Vangsted A J, Clausen H, Kjeldsen T B, White T, Sweeney B, Hakomori S, Drivsholm L, Zeuthen J
Department of Tumor Cell Biology, Fibiger Institute, Danish Cancer Society, Copenhagen, Denmark.
Cancer Res. 1991 Jun 1;51(11):2879-84.
Recently, the ganglioside FucGM1 (Fuc alpha 1-2Gal beta 1-3GalNAc beta 1-4[NeuAc alpha 2-3]-Gal beta 1-4Glc beta 1-1 Cer) was identified as a small cell lung cancer (SCLC) marker both in chemical and histochemical studies. In order to further determine whether the FucGM1 ganglioside is shed from the tumor site and consequently is present in the serum of SCLC patients, we produced a series of new monoclonal antibodies raised against FucGM1 and related glycolipids. Shedding of the FucGM1 ganglioside was studied both in vitro and in vivo using SCLC cell lines and nude mice xenografts of SCLC cells as model systems, and finally immunochemical analyses were performed on serum samples from patients with SCLC. High-performance thin-layer chromatography immunostaining demonstrated the presence of FucGM1 in conditioned culture media obtained from FucGM1-positive SCLC cell lines. Furthermore, tumor extracts of SCLC cell line xenografts in nude mice were positive for the FucGM1 marker, and more importantly the marker was also present in serum samples from these mice. Twenty serum samples were obtained from patients with histologically verified SCLC. Eight patients had localized disease, and the remaining patients had disseminated cancer involving metastases to other organ sites. Sera from 4 of these patients were clearly positive, and 2 additional cases were found to be weakly positive. The positive patient sera were all from patients with extensive disease. Sera from 12 patients with non-SCLC and 20 healthy individuals were all found to be negative. These results clearly establish the FucGM1 glycolipid as a potential serum marker of SCLC for which a sensitive immunoassay should be developed and tested using a larger series of serum samples.
最近,在化学和组织化学研究中,神经节苷脂FucGM1(岩藻糖α1-2半乳糖β1-3N-乙酰半乳糖胺β1-4[唾液酸α2-3]-半乳糖β1-4葡萄糖β1-1神经酰胺)被鉴定为小细胞肺癌(SCLC)标志物。为了进一步确定FucGM1神经节苷脂是否从肿瘤部位脱落并因此存在于SCLC患者的血清中,我们制备了一系列针对FucGM1和相关糖脂的新单克隆抗体。使用SCLC细胞系和SCLC细胞的裸鼠异种移植作为模型系统,在体外和体内研究了FucGM1神经节苷脂的脱落情况,最后对SCLC患者的血清样本进行了免疫化学分析。高效薄层色谱免疫染色显示,从FucGM1阳性SCLC细胞系获得的条件培养基中存在FucGM1。此外,裸鼠中SCLC细胞系异种移植的肿瘤提取物对FucGM1标志物呈阳性,更重要的是,该标志物也存在于这些小鼠的血清样本中。从组织学确诊的SCLC患者中获得了20份血清样本。8例患者患有局限性疾病,其余患者患有扩散性癌症,已转移至其他器官部位。其中4例患者的血清明显呈阳性,另外2例弱阳性。阳性患者血清均来自患有广泛性疾病的患者。12例非SCLC患者和20名健康个体的血清均为阴性。这些结果明确证实FucGM1糖脂是SCLC的潜在血清标志物,应开发一种灵敏的免疫测定方法,并使用更多系列的血清样本进行检测。