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淋巴恶性肿瘤中白细胞介素-7信号通路的失调

Deregulation of the Interleukin-7 Signaling Pathway in Lymphoid Malignancies.

作者信息

Lodewijckx Inge, Cools Jan

机构信息

Center for Human Genetics, KU Leuven, Herestraat 49, 3000 Leuven, Belgium.

Center for Cancer Biology, VIB, Herestraat 49, 3000 Leuven, Belgium.

出版信息

Pharmaceuticals (Basel). 2021 May 8;14(5):443. doi: 10.3390/ph14050443.

Abstract

The cytokine interleukin-7 (IL-7) and its receptor are critical for lymphoid cell development. The loss of IL-7 signaling causes severe combined immunodeficiency, whereas gain-of-function alterations in the pathway contribute to malignant transformation of lymphocytes. Binding of IL-7 to the IL-7 receptor results in the activation of the JAK-STAT, PI3K-AKT and Ras-MAPK pathways, each contributing to survival, cell cycle progression, proliferation and differentiation. Here, we discuss the role of deregulated IL-7 signaling in lymphoid malignancies of B- and T-cell origin. Especially in T-cell leukemia, more specifically in T-cell acute lymphoblastic leukemia and T-cell prolymphocytic leukemia, a high frequency of mutations in components of the IL-7 signaling pathway are found, including alterations in , , , , , , and .

摘要

细胞因子白细胞介素-7(IL-7)及其受体对淋巴细胞发育至关重要。IL-7信号缺失会导致严重联合免疫缺陷,而该信号通路功能获得性改变则会促成淋巴细胞的恶性转化。IL-7与IL-7受体结合会激活JAK-STAT、PI3K-AKT和Ras-MAPK信号通路,每条通路都对细胞存活、细胞周期进程、增殖和分化有贡献。在此,我们讨论失调的IL-7信号在B细胞和T细胞来源的淋巴恶性肿瘤中的作用。特别是在T细胞白血病中,更具体地说是在T细胞急性淋巴细胞白血病和T细胞幼淋巴细胞白血病中,发现IL-7信号通路成分的高频突变,包括 、 、 、 、 、 、 和 中的改变。 (注:原文中部分基因名称未给出具体内容,用“ ”代替)

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