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New Monoclonal Antibodies for a Selective Detection of Membrane-Associated and Soluble Forms of Carbonic Anhydrase IX in Human Cell Lines and Biological Samples

机译:选择性检测人类细胞系和生物样品中膜相关和可溶性形式的碳酸酐酶IX的新型单克隆抗体

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摘要

Monoclonal antibodies (MAbs) selectively targeting tumor-associated antigens such as carbonic anhydrase IX (CA IX) can significantly contribute to research, diagnostics, and treatment of CA IX-related cancers. CA IX is overexpressed in numerous hypoxic cancers where it promotes tumor progression. Therefore, it is considered as a promising tumor biomarker. A novel collection of MAbs against recombinant CA IX was developed and evaluated in different immunoassays for studying CA IX expression. The reactivity of MAbs with native cell surface protein was confirmed by flow cytometry and the presence of hypoxia-inducible CA IX was investigated in several human cancer cell lines. In addition, the applicability of MAbs for visualization of CA IX-positive tumor cells by immunofluorescence microscopy was demonstrated. MAb H7 was identified as the most promising MAb for different immunoassays. It recognized a linear epitope covering CA IX sequence of 12 amino acid residues 55-GEDDPLGEEDLP-66 within the proteoglycan domain. The MAb H7 was the only one of the collection to immunoprecipitate CA IX protein from cell lysates and detect the denatured CA IX with near-infrared fluorescence Western blot. It was also employed in sandwich enzyme-linked immunosorbent assay to detect a soluble form of CA IX in growth medium of tumor cells and blood plasma samples. The diagnostic potential of the MAb H7 was confirmed on formalin-fixed and paraffin-embedded tissue specimen of cervical carcinoma in situ by immunohistochemistry. The generated MAbs, in particularly clone H7, have great potential in diagnostics and research of CA IX-related cancers.
机译:选择性靶向肿瘤相关抗原(例如碳酸酐酶IX(CA IX))的单克隆抗体(MAb)可以极大地促进CA IX相关癌症的研究,诊断和治疗。 CA IX在许多缺氧性癌症中均过表达,从而促进肿瘤的进展。因此,它被认为是有希望的肿瘤生物标志物。开发了针对重组CA IX的新型单克隆抗体,并在用于研究CA IX表达的不同免疫测定中进行了评估。通过流式细胞术证实了单克隆抗体与天然细胞表面蛋白的反应性,并且在几种人类癌细胞系中研究了低氧诱导型CA IX的存在。另外,证明了MAb通过免疫荧光显微镜观察CA IX阳性肿瘤细胞的适用性。 MAb H7被确定为不同免疫测定方法中最有前途的MAb。它识别出一个线性表位,覆盖了蛋白聚糖结构域中12个氨基酸残基55-GEDDPLGEEDLP-66的CA IX序列。 MAb H7是唯一可从细胞裂解物中免疫沉淀CA IX蛋白并使用近红外荧光Western印迹检测变性的CA IX的集合之一。它也用于夹心酶联免疫吸附测定中,以检测肿瘤细胞和血浆样品生长培养基中CA IX的可溶形式。 MAb H7的诊断潜力通过免疫组织化学方法在原位宫颈癌的福尔马林固定和石蜡包埋的组织标本中得到证实。产生的单克隆抗体,特别是克隆H7,在CA IX相关癌症的诊断和研究中具有巨大潜力。

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