Literature DB >> 28720310

Epithelial membrane protein 2: Molecular interactions and clinical implications.

Lawrance K Chung1, Nikhilesh S Bhatt1, Carlito Lagman1, Panayiotis E Pelargos1, Yu Qin2, Lynn K Gordon3, Madhuri Wadehra4, Isaac Yang5.   

Abstract

Epithelial membrane protein 2 (EMP2) is a cell surface protein that has recently emerged as an object of neuro-oncological interest due to its potential to be utilized as a biomarker and target for antibody therapies. Preclinical studies have demonstrated that EMP2 is associated with disease prognosis in a number of human cancers, including glioblastoma. The four large extracellular domains of EMP2 and its association with the extracellular matrix makes it an attractive target for future cancer therapies. Translational research suggests that EMP2 may be targeted with antibodies to improve tumor control and survival in a variety of murine models and cancer types. However, in order to translate these preclinical findings into the clinic, future research will need to focus on elucidating the role EMP2 in the normal human body by better understanding its molecular and chemical interactions. The focus of this review is to provide a comprehensive insight into current research endeavors, discuss the potential for clinically translatable applications, and predict the future directions of such research.
Copyright © 2017. Published by Elsevier Ltd.

Entities:  

Keywords:  Antibody therapy; EMP2; Epithelial membrane protein 2; Glioblastoma

Mesh:

Substances:

Year:  2017        PMID: 28720310     DOI: 10.1016/j.jocn.2017.06.044

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  6 in total

1.  Epithelial membrane protein 2 governs transepithelial migration of neutrophils into the airspace.

Authors:  Wan-Chi Lin; Kymberly M Gowdy; Jennifer H Madenspacher; Rachel L Zemans; Kazuko Yamamoto; Miranda Lyons-Cohen; Hideki Nakano; Kyathanahalli Janardhan; Carmen J Williams; Donald N Cook; Joseph P Mizgerd; Michael B Fessler
Journal:  J Clin Invest       Date:  2020-01-02       Impact factor: 14.808

2.  miR-340-5p mediates the therapeutic effect of mesenchymal stem cells on corneal neovascularization.

Authors:  Jian Pan; Xu Luo; Shujue Zhao; Jianmin Li; Zipei Jiang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2021-09-08       Impact factor: 3.535

3.  RNF8 is responsible for ATRA resistance in variant acute promyelocytic leukemia with GTF2I/RARA fusion, and inhibition of the ubiquitin-proteasome pathway contributes to the reversion of ATRA resistance.

Authors:  Wenzhe Yan; Ji Li; Yang Zhang; Yafei Yin; Zhao Cheng; Jiayi Wang; Guoyu Hu; Sufang Liu; Yewei Wang; Yunxiao Xu; Hongling Peng; Guangsen Zhang
Journal:  Cancer Cell Int       Date:  2019-04-04       Impact factor: 5.722

4.  Full-length transcriptome of Misgurnus anguillicaudatus provides insights into evolution of genus Misgurnus.

Authors:  Shaokui Yi; Xiaoyun Zhou; Jie Li; Manman Zhang; Shuangshuang Luo
Journal:  Sci Rep       Date:  2018-08-03       Impact factor: 4.379

5.  Epithelial Membrane Protein-2 (EMP2) Antibody Blockade Reduces Corneal Neovascularization in an In Vivo Model.

Authors:  Michel M Sun; Ann M Chan; Samuel M Law; Sergio Duarte; Daniel Diaz-Aguilar; Madhuri Wadehra; Lynn K Gordon
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-01-02       Impact factor: 4.799

6.  Genetic Deletion of Emp2 Does Not Cause Proteinuric Kidney Disease in Mice.

Authors:  Michael D Donnan; Rizaldy P Scott; Tuncer Onay; Antoine Tarjus; Ummiye Venus Onay; Susan E Quaggin
Journal:  Front Med (Lausanne)       Date:  2019-08-27
  6 in total

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