The Role of RNA-Binding Proteins in Hematological Malignancies

被引:13
作者
Aguilar-Garrido, Pedro [1 ,2 ]
Otero-Sobrino, Alvaro [1 ,2 ]
Angel Navarro-Aguadero, Miguel [1 ,2 ]
Velasco-Estevez, Maria [1 ,2 ]
Gallardo, Miguel [1 ,2 ]
机构
[1] CNIO, H12O CNIO Hematol Malignancies Clin Res Unit, Madrid 28029, Spain
[2] Hosp Univ 12 Octubre, Inst Invest Sanitaria Hosp Octubre Imas12 12, Dept Hematol, Madrid 28041, Spain
基金
欧盟地平线“2020”;
关键词
RNA-binding proteins; leukemia; lymphoma; myeloma; dysplasia; NUCLEAR RIBONUCLEOPROTEIN K; MESSENGER-RNA; HNRNP-K; CRYSTAL-STRUCTURE; TRANSCRIPTIONAL COACTIVATOR; TUMOR-SUPPRESSOR; NMR STRUCTURE; DOMAINS; CANCER; CELLS;
D O I
10.3390/ijms23179552
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
Hematological malignancies comprise a plethora of different neoplasms, such as leukemia, lymphoma, and myeloma, plus a myriad of dysplasia, such as myelodysplastic syndromes or anemias. Despite all the advances in patient care and the development of new therapies, some of these malignancies remain incurable, mainly due to resistance and refractoriness to treatment. Therefore, there is an unmet clinical need to identify new biomarkers and potential therapeutic targets that play a role in treatment resistance and contribute to the poor outcomes of these tumors. RNA-binding proteins (RBPs) are a diverse class of proteins that interact with transcripts and noncoding RNAs and are involved in every step of the post-transcriptional processing of transcripts. Dysregulation of RBPs has been associated with the development of hematological malignancies, making them potential valuable biomarkers and potential therapeutic targets. Although a number of dysregulated RBPs have been identified in hematological malignancies, there is a critical need to understand the biology underlying their contribution to pathology, such as the spatiotemporal context and molecular mechanisms involved. In this review, we emphasize the importance of deciphering the regulatory mechanisms of RBPs to pinpoint novel therapeutic targets that could drive or contribute to hematological malignancy biology.
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页数:18
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