Venugopal M, Callaway A, Snyderwine E G
Chemical Carcinogenesis Section, Laboratory of Experimental Carcinogenesis, Division of Basic Sciences, National Cancer Institute, Bethesda, MD 20892-4255, USA.
Carcinogenesis. 1999 Jul;20(7):1309-14. doi: 10.1093/carcin/20.7.1309.
2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), a compound from cooked meat, is an established mammary gland carcinogen in female rats. Four doses of PhIP (150 mg/kg, p.o., once per day) were given to lactating Sprague-Dawley rats separated from their 10-day-old pups to initiate involution of the gland. Twenty-four hours after the last dose, apoptotic index in the mammary gland, as measured by the TUNEL assay, was significantly higher in the gland from control rats than in the PhIP-treated rats (4.757 +/- 1.066 versus 1.905 +/- 0.248%; P < 0.05). In comparison with controls, alveoli in the mammary gland of PhIP-treated rats were also visibly larger and contained more secretory epithelial cells. The expression of Bax, a stimulator of apoptosis, and Bcl-2, an inhibitor of apoptosis, were quantitated by western blotting. Accordingly, Bax expression was 2.7-fold higher in control rats, whereas Bcl-2 expression was 3.1-fold higher in PhIP-treated rats, both changes being statistically different (Student's t-test, P < 0.05). Immunohistochemistry further confirmed a lower expression of Bax and higher expression of Bcl-2 in secretory alveolar epithelial cells of the PhIP-treated mammary gland. The findings are consistent with the notion that exposure to PhIP retarded involution via partial inhibition of programmed cell death. To investigate possible mechanisms for the inhibitory effects of PhIP on mammary gland involution, serum levels of prolactin, an important hormone for the maintenance of lactation, were measured in virgin rats with regular estrous cycles given PhIP (150 mg/kg, p.o.) on the morning of diestrous. After one estrous cycle, on proestrous morning, serum prolactin levels were 1.3-fold higher after PhIP than after control vehicle (one-way ANOVA, Fisher LSD multiple comparison test, P < 0. 05). PhIP exposure during involution was associated with the induction of benign mammary tumors. Seven out of 12 rats developed fibroadenomas, and one developed a tubulopapillary carcinoma within 1 year of receiving PhIP administration during involution (150 mg/kg, p.o., once per day for 5 days), and a high-fat diet (23.5% corn oil). An increase in serum prolactin level and the effects on mammary gland apoptosis seen with PhIP may have implications for the mechanisms of carcinogenic targeting of PhIP to the mammary gland.
2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)是一种来自熟肉的化合物,是已确定的雌性大鼠乳腺致癌物。给与10日龄幼崽分离的哺乳期斯普拉格-道利大鼠灌胃四剂PhIP(150mg/kg,口服,每日一次)以启动乳腺退化。最后一剂后24小时,通过TUNEL检测法测得,对照大鼠乳腺中的凋亡指数显著高于PhIP处理组大鼠(4.757±1.066对1.905±0.248%;P<0.05)。与对照组相比,PhIP处理组大鼠乳腺中的肺泡也明显更大,且含有更多分泌性上皮细胞。通过蛋白质免疫印迹法定量检测凋亡刺激因子Bax和凋亡抑制因子Bcl-2的表达。结果显示,对照大鼠中Bax表达高2.7倍,而PhIP处理组大鼠中Bcl-2表达高3.1倍,两者变化均具有统计学差异(学生t检验,P<0.05)。免疫组织化学进一步证实,PhIP处理的乳腺分泌性肺泡上皮细胞中Bax表达较低,Bcl-2表达较高。这些发现与以下观点一致,即接触PhIP通过部分抑制程序性细胞死亡延缓了乳腺退化。为了研究PhIP对乳腺退化抑制作用的可能机制,在动情后期早晨给有规律动情周期的处女大鼠灌胃PhIP(150mg/kg,口服),并检测血清催乳素水平,催乳素是维持泌乳的重要激素。经过一个动情周期后,在动情前期早晨,PhIP处理组大鼠血清催乳素水平比对照载体处理组高1.3倍(单因素方差分析,Fisher LSD多重比较检验,P<0.05)。在乳腺退化期间接触PhIP与良性乳腺肿瘤的诱导有关。在接受退化期PhIP给药(150mg/kg,口服,每日一次,共5天)和高脂饮食(23.5%玉米油)的12只大鼠中,有7只发生了纤维腺瘤,1只在1年内发生了管状乳头状癌。PhIP导致的血清催乳素水平升高以及对乳腺细胞凋亡的影响可能与PhIP对乳腺致癌靶向作用的机制有关。