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B细胞祖细胞急性淋巴细胞白血病的幕后操纵者:前B细胞受体和白细胞介素7受体α

Puppet masters of B-cell progenitor acute lymphoblastic leukemia: The preB cell receptor and the interleukin 7 receptor α.

作者信息

Das Gupta Dennis, Lohoff Michael

机构信息

Institute for Medical Microbiology & Hospital Hygiene, Philipps University Marburg, Marburg, Germany.

Medical Department II, Hematology and Oncology, University Medical Center Schleswig-Holstein, Kiel, Germany.

出版信息

Eur J Immunol. 2023 Apr;53(4):e2250093. doi: 10.1002/eji.202250093. Epub 2023 Mar 9.

Abstract

B-cell progenitor acute lymphoblastic leukemia (BCP-ALL) is enriched for a preB cell phenotype, hinting at a specific vulnerability of this cell stage. Two signaling pathways via the preB cell receptor (preBCR) and the interleukin 7 receptor α (IL-7Rα) chain govern the balance between differentiation and proliferation at this stage and both receptor pathways are routinely altered in human BCP-ALL. Here, we review the immunobiology of both the preBCR as well as the IL-7Rα and analyze the human BCP-ALL spectrum in the light of these signaling complexes. Finally, we present a terminology for preBCR signaling modules that distinguishes a pro-proliferative "phase-I" module from a pro-differentiative "phase-II" module. This terminology might serve as a framework to better address shared oncogenic mechanics of preB cell stage BCP-ALL.

摘要

B细胞祖细胞急性淋巴细胞白血病(BCP-ALL)富含前B细胞表型,这暗示了该细胞阶段的特定脆弱性。通过前B细胞受体(preBCR)和白细胞介素7受体α(IL-7Rα)链的两条信号通路在此阶段控制分化与增殖之间的平衡,并且这两条受体通路在人类BCP-ALL中经常发生改变。在这里,我们综述了preBCR以及IL-7Rα的免疫生物学,并根据这些信号复合物分析人类BCP-ALL谱。最后,我们提出了一种preBCR信号模块的术语,该术语将促增殖的“阶段I”模块与促分化的“阶段II”模块区分开来。这种术语可能作为一个框架,以更好地解决前B细胞阶段BCP-ALL的共同致癌机制。

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