Department of Surgery, Norris Cancer Center, Keck School of Medicine, University of Southern California, 1441 Eastlake Ave, NOR 6420, Los Angeles, CA 90089-9176, USA.
Mol Cancer. 2011 Mar 30;10:33. doi: 10.1186/1476-4598-10-33.
Small-cell lung cancer (SCLC) is the most aggressive lung cancer subtype and lacks effective early detection methods and therapies. A number of rare paraneoplastic neurologic autoimmune diseases are strongly associated with SCLC. Most patients with such paraneoplastic syndromes harbor high titers of antibodies against neuronal proteins that are abnormally expressed in SCLC tumors. These autoantibodies may cross-react with the nervous system, possibly contributing to autoimmune disease development. Importantly, similar antibodies are present in many SCLC patients without autoimmune disease, albeit at lower titers. The timing of autoantibody development relative to cancer and the nature of the immune trigger remain to be elucidated. Here we review what is currently known about SCLC-associated autoantibodies, and describe a recently developed mouse model system of SCLC that appears to lend itself well to the study of the SCLC-associated immune response. We also discuss potential clinical applications for these autoantibodies, such as SCLC diagnosis, early detection, and therapy.
小细胞肺癌(SCLC)是最具侵袭性的肺癌亚型,缺乏有效的早期检测方法和治疗手段。一些罕见的副肿瘤性神经自身免疫性疾病与 SCLC 强烈相关。大多数患有此类副肿瘤综合征的患者都携带有针对神经元蛋白的高滴度抗体,这些蛋白在 SCLC 肿瘤中异常表达。这些自身抗体可能与神经系统发生交叉反应,从而可能导致自身免疫性疾病的发展。重要的是,许多没有自身免疫性疾病的 SCLC 患者也存在类似的抗体,尽管滴度较低。自身抗体相对于癌症的发展时间和免疫触发的性质仍有待阐明。本文综述了目前已知的与 SCLC 相关的自身抗体,并描述了一种最近开发的 SCLC 小鼠模型系统,该系统似乎非常适合研究 SCLC 相关的免疫反应。我们还讨论了这些自身抗体的潜在临床应用,如 SCLC 的诊断、早期检测和治疗。