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Lysyl oxidase (LOX) and hypoxia-induced metastases.

机译:赖氨酰氧化酶(LOX)和缺氧引起的转移。

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摘要

Angiogenesis is a critical process in the transition of tumors from a localized, primary site to a distant site of metastases. Hypoxic conditions within the tumor mass lead to the activation of signalling pathways which initiate tumor cell invasion, migration, adhesion and subsequent angiogenesis. Several key molecular players in hypoxia-induced tumor progression are well-described, e.g., hypoxia-inducible factor-1 (HIF-1) and angiopoietin-2; however, drug development aimed at suppressing individual members of this signalling cascade has proven to be challenging. The article by Erler et al. published in Nature (Vol. 440, April 2006) identifies lysyl oxidase (LOX) as an essential enzyme for hypoxia-induced metastases. This Journal Club reviews the findings presented by Erler and colleagues and briefly discusses the implications of LOX in cancer.
机译:血管生成是肿瘤从局部转移灶转移到远处转移的关键过程。肿瘤块内的低氧条件导致信号传导通路的激活,从而启动肿瘤细胞的侵袭,迁移,粘附和随后的血管生成。充分描述了缺氧诱导的肿瘤进展的几种关键分子参与者,例如,缺氧诱导因子-1(HIF-1)和血管生成素-2。然而,事实证明,旨在抑制该信号级联反应的各个成员的药物开发具有挑战性。 Erler等人的文章。发表于《自然》(第440卷,2006年4月)上的文章将赖氨酰氧化酶(LOX)鉴定为低氧诱导的转移的必需酶。该期刊俱乐部回顾了Erler及其同事提出的发现,并简要讨论了LOX在癌症中的意义。

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