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致癌激酶融合:一个充满创新临床机遇的不断发展的领域。

Oncogenic kinase fusions: an evolving arena with innovative clinical opportunities.

作者信息

Tabbò Fabrizio, Pizzi Marco, Kyriakides Peter W, Ruggeri Bruce, Inghirami Giorgio

机构信息

Department of Molecular Biotechnology and Health Science and Center for Experimental Research and Medical Studies (CeRMS), University of Torino, Torino, Italy.

Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.

出版信息

Oncotarget. 2016 May 3;7(18):25064-86. doi: 10.18632/oncotarget.7853.

Abstract

Cancer biology relies on intrinsic and extrinsic deregulated pathways, involving a plethora of intra-cellular and extra-cellular components. Tyrosine kinases are frequently deregulated genes, whose aberrant expression is often caused by major cytogenetic events (e.g. chromosomal translocations). The resulting tyrosine kinase fusions (TKFs) prompt the activation of oncogenic pathways, determining the biological and clinical features of the associated tumors. First reported half a century ago, oncogenic TKFs are now found in a large series of hematologic and solid tumors. The molecular basis of TKFs has been thoroughly investigated and tailored therapies against recurrent TKFs have recently been developed. This review illustrates the biology of oncogenic TKFs and their role in solid as well as hematological malignancies. We also address the therapeutic implications of TKFs and the many open issues concerning their clinical impact.

摘要

癌症生物学依赖于内在和外在失调的信号通路,涉及大量细胞内和细胞外成分。酪氨酸激酶是经常失调的基因,其异常表达通常由主要的细胞遗传学事件(如染色体易位)引起。由此产生的酪氨酸激酶融合蛋白(TKFs)促使致癌信号通路激活,决定了相关肿瘤的生物学和临床特征。致癌性TKFs在半个世纪前首次被报道,如今在大量血液系统肿瘤和实体瘤中均有发现。TKFs的分子基础已得到深入研究,针对复发性TKFs的靶向治疗也已开发出来。本综述阐述了致癌性TKFs的生物学特性及其在实体瘤和血液系统恶性肿瘤中的作用。我们还探讨了TKFs的治疗意义以及有关其临床影响的诸多未决问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebb9/5041889/1fa313175795/oncotarget-07-25064-g001.jpg

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