Hauser-Urfer I H, Stauffer J
Cytogenet Cell Genet. 1985;39(1):35-9. doi: 10.1159/000132100.
The chromosomes of nine cell lines from human squamous cell carcinomas of the head and neck were examined. Five of the lines were derived from patients who had received chemotherapy and radiotherapy, one line was derived from a lymph-node metastasis from one of these patients, and three lines were from patients who had not been treated. The cell lines from the untreated patients had lower modal chromosome numbers than those of all but one of the lines from the treated patients. A structural abnormality involving chromosome 1 with breakpoints located in p13, p22, q21, or q32 was found in all cases. The NRAS and SK oncogenes are located in or near some of these segments. In four of the cell lines the nucleolus organizer regions (NORs) were 10-30 times larger than the NORs of the normal human chromosomes. Double minutes (DM) and homogeneously staining regions (HSR) were found in four of the lines.
对9株来自头颈部鳞状细胞癌的细胞系的染色体进行了检查。其中5株细胞系来自接受过化疗和放疗的患者,1株细胞系来自其中1例患者的淋巴结转移灶,3株细胞系来自未接受过治疗的患者。未接受治疗患者的细胞系的众数染色体数低于除1株接受治疗患者的细胞系外的所有其他接受治疗患者的细胞系。在所有病例中均发现了涉及1号染色体的结构异常,其断点位于p13、p22、q21或q32。NRAS和SK癌基因位于其中一些区段内或附近。在4株细胞系中,核仁组织区(NORs)比正常人染色体的NORs大10 - 30倍。在4株细胞系中发现了双微体(DM)和均匀染色区(HSR)。