促炎细胞因子
癌变
巨噬细胞移动抑制因子
细胞因子
生物
抑制器
炎症
细胞生物学
激活剂(遗传学)
癌症研究
细胞凋亡
免疫学
基因
遗传学
作者
James D. Hudson,M. A. Shoaibi,Roberta Maestro,Amancio Carnero,Gregory J. Hannon,David Beach
标识
DOI:10.1084/jem.190.10.1375
摘要
p53 has a key role in the negative regulation of cell proliferation, in the maintenance of genomic stability, and in the suppression of transformation and tumorigenesis. To identify novel regulators of p53, we undertook two functional screens to isolate genes which bypassed either p53-mediated growth arrest or apoptosis. In both screens, we isolated cDNAs encoding macrophage migration inhibitory factor (MIF), a cytokine that was shown previously to exert both local and systemic proinflammatory activities. Treatment with MIF overcame p53 activity in three different biological assays, and suppressed its activity as a transcriptional activator. The observation that a proinflammatory cytokine, MIF, is capable of functionally inactivating a tumor suppressor, p53, may provide a link between inflammation and tumorigenesis.
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