Chandar N, Lombardi B, Schulz W, Locker J
Department of Pathology, University of Pittsburgh, School of Medicine, PA 15261.
Am J Pathol. 1987 Nov;129(2):232-41.
After long-term feeding of a choline-devoid diet to rats, the authors analyzed rasK, rasH, and rasN transcripts and gene structure in livers and liver tumors. They controlled their analysis by studying cell lines derived from chemically induced hepatomas. Transcripts from all three genes were elevated in all tumors, but not in the livers from which they arose. The transcript elevations may represent an effect of active cell proliferation in the tumors. Clone HiHi-3, derived from the Kirsten murine sarcoma virus, detected a large number of hybridization bands, most of which were not part of the rasK-p21 gene. Most tumors had an altered band at 2.6 kb; some had other altered bands. No alterations were seen in liver DNA, and none of the cell lines showed the 2.6 kb band. At low stringency, a rasH probe, which contains a short segment of a similar viral sequence, also detected altered bands in tumors and a single treated liver. These changes in endogenous viral sequences of the rat genome appear to be characteristic of carcinogenesis by a choline-devoid diet.
在给大鼠长期喂食缺乏胆碱的饮食后,作者分析了肝脏和肝肿瘤中rasK、rasH和rasN转录本及基因结构。他们通过研究化学诱导肝癌衍生的细胞系来控制分析。所有三种基因的转录本在所有肿瘤中均升高,但在产生肿瘤的肝脏中未升高。转录本升高可能代表肿瘤中活跃细胞增殖的一种效应。源自 Kirsten 小鼠肉瘤病毒的克隆HiHi-3检测到大量杂交带,其中大多数不是rasK-p21基因的一部分。大多数肿瘤在2.6 kb处有一条改变的带;一些有其他改变的带。在肝脏DNA中未观察到改变,并且没有细胞系显示出2.6 kb的带。在低严谨度下,一个含有相似病毒序列短片段的rasH探针也在肿瘤和一个经处理的肝脏中检测到改变的带。大鼠基因组内源性病毒序列的这些变化似乎是缺乏胆碱饮食致癌的特征。