Asanuma Koichi, Kobayashi Daisuke, Furuya Daisuke, Tsuji Naoki, Yagihashi Atsuhito, Watanabe Naoki
Division of Laboratory Diagnosis, Sapporo Medical University School of Medicine, Chuo-ku, Sapporo 060-8543, Japan.
Jpn J Cancer Res. 2002 Sep;93(9):1057-62. doi: 10.1111/j.1349-7006.2002.tb02483.x.
Using gene-transduced pancreatic cancer cells, we examined whether survivin expression is directly involved in regulation of radiosensitivity. Ordinarily radiosensitive MIAPaCa-2 cells transduced with wild-type survivin gene (MS cells) proliferated more rapidly than cells transduced with control vector. MS cells were significantly less radiosensitive than control vector-transduced cells. Radiation-induced activity of caspase-3, but not caspase-7, was significantly inhibited in MS cells. On the other hand, transduction of a dominant-negative mutant survivin gene into radioresistant PANC-1 cells augmented radiosensitivity. Further, the radiation-induced increase in caspase-3 activity was enhanced, indicating that survivin function was truly inhibited. These results indicate that survivin expression directly down-regulates radiosensitivity.
利用基因转导的胰腺癌细胞,我们研究了生存素表达是否直接参与放射敏感性的调节。通常对放射敏感的MIAPaCa - 2细胞转导野生型生存素基因(MS细胞)后,其增殖速度比转导对照载体的细胞更快。MS细胞的放射敏感性明显低于转导对照载体的细胞。在MS细胞中,辐射诱导的半胱天冬酶-3活性受到显著抑制,但半胱天冬酶-7活性未受抑制。另一方面,将显性负性突变生存素基因转导至放射抗性的PANC - 1细胞中可增强放射敏感性。此外,辐射诱导的半胱天冬酶-3活性增加得到增强,表明生存素功能确实受到抑制。这些结果表明生存素表达直接下调放射敏感性。