Recent patents concerning targeted therapy of apoptosis resistance in pancreatic cancer.

Kristin Werner, Felix Rückert, Hans-Detlev Saeger, Robert Grützmann, Christian Pilarsky
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引用次数: 7

Abstract

Pancreatic cancer is one of the most malignant forms of cancer. Due to numerous defects of the apoptosis machinery this tumor shows a high resistance towards conventional oncological therapies. On the level of the extrinsic pathway, signal transduction is flawed by over-expression of decoy receptors but also by a dysfunctional death inducing signaling complex (DISC). The mitochondrial pathway, normally stimulated by cell stress and toxic agents is impeded by over-expression of anti-apoptotic members of the Bcl 2 protein family and the so-called inhibitor of apoptosis proteins (IAPs). To overcome the dysfunction of the apoptosis pathway, new therapeutics focus on molecular targets within the apoptosis pathway. Recently, many new treatment modalities have been reported like recombinant ligands of the cell death receptors or inhibitors of anti-apoptotic Bcl-2 members. Furthermore, various substances for the direct activation of the caspase cascade were patented and the over-expression of IAPs could be treated by binding inhibitors or using RNA interference techniques. The present review aims at giving an overview on these new treatment modalities.

胰腺癌细胞凋亡耐药靶向治疗新专利。
胰腺癌是最恶性的癌症之一。由于细胞凋亡机制的许多缺陷,这种肿瘤对常规肿瘤治疗表现出很高的耐药性。在外在通路的水平上,信号转导由于诱饵受体的过度表达以及功能失调的死亡诱导信号复合体(DISC)而存在缺陷。线粒体途径通常受到细胞应激和有毒物质的刺激,但被Bcl 2蛋白家族抗凋亡成员和所谓的凋亡抑制蛋白(IAPs)的过度表达所阻碍。为了克服细胞凋亡途径的功能障碍,新的治疗方法关注细胞凋亡途径中的分子靶点。最近,许多新的治疗方式被报道,如细胞死亡受体的重组配体或抗凋亡Bcl-2成员的抑制剂。此外,用于直接激活caspase级联的各种物质已获得专利,IAPs的过表达可以通过结合抑制剂或RNA干扰技术进行处理。本综述旨在对这些新的治疗方式进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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