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MOLECULAR PHARMACOLOGY
Copyright 2006 The American Society for Pharmacology and Experimental Therapeutics
Mol Pharmacol 70:14691480, 2006
Vol. 70, No. 5

27029/3145820
Printed in U.S.A.
MINIREVIEW
Hypoxia-Inducible Factor-1 (HIF-1)

Qingdong Ke and Max Costa
Nelson Institute of Environmental Medicine, New York University, School of Medicine, Tuxedo, New York
Received May 25, 2006; accepted August 2, 2006
The transcription factor hypoxia-inducible factor-1 (HIF-1)

is a key regulator responsible for the induction of genes that
facilitate adaptation and survival of cells and the whole organism from normoxia (21% O2) to hypoxia (1% O2)
(Wang et al., 1995; Semenza, 1998). Since the identification
of HIF, 2 decades ago, our knowledge of it has grown exponentially. Because of the realization that hypoxia has a
strong impact, via gene expression, on cell biology and mammalian physiology, there has been enormous growing interest in the biology of the HIF-1 pathway and its role in human
diseases such as cancer. Therefore, this review considers
what has been learned about HIF-1: its discovery, its regulation, its target gene, its role in development and disease,
and its implication for therapy.
Article, publication date, and citation information can be found at

http://molpharm.aspetjournals.org.
doi:10.1124/mol.106.027029.
droxylation of two proline residues and acetylation of a lysine

residue at the oxygen-dependent degradation domain (ODDD)
of HIF-1 trigger its association with pVHL E3 ligase complex,
leading to HIF-1 degradation via ubiquitin-proteasome pathway. In hypoxia, the HIF-1 subunit becomes stable and interacts with coactivators such as cAMP response element-binding protein binding protein/p300 and regulates the expression
of target genes. Overexpression of HIF-1 has been found in
various cancers, and targeting HIF-1 could represent a novel
approach to cancer therapy.
The Discovery of HIF-1

HIF-1. HIF-1 was discovered by the identification of a
hypoxia response element (HRE; 5-RCGTG-3) in the 3 enhancer of the gene for erythropoietin (EPO), a hormone that
stimulates erythrocyte proliferation and undergoes hypoxiainduced transcription (Goldberg et al., 1988; Semenza et al.,
1991). Subsequent studies have revealed the protein that
binds to the HRE under hypoxic conditions as HIF-1, a heterodimeric complex consisting of a hypoxically inducible subunit HIF-1 and a constitutively expressed subunit HIF-1
(Wang et al., 1995). HIF-1 is also known as the aryl hydrocarbon nuclear translocator (ARNT), which was originally
identified as a binding partner of the aryl hydrocarbon receptor (Reyes et al., 1992), whereas HIF-1 was newly discovered. These proteins belong to the basic helix-loop-helix
Per-ARNT-Sim (bHLHPAS) protein family (Fig. 1) (Wang et
al., 1995). The bHLH and PAS motifs are required for heterodimer formation between the HIF-1 and HIF-1 subunits, and the downstream basic region affords specific bind-
ABBREVIATIONS: HIF-1, hypoxia-inducible factor-1; HRE, hypoxia response element; ARNT, aryl hydrocarbon nuclear translocator; PAS,
Per-ARNT-Sim; bHLH, basic helix-loop-helix; TAD, transactivation domains; CBP/p300, cAMP response element-binding protein binding protein;
ODDD, oxygen-dependent degradation domain; 2-OG, 2-oxoglutarate; PHD, prolyl hydroxylase domain; VHL, von Hippel-Lindau; FIH-1, factor
inhibiting HIF-1; ARD1, arrest-defective-1; MAPK, mitogen-activated protein kinase; VEGF, vascular endothelial cell growth factor; PTEN,
phosphatase and tensin homolog deleted on chromosome 10; LY294002, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one; PD98095, 2-(2amino-3-methoxyphenyl)-oxanphthalen-4-one; PI3K, phosphoinositide-3 kinase; YC-1, 3-(5-hydroxy-methyl-2-furyl)-1-benzylindazole.
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ABSTRACT
Adaptation to low oxygen tension (hypoxia) in cells and tissues
leads to the transcriptional induction of a series of genes that
participate in angiogenesis, iron metabolism, glucose metabolism, and cell proliferation/survival. The primary factor mediating this response is the hypoxia-inducible factor-1 (HIF-1), an
oxygen-sensitive transcriptional activator. HIF-1 consists of a
constitutively expressed subunit HIF-1 and an oxygen-regulated subunit HIF-1 (or its paralogs HIF-2 and HIF-3). The
stability and activity of the subunit of HIF are regulated by its
post-translational modifications such as hydroxylation, ubiquitination, acetylation, and phosphorylation. In normoxia, hy-
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The Regulation of HIF-1

