Hlavatý J, Tyukosova S, Bies J, Hlubinova K, Altaner C
Cancer Research Institute, Slovak Academy of Sciences, Bratislava.
Neoplasma. 2000;47(4):204-11.
A retroviral vector containing wild-type p53 tumor suppressor gene (wt-p53) under the control of viral LTR sequences was constructed and transfected into packaging cell line GP+envAm12. Virus producing single cell clone GP+envAm12/ p53clC8 (8 x 10(5) cfu/ml, determined on NIH 3T3 cells) was isolated and used to transfer wt-p53 gene into human glioma cell lines in vitro. Decreased viability in p53-infected cells as compared to uninfected or empty virus infected cells was observed.
构建了一种逆转录病毒载体,其在病毒长末端重复序列(LTR)序列的控制下含有野生型p53肿瘤抑制基因(wt-p53),并将其转染到包装细胞系GP + envAm12中。分离出产生病毒的单细胞克隆GP + envAm12 / p53clC8(在NIH 3T3细胞上测定为8×10⁵ cfu/ml),并用于在体外将wt-p53基因转移到人胶质瘤细胞系中。与未感染或空病毒感染的细胞相比,观察到p53感染细胞的活力降低。