Bose Anamika, Haque Enamul, Baral Rathindranath
Department of Immunoregulation and Immunodiagnostics, Chittaranjan National Cancer Institute, 37, S. P. Mookherjee Road, Kolkata 700026, India.
Phytother Res. 2007 Oct;21(10):914-20. doi: 10.1002/ptr.2185.
A neem leaf preparation (NLP) was investigated for its role in the induction of tumor cell apoptosis to elucidate the mechanism of NLP mediated immunoprophylaxis in tumor growth restriction. As NLP did not induce direct apoptosis of human tumor cell lines KB, MCF7 and K562, it was used instead to stimulate human peripheral blood mononuclear cells (PBMC) for 72 h. The PBMC derived culture supernatant (NLP-CS) was observed to induce the restriction of tumor cell proliferation as well as apoptosis. An enzyme linked immunosorbant assay revealed the presence of cytotoxic cytokines, IFN-gamma and TNF-alpha, in the NLP-CS. The inhibition of secretion of IFN-gamma and TNF-alpha in NLP-CS caused a significant decrease in tumor cell apoptosis. Furthermore, stimulation of these tumor cells with NLP-CS resulted in upregulation of the caspase 3 and downregulation of the Bcl 2 and cyclin D1. These observations suggested that NLP could induce tumor cellular apoptosis by releasing cytotoxic cytokines from human PBMC.
为了阐明印楝叶制剂(NLP)介导的免疫预防在肿瘤生长抑制中的机制,对其在诱导肿瘤细胞凋亡中的作用进行了研究。由于NLP不会诱导人肿瘤细胞系KB、MCF7和K562直接凋亡,因此用它来刺激人外周血单个核细胞(PBMC)72小时。观察到PBMC来源的培养上清液(NLP-CS)可诱导肿瘤细胞增殖受限以及凋亡。酶联免疫吸附测定显示NLP-CS中存在细胞毒性细胞因子IFN-γ和TNF-α。NLP-CS中IFN-γ和TNF-α分泌的抑制导致肿瘤细胞凋亡显著减少。此外,用NLP-CS刺激这些肿瘤细胞导致caspase 3上调以及Bcl 2和细胞周期蛋白D1下调。这些观察结果表明,NLP可通过从人PBMC释放细胞毒性细胞因子来诱导肿瘤细胞凋亡。