Although HIF-1 is constitutively expressed and its mRNA
and protein are maintained at constant levels regardless of
oxygen availability (Kallio et al., 1997), HIF-1 protein has a
short half-life (t1/2 5 min) and is highly regulated by oxygen
(Salceda and Caro, 1997) (Fig. 2). The transcription and
synthesis of HIF-1 are constitutive and seem not to be
affected by oxygen (Wang et al., 1995; Kallio et al., 1997;
Wiesener et al., 1998). However, in normoxia, the HIF-1
proteins are rapidly degraded, resulting in essentially no
detectable HIF-1 protein (Wang et al., 1995). During hypoxia, HIF-1 becomes stabilized and translocates from the
cytoplasm to the nucleus, where it dimerizes with HIF-1,
and the HIF complex formed becomes transcriptionally active (Huang et al., 1996; Kallio et al., 1997). The activated
HIF complex then associates with HREs in the regulatory
regions of target genes and binds the transcriptional coactivators to induce gene expression (Lando et al., 2002b). Tight
regulation of the stability and subsequent transactivational
function of HIF-1 is chiefly controlled by its post-translational modifications, such as hydroxylation, ubiquitination,
acetylation, and phosphorylation (Brahimi-Horn et al., 2005).
The modification of HIF-1 occurs within several domains.
In normoxia, hydroxylation of two proline residues and acetylation of a lysine residue in its ODDD promote interaction of
HIF-1 with the von Hippel-Lindau (pVHL) ubiquitin E3
ligase complex (Srinivas et al., 1999; Masson et al., 2001).
pVHL complex tags HIF-1 with ubiquitin and thereby
marks it for degradation by the 26S proteasome. In addition,
hydroxylation of an asparagine residue in the C-TAD inhibits
the association of HIF-1 with CBP/p300 and thus inhibits
its transcriptional activity (Lando et al., 2002a).
Prolyl Hydroxylation by PHDsSignaling for Polyubiquitination. De novo synthesized cytoplasmic HIF-1 is
rapidly hydroxylated by a family of 2-oxoglutarate (2-OG)dependent dioxygenases on proline 402 (Pro402) and 564
(Pro564) located within ODDD (Srinivas et al., 1999; Masson
et al., 2001; Masson and Ratcliffe, 2003). The proline residues
are conserved in HIF-2 (Pro405 and Pro530) and HIF-3.
They are also part of a consensus sequence, LXXLAP, that is
conserved for the two sites of all the isoforms except for the
second proline of HIF-3, which has the sequence LXXLHP
Fig. 1. Domain structure of human HIF- and HIF-1.

HIF- (HIF-1, HIF-2, HIF-3, IPAS) and HIF-1 belong
to the bHLH and PAS protein family. HIF- contains an
ODDD that mediates oxygen-regulated stability through
the hydroxylation of two proline (P) residues and the acetylation of a lysine (K). The proline residues are conserved
in HIF-2 and HIF-3. HIF-1 and HIF-2 also contain
two transaction domains (C-TAD and N-TAD), whereas
HIF-1 has only one TAD. The total number of amino acids
of each subunit is marked at the end of the domain structure.
ing to the HRE DNA sequence (Crews, 1998). Two

transactivation (stimulation of transcription) domains, Nterminal (N-TAD) and C-terminal (C-TAD), in the C-terminal half of the HIF-1 protein were identified later (Ruas et
al., 2002). The C-TAD in particular has been shown to interact with coactivators such as CBP/p300 to activate gene
transcription (Lando et al., 2002b). HIF-1 also contains an
oxygen-dependent degradation domain (ODDD) that mediates oxygen-regulated stability (Pugh et al., 1997). Later
work revealed that HIF-1 is ubiquitously expressed in human and mouse tissues and has a general role in multiple
physiological responses to hypoxia, such as erythropoiesis
and glycolysis, which quickly counteract oxygen deficiency,
and angiogenesis, which provides a long-term solution (Semenza, 1998).
HIF-2. Shortly after the cloning of HIF-1, a closely
related protein, HIF-2 [also termed endothelial PAS protein, HIF-like factor (HLF), HIF-related factor (HRF), and
member of the PAS superfamily 2 (MOP2)] was identified
and cloned (Ema et al., 1997; Flamme et al., 1997; Hogenesch
et al., 1997; Tian et al., 1997). HIF-2 shares 48% amino acid
sequence identity with HIF-1 and accordingly shares a
number of structural and biochemical similarities with
HIF-1 (for instance, heterodimerization with HIF-1 and
binding HREs). In contrast to ubiquitously expressed HIF1, though, HIF-2 is predominantly expressed in the lung,
endothelium, and carotid body (Ema et al., 1997; Tian et al.,
1997, 1998).
HIF-3. HIF-3, which was discovered later, is also expressed in a variety of tissues, dimerizes with HIF-1, and
binds to HREs (Gu et al., 1998). In addition, a splice variant
of HIF-3, inhibitory PAS (IPAS), which is predominantly
expressed in the Purkinje cells of the cerebellum and corneal
epithelium, was subsequently discovered (Makino et al.,
2001). IPAS possesses no endogenous transactivation activity; rather, it interacts with the amino-terminal region of
HIF-1 and prevents its DNA binding, acting as a dominantnegative regulator of HIF-1 (Makino et al., 2001). However,
IPAS can also be induced by hypoxia in the heart and lung,
contributing to a negative feedback loop for HIF-1 activity in
these tissues (Makino et al., 2002). HIF-1 and HIF-2 have
been more extensively studied, whereas research on HIF-3
and other HIF isoforms is relatively scarce.
HIF-1, A New Target for Therapy
(Bruick and McKnight, 2001; Masson et al., 2001). Mutation

of both proline residues disrupted the interaction of HIF-1
with pVHL and increased its stability in the presence of
normal oxygen levels, whereas mutation of either proline
alone only partially stabilized HIF-1 (Masson et al., 2001).
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Human HIF- dioxygenase was termed prolyl hydroxylase

domain (PHD), HIF-prolyl hydroxylase (HPH), or Egg-laying
Nine (EGLN), and three isoforms have been reported: PHD1/
HPH3/EGLN2, PHD2/HPH2/EGLN1, and PHD3/HPH1/
EGLN3 (Bruick and McKnight, 2001; Epstein et al., 2001;

