Chaudhary K S, Abel P D, Lalani E N
Department of Histopathology, Imperial College School of Medicine, Hammersmith Campus, London, United Kingdom.
Environ Health Perspect. 1999 Feb;107 Suppl 1(Suppl 1):49-57. doi: 10.1289/ehp.99107s149.
Prostate cancer (PC) is an escalating health burden in the western world. A large number of patients still present with extraprostatic (i.e., T3/T4, N0, M0/M1 or any T category and M1 disease or involved lymph nodes) and therefore incurable disease. Since the work of Huggins in 1940, there have been no major therapeutic advances and androgen ablation remains the best treatment option for extraprostatic androgen-responsive PC. Eighty to ninety percent of PC patients respond well to this form of treatment initially. After a median time of approximately 2 years, however, relapse to an androgen-independent (AI) state occurs, followed by death after a further median 6 months. Androgen ablation is rarely curative. The major molecular defect in extraprostatic and AI PC is the inability of PC cells to initiate apoptosis in response to a variety of stimuli, including different forms of androgen ablation and cytotoxic agents. The balance between cellular proliferation and cell death is regulated by multiple genes or families of genes through the cell cycle. The exact mechanisms governing this intricate and complex process are as yet not fully understood. One family of genes involved in cell survival/death control is the Bcl-2 gene family, which consists of homologous proteins that function to regulate distal and crucial commitment steps of the apoptotic pathway. The Bcl-2 family constitutes both agonists and antagonists of apoptosis that function at least in part through protein-protein interactions between various members of the family. The final outcome depends on the relative ratio of death agonists and antagonists. Bcl-2 expression has been closely associated with the AI phenotype of PC. Cytotoxic chemotherapy may be used as palliative therapy in AI PC but has not been found effective. Most chemotherapeutic cytotoxic agents induce apoptosis in cancer cells by direct and indirect action on the cell cycle. In vitro and in vivo studies have established that Bcl-2 expression confers an antiapoptotic activity against androgen withdrawal and cytotoxic chemotherapy. It thus offers a tempting potential target for therapeutic manipulations of PC.
前列腺癌(PC)在西方世界正成为日益严重的健康负担。仍有大量患者表现为前列腺外侵犯(即T3/T4、N0、M0/M1或任何T分期及M1期疾病或伴有淋巴结转移),因此属于无法治愈的疾病。自1940年哈金斯的研究以来,一直没有重大的治疗进展,雄激素剥夺仍然是前列腺外雄激素反应性PC的最佳治疗选择。80%至90%的PC患者最初对这种治疗形式反应良好。然而,在大约2年的中位时间后,会复发至雄激素非依赖(AI)状态,随后在又经过6个月的中位时间后死亡。雄激素剥夺很少能治愈疾病。前列腺外及AI PC的主要分子缺陷是PC细胞无法响应多种刺激(包括不同形式的雄激素剥夺和细胞毒性药物)启动细胞凋亡。细胞增殖与细胞死亡之间的平衡由多个基因或基因家族通过细胞周期进行调节。控制这一复杂过程的确切机制尚未完全明确。参与细胞存活/死亡控制的一个基因家族是Bcl-2基因家族,它由同源蛋白组成,这些蛋白的功能是调节凋亡途径的远端和关键决定性步骤。Bcl-2家族既包含凋亡的激动剂,也包含拮抗剂,它们至少部分通过家族成员之间的蛋白质-蛋白质相互作用发挥作用。最终结果取决于死亡激动剂和拮抗剂的相对比例。Bcl-2表达与PC的AI表型密切相关。细胞毒性化疗可作为AI PC的姑息治疗,但尚未发现其有效。大多数化疗细胞毒性药物通过对细胞周期的直接和间接作用诱导癌细胞凋亡。体外和体内研究已证实,Bcl-2表达赋予了对雄激素撤除和细胞毒性化疗的抗凋亡活性。因此,它为PC的治疗操作提供了一个诱人的潜在靶点。