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PTIP抑制食管鳞状细胞癌中的细胞侵袭:EphA2表达的调节

PTIP Inhibits Cell Invasion in Esophageal Squamous Cell Carcinoma Modulation of EphA2 Expression.

作者信息

Han Xiao, Zhu Yaning, Shen Li, Zhou Yu, Pang Liqun, Zhou Wubi, Gu Hao, Han Kairong, Yang Yijun, Jiang Chao, Xie Jun, Zhang Chengwan, Ding Lianshu

机构信息

Department of Central Laboratory, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huai'an, China.

Department of Pathology, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huai'an, China.

出版信息

Front Oncol. 2021 Mar 23;11:629916. doi: 10.3389/fonc.2021.629916. eCollection 2021.

Abstract

Esophageal squamous cell carcinoma (ESCC) is a highly aggressive malignancy and treatment failure is largely due to metastasis and invasion. Aberrant tumor cell adhesion is often associated with tumor progression and metastasis. However, the exact details of cell adhesion in ESCC progression have yet to be determined. In our study, the clinical relevance of Pax2 transactivation domain-interacting protein (PTIP/PAXIP1) was analyzed by immunohistochemistry of ESCC tissues. We found that low expression of PTIP was associated with lymph node metastasis in ESCC, and loss-of-function approaches showed that depletion of PTIP promoted ESCC cell migration and invasion both and . Analysis integrating RNA-seq and ChIP-seq data revealed that PTIP directly regulated ephrin type-A receptor 2 (EphA2) expression in ESCC cells. Moreover, PTIP inhibited EphA2 expression by competing with Fosl2, which attenuated the invasion ability of ESCC cells. These results collectively suggest that PTIP regulates ESCC invasion through modulation of EphA2 expression and hence presents a potential therapeutic target for its treatment.

摘要

食管鳞状细胞癌(ESCC)是一种侵袭性很强的恶性肿瘤,治疗失败主要归因于转移和侵袭。异常的肿瘤细胞黏附通常与肿瘤进展和转移相关。然而,ESCC进展过程中细胞黏附的确切细节尚未确定。在我们的研究中,通过对ESCC组织进行免疫组织化学分析,探讨了PAX2反式激活结构域相互作用蛋白(PTIP/PAXIP1)的临床相关性。我们发现,PTIP低表达与ESCC的淋巴结转移相关,功能缺失实验表明,PTIP缺失促进了ESCC细胞的迁移和侵袭。整合RNA测序和染色质免疫沉淀测序数据的分析显示,PTIP直接调控ESCC细胞中ephrin A型受体2(EphA2)的表达。此外,PTIP通过与Fosl2竞争抑制EphA2表达,从而减弱ESCC细胞的侵袭能力。这些结果共同表明,PTIP通过调节EphA2表达来调控ESCC侵袭,因此是ESCC治疗的一个潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d9/8021923/a61aff0e90f4/fonc-11-629916-g001.jpg

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