Boukamp P, Tilgen W, Dzarlieva R T, Breitkreutz D, Haag D, Riehl R K, Bohnert A, Fusenig N E
J Natl Cancer Inst. 1982 Mar;68(3):415-27.
A human cell line (SCL-1) from a poorly differentiating cutaneous squamous cell carcinoma (SCC) ws studied through 20 passages during 2 years. Cells maintained their original morphology with low degree of keratinization, as indicated by light and electron microscopy. The keratin peptide pattern resembled the type in SCC tumors, and the corresponding filaments were detected by immunofluorescence at all passage levels. Cells did not grow in soft agar but formed tumor-like nodules in an "organotypic" culture assay (on lifted collagen gels) and grew invasively after transplantation to immunosuppressed inbred C3H mice. After injection into BALB/c nu/nu mice, tumors of SCC morphology were formed. The hypodiploid tumor stem-line was maintained for about 10 passages, when a shift to hyperploidy started, as determined by chromosome and DNA flow microfluorometric analyses. Two stable marker chromosomes (in 100 and 70% of the metaphases, respectively), involving chromosomes 7 and 9, strongly indicated a monoclonal origin of this cell line.
对一株来自低分化皮肤鳞状细胞癌(SCC)的人细胞系(SCL-1)进行了为期2年的20代研究。光镜和电镜检查表明,细胞保持了低角化程度的原始形态。角蛋白肽模式类似于SCC肿瘤中的类型,并且在所有传代水平通过免疫荧光检测到相应的细丝。细胞在软琼脂中不生长,但在“器官型”培养试验(在悬浮的胶原凝胶上)中形成肿瘤样结节,并且在移植到免疫抑制的近交C3H小鼠后具有侵袭性生长。注射到BALB/c nu/nu小鼠体内后,形成了SCC形态的肿瘤。通过染色体和DNA流式细胞荧光分析确定,亚二倍体肿瘤干细胞系维持了约10代,之后开始向超倍体转变。两条稳定的标记染色体(分别在100%和70%的中期),涉及7号和9号染色体,强烈表明该细胞系起源于单克隆。