Circular RNAs Could Encode Unique Proteins and Affect Cancer Pathways

Author:

Crudele Francesca12ORCID,Bianchi Nicoletta1ORCID,Terrazzan Anna13ORCID,Ancona Pietro1ORCID,Frassoldati Antonio4,Gasparini Paolo2,D’Adamo Adamo P.2,Papaioannou Dimitrios5,Garzon Ramiro6,Wójcicka Anna7,Gaj Paweł7,Jażdżewski Krystian8,Palatini Jeffrey9,Volinia Stefano1310

Affiliation:

1. Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy

2. Genetics Unit, Institute for Maternal and Child Health, Scientific Institute for Research, Hospitalization and Healthcare (IRCCS) Burlo Garofolo, 34137 Trieste, Italy

3. Laboratory for Advanced Therapy Technologies (LTTA), University of Ferrara, 44121 Ferrara, Italy

4. Department of Oncology, Azienda Ospedaliero-Universitaria St. Anna di Ferrara, 44124 Ferrara, Italy

5. Laura and Isaac Perlmutter Cancer Center, New York University School of Medicine, NYU Langone Health, New York, NY 10016, USA

6. Division of Hematology and Hematological Malignancies, University of Utah, Salt Lake City, UT 84112, USA

7. Warsaw Genomics INC, 01-682 Warszawa, Poland

8. Human Cancer Genetics, Biological and Chemical Research Centre, University of Warsaw, 02-089 Warsaw, Poland

9. Genomics Core Facility, Centre of New Technologies, University of Warsaw, 02-097 Warsaw, Poland

10. CNBCh, Biological and Chemical Research Centre, University of Warsaw, 02-089 Warsaw, Poland

Abstract

circRNAs constitute a novel class of RNA, generally considered as non-coding RNAs; nonetheless, their coding potential has been under scrutiny. In this work, we systematically explored the predicted proteins of more than 160,000 circRNAs detected by exome capture RNA-sequencing and collected in the MiOncoCirc pan-cancer compendium, including normal and cancer samples from different types of tissues. For the functional evaluation, we compared their primary structure and domain composition with those derived from the same linear mRNAs. Among the 4362 circRNAs potentially encoding proteins with a unique primary structure and 1179 encoding proteins with a novel domain composition, 183 were differentially expressed in cancer. In particular, eight were associated with prognosis in acute myeloid leukemia. The functional classification of the dysregulated circRNA-encoded polypeptides showed an enrichment in the heme and cancer signaling, DNA-binding, and phosphorylation processes, and disclosed the roles of some circRNA-based effectors in cancer.

Funder

University of Ferrara

Publisher

MDPI AG

Subject

General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology

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