Expression of circular RNA CDR1‑AS in colon cancer cells increases cell surface PD‑L1 protein levels.
Animals
B7-H1 Antigen
/ biosynthesis
Caco-2 Cells
Cell Growth Processes
/ physiology
Cell Line, Tumor
Colorectal Neoplasms
/ genetics
HEK293 Cells
Humans
Immunohistochemistry
MARVEL Domain-Containing Proteins
/ biosynthesis
Male
Membrane Proteins
/ biosynthesis
Mice
Mice, Inbred BALB C
Mice, Nude
MicroRNAs
/ antagonists & inhibitors
Myelin Proteins
Neoplasm Invasiveness
Prognosis
RNA, Long Noncoding
/ biosynthesis
RNA, Messenger
/ genetics
Journal
Oncology reports
ISSN: 1791-2431
Titre abrégé: Oncol Rep
Pays: Greece
ID NLM: 9422756
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
10
02
2019
accepted:
07
06
2019
pubmed:
20
7
2019
medline:
23
10
2019
entrez:
20
7
2019
Statut:
ppublish
Résumé
The expression of CDR1‑AS, a representative circular RNA, is closely linked with poor prognosis in gastrointestinal cancers, such as colon, liver, and pancreatic cancers. Although it is well known that CDR1‑AS antagonizes microRNA‑7 function through its sequence similarities in the brain, its biological function and link with the malignant potential of cancer cells remain unclear, partly due to the difficulties of ectopic expression of circular RNAs. In the present study, SW620, a colon cancer cell line that stably expresses CDR1‑AS RNA circularized, was established using the laccase 2 gene cassette, and its biological function associated with malignant behavior was determined. In contrast to previous studies, cell growth or invasion ability was not altered by CDR1‑AS expression. However, the expression levels of CMTM4 and CMTM6, which were recently recognized as critical regulators of PD‑L1 protein expression at the cell surface, were significantly increased. Accordingly, the cell surface PD‑L1 protein levels were increased in CDR1‑AS‑expressing cells. Notably, the effects were not canceled out by overexpressing microRNA‑7, indicating that the increase in cell surface PD‑L1 in CDR1‑AS‑expressing cells was not dependent on microRNA‑7 function. These results indicated that expression of this circular RNA in cancer cells may lead to poor prognosis by increasing cell surface PD‑L1 levels through microRNA‑7‑independent mechanisms.
Identifiants
pubmed: 31322270
doi: 10.3892/or.2019.7244
doi:
Substances chimiques
B7-H1 Antigen
0
CD274 protein, human
0
CMTM4 protein, human
0
CMTM6 protein, human
0
MARVEL Domain-Containing Proteins
0
MIRN7 microRNA, human
0
Membrane Proteins
0
MicroRNAs
0
Myelin Proteins
0
RNA, Long Noncoding
0
RNA, Messenger
0
long non-coding RNA CDR1AS, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM