Laderoute K R, Ausserer W A, Knapp A M, Grant T D, Sutherland R M
Life Sciences Division, SRI International, Menlo Park, California 94025.
Cancer Res. 1994 Mar 15;54(6):1407-11.
Epidermal growth factor (EGF) has been shown to radiosensitize A431 and other human squamous carcinoma cells with high numbers of surface EGF receptors. In this study of the mechanistic basis of EGF-induced radiosensitization, both EGF and ionizing radiation caused G1 phase arrests in cycling A431 cells, but only radiation caused a G2-M arrest. However, EGF enhanced the magnitude of this G2-M arrest, suggesting an interaction of signaling pathways involved in cellular responses to EGF and radiation damage. EGF and radiation also uniquely perturbed cyclin A and B1 mRNA levels during the time of maximum radiation-induced G2-M arrest. The effects of EGF on G2-M events probably originated in cells in G1. It is possible that aberrant EGF signal transduction in human squamous carcinoma cells may be exploited as a novel strategy for radiotherapy.
表皮生长因子(EGF)已被证明可使具有大量表面EGF受体的A431细胞和其他人类鳞状癌细胞对辐射敏感。在这项关于EGF诱导辐射增敏机制基础的研究中,EGF和电离辐射均可使处于周期中的A431细胞停滞于G1期,但只有辐射会导致G2-M期停滞。然而,EGF增强了这种G2-M期停滞的程度,表明参与细胞对EGF和辐射损伤反应的信号通路之间存在相互作用。在辐射诱导的G2-M期停滞达到最大值时,EGF和辐射还分别对细胞周期蛋白A和B1的mRNA水平产生了独特的影响。EGF对G2-M期事件的影响可能起源于G1期的细胞。人类鳞状癌细胞中异常的EGF信号转导有可能被开发为一种新的放射治疗策略。