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Carbonic anhydrase IX correlates with survival and is a potential therapeutic target for neuroblastoma

机译:碳酸酐酶IX与生存有关,是神经母细胞瘤的潜在治疗靶标

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Abstract Carbonic anhydrase IX (CAIX) is involved in pathological processes including tumorgenicity, metastases and poor survival in solid tumors. Twenty-two neuroblastoma samples of patients who were surgically treated at the University Medical Center Hamburg-Eppendorf were evaluated immunohistochemically for expression of CAIX. Results were correlated with clinical parameters and outcome. Neuroblastoma Kelly and SH-EP-Tet-21/N cells were examined for CAIX expression and inhibited with specific inhibitors, FC5-207A and FC8-325A. 32% of neuroblastoma tumors expressed CAIX. This was significantly associated with poorer survival. Kelly and SH-EP-Tet-21/N cells showed a major increase of CAIX RNA under hypoxic conditions. Proliferation of Kelly cells was significantly decreased by CAIX inhibitors, FC5-207A and FC8-325A, while proliferation of SH-EP-Tet-21/N cells was only significantly affected by FC8-325A. CAIX is a potent biomarker that predicts survival in neuroblastoma patients. CAIX-targeted therapy in neuroblastoma cell lines is highly effective and strengthens the potential of CAIX as a clinical therapeutic target in a selected patient collective.
机译:摘要碳酸酐酶IX(CAIX)参与病理过程,包括实体瘤的致瘤性,转移和不良生存。在汉堡-埃彭多夫大学医学中心接受手术治疗的22例神经母细胞瘤样品中,采用免疫组织化学方法评估了CAIX的表达。结果与临床参数和结果相关。检查神经母细胞瘤凯利和SH-EP-Tet-21 / N细胞的CAIX表达,并用特异性抑制剂FC5-207A和FC8-325A抑制。 32%的神经母细胞瘤肿瘤表达CAIX。这与较差的存活率显着相关。 Kelly和SH-EP-Tet-21 / N细胞在缺氧条件下显示出CAIX RNA的大量增加。 CAIX抑制剂FC5-207A和FC8-325A显着降低了Kelly细胞的增殖,而SH-EP-Tet-21 / N细胞的增殖仅受FC8-325A显着影响。 CAIX是预测神经母细胞瘤患者生存的有效生物标志物。针对神经母细胞瘤细胞系的CAIX靶向疗法非常有效,并增强了CAIX作为选定患者群体中临床治疗靶标的潜力。

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