Dana-Farber Cancer Institute, 44 Binney St, Dana 520C, Boston, MA 02115, USA.
J Clin Oncol. 2010 Sep 10;28(26):4045-51. doi: 10.1200/JCO.2010.27.9992. Epub 2010 Jul 19.
Histopathologic examination reveals that most human tumors are associated with diverse immune cell infiltrates, but the roles of host reactions in disease pathogenesis and prognosis remain to be fully clarified. Recent investigations in genetically engineered murine tumor models have uncovered dual functions for immune responses during cancer development and progression. Alterations in tumor cell gene expression profiles and coding sequences may trigger the activation of cytotoxic lymphocytes, which act to restrain tumor growth. In contrast, persistent inflammatory reactions, which may be driven by infection, environmental toxins, or impaired immune regulation, create a microenvironment that fosters tumor cell growth, survival, invasion, and dissemination. The dynamic interplay of these competing responses appears to be a critical event in cancer pathogenesis, with tumor promotion and immune evasion proving dominant in clinically evident disease. Nonetheless, longitudinal studies of patient cohorts have demonstrated that particular histopathologic and genetic signatures of cytotoxic lymphocyte reactions provide important prognostic information. Here, we discuss the dual roles of immunity in cancer development, focusing on gastrointestinal malignancies, given the depth of recent insights into the mechanisms underlying these tumors.
组织病理学检查显示,大多数人类肿瘤都与多种免疫细胞浸润有关,但宿主反应在疾病发病机制和预后中的作用仍有待充分阐明。最近在基因工程小鼠肿瘤模型中的研究揭示了免疫反应在癌症发展和进展过程中的双重功能。肿瘤细胞基因表达谱和编码序列的改变可能会触发细胞毒性淋巴细胞的激活,从而抑制肿瘤生长。相比之下,持续的炎症反应可能由感染、环境毒素或免疫调节受损驱动,形成促进肿瘤细胞生长、存活、侵袭和扩散的微环境。这些相互竞争的反应的动态相互作用似乎是癌症发病机制中的一个关键事件,肿瘤促进和免疫逃逸在临床上明显的疾病中占主导地位。尽管如此,对患者队列的纵向研究表明,细胞毒性淋巴细胞反应的特定组织病理学和遗传特征提供了重要的预后信息。在这里,我们讨论了免疫在癌症发展中的双重作用,重点关注胃肠道恶性肿瘤,因为最近对这些肿瘤的机制有了更深入的了解。