(TG)的抗性作为遗传标记,比较了6例双侧RB患者和3例正常个体的成纤维细胞对钴60诱变作用的敏感性。结果显示两种细胞系之间无统计学显著差异。代表RB群体中诱导的TG抗性细胞频率作为剂量函数的加权最小二乘线的斜率为17±6(标准误)/10⁶细胞/戈瑞,截距为0.09戈瑞;正常细胞的斜率为17±7/10⁶细胞/戈瑞,截距为0.14戈瑞。我们还以集落形成能力的存活率为指标,比较了8个双侧RB细胞系和9个年龄匹配的正常细胞系对⁶⁰Co细胞毒性作用的敏感性。未照射的RB细胞系的克隆效率范围为22%至76%,平均为52%;正常细胞系的克隆效率范围为21%至89%,平均为64%。结果显示RB细胞比正常细胞稍敏感。RB细胞系的平均D0范围为0.99±0.01(标准误)至1.69±0.04戈瑞,加权平均值为1.44±0.08戈瑞;正常细胞系的平均D0范围为1.42±0.17至2.24±0.10戈瑞,加权平均值为1.79±0.11戈瑞。均值差异估计为0.34±0.14。RB细胞系的均值在统计学上显著低于正常细胞系的均值,显著性水平约为1%。