Liu J, Albert J, Geller J
Prostate. 1986;9(2):199-205. doi: 10.1002/pros.2990090210.
We studied the effects of megestrol acetate (MA) and ketoconazole (KC) on protein synthesis of epithelial and stromal cells of human prostate. Patients with benign prostatic hypertrophy (BPH) were treated with MA (160 mg/day) plus KC (1,200 mg/day) for 7 days. Prostate tissues obtained from transurethral resection (TURP) were separated into epithelial and stromal cells with 0.5% collagenase. The separated cells were incubated with L-35S-methionine in methionine-free MEM at 37 degrees C for 3 hr. The protein synthesis in both epithelial and stromal cells was significantly inhibited in the group treated with MA and KC when compared to a control group (p less than 0.05). The proteins incorporated with L-35S-methionine were analyzed by SDS-PAGE and autoradiography. The molecular weights of the epithelial and stromal proteins inhibited ranged between 35-55K.
我们研究了醋酸甲地孕酮(MA)和酮康唑(KC)对人前列腺上皮细胞和基质细胞蛋白质合成的影响。良性前列腺增生(BPH)患者接受MA(160毫克/天)加KC(1200毫克/天)治疗7天。经尿道前列腺切除术(TURP)获取的前列腺组织用0.5%胶原酶分离为上皮细胞和基质细胞。分离出的细胞在无蛋氨酸的MEM中与L-35S-甲硫氨酸于37℃孵育3小时。与对照组相比,MA和KC治疗组的上皮细胞和基质细胞中的蛋白质合成均受到显著抑制(p<0.05)。通过SDS-PAGE和放射自显影分析掺入L-35S-甲硫氨酸的蛋白质。被抑制的上皮细胞和基质细胞蛋白质的分子量在35 - 55K之间。