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EphB6通过调节EphA2信号传导促进失巢凋亡。

EphB6 promotes anoikis by modulating EphA2 signaling.

作者信息

Akada Mai, Harada Kohei, Negishi Manabu, Katoh Hironori

机构信息

Laboratory of Molecular Neurobiology, Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.

Laboratory of Molecular Neurobiology, Graduate School of Biostudies, Kyoto University, Yoshidakonoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

Cell Signal. 2014 Dec;26(12):2879-84. doi: 10.1016/j.cellsig.2014.08.031. Epub 2014 Sep 17.

Abstract

Anoikis is a specific type of apoptosis induced by detachment of epithelial cells from extracellular matrix, and acquiring resistance to anoikis is an important step that enables cancer cells to metastasize. EphA2, which is overexpressed in a variety of human cancers, is phosphorylated by Akt on serine 897 and mediates ligand ephrin-independent promotion of anoikis resistance through the RhoG activator Ephexin4. EphB6 is frequently silenced in invasive and metastatic cancers; however, its role in cancer progression is poorly understood. Here we show that EphB6 interacts with EphA2 and suppresses EphA2-mediated promotion of anoikis resistance in MCF7 breast cancer cells. On the other hand, knockdown of EphB6 promotes anoikis resistance. We further show that expression of EphB6 decreases serine 897 phosphorylation of EphA2 and suppresses EphA2-Ephexin4 interaction and the RhoG activation. These findings implicate EphB6 as a negative regulator of EphA2 oncogenic signaling.

摘要

失巢凋亡是上皮细胞与细胞外基质脱离所诱导的一种特定类型的细胞凋亡,而获得对失巢凋亡的抗性是癌细胞发生转移的重要步骤。EphA2在多种人类癌症中过表达,其在丝氨酸897位点被Akt磷酸化,并通过RhoG激活剂Ephexin4介导非配体依赖性促失巢凋亡抗性。EphB6在侵袭性和转移性癌症中经常沉默;然而,其在癌症进展中的作用尚不清楚。在此我们表明,EphB6与EphA2相互作用,并在MCF7乳腺癌细胞中抑制EphA2介导的促失巢凋亡抗性。另一方面,敲低EphB6可促进失巢凋亡抗性。我们进一步表明,EphB6的表达降低了EphA2的丝氨酸897磷酸化,并抑制了EphA2-Ephexin4相互作用以及RhoG激活。这些发现表明EphB6是EphA2致癌信号传导的负调节因子。

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