Fig. 2. Oxygen-dependent regulation of HIF-1 stabilization and transactivation. In normoxia (left), two proline residues of HIF-1 (P402 and P564) and
asparagine (N803) are hydroxylated by PHDs and FIH-1, respectively, in an O2, 2-OG, and Fe2-dependent manner. Hydroxylated HIF-1 proteins
bind to the E3 ubiquitin ligase VHL complex, leading to its degradation by the proteasome. Acetylation of lysine (K532) by ARD1 favors the interaction
of HIF-1 with VHL. Hydroxylated N803 blocks the recruitment of transcriptional coactivator CBP/p300. In hypoxia (right), the activities of PHDs and
FIH-1 are inhibited due to lack of O2, resulted in no proline and asparagine hydroxylation. Therefore, there is no VHL binding and HIF-1 is stabilized.
Stabilized HIF-1 proteins translocate to the nucleus and bind to HIF-1. HIF-1 may bind preferentially to the MAPK-induced phosphorylated form
of HIF-1. Nonhydroxylated N803 of HIF-1 allows CBP/p300 recruitment to the target genes, resulting in gene transcription. In addition, the
expression of ARD1 is decreased under hypoxia, causing less acetylated HIF-1.
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have also been shown to modify the activity of PHDs (Appelhoff et al., 2004; Hirota et al., 2004; Temes et al., 2005).
In the presence of oxygen, the PHDs are active and hydroxylate the prolines of HIF-1, constituting a recognition
signal for binding of pVHL and subsequent ubiquitination,
followed by degradation of HIF-1 (Ivan et al., 2001;
Jaakkola et al., 2001). The absence of oxygen causes no
enzyme activity, no modification of proline, and no pVHL/
HIF binding, resulting in HIF-1 stabilization and accumulation in the cell. The absolute requirement of oxygen as a
cosubstrate suggests PHDs as the oxygen sensor in cells
(Epstein et al., 2001).
Polyubiquitination by pVHLSignaling for Degradation. Once the two proline residues of HIF-1 are converted to hydroxyproline, pVHL then captures HIF-1. X-ray
crystallographic studies of the pVHL/HIF-1 complex have
revealed that pVHL has a surface pocket into which the
hydroxyproline fits accurately, and the overall binding configuration is highly specific (Hon et al., 2002; Min et al.,
2002). The pVHL associates with the proteins elongin C,
elongin B, cullin-2, and Rbx1 to form the VCB-Cul2 E3 ligase
complex (Ivan and Kaelin, 2001). Binding of HIF-1 to this
multiprotein E3 complex causes polyubiquitination of HIF1, ultimately leading to its degradation by the proteasome
(Kamura et al., 2000). However, the exact lysine residue(s)
ubiquitinated have not yet been identified.
The pVHL was first described in von Hippel-Lindau (VHL)
disease, an inherited human cancer syndrome that is characterized by the development of multiple tumors, such as
clear-cell renal carcinomas, pheochromocytomas, and hemangioblastomas in the retina and central nervous system
(Ivan and Kaelin, 2001). The VHL gene encodes a full-length
(213 amino acids) and an N-terminally truncated protein
(amino acids 54213). Because both proteins show similar
functions, they are often collectively referred to as pVHL.
Mutations in the VHL gene, the product of which functions as
a tumor suppressor, were found in the diseases discussed
above (Iliopoulos et al., 1998; Schoenfeld et al., 1998). In cells
lacking wild-type pVHL, HIF-1 and HIF-2 are stable and
active under normoxia, resulting in the over-production of
hypoxia-inducible genes (Iliopoulos et al., 1996). Restoration
of pVHL function by stable transfection reversed normoxic
HIF- protein stability and the aberrant increase of genes
(Iliopoulos et al., 1996). Therefore, one mechanism by which
mutations in pVHL might cause tumor formation is by permitting the stability and activity of HIF- under normal
oxygen tensions, resulting in the subsequent expression of
genes encoding angiogenic factors even before cells are exposed to a hypoxic stress.
The pVHL E3 ligase complex is ubiquitously expressed in
different tissues and predominantly localized to the cytoplasm. Its shuttling between the cytoplasm and nucleus enables HIF-1 degradation in both compartments (Berra et
al., 2001; Groulx and Lee, 2002).
However, the pVHL-dependent pathway may not be the
only pathway leading to degradation of HIF-1. In addition
to pVHL, a number of other proteins have been reported to
affect HIF-1 ubiquitination and stability. For example, the
oncogenic E3 ubiquitin ligase murine double minute 2
(MDM2) has been suggested to bring about ubiquitination of
HIF-1 in a p53-dependent fashion (Ravi et al., 2000). The
protein Jab1, a transcriptional coactivator of c-Jun and Jun
Huang et al., 2002). The biochemical characteristics of the

