Ananthaswamy H N
Photodermatol. 1984 Dec;1(6):265-76.
The wavelength dependence for cell killing and induction of oncogenic transformation in 10T1/2 cells, a C3H mouse embryo fibroblast cell line, was investigated. Ultraviolet radiation (UV) in the UVA (315-400 nm), UVB (280-340 nm), and UVC (254 nm) regions of the electromagnetic spectrum caused cell death and induced neoplastic transformation of 10T1/2 cells. Lethality and transformation induced by 3 different types of light source encompassing 4 ranges of wavelength were compared, using several parameters. The total energy required to reduce cell survival and to induce a given transformation frequency (e.g., 10(-3) transformants/surviving cell) increased with longer wavelengths, indicating that longer wavelengths are less cytotoxic and carcinogenic than the same dose of radiation at shorter wavelengths. However, when the frequency of transformation was calculated per lethal event (delta T values), all the wavelength ranges tested were found to be similarly effective in inducing transformation. This suggests that the lesions in DNA responsible for oncogenic transformation and lethality are the same for all the wavelength ranges tested. Although wavelengths above 300 nm are inefficient in their ability to induce transformation, their abundance in sunlight may make them a significant factor in carcinogenesis.
对C3H小鼠胚胎成纤维细胞系10T1/2细胞进行细胞杀伤和致癌转化诱导的波长依赖性进行了研究。电磁光谱中UVA(315 - 400nm)、UVB(280 - 340nm)和UVC(254nm)区域的紫外线辐射(UV)导致10T1/2细胞死亡并诱导其发生肿瘤转化。使用几个参数比较了涵盖4个波长范围的3种不同类型光源诱导的致死率和转化情况。降低细胞存活率并诱导给定转化频率(例如,10^(-3)个转化子/存活细胞)所需的总能量随波长增加而增加,这表明较长波长的细胞毒性和致癌性低于相同剂量的较短波长辐射。然而,当按每个致死事件计算转化频率(δT值)时,发现所有测试的波长范围在诱导转化方面同样有效。这表明在所有测试波长范围内,导致致癌转化和致死的DNA损伤是相同的。尽管波长大于300nm的光诱导转化的能力较低,但其在阳光中的丰度可能使其成为致癌作用的一个重要因素。