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Regulation of apoptosis in health and disease: the balancing act of BCL-2 family proteins

机译:健康与疾病细胞凋亡的调节:BCL-2家族蛋白的平衡学

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The loss of vital cells within healthy tissues contributes to the development, progression and treatment outcomes of many human disorders, including neurological and infectious diseases as well as environmental and medical toxicities. Conversely, the abnormal survival and accumulation of damaged or superfluous cells drive prominent human pathologies such as cancers and autoimmune diseases. Apoptosis is an evolutionarily conserved cell death pathway that is responsible for the programmed culling of cells during normal eukaryotic development and maintenance of organismal homeostasis. This pathway is controlled by the BCL-2 family of proteins, which contains both pro-apoptotic and pro-survival members that balance the decision between cellular life and death. Recent insights into the dynamic interactions between BCL-2 family proteins and how they control apoptotic cell death in healthy and diseased cells have uncovered novel opportunities for therapeutic intervention. Importantly, the development of both positive and negative small-molecule modulators of apoptosis is now enabling researchers to translate the discoveries that have been made in the laboratory into clinical practice to positively impact human health.
机译:健康组织内的重要细胞丧失有助于许多人类疾病的发展,进展和治疗结果,包括神经和传染病以及环境和医学毒性。相反,损坏或多余细胞的异常存活率和积累使突出的人类病理如癌症和自身免疫性疾病。细胞凋亡是一种进化的保守细胞死亡途径,该途径负责在正常真核发育和维持有机体稳态期间细胞的编程剔除。该途径由BCL-2蛋白质系列控制,该蛋白质含有促凋亡和潜水期成员,这些成员平衡了细胞生死之间的决定。最近对BCL-2家族蛋白质之间的动态相互作用以及它们在健康和患病细胞中控制凋亡细胞死亡的动态相互作用已经发现了对治疗干预的新机遇。重要的是,凋亡的阳性和阴性小分子调节剂的发展现在使研究人员能够将在实验室中所做的发现转化为临床实践,以积极影响人类健康。

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