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Characterization of the AGR2-NPM3 axis uncovers the AGR2 involvement in PD-L1 regulation in colorectal cancer
A. Martisova, J. Faktor, T. Sosolikova, I. Klemesova, T. Kolarova, J. Holcakova, R. Hrstka
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
MMCI, 00209805
MH CZ - DRO
P JAC; reg. no. CZ.02.01.01/00/22_008/0004644
Ministerstvo Školství, Mládeže a Tělovýchovy
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2011
Nature Open Access
od 2011-12-01
PubMed Central
od 2011
Europe PubMed Central
od 2011
ProQuest Central
od 2011-01-01
Open Access Digital Library
od 2011-01-01
Open Access Digital Library
od 2011-01-01
Health & Medicine (ProQuest)
od 2011-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2011
- MeSH
- antigeny CD274 * metabolismus genetika MeSH
- jaderné proteiny metabolismus genetika MeSH
- kolorektální nádory * genetika metabolismus patologie MeSH
- lidé MeSH
- mukoproteiny * metabolismus genetika MeSH
- nádorové buněčné linie MeSH
- nukleofosmin * MeSH
- onkogenní proteiny * metabolismus genetika MeSH
- proteiny * metabolismus genetika MeSH
- regulace genové exprese u nádorů * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Despite extensive research, the molecular role of AGR2 in the progression and metastasis of colorectal cancer (CRC) has not been fully characterized. We used quantitative mass spectrometry (SWATH MS) to identify differentially expressed proteins in paired CRC cell models of the SW480 and SW620 cell lines in response to AGR2 protein level manipulation. Relying on the results from SWATH MS and subsequent immunochemical validation, we selected NMP3 as the top candidate protein associated with AGR2 in CRC tumour cells in our screen. RT‒qPCR and immunochemical analysis confirmed the involvement of AGR2-mediated regulation of NPM3 at the transcriptional and posttranscriptional levels. Since PD-L1 is a constituent of the NPM3 regulatory axis, we aimed to correlate the changes in PD-L1 to the differential expression of AGR2 in our cell models. We found that AGR2 positively regulates PD-L1 levels in both SW480 and SW620 cell lines; additionally, several different CRC patient transcriptome cohorts confirmed the association of AGR2 with PD-L1. Our work reveals a new AGR2-NPM3 regulatory axis and the involvement of AGR2 in the regulation of PD-L1, which paves the way for the association of AGR2 with immune evasion in CRC cells.
Citace poskytuje Crossref.org
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