The role of SF3B1 and NOTCH1 in the pathogenesis of leukemia

被引:3
作者
Abolhasani, Shiva [1 ,2 ]
Hejazian, Seyyed Sina [1 ]
Karpisheh, Vahid [1 ]
Khodakarami, Atefeh [1 ]
Mohammadi, Hamed [3 ]
Navashenaq, Jamshid Gholizadeh [4 ]
Hojjat-Farsangi, Mohammad [5 ,6 ]
Jadidi-Niaragh, Farhad [1 ,7 ,8 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[3] Alborz Univ Med Sci, Noncommunicable Dis Res Ctr, Karaj, Iran
[4] Bam Univ Med Sci, Noncommunicable Dis Res Ctr, Bam, Iran
[5] Karolinska Inst, Dept Oncol Pathol, Bioclinicum, Stockholm, Sweden
[6] Bushehr Univ Med Sci, Persian Gulf Marine Biotechnol Med Res Ctr, Bushehr, Iran
[7] Tabriz Univ Med Sci, Fac Med, Dept Immunol, Tabriz, Iran
[8] Tabriz Univ Med Sci, Res Ctr Integrat Med Aging, Aging Res Inst, Tabriz, Iran
关键词
leukemia; NOTCH1; targeted therapy; therapeutic resistance; CHRONIC LYMPHOCYTIC-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; SECRETASE INHIBITOR PF-03084014; SPLICING FACTOR SF3B1; KAPPA-B ACTIVITY; GAMMA-SECRETASE; T-ALL; RECURRENT MUTATIONS; C-MYC;
D O I
10.1002/iub.2660
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The discovery of new genes/pathways improves our knowledge of cancer pathogenesis and presents novel potential therapeutic options. For instance, splicing factor 3b subunit 1 (SF3B1) and NOTCH1 genetic alterations have been identified at a high frequency in hematological malignancies, such as leukemia, and may be related to the prognosis of involved patients because they change the nature of malignancies in different ways like mediating therapeutic resistance; therefore, studying these gene/pathways is essential. This review aims to discuss SF3B1 and NOTCH1 roles in the pathogenesis of various types of leukemia and the therapeutic potential of targeting these genes or their mutations to provide a foundation for leukemia treatment.
引用
收藏
页码:257 / 278
页数:22
相关论文
共 206 条
[1]   Therapeutic antibody targeting of Notch1 in T-acute lymphoblastic leukemia xenografts [J].
Agnusdei, V. ;
Minuzzo, S. ;
Frasson, C. ;
Grassi, A. ;
Axelrod, F. ;
Satyal, S. ;
Gurney, A. ;
Hoey, T. ;
Seganfreddo, E. ;
Basso, G. ;
Valtorta, S. ;
Moresco, R. M. ;
Amadori, A. ;
Indraccolo, S. .
LEUKEMIA, 2014, 28 (02) :278-288
[2]   Novel SF3B1 in-frame deletions result in aberrant RNA splicing in CLL patients [J].
Agrawal, Anant A. ;
Seiler, Michael ;
Brinton, Lindsey T. ;
Mantel, Rose ;
Lapalombella, Rosa ;
Woyach, Jennifer A. ;
Johnson, Amy J. ;
Zhu, Ping ;
Warmuth, Markus ;
Yu, Lihua ;
Byrd, John C. ;
Smith, Peter G. ;
Blachly, James S. ;
Buonamici, Silvia .
BLOOD ADVANCES, 2017, 1 (15) :995-1000
[3]   Notch signaling: simplicity in design, versatility in function [J].
Andersson, Emma R. ;
Sandberg, Rickard ;
Lendahl, Urban .
DEVELOPMENT, 2011, 138 (17) :3593-3612
[4]  
Aref Salah, 2020, Asian Pac J Cancer Prev, V21, P1987, DOI 10.31557/APJCP.2020.21.7.1987
[5]   Significance of NOTCH1 mutations detections in T-acute lymphoblastic leukemia patients [J].
Aref, Salah ;
El Agdar, Mohammed ;
Salama, Osama ;
Zeid, Tarek Abouzeid ;
Sabry, Mohamed .
CANCER BIOMARKERS, 2020, 27 (02) :157-162
[6]   Structure-Activity Relationship (SAR) Study of Ethyl 2-Amino-6-(3,5-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate (CXL017) and the Potential of the Lead against Multidrug Resistance in Cancer Treatment [J].
Aridoss, Gopalakrishnan ;
Zhou, Bo ;
Hermanson, David L. ;
Bleeker, Nicholas P. ;
Xing, Chengguo .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (11) :5566-5581
[7]   Mutations in NOTCH1 PEST domain orchestrate CCL19-driven homing of chronic lymphocytic leukemia cells by modulating the tumor suppressor gene DUSP22 [J].
Arruga, F. ;
Gizdic, B. ;
Bologna, C. ;
Cignetto, S. ;
Buonincontri, R. ;
Serra, S. ;
Vaisitti, T. ;
Gizzi, K. ;
Vitale, N. ;
Garaffo, G. ;
Mereu, E. ;
Diop, F. ;
Neri, F. ;
Incarnato, D. ;
Coscia, M. ;
Allan, J. ;
Piva, R. ;
Oliviero, S. ;
Furman, R. R. ;
Rossi, D. ;
Gaidano, G. ;
Deaglio, S. .
LEUKEMIA, 2017, 31 (09) :1882-1893
[8]   Functional impact of NOTCH1 mutations in chronic lymphocytic leukemia [J].
Arruga, F. ;
Gizdic, B. ;
Serra, S. ;
Vaisitti, T. ;
Ciardullo, C. ;
Coscia, M. ;
Laurenti, L. ;
D'Arena, G. ;
Jaksic, O. ;
Inghirami, G. ;
Rossi, D. ;
Gaidano, G. ;
Deaglio, S. .
LEUKEMIA, 2014, 28 (05) :1060-1070
[9]   Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter's syndrome: therapeutic implications [J].
Arruga, Francesca ;
Bracciama, Valeria ;
Vitale, Nicoletta ;
Vaisitti, Tiziana ;
Gizzi, Katiuscia ;
Yeomans, Alison ;
Coscia, Marta ;
D'Arena, Giovanni ;
Gaidano, Gianluca ;
Allan, John N. ;
Furman, Richard R. ;
Packham, Graham ;
Forconi, Francesco ;
Deaglio, Silvia .
LEUKEMIA, 2020, 34 (02) :462-477
[10]   NOTCH1/FBXW7 mutation identifies a large subgroup with favorable outcome in adult T-cell acute lymphoblastic leukemia (T-ALL): a Group for Research on Adult Acute Lymphoblastic Leukemia (GRAALL) study [J].
Asnafi, Vahid ;
Buzyn, Agnes ;
Le Noir, Sandrine ;
Baleydier, Frederic ;
Simon, Arnauld ;
Beldjord, Kheira ;
Reman, Oumedaly ;
Witz, Francis ;
Fagot, Thierry ;
Tavernier, Emmanuelle ;
Turlure, Pascal ;
Leguay, Thibaut ;
Huguet, Francoise ;
Vernant, Jean-Paul ;
Daniel, Francis ;
Bene, Marie-Christine ;
Ifrah, Norbert ;
Thomas, Xavier ;
Dombret, Herve ;
Macintyre, Elizabeth .
BLOOD, 2009, 113 (17) :3918-3924