Sinicrope Frank A, Rego Rafaela L, Foster Nathan R, Thibodeau Stephen N, Alberts Steven R, Windschitl Harold E, Sargent Daniel J
Division of Oncology, Mayo Clinic, Guggenheim 10-11C, 200 1st Street Southwest, Rochester, MN 55905, USA.
Clin Cancer Res. 2008 Jul 1;14(13):4128-33. doi: 10.1158/1078-0432.CCR-07-5160.
Proapoptotic BH3-only proteins Bad and Bid initiate apoptosis by binding to regulatory sites on prosurvival Bcl-2 proteins to directly neutralize their function. We determined if expression of these proteins in colon cancers may account for differences in patient survival.
Tumor-node-metastasis stages II and III primary colon carcinomas from patients treated in 5-fluorouracil-based adjuvant therapy trials were studied. Immunohistochemical analysis of Bad and Bid proteins was done in tumors (n = 379) and adjacent normal mucosa. Expression was correlated with clinicopathologic variables, disease-free survival rates (DFS), and overall survival (OS) rates.
High expression of the Bad protein [hazard ratio (HR), 0.64; 95% confidence interval (95% CI), 0.43-0.96; P = 0.031] in the cytoplasm of tumor cells was significantly associated with more favorable OS in a univariate analysis. The combined Bad and Bid variable was prognostic for DFS (P = 0.027) and OS (P = 0.006). Stage and histologic grade, but not DNA mismatch repair status, were also prognostic for OS. Multivariate Cox analysis showed that high expression of Bad (HR, 0.64; 95% CI, 0.43-0.97; P = 0.027) and Bid (HR, 0.68; 95% CI, 0.49-0.97; P = 0.034) were independent predictors of OS after adjustment for stage, grade, age, treatment, and study. The combined variable of Bad + Bid was independently associated with DFS (P = 0.020) and OS (P = 0.004).
Proapoptotic Bad and Bid proteins are independent prognostic variables in colon cancer patients receiving adjuvant treatment. If validated, Bad and Bid expression may assist in risk stratification and selection of patients to receive adjuvant chemotherapy.
仅含BH3结构域的促凋亡蛋白Bad和Bid通过与抗凋亡Bcl-2蛋白上的调控位点结合,直接中和其功能,从而启动细胞凋亡。我们研究了这些蛋白在结肠癌中的表达是否可以解释患者生存率的差异。
对在基于5-氟尿嘧啶的辅助治疗试验中接受治疗的患者的II期和III期原发性结肠癌进行肿瘤-淋巴结-转移分期研究。对379例肿瘤及相邻正常黏膜进行Bad和Bid蛋白的免疫组织化学分析。将表达与临床病理变量、无病生存率(DFS)和总生存率(OS)进行关联分析。
在单因素分析中,肿瘤细胞胞质中Bad蛋白的高表达[风险比(HR),0.64;95%置信区间(95%CI),0.43 - 0.96;P = 0.031]与更有利的总生存率显著相关。Bad和Bid的联合变量对DFS(P = 0.027)和OS(P = 0.006)具有预后价值。分期和组织学分级对OS也具有预后价值,但DNA错配修复状态无此作用。多因素Cox分析显示,在对分期、分级、年龄、治疗和研究进行校正后,Bad(HR,0.64;95%CI,0.43 - 0.97;P = 0.027)和Bid(HR,0.68;95%CI,0.49 - 0.97;P = 0.034)的高表达是OS的独立预测因素。Bad + Bid的联合变量与DFS(P = 0.020)和OS(P = 0.004)独立相关。
促凋亡的Bad和Bid蛋白是接受辅助治疗的结肠癌患者的独立预后变量。如果得到验证,Bad和Bid的表达可能有助于风险分层以及选择接受辅助化疗的患者。