HIF-1 at the crossroads of hypoxia, inflammation, and cancer

被引:520
作者
Balamurugan, Kuppusamy [1 ,2 ]
机构
[1] NCI, Lab Cell & Dev Signaling, Ctr Canc Res, 1050 Boyles St, Frederick, MD 21702 USA
[2] NCI, 1050 Boyles St, Frederick, MD 21702 USA
关键词
hypoxia; inflammation; HIF-1; microenvironment; cancer stem cells; drug resistance; EPITHELIAL-MESENCHYMAL TRANSITION; NF-KAPPA-B; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR 1-ALPHA; TUMOR-ASSOCIATED MACROPHAGES; ACUTE MYELOID-LEUKEMIA; CARBONIC-ANHYDRASE-IX; BREAST-CANCER; STEM-CELLS; PYRUVATE-KINASE;
D O I
10.1002/ijc.29519
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The complex cross-talk of intricate intercellular signaling networks between the tumor and stromal cells promotes cancer progression. Hypoxia is one of the most common conditions encountered within the tumor microenvironment that drives tumorigenesis. Most responses to hypoxia are elicited by a family of transcription factors called hypoxia-inducible factors (HIFs), which induce expression of a diverse set of genes that assist cells to adapt to hypoxic environments. Among the three HIF protein family members, the role of HIF-1 is well established in cancer progression. HIF-1 functions as a signaling hub to coordinate the activities of many transcription factors and signaling molecules that impact tumorigenesis. This mini review discusses the complex role of HIF-1 and its context-dependent partners under various cancer-promoting events including inflammation and generation of cancer stem cells, which are implicated in tumor metastasis and relapse. In addition, the review highlights the importance of therapeutic targeting of HIF-1 for cancer prevention.
引用
收藏
页码:1058 / 1066
页数:9
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