Otsuka F, Nashiro K, Kobayashi K, Ishibashi Y
Department of Dermatology, Tokyo University Branch Hospital, Japan.
Cancer Genet Cytogenet. 1991 Oct 15;56(2):163-9. doi: 10.1016/0165-4608(91)90166-r.
Cultured epidermal keratinocytes and dermal fibroblasts derived from porokeratosis (PK) patients' skin lesions or normal-appearing skin had numerical and sometimes structural chromosomal abnormalities. Such abnormal cells were seen in 4.08% and 0.375% of all the studied epidermal keratinocytes derived from affected skin and normal-appearing skin, respectively. Similar abnormalities were present in 1.70% and 3.67% of the dermal fibroblasts from the patients' affected skin and normal-appearing skin, respectively. Chromosomal abnormalities were more frequent in keratinocytes and fibroblasts from the patients' skin than in keratinocytes (0.429%) or in fibroblasts (1.22%) derived from normal control donors. Clonal proliferation of such abnormal cells was frequently seen in keratinocytes from the patients' affected skin. The frequent appearance of chromosomal abnormalities and clonal proliferation in epidermal keratinocytes may explain skin lesion formation and skin cancer development in PK patients.
从汗孔角化症(PK)患者皮肤病变部位或外观正常皮肤中获取的培养表皮角质形成细胞和真皮成纤维细胞存在染色体数目异常,有时还伴有结构异常。在所有研究的来自患病皮肤和外观正常皮肤的表皮角质形成细胞中,此类异常细胞分别占4.08%和0.375%。在患者患病皮肤和外观正常皮肤的真皮成纤维细胞中,类似异常分别占1.70%和3.67%。与来自正常对照供体的角质形成细胞(0.429%)或成纤维细胞(1.22%)相比,患者皮肤中的角质形成细胞和成纤维细胞染色体异常更为频繁。在患者患病皮肤的角质形成细胞中经常可见此类异常细胞的克隆性增殖。表皮角质形成细胞中染色体异常和克隆性增殖的频繁出现可能解释了PK患者皮肤病变的形成和皮肤癌的发生。