Watanabe R, Otsuka F
Department of Dermatology, Faculty of Medicine, University of Tokyo, Japan.
Exp Dermatol. 1993 Aug;2(4):175-8. doi: 10.1111/j.1600-0625.1993.tb00029.x.
Disseminated superficial actinic porokeratosis (DSAP), skin lesions of which are known to be induced by ultraviolet (UV) light, does not develop into skin cancer as frequently as other types of porokeratosis (PK). To establish the cellular basis of this characteristic of DSAP, we examined the colony-forming ability of UVC light- or X-ray-irradiated cultured fibroblasts derived from DSAP patients' skin. Sensitivity to the lethal effects of UV light was not significantly different between 3 DSAP and 5 control cell strains. In contrast, DSAP cell strains were significantly hypersensitive to the lethal effects of X-radiation, although the sensitivity was less than that of cell strains from other types of PK patients. The results indicate that the actinic character of DSAP is not reflected in the cellular response to the lethal effects of UV light, but suggest that DSAP shares X-ray sensitivity, which is probably associated with the cancer-prone nature of PK.
播散性浅表性光化性汗孔角化症(DSAP)的皮肤病变已知是由紫外线(UV)诱导的,它不像其他类型的汗孔角化症(PK)那样频繁地发展为皮肤癌。为了确定DSAP这一特征的细胞基础,我们检测了来自DSAP患者皮肤的经紫外线C光或X射线照射的培养成纤维细胞的集落形成能力。3株DSAP细胞株和5株对照细胞株对紫外线致死效应的敏感性没有显著差异。相比之下,DSAP细胞株对X射线的致死效应明显超敏,尽管其敏感性低于其他类型PK患者的细胞株。结果表明,DSAP的光化性特征并未反映在细胞对紫外线致死效应的反应中,但提示DSAP具有X射线敏感性,这可能与PK的癌症易发性有关。