Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo 113‑8655, Japan.
Oncol Rep. 2019 Oct;42(4):1459-1466. doi: 10.3892/or.2019.7244. Epub 2019 Jul 19.
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.
CDR1-AS 的表达与胃肠道癌(如结肠癌、肝癌和胰腺癌)的预后不良密切相关,它是一种代表性的环状 RNA。尽管众所周知,CDR1-AS 通过其在脑中的序列相似性拮抗 microRNA-7 的功能,但由于环状 RNA 的异位表达存在困难,其生物学功能及其与癌细胞恶性潜能的联系仍不清楚。在本研究中,使用漆酶 2 基因盒建立了稳定表达 CDR1-AS RNA 环状物的 SW620 结肠癌细胞系,并确定了其与恶性行为相关的生物学功能。与之前的研究不同,CDR1-AS 的表达并未改变细胞生长或侵袭能力。然而,CMTM4 和 CMTM6 的表达水平显著增加,CMTM4 和 CMTM6 最近被认为是细胞表面 PD-L1 蛋白表达的关键调节因子。因此,在表达 CDR1-AS 的细胞中细胞表面 PD-L1 蛋白水平增加。值得注意的是,过表达 microRNA-7 并没有消除这些作用,这表明表达 CDR1-AS 的细胞中细胞表面 PD-L1 的增加不依赖于 microRNA-7 的功能。这些结果表明,癌细胞中这种环状 RNA 的表达可能通过 microRNA-7 独立机制增加细胞表面 PD-L1 水平,从而导致预后不良。