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CD147 a direct target of miR-146a supports energy metabolism and promotes tumor growth in ALK+ ALCL.

Authors :
Montes-Mojarro IA
Steinhilber J
Griessinger CM
Rau A
Gersmann AK
Kohlhofer U
Fallier-Becker P
Liang HC
Hofmann U
Haag M
Klapper W
Schaeffeler E
Pichler BJ
Schwab M
Fend F
Bonzheim I
Quintanilla-Martinez L
Source :
Leukemia [Leukemia] 2022 Aug; Vol. 36 (8), pp. 2050-2063. Date of Electronic Publication: 2022 Jun 08.
Publication Year :
2022

Abstract

We recently reported that miR-146a is differentially expressed in ALK+ and ALK- anaplastic large cell lymphoma (ALCL). In this study, the downstream targets of miR-146a in ALK+ ALCL were investigated by transcriptome analysis, identifying CD147 as potential target gene. Because CD147 is differentially expressed in ALK+ ALCL versus ALK- ALCL and normal T cells, this gene emerged as a strong candidate for the pathogenesis of this tumor. Here we demonstrate that CD147 is a direct target of miR-146 and contributes to the survival and proliferation of ALK+ ALCL cells in vitro and to the engraftment and tumor growth in vivo in an ALK+ ALCL-xenotransplant mouse model. CD147 knockdown in ALK+ ALCL cells resulted in loss of monocarboxylate transporter 1 (MCT1) expression, reduced glucose consumption and tumor growth retardation, as demonstrated by [ <superscript>18</superscript> F]FDG-PET/MRI analysis. Investigation of metabolism in vitro and in vivo supported these findings, revealing reduced aerobic glycolysis and increased basal respiration in CD147 knockdown. In conclusion, our findings indicate that CD147 is of vital importance for ALK+ ALCL to maintain the high energy demand of rapid cell proliferation, promoting lactate export, and tumor growth. Furthermore, CD147 has the potential to serve as a novel therapeutic target in ALK+ ALCL, and warrants further investigation.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1476-5551
Volume :
36
Issue :
8
Database :
MEDLINE
Journal :
Leukemia
Publication Type :
Academic Journal
Accession number :
35676454
Full Text :
https://doi.org/10.1038/s41375-022-01617-x