Cheda Aneta, Wrembel-Wargocka Jolanta, Lisiak Emil, Nowosielska Ewa M, Marciniak Maria, Janiak Marek K
Department of Radiobiology and Radiation Protection, Military Institute of Hygiene and Epidemiology, 01-163 Warsaw, Poland.
Radiat Res. 2004 Mar;161(3):335-40. doi: 10.1667/rr3123.
There is evidence indicating that low-level exposures to low- LET radiation may inhibit the development of tumors, but the mechanism of this effect is virtually unknown. In the present study, BALB/c mice were irradiated with single doses of 0.1 or 0.2 Gy X rays and injected intravenously 2 h later with syngeneic L1 sarcoma cells. Compared to the values obtained for sham-irradiated control mice, the numbers of pulmonary tumor colonies were significantly reduced in the animals exposed to either 0.1 or 0.2 Gy X rays. Concurrently, a significant stimulation of NK cell-mediated cytotoxic activity was detected in splenocyte suspensions obtained from irradiated mice compared to sham-exposed mice. Intraperitoneal injection of the NK-suppressive anti-asialo GM1 antibody totally abrogated the tumor inhibitory effect of the exposures to 0.1 and 0.2 Gy X rays. These results indicate that single irradiations of mice with either 0.1 or 0.2 Gy X rays suppress the development of experimental tumor metastases primarily due to the stimulation of the cytolytic function of NK cells by radiation.
有证据表明,低剂量接触低传能线密度辐射可能会抑制肿瘤的发展,但其作用机制几乎尚不明确。在本研究中,对BALB/c小鼠进行单次0.1或0.2 Gy X射线照射,2小时后静脉注射同基因L1肉瘤细胞。与假照射对照小鼠相比,接受0.1或0.2 Gy X射线照射的动物肺部肿瘤集落数量显著减少。同时,与假照射小鼠相比,在从照射小鼠获得的脾细胞悬液中检测到自然杀伤(NK)细胞介导的细胞毒性活性显著增强。腹腔注射NK抑制性抗去唾液酸GM1抗体完全消除了0.1和0.2 Gy X射线照射对肿瘤的抑制作用。这些结果表明,单次用0.1或0.2 Gy X射线照射小鼠主要通过辐射刺激NK细胞的溶细胞功能来抑制实验性肿瘤转移的发展。