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neu不参与N-[4-(5-硝基-2-呋喃基)-2-噻唑基]-甲酰胺诱导的大鼠膀胱癌或2-氨基-4-(5-硝基-2-呋喃基)噻唑对大鼠膀胱上皮细胞的转化。

neu is not involved in N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide-induced bladder carcinoma or 2-amino-4-(5-nitro-2-furyl)thiazole transformation of rat bladder epithelial cells.

作者信息

Mann A M, Asamoto M, Masui T, Macatee T, Eklund S H, Cohen S M

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha 68198-3135.

出版信息

Cancer Lett. 1994 Sep 15;84(2):125-31. doi: 10.1016/0304-3835(94)90366-2.

Abstract

Enhanced c-erbB-2/neu expression has been linked with a poor prognosis in human bladder cancer. Previous reports have shown that a point mutation at nucleotide T2012 in the coding region of the transmembrane domain of the rat gene is sufficient to confer transformation potential on this gene. We examined the comparative levels of p185neu as well as the sequence around the hotspot (T2012) of the neu gene of rat bladder cells transformed by 2-amino-4-(5-nitro-2-furyl)thiazole (ANFT) or established in culture from N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT)-induced rat bladder tumors. We concluded that increased p185neu expression did not correlate significantly with tumorigenicity. No alterations in nucleotide sequences of the neu gene were observed in either in vitro model.

摘要

增强的c-erbB-2/neu表达与人类膀胱癌的不良预后相关。先前的报告表明,大鼠基因跨膜结构域编码区核苷酸T2012处的点突变足以赋予该基因转化潜能。我们检测了经2-氨基-4-(5-硝基-2-呋喃基)噻唑(ANFT)转化或从N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺(FANFT)诱导的大鼠膀胱肿瘤培养建立的大鼠膀胱细胞中p185neu的相对水平以及neu基因热点(T2012)周围的序列。我们得出结论,p185neu表达增加与致瘤性无显著相关性。在两种体外模型中均未观察到neu基因核苷酸序列的改变。

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In vitro transformation of rat bladder epithelium by 2-amino-4-(5-nitro-2-furyl)thiazole.
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