Krajewska Maryla, Zapata Juan M, Meinhold-Heerlein Ivo, Hedayat Hirad, Monks Anne, Bettendorf Herta, Shabaik Ahmed, Bubendorf Lukas, Kallioniemi Olli-P, Kim Hoguen, Reifenberger Guido, Reed John C, Krajewski Stanislaw
The Burnham Institute, Program on Apoptosis and Cell Death Regulation, La Jolla, CA 92037, USA.
Neoplasia. 2002 Mar-Apr;4(2):129-40. doi: 10.1038/sj.neo.7900222.
Bid is the only known Bcl-2 family member that can function as an agonist of proapoptotic Bcl-2-related proteins such as Bax and Bak. Expression of the proapoptotic Bcl-2 family protein Bid was assessed by immunoblotting and immunohistochemical methods in normal murine and human tissues, and in several types of human cancers and tumor cell lines. Bid expression in normal tissues varied widely, with prominent Bid immunostaining occurring in several types of short-lived cells (e.g., germinal center B cells, peripheral blood granulocytes, differentiated keratinocytes) and in apoptosis-sensitive cells (e.g., adult neurons). Analysis of Bid expression by immunostaining of 100 colon, 95 ovarian, and 254 prostate cancers, as well as 59 brain tumors and 50 lymphomas, revealed evidence of altered Bid regulation in some types of cancers. Correlations with clinical outcome data revealed association of higher levels of Bid with longer recurrence-free survival in men with locally advanced (T3 stage) prostate cancer (P=0.04). Immunoblot analysis of Bid protein levels in the NCI's panel of 60 human tumor cell lines revealed a correlation between higher levels of Bid and sensitivity to ribonucleotide reductase (RR)-inhibiting drugs (P<0.0005). Overexpression of Bid in a model tumor cell line by gene transfection resulted in increased sensitivity to apoptosis induction by a RR inhibitor. Taken together, these observations suggest a potential role for Bid in tumor responses to specific chemotherapeutic drugs, and lay a foundation for future investigations of this member of the Bcl-2 family in healthy and diseased tissues.
Bid是已知唯一能作为促凋亡的Bcl-2相关蛋白(如Bax和Bak)激动剂的Bcl-2家族成员。通过免疫印迹和免疫组化方法,在正常小鼠和人类组织、几种人类癌症及肿瘤细胞系中评估了促凋亡Bcl-2家族蛋白Bid的表达。Bid在正常组织中的表达差异很大,在几种类型的短命细胞(如生发中心B细胞、外周血粒细胞、分化的角质形成细胞)和凋亡敏感细胞(如成年神经元)中出现明显的Bid免疫染色。对100例结肠癌、95例卵巢癌、254例前列腺癌以及59例脑肿瘤和50例淋巴瘤进行免疫染色分析Bid表达,结果显示在某些类型的癌症中存在Bid调控改变的证据。与临床结局数据的相关性分析显示,在局部晚期(T3期)前列腺癌男性患者中,Bid水平较高与无复发生存期较长相关(P = 0.04)。对美国国立癌症研究所的60种人类肿瘤细胞系进行Bid蛋白水平的免疫印迹分析发现,Bid水平较高与对核糖核苷酸还原酶(RR)抑制药物的敏感性相关(P < 0.0005)。通过基因转染在模型肿瘤细胞系中过表达Bid,可导致对RR抑制剂诱导的凋亡敏感性增加。综上所述,这些观察结果提示Bid在肿瘤对特定化疗药物的反应中可能发挥作用,并为未来在健康和患病组织中研究这个Bcl-2家族成员奠定了基础。