Epithelial Membrane Protein 2 Suppresses Non-Small Cell Lung Cancer Cell Growth by Inhibition of MAPK Pathway

GND
1151165832
ORCID
0000-0001-7409-4001
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Ma, Yunxia;
GND
1230903917
ORCID
0000-0001-8274-8271
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Schröder, Desiree Charlotte;
GND
1230904492
ORCID
0000-0001-7976-2611
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Nenkov, Miljana;
GND
1230905170
ORCID
0000-0002-8931-5396
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Rizwan, Maryam Noor;
GND
1230905855
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Abubrig, Mohamed;
GND
1230907351
ORCID
0000-0003-2993-9161
Zugehörigkeit
Jena University Hospital
Sonnemann, Jürgen;
GND
121666272X
ORCID
0000-0003-4093-1419
Zugehörigkeit
Jena University Hospital
Murrieta-Coxca, José M.;
GND
1029632839
ORCID
0000-0002-7348-059X
Zugehörigkeit
Jena University Hospital
Morales-Prieto, Diana M.;
GND
1230908374
Zugehörigkeit
Jena University Hospital
Westermann, Martin;
GND
1076884180
Zugehörigkeit
Jena University Hospital, Friedrich Schiller University Jena
Gaßler, Nikolaus;
GND
124313329
ORCID
0000-0002-4752-9222
Zugehörigkeit
Section Pathology of the Institute of Forensic Medicine, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747 Jena, Germany,
Chen, Yuan

Epithelial membrane proteins (EMP1-3) are involved in epithelial differentiation and carcinogenesis. Dysregulated expression of EMP2 was observed in various cancers, but its role in human lung cancer is not yet clarified. In this study, we analyzed the expression of EMP1-3 and investigated the biological function of EMP2 in non-small cell lung cancer (NSCLC). The results showed that lower expression of EMP1 was significantly correlated with tumor size in primary lung tumors (p = 0.004). Overexpression of EMP2 suppressed tumor cell growth, migration, and invasion, resulting in a G1 cell cycle arrest, with knockdown of EMP2 leading to enhanced cell migration, related to MAPK pathway alterations and disruption of cell cycle regulatory genes. Exosomes isolated from transfected cells were taken up by tumor cells, carrying EMP2-downregulated microRNAs (miRNAs) which participated in regulation of the tumor microenvironment. Our data suggest that decreased EMP1 expression is significantly related to increased tumor size in NSCLC. EMP2 suppresses NSCLC cell growth mainly by inhibiting the MAPK pathway. EMP2 might further affect the tumor microenvironment by regulating tumor microenvironment-associated miRNAs.

Zitieren

Zitierform:
Zitierform konnte nicht geladen werden.

Rechte

Rechteinhaber: © 1996-2021 MDPI (Basel, Switzerland)

Nutzung und Vervielfältigung: