The role of hypoxia-inducible factor-2 in digestive system cancers

被引:95
作者
Zhao, J. [1 ,2 ]
Du, F. [1 ]
Shen, G. [2 ]
Zheng, F. [2 ]
Xu, B. [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll, Canc Inst & Hosp, Dept Med Oncol, Beijing 100021, Peoples R China
[2] Qinghai Univ, Affiliated Hosp, High Altitude Med Res Ctr, Xining, Peoples R China
基金
中国国家自然科学基金;
关键词
ENDOTHELIAL GROWTH-FACTOR; HIPPEL-LINDAU PROTEIN; PAS DOMAIN PROTEIN-1; RENAL-CELL CARCINOMA; CHEMOKINE RECEPTOR CXCR4; TRANSCRIPTION FACTOR; STEM-CELLS; HEPATOCELLULAR-CARCINOMA; COLON-CANCER; C-MYC;
D O I
10.1038/cddis.2014.565
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hypoxia is an all but ubiquitous phenomenon in cancers. Two known hypoxia-inducible factors (HIFs), HIF-1 alpha and HIF-2 alpha, primarily mediate the transcriptional response to hypoxia. Despite the high homology between HIF-1 alpha and HIF-2 alpha, emerging evidence suggests differences between both molecules in terms of transcriptional targets as well as impact on multiple physiological pathways and tumorigenesis. To date, much progress has been made toward understanding the roles of HIF-2 alpha in digestive system cancers. Indeed, HIF-2 alpha has been shown to regulate multiple aspects of digestive system cancers, including cell proliferation, angiogenesis and apoptosis, metabolism, metastasis and resistance to chemotherapy. These findings make HIF-2 alpha a critical regulator of this malignant phenotype. Here we summarize the function of HIF-2 during cancer development as well as its contribution to tumorigenesis in digestive system malignancies.
引用
收藏
页码:e1600 / e1600
页数:9
相关论文
共 109 条
[81]   Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1-/- mice [J].
Scortegagna, M ;
Ding, K ;
Oktay, Y ;
Gaur, A ;
Thurmond, F ;
Yan, LJ ;
Marck, BT ;
Matsumoto, AM ;
Shelton, JM ;
Richardson, JA ;
Bennett, MJ ;
Garcia, JA .
NATURE GENETICS, 2003, 35 (04) :331-340
[82]   Defining the role of hypoxia-inducible factor 1 in cancer biology and therapeutics [J].
Semenza, G. L. .
ONCOGENE, 2010, 29 (05) :625-634
[83]   Glucose metabolism and cancer [J].
Shaw, Reuben J. .
CURRENT OPINION IN CELL BIOLOGY, 2006, 18 (06) :598-608
[84]   HIF1 Contributes to Hypoxia-Induced Pancreatic Cancer Cells Invasion via Promoting QSOX1 Expression [J].
Shi, Chen-Ye ;
Fan, Yue ;
Liu, Bin ;
Lou, Wen-Hui .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2013, 32 (03) :561-568
[85]   Chemokine receptor CXCR4 downregulated by von Hippel-Lindau tumour suppressor pVHL [J].
Staller, P ;
Sulitkova, J ;
Liszlwan, J ;
Moch, H ;
Oakeley, EJ ;
Krek, W .
NATURE, 2003, 425 (6955) :307-311
[86]   Hypoxia inducible factor 2 alpha inhibits hepatocellular carcinoma growth through the transcription factor dimerization partner 3/E2F transcription factor 1-dependent apoptotic pathway [J].
Sun, Hai-Xiang ;
Xu, Yang ;
Yang, Xin-Rong ;
Wang, Wei-Min ;
Bai, Haibo ;
Shi, Ruo-Yu ;
Nayar, Suresh K. ;
Devbhandari, Ranjan P. ;
He, Yi-zhou ;
Zhu, Qin-Feng ;
Sun, Yun-Fan ;
Hu, Bo ;
Khan, Mehtab ;
Anders, Robert A. ;
Fan, Jia .
HEPATOLOGY, 2013, 57 (03) :1088-1097
[87]   The expression and distribution of the hypoxia-inducible factors HIF-1α and HIF-2α in normal human tissues, cancers, and tumor-associated macrophages [J].
Talks, KL ;
Turley, H ;
Gatter, KC ;
Maxwell, PH ;
Pugh, CW ;
Ratcliffe, PJ ;
Harris, AL .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :411-421
[88]   Loss of HIF-1α in endothelial cells disrupts a hypoxia-driven VEGF autocrine loop necessary for tumorigenesis [J].
Tang, N ;
Wang, LC ;
Esko, J ;
Giordano, FJ ;
Huang, Y ;
Gerber, HP ;
Ferrara, N ;
Johnson, RS .
CANCER CELL, 2004, 6 (05) :485-495
[89]   Endothelial PAS domain protein 1 (EPAS1), a transcription factor selectively expressed in endothelial cells [J].
Tian, H ;
McKnight, SL ;
Russell, DW .
GENES & DEVELOPMENT, 1997, 11 (01) :72-82
[90]   The hypoxia-responsive transcription factor EPAS1 is essential for catecholamine homeostasis and protection against heart failure during embryonic development [J].
Tian, H ;
Hammer, RE ;
Matsumoto, AM ;
Russell, DW ;
McKnight, SL .
GENES & DEVELOPMENT, 1998, 12 (21) :3320-3324