PHDs are similar to the collagen prolyl-4-hydroxylases,
which are also 2-OG-dependent dioxygenases and require
oxygen (O2) for hydroxylation as well as Fe2 and ascorbate
as cofactors (Schofield and Zhang, 1999). The collagen prolyl4-hydroxylases, however, are not able to catalyze HIF-1/
HIF-2 proline hydroxylation (Jaakkola et al., 2001). The
hydroxylation process splits O2; one oxygen atom is transferred to the proline residue and the other reacts with 2-OG
to generate succinate and CO2 (Bruick and McKnight, 2001;
Masson and Ratcliffe, 2003). Inactivation of the PHDs by
2-OG analogs can increase the half-life of HIF-1 (Jaakkola
et al., 2001; Ivan et al., 2002). Fe2 at the active site of the
PHDs is loosely bound by two histidine residues and one
aspartic acid, forming a 2-histidine-1-carboxylate coordination motif. The requirement of Fe2 for PHDs was demonstrated in the observation that iron chelators and metal irons
(such as Co2, Ni2, and Mn2) are able to stabilize HIF-1,
probably by diminishing the availability of Fe2 for the enzyme or substituting Fe2 from the Fe2-binding site (Masson and Ratcliffe, 2003; Yuan et al., 2003). Ascorbate helps to
maintain Fe in the ferrous (Fe2) state and is important in
maintaining and achieving full activity of the PHDs (Bruick
and McKnight, 2001; Epstein et al., 2001).
All three PHDs have the potential to hydroxylate HIF- in
vitro with their relative activities as PHD2 PHD3
PHD1, and PHD2 was shown to be the key limiting enzyme
that controls the HIF-1 turnover in vivo (Huang et al., 2002;
Berra et al., 2003). Knockdown of PHD2 by its specific small
interfering RNA is sufficient to stabilize HIF-1 levels under
normoxia, whereas small interfering RNA silencing of either
PHD1 or PHD3 is unable to produce similar effects on
HIF-1 (Berra et al., 2003). In addition, it was found that the
mRNA and protein of PHD2 were induced during a hypoxia
challenge, and the mRNA of PHD3 was up-regulated as well,
whereas that of PHD1 remained unaffected (Epstein et al.,
2001; Metzen et al., 2003a). This may represent a way by
which HIF-1 self-regulates its expression. Furthermore,
Siah1 and -2, the specific E3 ligases of PHD1 and -3, are
transcriptionally up-regulated during hypoxia, thereby elevating the degradation of these PHDs by the proteasome
(Nakayama and Ronai, 2004). When overexpressed as tagged
proteins in transfected cells, PHD2 was found to be localized
primarily in the cytoplasm, whereas PHD1 localized in the
nucleus and PHD3 was in both compartments (Metzen et al.,
2003a). Despite its primary localization in the cytoplasm,
PHD2 is able to shuttle between the cytoplasm and the
nucleus, thereby contributing to HIF-1 degradation in both
compartments. Although all three enzymes are widely expressed in many tissues, they exhibit tissue-specific overexpression. PHD2 was abundant in adipose tissue (Oehme et
al., 2002), PHD3 in the heart and placenta (Lieb et al., 2002;
Oehme et al., 2002), and PHD1 in the testis (Lieb et al.,
2002). The differences of the enzyme activity of PHDs, subcellular localization, and tissue distribution may enable a
graded or tissue-specific response to hypoxia. Some proteins,
such as OS-9, the protein product of a widely expressed gene
with unclear function, have been shown to promote prolyl
hydroxylation by interacting with both HIF-1 and PHDs,
thereby promoting the O2-dependent degradation of HIF-1
(Baek et al., 2005). In addition, several second messengers
oxygen as a substrate allows FIH-1 to serve as a second

oxygen sensor.
Phosphorylation by MAPKEnhancing Transactivation. Despite the central importance of hydroxylases in
sensing oxygen tension and regulating HIF-1 activity, there
are other mechanisms that contribute to the control of HIF-1.
Phosphorylation is well known to be crucial in controlling
protein activities. Direct phosphorylation of HIF-1 has been
reported, and the mitogen-activated protein kinase (MAPK)
pathway seems to play a role (Richard et al., 1999; Sodhi et
al., 2000; Minet et al., 2001). It has been shown that p42/44
and p38 kinase phosphorylated HIF-1/HIF-2 in vitro
(Richard et al., 1999; Sodhi et al., 2000). In addition, inhibitors of p42/44 and p38 blocked HIF-1-mediated reporter
gene expression (Hur et al., 2001). Transfection with active
forms of p42/44 kinase stimulated HIF-1 transcription activity without affecting HIF-1 stability. Moreover, HIF-1/
HIF-2 transaction during hypoxia required p42/44 MAPKs
(Conrad et al., 1999; Minet et al., 2000; Hofer et al., 2001;
Hur et al., 2001). It seems that phosphorylation does not
affect stability or DNA binding of HIF-1; rather, it increases
the transcriptional activity of HIF-1 (Richard et al., 1999).
One explanation could be that HIF-1 binds preferentially to
the phosphorylated form of HIF-1 (Suzuki et al., 2001).
Although the functionally relevant phosphorylation sites remain to be identified, threonine 796 in HIF-1 and 844 in
HIF-2 are candidate sites (Gradin et al., 2002).
In addition to the post-translational modification of
HIF-1 described above, SUMOylation of HIF-1 has also
been reported to contribute to repressing transactivation
(Brahimi-Horn et al., 2005). Moreover, S-nitrosation on cysteine 800 of HIF-1 has been shown to increase its transactivation through its interaction with CBP/p300 (Yasinska
and Sumbayev, 2003).
Besides hypoxia, HIF-1 is also regulated in an oxygenindependent manner. Cytokines, growth factors, environmental stimuli, and other signaling molecules have been
implicated in controlling HIF-1 under nonhypoxic condition
(Table 1) (Feldser et al., 1999; Hellwig-Burgel et al., 1999;
Richard et al., 2000; Salnikow et al., 2000; Gorlach et al.,
2001; Haddad and Land, 2001; Stiehl et al., 2002; Li et al.,
2004). Although complex and cell-type dependent, some have
been shown to stimulate HIF-1 transactivation or synthesis by
activation of the MAPK or the phosphatidylinositol 3-kinase
(PI3K) signaling pathways (Zelzer et al., 1998; Li et al., 2004).
The Target Gene of HIF-1

