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Apoptotic and Non-Apoptotic Modalities of Thymoquinone-Induced Lymphoma Cell Death: Highlight of the Role of Cytosolic Calcium and Necroptosis

机译:胸腺酮诱导的淋巴瘤细胞死亡的凋亡和非凋亡方式:突出细胞溶质钙和坏凋亡的作用

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摘要

Diffuse large B cell lymphoma (DLBCL) represents the most common type of non-Hodgkin lymphoma with a high curability rate. However, 40% of patients will relapse or exhibit refractory disease, and compromised apoptotic pathways is among the prognosis-worsening factors. Therefore, drugging non-apoptotic modalities might be therapeutically promising. Thymoquinone (TQ) has been reported to promote apoptosis in cancer cells. Herein, we show that TQ selectively kills DLBCL cells, either cell lines or primary lymphoma cells bearing resistance features to standard treatment. Investigations show that, although TQ induced apoptotic markers, non-apoptotic death was the major mechanism responsible for TQ-induced cellular demise. We demonstrate critical and selective roles of cytosolic calcium and necroptosis in TQ-induced non-apoptotic cell death. Finally, TQ exhibits an improved selectivity profile over conventional chemotherapy. Collectively, this work provides new insights into the mode of action of TQ and points to the therapeutic relevance of non-apoptotic modalities as a fail-safe mechanism for pro-apoptotic DLBCL therapies.
机译:弥漫性大B细胞淋巴瘤(DLBCL)代表具有高可固化率的非霍奇金淋巴瘤类型。然而,40%的患者将复发或表现出耐火性疾病,并且受损的凋亡途径是预后恶化因素。因此,药物的非凋亡方式可能具有治疗上有前途。据报道,替米醌(TQ)促进癌细胞中的凋亡。在此,我们表明TQ选择性地杀死DLBCL细胞,细胞系或初级淋巴瘤细胞承载阻力特征以标准处理。调查表明,尽管TQ诱导凋亡标记,灭绝凋亡死亡是负责TQ诱导的细胞消亡的主要机制。我们展示了TQ诱导的非凋亡细胞死亡中的细胞溶质钙和坏死性的关键和选择性作用。最后,TQ在常规化疗中表现出改进的选择性概况。统称,这项工作为TQ的作用方式提供了新的见解,并指向非凋亡方式作为促凋亡DLBCL疗法的故障安全机制的治疗相关性。

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