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EGFR 与 EphA2 之间的相互作用通过 Ephexin1 的作用促进肿瘤发生。

Interactions between EGFR and EphA2 promote tumorigenesis through the action of Ephexin1.

机构信息

Laboratory of Genomic Instability and Cancer therapeutics, Chosun University School of medicine, 375 Seosuk-dong, Gwangju, 501-759, South Korea.

Department of Pharmacology, Chosun University School of medicine, 375 Seosuk-dong, Gwangju, 501-759, South Korea.

出版信息

Cell Death Dis. 2022 Jun 6;13(6):528. doi: 10.1038/s41419-022-04984-6.

DOI:10.1038/s41419-022-04984-6
PMID:35668076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9170705/
Abstract

The cell signaling factors EGFR, EphA2, and Ephexin1 are associated with lung and colorectal cancer and play an important role in tumorigenesis. Although the respective functional roles of EGFR and EphA2 are well known, interactions between these proteins and a functional role for the complex is not understood. Here, we showed that Ephexin1, EphA2, and EGFR are each expressed at higher levels in lung and colorectal cancer patient tissues, and binding of EGFR to EphA2 was associated with both increased tumor grade and metastatic cases in both cancer types. Treatment with Epidermal Growth Factor (EGF) induced binding of the RR domain of EGFR to the kinase domain of EphA2, and this binding was promoted by Ephexin1. Additionally, the AKT-mediated phosphorylation of EphA2 (at Ser897) promoted interactions with EGFR, pointing to the importance of this pathway. Two mutations in EGFR, L858R and T790M, that are frequently observed in lung cancer patients, promoted binding to EphA2, and this binding was dependent on Ephexin1. Our results indicate that the formation of a complex between EGFR, EphA2, and Ephexin1 plays an important role in lung and colorectal cancers, and that inhibition of this complex may be an effective target for cancer therapy.

摘要

细胞信号因子 EGFR、EphA2 和 Ephexin1 与肺癌和结直肠癌相关,并在肿瘤发生中发挥重要作用。尽管 EGFR 和 EphA2 的各自功能作用已经众所周知,但这些蛋白质之间的相互作用及其复合物的功能作用尚不清楚。在这里,我们表明 Ephexin1、EphA2 和 EGFR 在肺癌和结直肠癌患者组织中的表达水平均较高,EGFR 与 EphA2 的结合与这两种癌症类型的肿瘤分级增加和转移病例均相关。表皮生长因子 (EGF) 的治疗诱导了 EGFR 的 RR 结构域与 EphA2 的激酶结构域的结合,而 Ephexin1 促进了这种结合。此外,EphA2 的 AKT 介导的磷酸化 (在 Ser897 处) 促进了与 EGFR 的相互作用,这表明了该途径的重要性。在肺癌患者中经常观察到的 EGFR 的两种突变,L858R 和 T790M,促进了与 EphA2 的结合,这种结合依赖于 Ephexin1。我们的结果表明,EGFR、EphA2 和 Ephexin1 之间复合物的形成在肺癌和结直肠癌中发挥着重要作用,抑制该复合物可能是癌症治疗的有效靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/8df5f255928d/41419_2022_4984_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/7de812cee068/41419_2022_4984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/db853b28cc92/41419_2022_4984_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/360c8622e944/41419_2022_4984_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/a7ce8ca40612/41419_2022_4984_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/b77d73bb9875/41419_2022_4984_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/8df5f255928d/41419_2022_4984_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/7de812cee068/41419_2022_4984_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/db853b28cc92/41419_2022_4984_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/360c8622e944/41419_2022_4984_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/a7ce8ca40612/41419_2022_4984_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/b77d73bb9875/41419_2022_4984_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/9170705/8df5f255928d/41419_2022_4984_Fig6_HTML.jpg

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