Lodewijckx Inge, Cools Jan
Center for Human Genetics, KU Leuven, Herestraat 49, 3000 Leuven, Belgium.
Center for Cancer Biology, VIB, Herestraat 49, 3000 Leuven, Belgium.
Pharmaceuticals (Basel). 2021 May 8;14(5):443. doi: 10.3390/ph14050443.
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 .
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)