Université de Picardie Jules Verne, UFR des Sciences, Laboratoire de Physiologie Cellulaire et Moléculaire (EA 4667), SFR CAP-SANTE (FED 4231), Amiens, France.
Department of Medical Biology L2-109, Academic Medical Center-University of Amsterdam, Meibergdreef 9, 1105AZ, Amsterdam, The Netherlands.
Cell Death Differ. 2018 Mar;25(4):693-707. doi: 10.1038/s41418-017-0007-1. Epub 2018 Jan 11.
Orai proteins are highly selective calcium channels playing an important role in calcium entry. Orai3 channels are overexpressed in breast cancer (BC) tissues, and involved in their proliferation, cell cycle progression and survival. Herein, we sought to address the involvement of Orai3 in resistance to chemotherapeutic drugs. Using high-throughput approaches, we investigated major changes induced by Orai3 overexpression, including downstream signaling mechanisms involved in BC chemotherapy resistance. Resistance was dependent on external calcium presence and thus Orai3 functionality. This effect allowed a downregulation of the p53 tumor suppressor protein expression via the pro-survival PI3K/Sgk-1/Sek-1 pathway. We demonstrated that p53 degradation occurred not only via Mdm2, but also via another unexpected E3 ubiquitin ligase, Nedd4-2. We found supporting bioinformatic evidence linking Orai3 overexpression and chemoresistance in large human BC data sets. Altogether, our results shed light on the molecular mechanisms activated in BC cells commonly found to overexpress Orai3, allowing resistance to chemotherapeutic drugs.
Orai 蛋白是高度选择性的钙离子通道,在钙离子内流中发挥重要作用。Orai3 通道在乳腺癌 (BC) 组织中过度表达,并参与其增殖、细胞周期进程和存活。在此,我们试图探讨 Orai3 在化疗药物耐药中的作用。我们使用高通量方法研究了 Orai3 过表达诱导的主要变化,包括参与 BC 化疗耐药的下游信号机制。耐药性依赖于外源性钙离子的存在和 Orai3 的功能。这种作用通过促进生存的 PI3K/Sgk-1/Sek-1 通路下调了抑癌蛋白 p53 的表达。我们证明了 p53 的降解不仅通过 Mdm2 发生,而且还通过另一种意想不到的 E3 泛素连接酶 Nedd4-2 发生。我们发现了支持生物信息学证据,将 Orai3 过表达与大型人类 BC 数据集中的化疗耐药联系起来。总之,我们的研究结果揭示了在普遍过度表达 Orai3 的 BC 细胞中激活的分子机制,导致对化疗药物的耐药性。