PDGF和FGF受体在癌症中的作用。

J B Demoulin, Sandrine Medves, Federica Toffalini, Ahmed Essaghir, Anders Kallin, Carmen Montano, Amélie Velghe, François Duhoux
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引用次数: 0

摘要

PDGF和FGF家族的生长因子通过受体酪氨酸激酶起作用。在嗜酸性粒细胞增多症相关的髓系肿瘤中,这些受体可被染色体重排激活。我们在一个血小板增多症患者中发现了KANK1和PDGFRbeta之间的一个新的融合基因。我们发现这种来自PDGF和FGF受体的融合癌蛋白逃脱了正常的降解途径,导致它们在细胞中积累。这个过程放大了导致细胞增殖的信号。利用微阵列和生物信息学,我们发现几种转录因子有助于控制细胞生长,包括STATS, FOXO和SREBP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Role of PDGF and FGF receptors in cancer].

Growth factors of the PDGF and FGF families act through receptor tyrosine kinases. These receptors can be activated by chromosomal rearrangements in myeloid neoplasms associated with hypereosinophilia. We identified a new fusion gene between KANK1 and PDGFRbeta in a patient with thrombocythemia. We showed that such fusion oncoproteins derived from PDGF and FGF receptors escape the normal degradation pathways, leading to their accumulation in cells. This process amplifies signalling leading to cell proliferation. Using microarrays and bioinformatics, we showed that several transcription factors contribute to the control cell growth, including STATS, FOXO and SREBP.

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