Johnson M I, Hamdy F C
Department of Surgery, School of Surgical Sciences, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, NE2 4HH, UK.
Oncol Rep. 1998 May-Jun;5(3):553-7. doi: 10.3892/or.5.3.553.
Prostatic adenocarcinoma is emerging as a major cause of morbidity and mortality in the male population in the western world. Programmed cell death (apoptosis) in the prostate is activated by hormone ablation and is under the control of several regulating genes including the tumour suppressor gene p53 and the proto-oncogene bcl-2. Bcl-2 belongs to a rapidly expanding family of genes which form two functionally antagonistic groups controlling cell death and survival. Apoptosis regulating genes appear to play an important role in the development and progression of prostatic adenocarcinoma and offer a potential target for future therapeutic strategies.
前列腺腺癌正成为西方世界男性人群发病和死亡的主要原因。前列腺中的程序性细胞死亡(凋亡)由激素去除激活,并受包括肿瘤抑制基因p53和原癌基因bcl-2在内的多个调控基因控制。Bcl-2属于一个迅速扩展的基因家族,该家族形成两个功能拮抗的组,控制细胞死亡和存活。凋亡调控基因似乎在前列腺腺癌的发生和发展中起重要作用,并为未来的治疗策略提供了一个潜在靶点。