Expression of circular RNA CDR1‑AS in colon cancer cells increases cell surface PD‑L1 protein levels

Eri Tanaka1, Yu Miyakawa1, Takahiro Kishikawa1

  • 1Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo 113‑8655, Japan.

Oncology Reports
|July 20, 2019
PubMed

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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