Tissue Culture Research Laboratory, Centre of Synthesis and Chemical Biology, Institute of Science, University Technology MARA, 40450 Shah Alam, Malaysia.
Molecules. 2010 Dec 17;15(12):9340-53. doi: 10.3390/molecules15129340.
The aim of this study was to investigate the in vitro cellular activity of novel spiroisoxazoline type compounds against normal and cancer cell lines from lung tissue (Hs888Lu), neuron-phenotypic cells (SH-SY5Y), neuroblastoma (SH-SY5Y), human histiocytic lymphoma (U937), lung cancer (A549), and leukaemia (HL-60). Our bioassay program revealed that the spiroisoxazoline type compounds show cytotoxicity only in lymphoma cell lines, which is in contrast with the pyrrolidine precursor of these spiroisoxazoline compounds, where significant cytotoxicity is seen in all normal and cancer cell lines. These data suggest a tumour-specific mechanism of action. In addition these data also show that spiroisoxazoline compounds are non-toxic in the human neuronphenotypic neuroblastoma SH-SY5Y cell line, and furthermore that they might protect cells from neurodegenerative disease.
本研究旨在研究新型螺环异恶唑啉类化合物对来自肺组织(Hs888Lu)、神经元表型细胞(SH-SY5Y)、神经母细胞瘤(SH-SY5Y)、人组织细胞淋巴瘤(U937)、肺癌(A549)和白血病(HL-60)的正常和癌细胞系的体外细胞活性。我们的生物测定计划显示,螺环异恶唑啉类化合物仅在淋巴瘤细胞系中表现出细胞毒性,这与这些螺环异恶唑啉化合物的吡咯烷前体形成对比,其中在所有正常和癌细胞系中均观察到显著的细胞毒性。这些数据表明存在肿瘤特异性作用机制。此外,这些数据还表明螺环异恶唑啉类化合物在人神经元表型神经母细胞瘤 SH-SY5Y 细胞系中无毒性,并且它们可能保护细胞免受神经退行性疾病的侵害。