Sarto F, Mazzotti D, Tomanin R, Corsi G C, Peserico A
Istituto di Medicina del Lavoro dell'Università di Padova, Italy.
Mutat Res. 1989 Jan-Feb;225(1-2):21-6. doi: 10.1016/0165-7992(89)90027-4.
The nevoid basal-cell carcinoma syndrome (NBCCS) is a rare multisystem disorder characterized by several alterations of the skin, skeletal, nervous, endocrine system. These patients are more susceptible to cancer and suggestions have been made about an association with the chromosomal breakage syndromes. We studied the induction of chromosomal aberrations by mitomycin C (MMC) and bleomycin and that of sister-chromatid exchanges by MMC and 4-nitroquinoline N-oxide in lymphocytes of 4 NBCCS patients. The frequencies of both spontaneous and induced cytogenetic effects were within normal ranges, suggesting that there is no chromosomal instability in NBCCS patients.
痣样基底细胞癌综合征(NBCCS)是一种罕见的多系统疾病,其特征为皮肤、骨骼、神经、内分泌系统的多种改变。这些患者更易患癌症,并且有人提出其与染色体断裂综合征有关联。我们研究了丝裂霉素C(MMC)和博来霉素对4例NBCCS患者淋巴细胞染色体畸变的诱导作用,以及MMC和4-硝基喹啉N-氧化物对姐妹染色单体交换的诱导作用。自发和诱导的细胞遗传学效应频率均在正常范围内,这表明NBCCS患者不存在染色体不稳定性。