The effects of RNA editing in cancer tissue at different stages in carcinogenesis

• Published in: RNA biology Vol. 18; no. 11; pp. 1524 - 1539
• Main Authors: Kurkowiak, Małgorzata, Arcimowicz, Łukasz, Chruściel, Elżbieta, Urban-Wójciuk, Zuzanna, Papak, Ines, Keegan, Liam, O'Connell, Mary, Kowalski, Jacek, Hupp, Ted, Marek-Trzonkowska, Natalia
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 02.11.2021
• Subjects: ADARs; Adenosine - genetics; Animals; cancer development; Carcinogenesis - genetics; Carcinogenesis - pathology; Humans; Inosine - genetics; Neoplasms - genetics; Neoplasms - metabolism; Neoplasms - pathology; Review; RNA Editing; RNA editing in cancer; RNA, Double-Stranded - genetics; RNA-Binding Proteins - genetics; RNA-Binding Proteins - metabolism; RNA editing; RNA editing in cancer; ADARs; cancer development
• ISSN: 1547-6286; 1555-8584
• DOI: 10.1080/15476286.2021.1877024

RNA editing is one of the most prevalent and abundant forms of post-transcriptional RNA modification observed in normal physiological processes and often aberrant in diseases including cancer. RNA editing changes the sequences of mRNAs, making them different from the source DNA sequence. Edited mRNAs can produce editing-recoded protein isoforms that are functionally different from the corresponding genome-encoded protein isoforms. The major type of RNA editing in mammals occurs by enzymatic deamination of adenosine to inosine (A-to-I) within double-stranded RNAs (dsRNAs) or hairpins in pre-mRNA transcripts. Enzymes that catalyse these processes belong to the adenosine deaminase acting on RNA (ADAR) family. The vast majority of knowledge on the RNA editing landscape relevant to human disease has been acquired using in vitro cancer cell culture models. The limitation of such in vitro models, however, is that the physiological or disease relevance of results obtained is not necessarily obvious. In this review we focus on discussing in vivo occurring RNA editing events that have been identified in human cancer tissue using samples surgically resected or clinically retrieved from patients. We discuss how RNA editing events occurring in tumours in vivo can identify pathological signalling mechanisms relevant to human cancer physiology which is linked to the different stages of cancer progression including initiation, promotion, survival, proliferation, immune escape and metastasis.