Department of Physiology and Medical Physics, Dublin, Ireland.
Br J Cancer. 2012 Apr 24;106(9):1499-1505. doi: 10.1038/bjc.2012.133.
Critical to successful execution of mitochondrial-mediated apoptosis is apoptosome formation and subsequent activation of caspases. Defects in this pathway have an important role in colorectal carcinogenesis and chemoresistance; therefore, the expression of apoptosome-associated proteins may be associated with clinical outcome and response to chemotherapy.
Here we performed a systematic analysis of the immunohistochemical expression of the key proteins involved in apoptosome-dependent caspase activation (APAF1, Pro-caspases 9 and 3, SMAC, and XIAP) in a cohort of Stage II and III colorectal cancer patients from a Phase III trial of adjuvant 5-fluorouracil-based chemotherapy vs postoperative observation alone.
Survival analysis indicated that of the apoptosome-associated proteins examined here, Pro-caspase 3 and APAF1 have potential clinical utility as predictive markers in Stage II and III colorectal cancer, respectively. Interestingly, we identified APAF1 staining to be associated with better recurrence-free and overall survival in patients receiving chemotherapy.
These studies reveal the importance of the apoptosome-dependent caspase activation pathway, specifically Pro-caspase 3 and APAF1 proteins, for predicting both prognosis and response to therapy.
成功执行线粒体介导的细胞凋亡的关键是凋亡小体的形成和随后的胱天蛋白酶的激活。该途径的缺陷在结直肠发生和化学抗性中起着重要作用;因此,凋亡小体相关蛋白的表达可能与临床结果和对化疗的反应有关。
在这里,我们对 III 期试验中接受辅助基于 5-氟尿嘧啶的化疗与单独术后观察的 II 期和 III 期结直肠癌患者队列中参与凋亡小体依赖性胱天蛋白酶激活的关键蛋白(APAF1、Pro-caspases 9 和 3、SMAC 和 XIAP)的免疫组织化学表达进行了系统分析。
生存分析表明,在研究的凋亡小体相关蛋白中,Pro-caspase 3 和 APAF1 分别作为 II 期和 III 期结直肠癌的预测标志物具有潜在的临床应用价值。有趣的是,我们发现 APAF1 染色与接受化疗的患者无复发生存和总生存的改善相关。
这些研究揭示了凋亡小体依赖性胱天蛋白酶激活途径的重要性,特别是 Pro-caspase 3 和 APAF1 蛋白,可预测预后和对治疗的反应。