Given that cells and organs need to adapt to changes in
oxygen supply, it would not be surprising to find that a
significant variety of the HIF-1 target genes are regulated in
a tissue-specific manner. To date, there are more than 100
HIF-1 downstream genes identified with varying functions
(Table 2). HIF-1 activates the expression of these genes by
binding to a 50-base pair cis-acting HRE located in their
enhancer and promoter regions (Semenza et al., 1991). Moreover, by using DNA microarrays, it has recently been reported that more than 2% of all human genes are regulated
by HIF-1 in arterial endothelial cells, directly or indirectly
(Manalo et al., 2005).
Erythropoiesis/Iron Metabolism. In response to hypoxia, the capacity of red blood cells to transport oxygen is
D, has also been shown to increase HIF-1 levels under

hypoxia, probably by competing with p53 for binding to
HIF-1 (Bae et al., 2002). In addition, pVHL has also been
shown to interact with other proteins involved in the HIF-1
signaling pathway and thus may regulate more than just
HIF-1 stability.
Lysine Acetylation by ARD1Facilitating pVHL
Binding. Lysine residue 532 (Lys532) located in the ODDD
domain of HIF-1 was reported to be acetylated by an acetyltransferase named arrest-defective-1 (ARD1) (Jeong et al.,
2002). ARD1 was originally identified in the yeast Saccharomyces cerevisiae, and its name came from the defective yeast
mutants in the mitotic cell cycle (Whiteway and Szostak,
1985). Acetylation of Lys532 favors the interaction of HIF-1
with pVHL, and thus destabilizes HIF-1 (Jeong et al., 2002).
Mutation of Lys532 to arginine resulted in increased stability
of HIF-1 (Tanimoto et al., 2000). In addition, artificial maintenance or increase of the acetylated state of HIF-1 by
butyric acid, a global inhibitor of deacetylases, caused decreased HIF-1 protein levels (Kim et al., 2001).
Because the activity of acetyltransferases is not influenced
by oxygen, ARD1 may be active and acetylate HIF-1 regardless of oxygen conditions. But the mRNA and protein levels of
ARD1 were decreased under hypoxia, which may cause less
acetylated HIF-1 in hypoxia than that in normoxia (Jeong
et al., 2002).
Asparagine Hydroxylation by FIH-1Preventing
CBP/p300 Binding. The post-translational modifications of
HIF-1 described above regulate the stabilization of HIF-1
protein. But the stabilization alone is not sufficient for full
transcriptional activation of HIF-1. The second major mechanism controlling HIF activity is through the modulation of
its transactivation domains N-TAD and C-TAD. These domains function by recruiting transcriptional coactivators
such as CBP/p300, SRC-1, and TIF2 (Arany et al., 1996;
Ebert and Bunn, 1998; Kallio et al., 1998; Ema et al., 1999;
Carrero et al., 2000). Under normal oxygen tension, hydroxylation of the asparagines residue 803 (Asn803) in the C-TAD
of HIF-1 (Asn851 in HIF-2) by factor inhibiting HIF-1
(FIH-1) prevented the interaction of HIF-1 with CBP/p300
(Hewitson et al., 2002; Lando et al., 2002b; Sang et al., 2002).
Hypoxia abrogated asparagine hydroxylation, which allowed
the C-TAD of HIF-1 to efficiently interact with CBP/p300
therein, activating the transcription of the respective target
genes (Lando et al., 2002a). Replacement of Asn803 with
alanine permitted coactivator binding with HIF-1 at normoxia (Lando et al., 2002b). In addition, it has been reported
that FIH-1 binds pVHL, forming a ternary complex with the
HIF-1 (Mahon et al., 2001). Although interaction with
pVHL was not required for FIH-1 activity, histone deacetylases recruited by pVHL interfered with the transcription
processes, facilitating FIH-1 to modulate HIF-1 transactivation (Hewitson et al., 2002; Sang et al., 2002). FIH-1 is
mainly located in the cytoplasm, but some fraction is likely to
reside in the nucleus as well (Metzen et al., 2003a). The
transcription of FIH-1 is independent of the oxygen concentration, and it does not influence HIF-1 stability (Metzen et
al., 2003a).
Like the PHDs, the asparaginyl hydroxylase FIH-1 is a
2-OG-dependent dioxygenase that also requires Fe2 and
ascorbate as cofactors (Lando et al., 2002a). Utilization of
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proangiogenic factors leads to an increase in the vascular

density and hence a decrease in the oxygen diffusion distance. In addition, HIF-1 regulates genes involved in governing the vascular tone such as nitric oxide synthase (NOS2)
(Melillo et al., 1995), heme oxygenease 1 (Lee et al., 1997),
endothelin 1 (ET1) (Hu et al., 1998), adrenomedulin (ADM)
(Nguyen and Claycomb, 1999), and the 1B-adrenergic receptor (Eckhart et al., 1997). Moreover, hypoxia induces genes
involved in matrix metabolism and vessel maturation such as
matrix metalloproteinases (MMPs) (Ben-Yosef et al., 2002),
plasminogen activator receptors and inhibitors (PAIs) (Kietzmann et al., 1999), and collagen prolyl hydroxylase (Takahashi et al., 2000).
Glucose Metabolism. Under low oxygen supply, cells
switch their glucose metabolism pathway away from the
oxygen-dependent tricarboxylic acid (TCA) cycle to the oxygen-independent glycolysis (Dang and Semenza, 1999; Seagroves et al., 2001). With only 2 ATP molecules from each
glucose molecule produced by glycolysis, instead of 38 ATP
provided by TCA cycle, hypoxic cells elevate their ability to
generate ATP by increasing the glucose uptake. This is
achieved by up-regulating the expression of glycolytic enzymes and glucose transporters (Wenger, 2002). Hypoxia and
HIF-1 increase virtually all the enzymes in the glycolytic
pathway, as well as the glucose transporters 1 and 3 (GLU1,
GLU3) (Chen et al., 2001). Furthermore, the glycolysis metabolic products, such as lactate and pyruvate, have been
reported to cause HIF-1 accumulation under normoxia and
TABLE 1
Environmental regulator of HIF-1
Regulator
2
Nickel (Ni
Cobalt (Co2)
Arsenite
Chromium
Vanadate
Desferrioxamine (DFO)
Insulin Interleukin-1 (IL-1)
Insulin-like growth factor
(IGF)-1, IGF-2
Fetal calf serum
Angiotensin II (Ang II)
Thrombin, Platelet-derived
growth factor (PDGF)
Nitric oxide (NO)
Nitric oxide (NO) under
hypoxia
TGF-
Function/Pathway Involved
Consequence
Increased HIF-1
Reference
Decreases cellular Fe level

