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一种新型 EHD1/CD44/Hippo/SP1 正反馈回路增强了肺腺癌的干性和转移能力。

A novel EHD1/CD44/Hippo/SP1 positive feedback loop potentiates stemness and metastasis in lung adenocarcinoma.

机构信息

The Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.

The First Department of Orthopedic Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

Clin Transl Med. 2022 Apr;12(4):e836. doi: 10.1002/ctm2.836.

Abstract

BACKGROUND

There is growing evidence that endocytosis plays a pivotal role in cancer metastasis. In this study, we first identified endocytic and metastasis-associated genes (EMGs) and then investigated the biological functions and mechanisms of EMGs.

METHODS

Cancer stem cells (CSCs)-like characteristics were evaluated by tumour limiting dilution assays, three-dimensional (3D) spheroid cancer models. Microarray analysis was used to identify the pathways significantly regulated by mammalian Eps15 homology domain protein 1 (EHD1) knockdown. Mass spectrometry (MS) was performed to identify EHD1-interacting proteins. The function of EHD1 as a regulator of cluster of differentiation 44 (CD44) endocytic recycling and lysosomal degradation was determined by CD44 biotinylation and recycling assays.

RESULTS

EHD1 was identified as a significant EMG. Knockdown of EHD1 suppressed CSCs-like characteristics, epithelial-mesenchymal transition (EMT), migration and invasion of lung adenocarcinoma (LUAD) cells by increasing Hippo kinase cascade activation. Conversely, EHD1 overexpression inhibited the Hippo pathway to promote cancer stemness and metastasis. Notably, utilising MS analysis, the CD44 protein was identified as a potential binding partner of EHD1. Furthermore, EHD1 enhanced CD44 recycling and stability. Indeed, silencing of CD44 or disruption of the EHD1/CD44 interaction enhanced Hippo pathway activity and reduced CSCs-like traits, EMT and metastasis. Interestingly, specificity protein 1 (SP1), a known downstream target gene of the Hippo-TEA-domain family members 1 (TEAD1) pathway, was found to directly bind to the EHD1 promoter region and induce its expression. Among clinical specimens, the EHD1 expression level in LUAD tissues of metastatic patients was higher than that of non-metastatic patients.

CONCLUSIONS

Our findings emphasise that EHD1 might be a potent anti-metastatic target and present a novel regulatory mechanism by which the EHD1/CD44/Hippo/SP1 positive feedback circuit plays pivotal roles in coupling modules of CSCs-like properties and EMT in LUAD. Targeting this loop may serve as a remedy for patients with advanced metastatic LUAD.

摘要

背景

越来越多的证据表明,内吞作用在癌症转移中起着关键作用。在这项研究中,我们首先鉴定了内吞作用和转移相关基因(EMGs),然后研究了 EMGs 的生物学功能和机制。

方法

通过肿瘤限制稀释测定、三维(3D)球体癌细胞模型评估癌症干细胞(CSCs)样特征。微阵列分析用于鉴定哺乳动物 Eps15 同源结构域蛋白 1(EHD1)敲低显著调节的途径。质谱(MS)用于鉴定 EHD1 相互作用蛋白。通过 CD44 生物素化和回收测定确定 EHD1 作为 CD44 内吞回收和溶酶体降解的调节剂的功能。

结果

EHD1 被鉴定为重要的 EMG。EHD1 的敲低通过增加 Hippo 激酶级联激活来抑制肺腺癌(LUAD)细胞的 CSCs 样特征、上皮-间充质转化(EMT)、迁移和侵袭。相反,EHD1 过表达抑制 Hippo 通路以促进癌症干性和转移。值得注意的是,利用 MS 分析,鉴定出 CD44 蛋白是 EHD1 的潜在结合伴侣。此外,EHD1 增强了 CD44 的回收和稳定性。事实上,沉默 CD44 或破坏 EHD1/CD44 相互作用增强了 Hippo 通路活性并降低了 CSCs 样特征、EMT 和转移。有趣的是,特异性蛋白 1(SP1),Hippo-TEA 结构域家族成员 1(TEAD1)通路的已知下游靶基因,被发现直接结合到 EHD1 启动子区域并诱导其表达。在临床标本中,转移性患者的 LUAD 组织中 EHD1 的表达水平高于非转移性患者。

结论

我们的研究结果强调 EHD1 可能是一种有效的抗转移靶标,并提出了一种新的调节机制,即 EHD1/CD44/Hippo/SP1 正反馈回路通过连接模块在 LUAD 中发挥关键作用,连接 CSCs 样特性和 EMT。靶向该循环可能为晚期转移性 LUAD 患者提供治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e5b/9786223/73faded7a7fc/CTM2-12-e836-g006.jpg

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