Hama S, Sadatomo T, Yoshioka H, Kurisu K, Tahara E, Naruse I, Heike Y, Saijo N
Department of Neurosurgery, Hiroshima University School of Medicine, Japan.
Anticancer Res. 1997 May-Jun;17(3C):1933-8.
We examined the genomic status of the p16 gene in 5 human glioma cell lines by Southern blot analysis. The p16 gene was located in the 9p21 chromosomal region and homozygous deletion was detected in 4 of 5 (80%) human glioma cell lines and 5 of 15 (33%) clinical samples. We transfected the full-length human p16 gene into p16-null human glioma cell line, U251MG cells, using the plasmid vector pRc/CMV-p16 and evaluated the effect of p16 gene transfer on the growth suppression of malignant glioma cells. The transfection of p16 cDNA caused growth suppression through G1 cell cycle arrest in U251MG cells. We also examined the effect of p16 gene transfer on the chemosensitivity to cis-diamminedichloroplatinum II (CDDP), 1-(4-amino-2-methyl-5-pyrimidinyl)methyl-3-(2-chloroethyl) -3-nitrosourea hydrochloride (ACNU), and 5'-azacytidine (AZC). We did not detect any change in them after p16 gene transfer. These results might suggest that deletion of p16 genes promoted unrestrained growth in human glioma but has no relationship to the chemosensitivity to CDDP, ACNU and AZC.
我们通过Southern印迹分析检测了5种人胶质瘤细胞系中p16基因的基因组状态。p16基因位于9p21染色体区域,在5种人胶质瘤细胞系中有4种(80%)以及15份临床样本中有5份(33%)检测到纯合缺失。我们使用质粒载体pRc/CMV-p16将全长人p16基因转染到p16基因缺失的人胶质瘤细胞系U251MG细胞中,并评估p16基因转移对恶性胶质瘤细胞生长抑制的影响。p16 cDNA的转染通过使U251MG细胞的G1期细胞周期停滞导致生长抑制。我们还检测了p16基因转移对顺二氯二氨铂(CDDP)、1-(4-氨基-2-甲基-5-嘧啶基)甲基-3-(2-氯乙基)-3-亚硝基脲盐酸盐(ACNU)和5'-氮杂胞苷(AZC)化疗敏感性的影响。p16基因转移后我们未检测到它们有任何变化。这些结果可能表明p16基因的缺失促进了人胶质瘤的无节制生长,但与对CDDP、ACNU和AZC的化疗敏感性无关。