Inhibits PHDs
Down-regulates the expression
of FIH-1 and ARD1
Depletes intracellular
ascorbate
PI3K/Akt
Replaces Fe
Down-regulates the expression
of FIH-1 and ARD1
Depletes intracellular
ascorbate
PI3K
ROS
p38 MAPK
p38 MAPK, ROS
PI3K/Akt, ROS
AMP-activated protein kinase
(AMPK)
Fe chelator
PI3K
ROS
Increased HIF-1
Increased HIF-1
Increased HIF-1
Wang and Semenza, 1993

Stiehl et al., 2002
Feldser et al., 1999
ROS
ROS
Increased HIF-1
Increased HIF-1
Richard et al., 2000

Gorlach et al., 2001
MAPK, PI3K
Inhibits PHDs
Inhibits mitochondrial O2
consumption
Increases intracellular Fe and
PHDs activity
ROS
Increased HIF-1
Kasuno et al., 2004

Metzen et al., 2003b
Hagen et al., 2003
Davidson et al., 2005

Ke et al., 2005
Salnikow et al., 2004
Increased HIF-1
Li et al., 2004
Yuan et al., 2003
Ke et al., 2005
Salnikow et al., 2004
Increased HIF-1
Increased HIF-1
Increased HIF-1
Decreased HIF-1
Gao et al., 2004

Duyndam et al., 2001
Duyndam et al., 2003
Gao et al., 2004
Gao et al., 2002
Hwang et al., 2004
Callapina et al., 2005

Increased HIF-1 translocation
and activity
Increased DNA binding
Haddad and Land, 2001

Hellwig-Burgel et al., 1999
up-regulated by the expression of genes involved in erythropoiesis and iron-metabolism. Hypoxia increases the expression of EPO, which is required for the formation of red blood
cells (Semenza et al., 1991). An increase in the number of
erythrocytes enhances the delivery of oxygen to tissues. Products of iron-metabolizing genes control the major erythropoietic rate-limiting step of heme production. Hypoxia up-regulates transferrin (Tf), which transports Fe3 into cells (Rolfs
et al., 1997); the transferring receptor (Tfr), which binds Tf
and enables cellular transferrin uptake (Bianchi et al., 1999;
Lok and Ponka, 1999; Tacchini et al., 1999); and ceruloplasmin (also known as a ferroxidase), which is required to oxidize ferrous (Fe2) to ferric (Fe3) iron (Lok and Ponka, 1999;
Mukhopadhyay et al., 2000). Increasing of these genes supports iron supply to erythroid tissues (Rolfs et al., 1997).
Angiogenesis. Angiogenesis is a complex process that
involves multiple gene products expressed by different cell
types (Conway et al., 2001). A large number of genes involved
in different steps of angiogenesis have been shown to increase by hypoxia challenge (Levy et al., 1995; Bunn and
Poyton, 1996; Forsythe et al., 1996; Berra et al., 2000; Giordano and Johnson, 2001; Semenza, 2002). Among them, the
vascular endothelial cell growth factor (VEGF) is the most
potent endothelial-specific mitogen, and it directly participates in angiogenesis by recruiting endothelial cells into
hypoxic and avascular area and stimulates their proliferation (Neufeld et al., 1999; Josko et al., 2000; Conway et al.,
2001). Therefore, the induction of VEGF and various other
(Volm and Koomagi, 2000). Moreover, hypoxia depressed the

antiapoptotic protein Bcl-2 (Carmeliet et al., 1998), whereas
the proapoptotic protein Bcl-2/adenovirus EIB 19-kDa interacting protein 3 (BNip3) and its homolog Nip3-like protein X
(NIX) were up-regulated in a HIF-dependent manner
(Bruick, 2000). Some genes involved in cell cycle control, such
as p53 and p21, were also found to be HIF-dependent (Carmeliet et al., 1998). In addition, p53 has been implicated in
regulating hypoxia-induced apoptosis through induction of
apoptosis-related genes such as Bax, NOXA, PUMA, and
PERP (Schuler and Green, 2001).
In addition to the above classes of genes, HIF-1 also regulated
many other target genes implicated in diverse processes such as
adipogenesis (Yun et al., 2002), carotide body formation (Kline
et al., 2002), B lymphocyte development (Kojima et al., 2002),
and immune reactions (Hellwig-Burgel et al., 2005).
Although there are some studies showing a role of HIF-2
in the VEGF induction (Akeno et al., 2001; Compernolle et
al., 2002), no bona fide target genes have yet been identified
for HIF-2 or HIF-3. However, a recent study using a genetic knock-in strategy has shown that targeted replacement of HIF-1 with HIF-2 results in expanded expression
of HIF-2-specific target genes (i.e., Oct-4, a transcription
factor essential for maintaining stem cell pluripotency) (Covello et al., 2006).
The Role of HIF-1 in Development and

