Expression of circular RNA CDR1‑AS in colon cancer cells increases cell surface PD‑L1 protein levels
Related Experiment Video
Updated: Jan 22, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Eri Tanaka1, Yu Miyakawa1, Takahiro Kishikawa1
1Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo 113‑8655, Japan.
Abstract:
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.
Insights
Circular RNA CDR1-AS expression in colon cancer cells increases cell surface PD-L1 levels independently of microRNA-7, potentially contributing to poor prognosis. This finding offers new insights into cancer progression and therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- RNA Biology
Background:
- Circular RNA CDR1-AS is linked to poor prognosis in gastrointestinal cancers.
- Its precise role in cancer cell malignancy and interaction with microRNA-7 is not fully understood.
- Difficulties in ectopic expression of circular RNAs hinder functional studies.
Purpose of the Study:
- To investigate the biological function of CDR1-AS in colon cancer cells.
- To determine the association between CDR1-AS expression and malignant potential.
- To elucidate the mechanism underlying CDR1-AS's effect on PD-L1 expression.
Main Methods:
- Established a colon cancer cell line (SW620) stably expressing CDR1-AS using a laccase 2 gene cassette.
- Assessed cell growth and invasion ability.
- Quantified expression levels of CMTM4, CMTM6, and cell surface PD-L1.
- Evaluated the effect of microRNA-7 overexpression.
Main Results:
- CDR1-AS expression did not alter cell growth or invasion.
- Expression of CMTM4 and CMTM6 was significantly increased in CDR1-AS-expressing cells.
- Cell surface PD-L1 protein levels were elevated.
- These effects were independent of microRNA-7 function.
Conclusions:
- CDR1-AS expression in cancer cells may promote poor prognosis by upregulating cell surface PD-L1.
- The mechanism involves microRNA-7-independent pathways, potentially through CMTM4 and CMTM6.
- This highlights a novel role for CDR1-AS in cancer progression.
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