Interaction studies of flavonoids with Bcl-2 protein to re-activate apoptosis in JurkatT-cells by induced TRAIL

Manjunatha Bukkambudi Krishnaswamy, V. Kanagasabapathy, A. Gomathi, Dr. Ramachandrappa, Pratheeksha Gurumurthy, R. Kumar, Urvi Narayan, Krithika Shanmugam, Girinath G. Pillai
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引用次数: 0

Abstract

Immune cell malignancy such as Acute T- cell Lymphoblastic Leukaemia is generally associated with high rate of relapse and often does not respond to salvage therapy. Thus, identification of novel treatment regimens or cell apoptosis pathways and therapeutic agents without major side effects is necessary. TRAIL-induced apoptotic pathway is one such pathway that is usually blocked by anti-apoptotic proteins like Bcl-2. This research estimated and compared the ability of few common flavonoids to re-activate TRAIL-induced apoptosis by blocking Bcl-2 protein. Studies were carried out to understand the interaction between binding energy of the Flavonoids with Bcl-2 protein in cancer cells. The pharmacokinetic and toxicity profiling was performed to study the potency of the flavonoids as a lead candidate. Baicalein was selected as lead molecule because of its lower binding energy and its ability to increase Mitochondrial Membrane Potential as studied from its ADME properties. For validation of apoptosis of Baicalein by TRAIL-induced owing to Bcl-2 analysis of cell cycle and Gene expression studies were carried out on Jurkat T cells.
黄酮类化合物与Bcl-2蛋白相互作用诱导TRAIL重新激活jurkat细胞凋亡的研究
免疫细胞恶性肿瘤,如急性T细胞淋巴细胞白血病,通常与高复发率相关,并且通常对挽救性治疗没有反应。因此,确定新的治疗方案或细胞凋亡途径和无主要副作用的治疗剂是必要的。trail诱导的凋亡途径就是其中一种,通常被Bcl-2等抗凋亡蛋白阻断。本研究估计并比较了几种常见的黄酮类化合物通过阻断Bcl-2蛋白重新激活trail诱导的细胞凋亡的能力。研究了黄酮类化合物的结合能与肿瘤细胞中Bcl-2蛋白的相互作用。通过药代动力学和毒性分析来研究黄酮类化合物作为主要候选物的效力。从黄芩素的ADME特性来看,黄芩素具有较低的结合能和增加线粒体膜电位的能力,因此被选为先导分子。为了验证trail诱导Bcl-2诱导黄芩素凋亡,我们在Jurkat T细胞上进行了细胞周期分析和基因表达研究。
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来源期刊
Asia-pacific Journal of Molecular Biology and Biotechnology
Asia-pacific Journal of Molecular Biology and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
0.90
自引率
0.00%
发文量
25
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