Diseases
Hypoxia and the HIF pathway have been linked to the
embryonic development and pathophysiology of numerous
TABLE 2
HIF-1 target genes
Function
Erythropoiesis/ iron metabolism
Angiogenesis
Vascular tone
Matrix metabolism
Glucose metabolism
Cell proliferation/survival
Apoptosis
Gene (abbreviation)
Erythropoietin (EPO)
Transferrin (Tf)
Transferrin receptor (Tfr)
Ceruloplasmin
Vascular endothelial growth factor (VEGF)
Endocrine-gland-derived VEGF (EG-VEGF)
Leptin (LEP)
Transforming growth factor-3 (TGF-3)
Nitric oxide synthase (NOS2)
Heme oxygenase 1
Endothelin 1 (ET1)
Adrenomedulin (ADM)
1B-Adrenergic receptor
Matrix metalloproteinases (MMPs)
Plasminogen activator receptors and inhibitors (PAIs)
Collagen prolyl hydroxylase
Adenylate kinase-3
Aldolase-A,C (ALDA,C)
Carbonic anhydrase-9
Enolase-1 (ENO1)
Glucose transporter-1,3 (GLU1,3)
Glyceraldehyde phosphate dehydrogenase (GAPDH)
Hexokinase 1,2 (HK1,2)
Lactate dehydrogenase-A (LDHA)
Pyruvate kinase M (PKM)
Phosphofructokinase L (PFKL)
Phosphoglycerate kinase 1 (PGK1)
6-phosphofructo-2-kinase/gructose-2,6-bisphosphate-3
(PFKFB3)
Insulin-like growth factor-2 (IGF2)
Transforming growth factor- (TGF- )
Adrenomedullin (ADM)
Bcl-2/adenovirus EIB 19kD-interacting protein 3 (BNip3)
Nip3-like protein X (NIX)
Reference
Semenza et al., 1991

Rolfs et al., 1997
Bianchi et al., 1999
Lok and Ponka, 1999
Levy et al., 1995
LeCouter et al., 2001
Grosfeld et al., 2002
Scheid et al., 2002
Melillo et al., 1995
Lee et al., 1997
Hu et al., 1998
Nguyen and Claycomb, 1999
Eckhart et al., 1997
Ben-Yosef et al., 2002
Kietzmann et al., 1999
Takahashi et al., 2000
ORourke et al., 1996
Wykoff et al., 2000
Chen et al., 2001
Graven et al., 1999
Mathupala et al., 2001
Minchenko et al., 2002
Feldser et al., 1999
Krishnamachary et al., 2003
Cormier-Regard et al., 1998
Carrero et al., 2000
Bruick, 2000
regulate hypoxia-inducible gene expression, hence establishing a potential positive feedback loop (Lu et al., 2002).
Cell Proliferation/Survival. Hypoxia and HIF-1 induce
growth factors, such as insulin-like growth factor-2 (IGF2)
and transforming growth factor- (TGF-) (Feldser et al.,
1999; Krishnamachary et al., 2003). Binding of such growth
factors to their cognate receptors activates signal transduction pathways that lead to cell proliferation/survival and
stimulates the expression of HIF-1 itself (Semenza, 2003).
As mentioned above, cytokines and growth factors, as well as
hypoxia in some cell types, can activate signaling pathways
MAPK and PI3K, which promote cell proliferation/survival
as well as contribute to HIF-1 activity. This leads to increased HIF-1 transcriptional activity of target genes, including those encoding IGF2 and TGF-, thereby contributing to
autocrine-signaling pathways that are crucial for cancer progression (Semenza, 2003).
Apoptosis. Paradoxically, cell adaptation to hypoxia leads
not only to cell proliferation/survival but also to cell death in
some circumstances. Hypoxia has been shown to induce
apoptosis, where HIF-1 plays a complex role (Carmeliet et
al., 1998). Genetic studies using embryonic stem cells harboring a deletion of HIF-1 showed decreased apoptosis compared with wild type when challenged with low oxygen
(Carmeliet et al., 1998). Activation of caspase-3 and Apaf-1mediated caspase-9, and the release of cytochrome c, have
been reported in several cell types under hypoxic conditions
(Brunelle and Chandel, 2002; McClintock et al., 2002). It has
also been demonstrated that the expression of HIF-1 and
HIF-1 significantly correlated with apoptosis and the proapoptotic factors, such as caspase-3, Fas, and Fas ligand
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Ke and Costa
There is a remarkable frequency of common genetic alterations in cancer cells associated with increased HIF-1 expression. As mentioned in VHL disease, for example, loss of
function of VHL resulted in constitutively expressed HIF-1
(Iliopoulos et al., 1996). In addition, loss of function of wildtype p53, which is inactivated in most of human cancers,
increased HIF-1 levels and enhanced HIF-dependent transcription in tumors (Ravi et al., 2000). Loss of function of
tumor suppressor gene PTEN in glioblastoma-derived cell
line resulted in increased HIF-1 levels and HIF-1-mediated
gene expression, probably via activating of the PI3K/AKT
signaling cascade (Zundel et al., 2000). The transforming
potential of the v-Src oncogene is thought to be due in part to
its induction of HIF and gain of function of v-SRC increased
expression of HIF-1 and HIF-dependent genes (Jiang et al.,
1997). Moreover, enhanced HER2 receptor tyrosine kinase
signaling has been shown to increase the rate of synthesis of
HIF-1 (Laughner et al., 2001). Increased activity of the
HER2 receptor tyrosine kinase is a prevalent and important
genetic alteration in breast cancer, correlating with tumor
aggressiveness and decreased patient survival. Therefore, it
seems that HIF-1 overexpression confers selective advantages to tumor cells. A correlation between HIF-1 overexpression and patient mortality, poor prognosis, or treatment resistance has been noted in many studies (Semenza, 2003).
Ischemic Disease. Activation of HIF activity has also
been demonstrated in a broad range of physiological responses to ischemic, hypoxic, and inflammatory conditions,
where it plays a positive role to respond to the damage to
organs or tissues. For example, the levels of HIF-1 and
VEGF were increased in the myocardium when patients developed acute coronary artery occlusion (Lee et al., 2000).
Effective vascular remodeling after ischemic injury depended
on an integrated program of HIF-dependent gene expression.
Increasing of HIF-1 expression and HIF-inducible genes
was also observed in sheep and rat models of myocardial and
cerebral ischemia (Martin et al., 1998; Bergeron et al., 1999).
In addition, induction of HIF-1 or HIF-2 and their target
genes has been shown in the pre-eclamptic placenta (Rajakumar et al., 2003), by macrophages in rheumatoid synovia
(Hollander et al., 2001), in the ischemic retina (Ozaki et al.,
1999; Grimm et al., 2002), as well as from wound healing
(Elson et al., 2000).
The Implication of HIF-1 in Therapy

