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A monoclonal antibody for detection of folylpolyglutamate synthetase in paraffin embedded tissues.

机译:用于检测石蜡包埋组织中叶酰聚谷氨酸合成酶的单克隆抗体。

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摘要

Folate biochemical pathway enzymes such as folylpolyglutamate synthetase (FPGS) are key elements in the folate pathway. The role of FPGS is to add glutamate residues to folates and antifolates, trapping them in the cell and increasing their affinity for subsequent enzymatic reactions. FPGS may also be an indicator of response to both clinically established and novel antifolate drugs such as pemetrexed; knowledge of their level of expression in tumors may enable their optimal use by identifying potentially responsive subgroups of patients. In spite of its key role in both nucleotide biosynthesis and possible role as a determinant of response in chemotherapy, monoclonal antibodies to FPGS suitable for immunohistochemical analysis of formalin fixed and paraffin embedded biopsy samples, or that can be used for Western blot analysis, are not commercially available. The aim of this study was to generate a monoclonal antibody that could be used to detect specific expression of FPGS in paraffin embedded tissues. A 228 amino acid region of the FPGS sequence was expressed as a recombinant fusion protein and used as an antigen to generate monoclonal antibodies. ELISA and Western blot studies identified specific reactivity of the NN3.2 antibody to the recombinant protein and a single 60 kDa protein in whole cell lysates from cell lines known to express FPGS. Immunohistochemical analysis of FPGS using hybridoma clone NN3.2 in a panel of normal tissues demonstrated wide expression including strong immunoreactivity in the brush border and crypts of colon, liver hepatocytes, and lymphoid cells. Analysis of a panel of malignant and benign tissues demonstrated wide expression with variable intensities of staining and patterns of cytoplasmic reactivity. Stronger staining was observed in malignant tissue compared with that of normal adjacent tissue, particularly in ovarian and colon adenocarcinoma cases. Our results show that clone NN3.2 is a sensitive tool for detection of FPGS in paraffin-embedded tissues.
机译:叶酸生化途径酶(例如叶酰聚谷氨酸合成酶(FPGS))是叶酸途径中的关键元素。 FPGS的作用是将谷氨酸残基添加到叶酸和抗叶酸中,将其捕获在细胞中并增加其对后续酶促反应的亲和力。 FPGS可能也是对临床确定的和新型抗叶酸药物(如培美曲塞)反应的指标。了解它们在肿瘤中的表达水平,可能会通过确定潜在的患者亚组使其最佳应用。尽管FPGS的单克隆抗体在核苷酸生物合成中起着关键作用,并可能在化学反应中起决定作用,但它并不适合用于福尔马林固定和石蜡包埋的活检样品的免疫组织化学分析或可用于蛋白质印迹分析的FPGS单克隆抗体。市售。这项研究的目的是产生一种单克隆抗体,该抗体可用于检测石蜡包埋组织中FPGS的特异性表达。 FPGS序列的228个氨基酸区域表达为重组融合蛋白,并用作产生单克隆抗体的抗原。 ELISA和Western blot研究鉴定了NN3.2抗体对重组蛋白和来自已知表达FPGS的细胞系的全细胞裂解物中的单个60 kDa蛋白的特异性反应性。在一组正常组织中使用杂交瘤克隆NN3.2对FPGS进行免疫组织化学分析,结果表明该蛋白的表达广泛,包括在刷状缘和结肠,肝肝细胞和淋巴样细胞的隐窝中具有强免疫反应性。对一组恶性和良性组织的分析表明,其表达广泛,具有不同的染色强度和胞浆反应性模式。与正常相邻组织相比,在恶性组织中观察到更强的染色,尤其是在卵巢和结肠腺癌病例中。我们的结果表明,克隆NN3.2是检测石蜡包埋组织中FPGS的灵敏工具。

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