Kharabi Masouleh Behzad, Chevet Eric, Panse Jens, Jost Edgar, O'Dwyer Michael, Bruemmendorf Tim H, Samali Afshin
Department of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Université Rennes 1 - ER_440 "Oncogenesis, Stress & Signaling", Centre de Lutte Contre le Cancer Eugène Marquis, Rennes, France.
J Hematol Oncol. 2015 Jul 16;8:87. doi: 10.1186/s13045-015-0184-7.
The unfolded protein response (UPR), an endoplasmic reticulum (ER) stress-induced signaling cascade, is mediated by three major stress sensors IRE-1α, PERK, and ATF6α. Studies described the UPR as a critical network in selection, adaptation, and survival of cancer cells. While previous reviews focused mainly on solid cancer cells, in this review, we summarize the recent findings focusing on acute leukemias. We take into account the impact of the underlying genetic alterations of acute leukemia cells, the leukemia stem cell pool, and provide an outline on the current genetic, clinical, and therapeutic findings. Furthermore, we shed light on the important oncogene-specific regulation of individual UPR signaling branches and the therapeutic relevance of this information to answer the question if the UPR could be an attractive novel target in acute leukemias.
未折叠蛋白反应(UPR)是一种由内质网(ER)应激诱导的信号级联反应,由三种主要的应激传感器IRE-1α、PERK和ATF6α介导。研究表明,UPR是癌细胞选择、适应和存活的关键网络。虽然之前的综述主要集中在实体癌细胞上,但在本综述中,我们总结了最近关于急性白血病的研究发现。我们考虑了急性白血病细胞潜在基因改变、白血病干细胞库的影响,并概述了当前的基因、临床和治疗研究结果。此外,我们阐明了单个UPR信号分支的重要癌基因特异性调控以及该信息的治疗相关性,以回答UPR是否可能成为急性白血病有吸引力的新靶点这一问题。