Speetjens Frank M, de Bruin Elza C, Morreau Hans, Zeestraten Eliane C M, Putter Hein, van Krieken J Han, van Buren Maaike M, van Velzen Monique, Dekker-Ensink N Geeske, van de Velde Cornelis J H, Kuppen Peter J K
Department of Surgery, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands.
Cancer Immunol Immunother. 2008 May;57(5):601-9. doi: 10.1007/s00262-007-0396-y. Epub 2007 Sep 15.
To determine the clinical impact of human leukocyte antigen (HLA) class I expression in irradiated and non-irradiated rectal carcinomas.
Tumor samples in tissue micro array format were collected from 1,135 patients. HLA class I expression was assessed after immunohistochemical staining with two antibodies (HCA2 and HC10).
Tumors were split into two groups: (1) tumors with >50% of tumor cells expressing HLA class I (high) and (2) tumors with < or =50% of tumor cells expressing HLA class I (low). No difference in distribution or prognosis of HLA class I expression was found between irradiated and non-irradiated patients. Patients with low expression of HLA class I (15% of all patients) showed an independent significantly worse prognosis with regard to overall survival and disease-free survival. HLA class I expression had no effect on cancer-specific survival or recurrence-free survival.
Down-regulation of HLA class I in rectal cancer is associated with poor prognosis. In contrast to our results, previous reports on HLA class I expression in colorectal cancer described a large population of patients with HLA class I negative tumors, having a good prognosis. This difference might be explained by the fact that a large proportion of HLA negative colon tumors are microsatellite instable (MSI). MSI tumors are associated with a better prognosis than microsatellite stable (MSS). As rectal tumors are mainly MSS, our results suggest that it is both, oncogenic pathway and HLA class I expression, that dictates patient's prognosis in colorectal cancer. Therefore, to prevent confounding in future prognostic analysis on the impact of HLA expression in colorectal tumors, separate analysis of MSI and MSS tumors should be performed.
确定人类白细胞抗原(HLA)I类分子表达在接受照射和未接受照射的直肠癌中的临床影响。
从1135例患者中收集组织微阵列形式的肿瘤样本。用两种抗体(HCA2和HC10)进行免疫组织化学染色后评估HLA I类分子表达。
肿瘤被分为两组:(1)肿瘤细胞中HLA I类分子表达>50%的肿瘤(高表达组)和(2)肿瘤细胞中HLA I类分子表达≤50%的肿瘤(低表达组)。在接受照射和未接受照射的患者之间,未发现HLA I类分子表达的分布或预后存在差异。HLA I类分子低表达的患者(占所有患者的15%)在总生存期和无病生存期方面显示出独立的显著较差的预后。HLA I类分子表达对癌症特异性生存期或无复发生存期没有影响。
直肠癌中HLA I类分子的下调与预后不良相关。与我们的结果相反,先前关于结直肠癌中HLA I类分子表达的报告描述了大量HLA I类分子阴性肿瘤患者预后良好。这种差异可能是由于很大一部分HLA阴性结肠肿瘤是微卫星不稳定(MSI)的。MSI肿瘤的预后比微卫星稳定(MSS)肿瘤更好。由于直肠肿瘤主要是MSS,我们的结果表明,致癌途径和HLA I类分子表达都决定了结直肠癌患者的预后。因此,为了避免在未来关于HLA表达对结直肠肿瘤影响的预后分析中产生混淆,应分别对MSI和MSS肿瘤进行分析。