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用于检测癌胚抗原(CEA)阳性癌细胞的绿色荧光共轭抗CEA单链抗体。

Green fluorescent-conjugated anti-CEA single chain antibody for the detection of CEA-positive cancer cells.

作者信息

Salavatifar Maryam, Amin Shadi, Jahromi Zahra Moghaddassi, Rasgoo Nasrin, Rastgoo Nasrin, Arbabi Mehdi

机构信息

Khatam Institute of Higher Education, Tehran, Iran.

出版信息

Hybridoma (Larchmt). 2011 Jun;30(3):229-38. doi: 10.1089/hyb.2011.0009.

Abstract

According to World Health Organization (WHO), cancer is a leading cause of death worldwide, accounting for 7.4 million deaths (around 13% of all deaths) in 2004. Monoclonal/recombinant antibodies, which specifically target clinical biomarkers of disease, have increasingly been applied as powerful tools in cancer imaging and therapy, a fact that is highlighted by some nine FDA-approved monoclonal antibodies (MAbs) or their immunoconjugates (as of December 2008) for use in cancer treatment. In this study, five monoclonal antibodies (MAbs) were generated and characterized against carcinoembryonic antigen (CEA), which is widely used clinically as both a blood and tissue tumor marker of epithelial malignancy. Variable domains (VH and VL) of one the stable MAbs with highest affinity were PCR-amplified and assembled as single-chain antibody fragment (scFv). Following the cloning and expression of scFv antibody fragments in Escherichia coli, the functional binding and specificity of the recombinant antibody were confirmed by ELISA. To develop a direct in vitro detection of CEA-positive cancer cells, scFv DNA was genetically fused to enhanced green fluorescent protein (EGFP) gene and expressed in bacteria. The chimeric fluorescent protein is able to specifically detect CEA-positive cell lines; no cross-reactivity was observed with a negative control cell line. This strategy will likely allow the establishment of a rapid, single-step detection assay of CEA, which is considered to be one of the best predictors of malignancy among all other tumor markers.

摘要

根据世界卫生组织(WHO)的数据,癌症是全球主要的死亡原因之一,2004年有740万人死于癌症(约占总死亡人数的13%)。单克隆/重组抗体能够特异性靶向疾病的临床生物标志物,越来越多地被用作癌症成像和治疗的有力工具,截至2008年12月,约有九种经美国食品药品监督管理局(FDA)批准的单克隆抗体(MAb)或其免疫缀合物用于癌症治疗,这一事实凸显了这一点。在本研究中,针对癌胚抗原(CEA)产生并鉴定了五种单克隆抗体(MAb),CEA在临床上广泛用作上皮恶性肿瘤的血液和组织肿瘤标志物。对一种亲和力最高的稳定单克隆抗体的可变区(VH和VL)进行PCR扩增,并组装成单链抗体片段(scFv)。在大肠杆菌中克隆和表达scFv抗体片段后,通过酶联免疫吸附测定(ELISA)确认了重组抗体的功能结合和特异性。为了开发一种直接体外检测CEA阳性癌细胞的方法,将scFv DNA与增强型绿色荧光蛋白(EGFP)基因进行基因融合,并在细菌中表达。嵌合荧光蛋白能够特异性检测CEA阳性细胞系;未观察到与阴性对照细胞系的交叉反应。这种策略可能会建立一种快速、单步的CEA检测方法,CEA被认为是所有其他肿瘤标志物中恶性肿瘤的最佳预测指标之一。

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