circRNA circ-MYBL2 is a novel tumor suppressor and potential biomarker in multiple myeloma

被引:28
作者
Yu, Shanshan [1 ]
Ai, Limei [1 ]
Wei, Wei [1 ]
Pan, Jing [1 ]
机构
[1] Jinzhou Med Univ, Dept Hematol, Affiliated Hosp 1, 2,Sect 5,Renmin St, Jinzhou 121000, Liaoning, Peoples R China
关键词
Multiple myeloma; Circular RNA; MYBL2; Biomarker; CIRCULAR RNA;
D O I
10.1007/s13577-020-00441-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Currently, multiple myeloma (MM) is still an incurable disease. Deciphering its pathogenesis will bring new targets for clinical diagnosis and treatment. In the present study, we identified a MM-associated circular RNA (circRNA), circ-MYBL2, which was dramatically decreased in MM tissue and serum samples in comparison to normal samples. Low circ-MYBL2 level was closely correlated with high clinical stage and unfavorable outcome, and serum circ-MYBL2 had excellent accuracy in diagnosing MM. Exogenous circ-MYBL2 expression notably repressed MM cell viability, DNA synthesis and cell cycle progression. Further exploration revealed that circ-MYBL2 exerted the tumor-inhibiting effect by affecting the phosphorylation level of its linear isoform, in which circ-MYBL2 facilitated the binding of Cyclin F to MYBL2, dampening MYBL2 phosphorylation and activation, thereby inhibiting the transcription of a number of well-known proliferation-related oncogenes. Importantly, overexpression of circ-MYBL2 significantly reduced the tumor size of subcutaneous xenografts in nude mice. Taken together, our data unveil a regulatory mechanism linking circ-MYBL2 and its host gene mediated by Cyclin F, providing a potential diagnostic, prognostic and therapeutic target for MM patients.
引用
收藏
页码:219 / 228
页数:10
相关论文
共 31 条
[1]   CircRNAs and cancer: Biomarkers and master regulators [J].
Arnaiz, Esther ;
Sole, Carla ;
Manterola, Lorea ;
Iparraguirre, Leire ;
Otaegui, David ;
Lawrie, Charles H. .
SEMINARS IN CANCER BIOLOGY, 2019, 58 :90-99
[2]   Circular RNAs in Cancer [J].
Bach, Duc-Hiep ;
Lee, Sang Kook ;
Sood, Anil K. .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2019, 16 :118-129
[3]   H-DrunkWalk: Collaborative and Adaptive Navigation for Heterogeneous MAV Swarm [J].
Chen, Xinlei ;
Ruiz, Carlos ;
Zeng, Sihan ;
Gao, Liyao ;
Purohit, Aveek ;
Carpin, Stefano ;
Zhang, Pei .
ACM TRANSACTIONS ON SENSOR NETWORKS, 2020, 16 (02)
[4]   Combined treatment for multiple myeloma [J].
Das, Manjulika .
LANCET ONCOLOGY, 2019, 20 (07) :E349-E349
[5]   Circular RNA Splicing [J].
Eger, Nicole ;
Schoppe, Laura ;
Schuster, Susanne ;
Laufs, Ulrich ;
Boeckel, Jes-Niels .
CIRCULAR RNAS: BIOGENESIS AND FUNCTIONS, 2018, 1087 :41-52
[6]  
Eslick R, 2013, AUST FAM PHYSICIAN, V42, P684
[7]   Circular RNA and its mechanisms in disease: From the bench to the clinic [J].
Han, Bing ;
Chao, Jie ;
Yao, Honghong .
PHARMACOLOGY & THERAPEUTICS, 2018, 187 :31-44
[8]   Cell cycle regulation by the B-Myb transcription factor [J].
Joaquin, M ;
Watson, RJ .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (11) :2389-2401
[9]   Cyclin F suppresses B-Myb activity to promote cell cycle checkpoint control [J].
Klein, Ditte Kjaersgaard ;
Hoffmann, Saskia ;
Ahlskog, Johanna K. ;
O'Hanlon, Karen ;
Quaas, Marianne ;
Larsen, Brian D. ;
Rolland, Baptiste ;
Rosner, Heike I. ;
Walter, David ;
Kousholt, Arne Nedergaard ;
Menzel, Tobias ;
Lees, Michael ;
Johansen, Jens Vilstrup ;
Rappsilber, Juri ;
Engeland, Kurt ;
Sorensen, Claus Storgaard .
NATURE COMMUNICATIONS, 2015, 6
[10]   Circular RNAs in cancer: opportunities and challenges in the field [J].
Kristensen, L. S. ;
Hansen, T. B. ;
Veno, M. T. ;
Kjems, J. .
ONCOGENE, 2018, 37 (05) :555-565