IL-2/IL-2R signaling and IL-2Rα-targeted therapy in anaplastic large cell lymphoma; [IL-2/IL-2R-Signalübertragung und gezielte IL-2Rα-Therapie bei anaplastischem großzelligem Lymphom]

被引:0
|
作者
Liang H.-C. [1 ]
机构
[1] Human Oncology & Pathogenesis Program (HOPP), Department of Pathology, Memorial Sloan Kettering Cancer Center, New York
关键词
Activator protein‑1; Anaplastic large cell lymphoma; BATF3 transcription factor; Interleukin‑2; receptor; α; Super-enhancer;
D O I
10.1007/s00292-022-01108-x
中图分类号
学科分类号
摘要
Anaplastic large cell lymphoma (ALCL) is a CD30-positive non-Hodgkin’s T‑cell lymphoma. Despite the implementation of CD30 antibody–drug conjugate-targeted therapy into front-line treatment regimens, the prognosis of some subtypes of the disease remains unsatisfactory. In the relapsed/refractory setting, effective second-line treatment options are still lacking. However, it has been reported that blockade of direct downstream targets of activator protein‑1 (AP-1) transcription factors, which are highly dysregulated in ALCL, results in complete and sustained remission in late-stage relapsed/refractory anaplastic lymphoma kinase (ALK)-positive ALCL patients. Moreover, it has been identified that involvement of the BATF3/AP‑1 module promotes lymphomagenesis via oncogenic BATF3/IL-2/IL-2R signaling through hyperphosphorylation of ERK1/2, STAT1, and STAT5 in ALCL cells regardless of their ALK status. Therefore, targeting BATF3/IL-2/IL-2R signaling may represent a novel therapeutic alternative for ALCL patients. © 2022, The Author(s), under exclusive licence to Springer Medizin Verlag GmbH, ein Teil von Springer Nature.
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页码:25 / 30
页数:5
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