Penhaligon M, Courtenay V D, Camplejohn R S
Richard Dimbleby Department of Cancer Research, United Medical School, St Thomas' Hospital, London, U.K.
Int J Radiat Biol Relat Stud Phys Chem Med. 1987 Oct;52(4):635-41. doi: 10.1080/09553008714552121.
The reduction in tumour growth rate seen when tumours are implanted into preirradiated sites, the tumour bed effect (TBE), is believed to be due to radiation damage to vascular stroma, leading to defective angiogenesis in the tumour. The present work examined whether or not the functional inadequacy of irradiated stroma was accompanied by an increased hypoxic fraction in tumours growing in irradiated beds. Mouse flank skin was given 0 or 20 Gy X-rays and RIF-1 fibrosarcoma cells were implanted i.d. into the centre of the treatment field one week later. Tumours of 200 mm3 were irradiated under clamped or unclamped conditions and the hypoxic fraction measured from the displacement of the corresponding survival curves, assayed in vitro. Results indicated a small increase in the hypoxic fraction. Averaging values from three independent experiments, the percentage of hypoxic cells increased from 2.5 per cent for cells in tumours growing in unirradiated beds to 4.6 per cent for those from tumours in beds given 20 Gy. Thus an irradiated vascular bed is still to some extent able to maintain the proportion of oxic: hypoxic tumour cells found in tumours growing in unirradiated beds, despite manifest changes in tumour necrosis and growth rate.
当肿瘤植入预先照射过的部位时,肿瘤生长速率会降低,即肿瘤床效应(TBE),据信这是由于血管基质受到辐射损伤,导致肿瘤血管生成缺陷。本研究探讨了在照射过的肿瘤床中生长的肿瘤,其受照射基质的功能不足是否伴随着缺氧部分的增加。对小鼠侧腹皮肤给予0或20 Gy的X射线照射,一周后将RIF-1纤维肉瘤细胞皮下注射到治疗区域中心。对体积为200 mm3的肿瘤在钳夹或未钳夹条件下进行照射,并通过相应存活曲线的位移在体外测定缺氧部分,结果显示缺氧部分略有增加。对三个独立实验的数据进行平均,缺氧细胞的百分比从未照射肿瘤床中生长的肿瘤细胞的2.5%增加到接受20 Gy照射的肿瘤床中肿瘤细胞的4.6%。因此,尽管肿瘤坏死和生长速率出现明显变化,但照射过的血管床在一定程度上仍能够维持未照射肿瘤床中生长的肿瘤所具有的有氧:缺氧肿瘤细胞比例。