Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai, India.
Oral Oncol. 2010 Sep;46(9):688-93. doi: 10.1016/j.oraloncology.2010.04.003. Epub 2010 Aug 21.
At our laboratory, we recently observed cell cycle and apoptosis-related proteins Myeloid Cell Leukemia-1 (Mcl-1) and Proliferating Cell Nuclear Antigen (PCNA) to be altered in oral tumours/cell lines. The present study aimed to evaluate the above proteins for predicting response and outcome in oral cancer patients treated with definitive radiotherapy. Pre-treatment oral cancer biopsy samples from 39 patients were examined for Mcl-1 and PCNA proteins using immunohistochemistry and correlated with clinico-pathological variables using disease-free survival (DFS) as the primary endpoint. We observed high expression of Mcl-1 in older versus younger patients (p=0.013) and in tobacco chewers+/-alcohol versus smokers+/-alcohol (p=0.037); and PCNA in node-positive versus node-negative tumours (p=0.037). On univariate analysis, high PCNA (p=0.007), Mcl-1 (p=0.050), node positivity (p=0.040) and co-expression of PCNA and Mcl-1 (p=0.008), had a significant impact on DFS. On multivariate analysis, low PCNA/Mcl-1 (p=0.006) co-expressing tumours were associated with improved DFS. Thus our study suggests that in patients undergoing primary radiotherapy, PCNA could be of potential predictive value to identify patients with risk of nodal metastases and in combination with Mcl-1 may have potential prognostic value to differentiate patients with poor DFS. These markers may be used for future trial patients requiring radiotherapy for their treatment.
在我们的实验室,我们最近观察到口腔肿瘤/细胞系中细胞周期和凋亡相关蛋白髓样细胞白血病-1 (Mcl-1) 和增殖细胞核抗原 (PCNA) 发生改变。本研究旨在评估这些蛋白在接受根治性放疗的口腔癌患者中的预测作用和预后。对 39 例口腔癌患者的治疗前口腔癌活检样本进行 Mcl-1 和 PCNA 蛋白的免疫组织化学检测,并结合无病生存 (DFS) 作为主要终点,与临床病理变量相关。我们观察到 Mcl-1 在老年患者中高表达,而在年轻患者中低表达 (p=0.013),在咀嚼烟草+/-饮酒者中高表达,而在吸烟者+/-饮酒者中低表达 (p=0.037);PCNA 在淋巴结阳性肿瘤中高表达,而在淋巴结阴性肿瘤中低表达 (p=0.037)。单因素分析显示,PCNA 高表达 (p=0.007)、Mcl-1 高表达 (p=0.050)、淋巴结阳性 (p=0.040) 和 PCNA 和 Mcl-1 共同表达 (p=0.008) 对 DFS 有显著影响。多因素分析显示,低 PCNA/Mcl-1 共同表达的肿瘤与 DFS 改善相关 (p=0.006)。因此,我们的研究表明,在接受根治性放疗的患者中,PCNA 可能具有潜在的预测价值,能够识别有淋巴结转移风险的患者,与 Mcl-1 联合使用可能具有潜在的预后价值,能够区分 DFS 较差的患者。这些标志物可能用于未来需要放疗治疗的试验患者。