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Defining Causative Factors Contributing in the Activation of Hedgehog Signaling in Diffuse Large B-Cell Lymphoma

机译:定义在弥漫性大B细胞淋巴瘤中刺激刺猬信号激活的致病因素

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摘要

Hedgehog (Hh) signaling pathway is activated in diffuse large B-cell lymphoma (DLBCL). Genetic abnormalities that explain activation of Hh signaling in DLBCL are unknown. We investigate the presence of amplifications of Hh genes that might result in activation of this pathway in DLBCL. Our data showed few extra copies of GLI1 and SMO due to chromosomal aneuploidies in a subset of DLBCL cell lines. We also showed that pharmacologic inhibition of PI3K/AKT and NF-KB pathways resulted in decreased expression of GLI1 and Hh ligands. In conclusion, our data support the hypothesis that aberrant activation of Hh signaling in DLBCL mainly results from integration of deregulated oncogenic signaling inputs converging into Hh signaling.
机译:刺猬(Hh)信号通路在弥漫性大B细胞淋巴瘤(DLBCL)中被激活。解释DLBCL中Hh信号激活的遗传异常是未知的。我们调查了可能导致DLBCL中该途径激活的Hh基因扩增的存在。我们的数据显示,由于一部分DLBCL细胞系中的染色体非整倍性,GLI1和SMO的额外拷贝很少。我们还显示,PI3K / AKT和NF-KB途径的药理抑制作用导致GLI1和Hh配体的表达降低。总之,我们的数据支持以下假设:DLBCL中Hh信号的异常激活主要是由于整合成Hh信号的失活的致癌信号输入的整合所致。

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