Division of Cancer Studies, King's College London, London SE1 1UL, UK.
Open Biol. 2013 Jun 5;3(6):120159. doi: 10.1098/rsob.120159.
During tumour progression, oxygen tension in the microenvironment surrounding tumour cells is reduced, resulting in hypoxia. It is well established that cancer cells resist the negative effects of hypoxia by inducing angiogenesis predominantly via the activity of transcription factor hypoxia-inducible factor-1 (HIF-1). However, more recently HIF-1α has also been linked to increased invasive potential, although the molecular mechanisms remain to be defined. Invasive cancer cells are thought to employ membrane protrusions, termed invadopodia, to achieve matrix degradation. While many invadopodia components have been identified, signalling pathways that link extracellular stimuli to invadopodia formation remain largely unknown. Indeed, the relationship between invadopodia formation and HIF-1α has not been explored. We now report that HIF-1α is a driver of invadopodia formation. Furthermore, we have identified an important, direct and novel link between the Rho family activator β-PIX, HIF-1α and invadopodia formation. Indeed, we find that β-PIX expression is essential for invadopodia formation. In conclusion, we identify a new HIF-1α mechanistic pathway and suggest that β-PIX is a novel downstream signalling mediator during invadopodia formation.
在肿瘤进展过程中,肿瘤细胞周围微环境中的氧张力降低,导致缺氧。众所周知,癌细胞通过转录因子缺氧诱导因子-1(HIF-1)的活性主要诱导血管生成来抵抗缺氧的负面影响。然而,最近也发现 HIF-1α 与侵袭潜能的增加有关,尽管分子机制尚待确定。侵袭性癌细胞被认为利用膜突起,称为侵袭伪足,来实现基质降解。虽然已经鉴定出许多侵袭伪足成分,但将细胞外刺激与侵袭伪足形成联系起来的信号通路仍知之甚少。事实上,侵袭伪足形成与 HIF-1α 之间的关系尚未被探索。我们现在报告 HIF-1α 是侵袭伪足形成的驱动因素。此外,我们已经确定了 Rho 家族激活剂 β-PIX、HIF-1α 和侵袭伪足形成之间的重要、直接和新的联系。事实上,我们发现 β-PIX 的表达对于侵袭伪足的形成是必不可少的。总之,我们确定了一个新的 HIF-1α 机制途径,并提出β-PIX 是侵袭伪足形成过程中的一个新的下游信号转导介质。