RNA editing contributes to epitranscriptome diversity in chronic lymphocytic leukemia

被引:20
作者
Gassner, Franz J. [1 ,2 ]
Zaborsky, Nadja [1 ,2 ]
Buchumenski, Ilana [3 ]
Levanon, Erez Y. [3 ]
Gatterbauer, Matthias [1 ,2 ,4 ]
Schubert, Maria [1 ,2 ,4 ]
Rauscher, Stefanie [1 ,2 ,4 ]
Hebenstreit, Daniel [5 ]
Nadeu, Ferran [6 ,7 ]
Campo, Elias [6 ,7 ,8 ]
Egle, Alexander [1 ,2 ,9 ]
Greil, Richard [1 ,2 ,9 ,10 ]
Geisberger, Roland [1 ,2 ]
机构
[1] Paracelsus Med Univ, Dept Internal Med Haematol Med Oncol Haemostaseol, Lab Immunol & Mol Canc Res SCRI LIMCR, Salzburg Canc Res Inst,Oncol Ctr, Salzburg, Austria
[2] Canc Cluster Salzburg, Salzburg, Austria
[3] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, IL-5290002 Ramat Gan, Israel
[4] Paris Lodron Univ Salzburg, Dept Biosci, Salzburg, Austria
[5] Univ Warwick, Sch Life Sci, Coventry, W Midlands, England
[6] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Mol Pathol Lymphoid Neoplasms Program, Barcelona, Spain
[7] Ctr Invest Biomed Red Canc CIBERONC, Madrid, Spain
[8] Univ Barcelona, Hosp Clin Barcelona, Hematopathol Sect, Barcelona, Spain
[9] Ctr Clin Canc & Immunol Trials CCCIT, Salzburg Canc Res Inst, Salzburg, Austria
[10] Austrian Grp Med Tumor Therapy AGMT, Salzburg, Austria
基金
英国生物技术与生命科学研究理事会; 奥地利科学基金会;
关键词
MUTATIONAL PROCESSES; CANCER; LANDSCAPE; ADAR1; SIGNATURES; EVOLUTION; CLL;
D O I
10.1038/s41375-020-0995-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RNA editing-primarily conversion of adenosine to inosine (A > I)-is a widespread posttranscriptional mechanism, mediated by Adenosine Deaminases acting on RNA (ADAR) enzymes to alter the RNA sequence of primary transcripts. Hence, in addition to somatic mutations and alternative RNA splicing, RNA editing can be a further source for recoding events. Although RNA editing has been detected in many solid cancers and normal tissue, RNA editing in chronic lymphocytic leukemia (CLL) has not been addressed so far. We determined global RNA editing and recurrent, recoding RNA editing events from matched RNA-sequencing and whole exome sequencing data in CLL samples from 45 untreated patients. RNA editing was verified in a validation cohort of 98 CLL patients and revealed substantially altered RNA editing profiles in CLL compared with normal B cells. We further found that RNA editing patterns were prognostically relevant. Finally, we showed that ADAR knockout decreased steady state viability of MEC1 cells and made them more susceptible to treatment with fludarabine and ibrutinib in vitro. We propose that RNA editing contributes to the pathophysiology of CLL and targeting the RNA editing machinery could be a future strategy to maximize treatment efficacy.
引用
收藏
页码:1053 / 1063
页数:11
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