Circular RNA plays key role in cancer biology and therapy

A new review article highlights the transformative role of circular RNA (circRNA) in cancer, revealing its potential as both a key player in tumor biology and a promising avenue for future therapies. Once thought to be noncoding RNA, circRNA has now been shown to encode functional proteins, challenging conventional RNA biology and opening up novel therapeutic possibilities.

Unlike traditional messenger RNA, circRNAs form a continuous loop, lacking the typical 5′ cap and 3′ tail. This unique structure was originally believed to preclude them from protein translation. However, recent discoveries demonstrate that specific internal ribosome entry sites (IRES) and N6-methyladenosine (m6A) modifications enable circRNAs to undergo cap-independent translation. The resulting proteins influence a range of cellular processes, including those linked to cancer progression and suppression.

Emerging evidence underscores the significance of circRNA-encoded proteins in multiple types of cancer, including glioblastoma, breast cancer, gastric cancer, liver cancer, and colorectal cancer. These proteins interact with critical signaling pathways, such as PI3K/Akt, Wnt/β-catenin, and TGF-β/Smad, influencing cell proliferation, migration, and apoptosis. In glioblastoma, for instance, circRNA-derived proteins contribute to tumorigenicity, while in colorectal cancer, they regulate metabolic processes that drive malignancy.

Beyond their role in cancer progression, translatable circRNAs are poised to redefine RNA-based therapeutics. Their stability and potential for long-lasting protein expression make them promising candidates for protein replacement therapies, vaccines, and targeted drug development. Advances in bioengineering have further enhanced circRNA synthesis, enabling more efficient protein production and laying the foundation for circRNA-based immunotherapies. These innovations could lead to highly potent treatments with improved delivery mechanisms and greater precision in targeting malignant cells.

Despite their vast potential, significant challenges remain in understanding the regulatory mechanisms governing circRNA translation. Key questions include how these proteins achieve tissue-specific functions and how circRNA synthesis can be optimized for clinical applications. Current research aims to refine the techniques used to design and manufacture artificial circRNAs, ensuring their efficacy and safety in medical treatments.

This new understanding of circRNAs as hidden protein sources represents a major shift in molecular biology and oncology. By further exploring their coding potential, researchers and clinicians may unlock new ways to detect, treat, and ultimately prevent cancer.