The role of hypoxia-inducible factors in cancer

被引：145

作者：

Maynard, M. A. ^{[1
]}

Ohh, M. ^{[1
]}

机构：

[1] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5S 1A8, Canada

来源：

CELLULAR AND MOLECULAR LIFE SCIENCES | 2007年 / 64卷 / 16期

关键词：

HIF; VHL; PI3K; MAPK; PHD;

D O I：

10.1007/s00018-007-7082-2

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Hypoxia-inducible factor (HIF) is a heterodimeric transcription factor that mediates the adaptive responses to hypoxia by effecting the transcription of numerous hypoxia-inducible genes. HIF is frequently overexpressed in solid tumors, and the transactivation of HIF targets in transformed cells provides a distinct survival advantage. Accordingly, the upregulation of HIF correlates with increased progression or aggressiveness of the cancer and poor prognosis. In addition to the induction of HIF by hypoxia, its expression is induced by the loss of tumor suppressors VHL, PTEN, TSC1/2, PML, and SDH, as well as by the increased activity of PI3K and/or MAPK signaling pathways, underscoring the significance of HIF in oncogenesis.

引用

页码：2170 / 2180

页数：11

共 149 条

[1] Genetic evidence for a tumor suppressor role of HIF-2α [J].

Acker, T ;

Diez-Juan, A ;

Aragones, J ;

Tjwa, M ;

Brusselmans, K ;

Moons, L ;

Fukumura, D ;

Moreno-Murciano, MP ;

Herbert, JM ;

Burger, A ;

Riedel, J ;

Elverl, G ;

Flamme, I ;

Maxwell, PH ;

Collen, D ;

Dewerchin, M ;

Jain, RK ;

Plate, KH ;

Carmeliet, P .

CANCER CELL, 2005, 8 (02) :131-141

[2]

Akakura N, 2001, CANCER RES, V61, P6548

[3] Role of ETS transcription factors in the hypoxia-inducible factor-2 target gene selection [J].

Aprelikova, Olga ;

Wood, Matthew ;

Tackett, Sean ;

Chandramouli, Gadisetti V. R. ;

Barrett, J. Carl .

CANCER RESEARCH, 2006, 66 (11) :5641-5647

[4] An essential role for p300/CBP in the cellular response to hypoxia [J].

Arany, Z ;

Huang, LE ;

Eckner, R ;

Bhattacharya, S ;

Jiang, C ;

Goldberg, MA ;

Bunn, HF ;

Livingston, DM .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :12969-12973

[5] Interaction between HIF-1α (ODD) and hARD1 does not induce acetylation and destabilization of HIF-1α [J].

Arnesen, T ;

Kong, X ;

Evjenth, R ;

Gromyko, D ;

Varhaug, JE ;

Lin, Z ;

Sang, NL ;

Caro, J ;

Lillehaug, JR .

FEBS LETTERS, 2005, 579 (28) :6428-6432

[6] Selective silencing of the hypoxia-inducible factor 1 target gene BNIP3 by histone deacetylation and methylation in colorectal cancer [J].

Bacon, A. L. ;

Fox, S. ;

Turley, H. ;

Harris, A. L. .

ONCOGENE, 2007, 26 (01) :132-141

[7] PML inhibits HIF-1α translation and neoangiogenesis through repression of mTOR [J].

Bernardi, Rosa ;

Guernah, Ilhem ;

Jin, David ;

Grisendi, Silvia ;

Alimonti, Andrea ;

Teruya-Feldstein, Julie ;

Cordon-Cardo, Carlos ;

Simon, M. Celeste ;

Rafii, Shahin ;

Pandolfi, Pier Paolo .

NATURE, 2006, 442 (7104) :779-785

[8] Arrest-defective-1 protein, an acetyltransferase, does not alter stability of hypoxia-inducible factor (HIF)-1α and is not induced by hypoxia or HIF [J].

Bilton, R ;

Mazure, N ;

Trottier, E ;

Hattab, M ;

Déry, MA ;

Richard, DE ;

Pouysségur, J ;

Brahimi-Horn, MC .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (35) :31132-31140

[9]

Birner P, 2000, CANCER RES, V60, P4693

[10]

Birner P, 2001, CLIN CANCER RES, V7, P1661

← 1 2 3 4 5 6 7 8 9 10 →