Hougaard S, Krarup M, Nørgaard P, Damstrup L, Spang-Thomsen M, Poulsen H S
Section for Radiation Biology, Finsen Center, University Hospital Copenhagen, Denmark.
Lung Cancer. 1998 Apr;20(1):65-9. doi: 10.1016/s0169-5002(98)00013-0.
Our panel of SCLC cell lines have previously been examined for their radiobiological characteristics and sensitivity to treatment with TGF beta 1. In this study we examined the possible correlations between radiobiological parameters and the expression of the TGF beta type II receptor (TGF beta-rII). We have, in other studies, shown that the presence of TGF beta-rII was mandatory for transmitting the growth inhibitory effect of TGF beta. The results showed a statistically significant difference in Dq, i.e. the shoulder width of the survival curve, between cell lines expressing TGF beta-rII and cell lines which did not express the receptor (P = 0.01). Cell lines expressing TGF beta-rII had a high Dq-value. TGF beta-rII expression did not correlate with any other radiobiological parameters. We suggest that an intact growth inhibitory pathway mediated by the TGF beta-rII may have a significant role for the repair of radiation induced DNA damage in SCLC.
我们之前已经对一组小细胞肺癌(SCLC)细胞系的放射生物学特性以及对转化生长因子β1(TGFβ1)治疗的敏感性进行了检测。在本研究中,我们检测了放射生物学参数与II型TGFβ受体(TGFβ-rII)表达之间可能存在的相关性。在其他研究中,我们已经表明TGFβ-rII的存在是传递TGFβ生长抑制作用所必需的。结果显示,表达TGFβ-rII的细胞系与不表达该受体的细胞系之间,在Dq(即存活曲线的肩宽)上存在统计学显著差异(P = 0.01)。表达TGFβ-rII的细胞系具有较高的Dq值。TGFβ-rII的表达与任何其他放射生物学参数均无相关性。我们认为,由TGFβ-rII介导的完整生长抑制途径可能在小细胞肺癌中辐射诱导的DNA损伤修复中发挥重要作用。