Abstract LB-248: A novel multiplex assay for detection and quantitation of fatty acid synthase (FASN) in serum or plasma samples

N. Venkateswaran, W. Nelson
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Abstract

Many cancers overexpress FASN which catalyzes the final synthetic step of de novo fatty acid synthesis pathway. FASN has been considered as a potential drug target for several decades now. Many publications provide evidence of the elevated FASN with aggressive tumors, but still, there are very few inhibitors of FASN that have successfully been utilized as therapeutics in the clinical arena. An accurate measurement of FASN in association with tumor-specific markers in solid tumors and serum may help to propel forward the therapeutic significance of FASN inhibitors. With this objective in mind, we are currently working on the development of a multiplex assay for detection and quantitation of FASN and Cripto-1 in serum samples. We have optimized a magnetic fluorescent bead based multiplex sandwich immunoassay for detection and quantitation of FASN and Cripto-1 (CR-1) in human serum and plasma samples. We selected Cripto-1 to pair with FASN because it is an EGF-like domain carrying growth factor associated with a number of different types of human carcinomas. We use two different monoclonal antibodies for FASN and one for CR-1 as capture antibodies covalently coupled to magnetic fluorescent beads and a mixture of two biotin-labeled detection antibodies in this assay. The streptavidin-phycoerythrin (SAPE) conjugate is used to report the positive capture of a target in this assay. We have also included various internal controls in this assay to monitor the assay performance and assure quality of the reagents used in each well. The dynamic range of this assay was determined to be 100pg/mL to 100 ng/mL using recombinant FASN and Cripto-1 from commercial sources. The R2 values were 0.98 and above for each of the analytes and recovery of each standard were between 90 % and 125%. We spiked recombinant FASN and Cripto-1 in normal human serum and plasma at different concentrations and spike recovery was between 70 % and 130 %. We further evaluated this assay with some commercially obtained clinical samples. This presentation includes detailed results of this study. Citation Format: Neeraja Venkateswaran, William M. Nelson. A novel multiplex assay for detection and quantitation of fatty acid synthase (FASN) in serum or plasma samples [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2019; 2019 Mar 29-Apr 3; Atlanta, GA. Philadelphia (PA): AACR; Cancer Res 2019;79(13 Suppl):Abstract nr LB-248.
LB-248:一种用于检测和定量血清或血浆样品中脂肪酸合成酶(FASN)的新型多重检测方法
许多癌症过度表达FASN,它催化了脂肪酸新合成途径的最后合成步骤。几十年来,FASN一直被认为是一种潜在的药物靶点。许多出版物提供了侵袭性肿瘤中FASN升高的证据,但仍然有很少的FASN抑制剂已成功地用于临床治疗领域。准确测量FASN与实体瘤和血清中肿瘤特异性标志物的关联,可能有助于推进FASN抑制剂的治疗意义。考虑到这一目标,我们目前正在开发一种用于检测和定量血清样本中FASN和Cripto-1的多重检测方法。我们优化了一种基于磁荧光珠的多重三明治免疫分析法,用于检测和定量人血清和血浆样品中的FASN和cr1。我们选择Cripto-1与FASN配对,因为它是一种携带egf样结构域的生长因子,与许多不同类型的人类癌症相关。我们使用两种不同的FASN单克隆抗体和一种CR-1单克隆抗体作为捕获抗体,共价偶联到磁荧光珠和两种生物素标记的检测抗体的混合物。链亲和素-植红蛋白(SAPE)偶联物用于报告在该试验中目标的阳性捕获。我们还在该分析中加入了各种内部控制,以监测分析性能并确保每个孔中使用的试剂的质量。利用商业来源的重组FASN和Cripto-1确定该检测的动态范围为100pg/mL至100ng /mL。各分析物的R2值均在0.98及以上,各标准品的回收率在90% ~ 125%之间。我们将重组FASN和Cripto-1以不同浓度加标于正常人血清和血浆中,加标回收率在70% ~ 130%之间。我们用一些商业获得的临床样本进一步评估了这种检测方法。本报告包括本研究的详细结果。引文格式:Neeraja Venkateswaran, William M. Nelson。一种用于检测和定量血清或血浆样品中脂肪酸合成酶(FASN)的新型多重检测方法[摘要]。摘自:2019年美国癌症研究协会年会论文集;2019年3月29日至4月3日;亚特兰大,乔治亚州。费城(PA): AACR;癌症杂志2019;79(13增刊):摘要nr LB-248。
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