Lurie A G, Rippey R M
Radiat Res. 1987 Feb;109(2):227-37.
Studies examined the effects of acute and fractionated low to moderate level X-ray exposures on hamster cheek pouch carcinogenesis in vivo by 7,12-dimethylbenz(a)anthracene (DMBA). Animals were grouped by treatment as follows: acute doses of 0.85-3.40 Gy X rays; 17 once weekly doses of 0.01-0.20 Gy X rays (fractionated radiation); topical DMBA for 10 weeks; DMBA plus fractionated radiation starting together; DMBA plus acute radiation in Week 1 or 10 of DMBA treatments; and sham irradiation, DMBA vehicle, or anesthesia controls. After 44 weeks, hamsters were sacrificed, and their cheek pouches were excised, serially sectioned, and examined by light microscopy for histopathology. No histologic changes were observed in radiation-only hamsters. Carcinoma incidences in DMBA-only groups ranged from 45 to 60%. Carcinoma incidences were greater in groups receiving DMBA plus fractionated radiation than in groups receiving either acute radiation + DMBA or DMBA alone. Carcinoma incidences in acute radiation plus DMBA groups were lower than those in DMBA-only groups. These results suggest complex interactions between radiation and DMBA, perhaps with radiogenic cell killing being a principal factor in acute radiation + DMBA groups, and reciprocal additive or synergistic effects of radiation and DMBA on cancer induction and manifestation in fractionated radiation + DMBA groups.
研究通过7,12-二甲基苯并(a)蒽(DMBA)检测了急性和分次低至中等剂量X射线照射对体内仓鼠颊囊致癌作用的影响。动物按治疗分组如下:急性剂量为0.85 - 3.40 Gy X射线;每周一次,共17次,每次剂量为0.01 - 0.20 Gy X射线(分次照射);局部涂抹DMBA 10周;DMBA与分次照射同时开始;在DMBA治疗的第1周或第10周给予DMBA加急性照射;以及假照射、DMBA赋形剂或麻醉对照。44周后,处死仓鼠,切除其颊囊,连续切片,并通过光学显微镜检查组织病理学。仅接受辐射的仓鼠未观察到组织学变化。仅接受DMBA的组中癌发生率在45%至60%之间。接受DMBA加分次照射的组中癌发生率高于接受急性照射+DMBA或仅接受DMBA的组。急性照射加DMBA组的癌发生率低于仅接受DMBA的组。这些结果表明辐射与DMBA之间存在复杂的相互作用,可能在急性照射+DMBA组中放射致细胞死亡是主要因素,而在分次照射+DMBA组中辐射与DMBA对癌症诱导和表现存在相互累加或协同作用。