Watson Nicholas F S, Durrant Lindy G, Madjd Zahra, Ellis Ian O, Scholefield John H, Spendlove Ian
Academic Department of Clinical Oncology, City Hospital, University of Nottingham, Hucknall Road, Nottingham, NG5 1PB, UK.
Cancer Immunol Immunother. 2006 Aug;55(8):973-80. doi: 10.1007/s00262-005-0055-0. Epub 2005 Sep 3.
It has been known for some time that the immune system can recognise growing tumours, and that tumours may respond by modulation of molecules, which make them resistant to further attack. Expression, over-expression, or loss of these molecules may function as markers of tumour progression and prognosis. Among such molecules are the membrane-bound complement regulatory proteins (mCRP), which protect cells from bystander attack by autologous complement. These include CD59 (protectin), which prevents formation of the MAC complex in the terminal stages of complement activation. In the present study, we evaluated immunohistochemical expression of CD59 in a series of over 460 well-characterised colorectal cancers using tissue microarrays (TMA), and related this information to known tumour and patient variables and to survival. The CD59 expression was observed in 69 (15%) of cases overall, and was significantly associated with tumour grade. In contrast, no associations were noted with tumour site, stage or histological type. On survival analysis, a further correlation was observed between expression of CD59 by the colorectal tumours and a reduction in disease-specific patient survival. This observation was strongest for patients with early stage disease. However, a negative impact on survival was also seen in those patients with late stage disease. These results indicate that TMA linked to good clinicopathological databases with good long term follow up are useful tools for determining new prognostic indicators that can be used in future patient management. Immune surveillance may result in immune-editing that induces variable expression of a range of target antigens, and these may be useful prognostic markers. This study has identified CD59 expression as a marker of poor prognosis in colorectal cancer patients.
免疫系统能够识别正在生长的肿瘤,且肿瘤可能通过调节分子作出反应,使其对进一步的攻击产生抗性,这一现象已为人所知有一段时间了。这些分子的表达、过表达或缺失可能作为肿瘤进展和预后的标志物。此类分子包括膜结合补体调节蛋白(mCRP),其可保护细胞免受自身补体的旁观者攻击。其中包括CD59(保护素),它可在补体激活的终末阶段阻止膜攻击复合物(MAC)的形成。在本研究中,我们使用组织微阵列(TMA)评估了460多例特征明确的结直肠癌中CD59的免疫组化表达,并将此信息与已知的肿瘤和患者变量以及生存率相关联。总体上在69例(15%)病例中观察到CD59表达,且其与肿瘤分级显著相关。相比之下,未发现与肿瘤部位、分期或组织学类型有关联。在生存分析中,观察到结直肠癌中CD59的表达与患者疾病特异性生存率降低之间存在进一步的相关性。这一观察结果在早期疾病患者中最为明显。然而,在晚期疾病患者中也观察到对生存有负面影响。这些结果表明,与良好的临床病理数据库相关联并进行长期良好随访的TMA是确定可用于未来患者管理的新预后指标的有用工具。免疫监视可能导致免疫编辑,从而诱导一系列靶抗原的可变表达,而这些可能是有用的预后标志物。本研究已确定CD59表达是结直肠癌患者预后不良的标志物。