摘要
分别将野生型和突变型p53基因导入鼻咽癌的体外培养细胞系CNE-3.裸鼠致瘤试验表明,导入野生型p53基因的细胞系,肿瘤生长速度明显低于对照细胞系及导入突变型p53基因的细胞系;导入突变型p53基因的细胞系肿瘤生长速度最快;导入野生型p53基因的细胞系肿瘤生长速度最慢,而且肿瘤出现时间也较导入突变型p53的细胞及对照细胞晚1~2周。这说明野生型p53基因能有效地抑制肿瘤的生长,而实变型p53基因则可以促进肿瘤生长。这是首次有关p53基因对鼻咽癌细胞作用的报道。这一研究更进一步说明了p53基因的功能,对于鼻咽癌发生机理的探讨以及肿瘤的防治具有重要意义。
Wild-type and mutant human P53 genes were transfected into the nasopharyngeal carcino-m3(NPC)cell line CNE-3.Tumorigenicity in nude mice showed that the tumor resulting from the cellstransfected with the wild-type P53 gene grew more slowly and was smaller than that from control CNE-3cells.In contrast,the tumor from the cells transfected with the mutant P53 gene grew faster than that pro-duced by cells transfected with the wild-type P53 gene and that producd by control CNE-3 cells.The re-sults demonstrate that the wild-type P53 gene could inhibit the NPC cell growth in nude mice and the mu-tant P53 gene could enhance the NPC cell growth in nude mice.The P53 gene may also play an importantrole in the pathogenesis of NPC.
出处
《癌症》
SCIE
CAS
CSCD
北大核心
1996年第1期11-14,共4页
Chinese Journal of Cancer