The importance of HIF-1 as a transcription factor and the
broad spectrum of processes influenced by HIF suggest that
it could have important clinical implications. The many aspects of HIF-1 regulation provide a variety of possibilities for
therapeutic intervention.
Cancer TherapyInhibiting HIF-1 Activity. First, immunohistochemical analysis of HIF-1 expression in tumor
biopsies may provide the prognostic information and thereby
identify subsets of patients requiring aggressive therapy
(Harris, 2002). To achieve high specificity to hypoxic tumor
regions or cells, HREs from hypoxia-responsive genes can be
used to express marker therapeutic genes selectively expressed in tumor cells that are hypoxic and overexpress
HIF-1 (Dachs et al., 1997).
It has been suggested that disruption of the HIF-1 pathway might be effective in the treatment of pancreatic cancer
human diseases. In order for solid tumors to grow, an increase of oxygen delivery to cells via angiogenesis and activation of glycolysis have been observed and named the Warburg effects (Seagroves et al., 2001). Given the importance of
HIF-1 in the activation of genes essential to these processes,
it is not surprising that both HIF-1 and HIF-2 have been
strongly implicated in tumor progression and grade, hence
conferring a selective advantage to tumor cells.
Development. Components of the HIF-1 system play essential roles in embryonic development. Knockout of either
HIF-1 (Iyer et al., 1998; Ryan et al., 1998; Kotch et al.,
1999), HIF-2 (Tian et al., 1998; Peng et al., 2000), or HIF-1
(Maltepe et al., 1997) resulted in abnormal vascular development and lethality in mice. HIF-1 expression increased
between embryonic days 8.5 and 9.5 in normal mouse embryos (Iyer et al., 1998). Embryos deficient in HIF-1 (HIF1/) died by embryonic day 11 as a consequence of lack of
blood vessel formation, defective formation of the neural fold,
and cardiovascular malformation (Iyer et al., 1998; Ryan et
al., 1998). Global hypoxia was also observed. In addition, the
rate of cell proliferation and the expression of hypoxia-inducible genes were decreased in HIF-1/ cells, compared with
those of wild-type cells (Iyer et al., 1998). Although heterozygous mice carrying a single HIF-1 gene (HIF1/) developed normally, they displayed impaired physiological responses when challenged by chronic hypoxia (Yu et al., 1999;
Kline et al., 2002).
Targeted inactivation of HIF-2 (HIF-2/) in mice resulted in rather different and variable phenotypes. HIF2/ mouse embryos died by E12.5-embryonic day 16.5 as a
result of inadequate blood vessel fusion and remodeling, impaired fetal lung maturation, and a very slow heart rate
because of insufficient catecholamine production (Tian et al.,
1998; Peng et al., 2000). Thus, it seems that HIF-1 and
HIF-2 have nonredundant functions in the regulation of
gene expression during development, despite their close similarity in terms of amino acid sequence, domain architecture,
DNA-binding capacity, and hypoxic activation.
HIF-1/ embryos died by embryonic day 10.5 and
showed defect in blood vessel formation, defective angiogenesis of the yolk sac and branchial arches, stunted development, and embryo wasting (Maltepe et al., 1997). In addition,
HIF-1/ cells failed to activate genes that normally respond to hypoxia and low glucose concentration (Maltepe et
al., 1997).
Cancer. Overexpression of HIF-1 and HIF-2 was found
in various human cancers, probably as a consequence of
intratumoral hypoxia or genetic alteration (Zhong et al.,
1999; Talks et al., 2000). The interior of the tumor mass
becomes progressively hypoxic as its size increases until adequate blood vessels are obtained by tumors. Hypoxic conditions within tumors can result in increased HIF-1 stability
and activity. Immunohistochemical analyses demonstrated
that there are detectable levels of HIF-1 protein in benign
tumors, elevated levels in primary malignant tumors, and a
marked amount in tumor metastases, in contrast to its absence in normal tissues (Zhong et al., 1999; Harris, 2002).
Expression of HIF target genes is generally consistent with
the levels of HIF-1. In addition, injection of HIF-1 (or
HIF-1) positive and deficient cells to immunocompromised
mice revealed that HIF-1 is a positive factor to tumorigenesis (Maxwell et al., 1997; Ryan et al., 2000).
Conclusion
Despite recent rapid advance in understanding the molecular mechanisms of the HIF pathway in response to hypoxia,
many important questions remain to be answered. For example, the distinct role of enzymes modifying HIF-1 posttranslationally, the interplay among the HIF-1 post-translational modifications, the identity of additional target genes
of HIF-1, the function of the paralogs of HIF-1 (such as
HIF-2 and HIF-3), the link between HIF-1 activation and

other oncogenic or tumor suppressor pathways, the mechanism by which the HIF-1 pathway contribute to tumor
growth and other pathological responses. Unraveling such
questions should provide new insights into cellular adaptation to hypoxia and aid to discover new therapeutic approaches to diverse human diseases.
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0026-895X/06/7005-1469 1480$20.

Vol. 70, No. 5

Hypoxia-Inducible Factor-1 (HIF-1)

The transcription factor hypoxia-inducible factor-1 (HIF-1)

Article, publication date, and citation information can be found at

droxylation of two proline residues and acetylation of a lysine

The Discovery of HIF-1

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The Regulation of HIF-1

Fig. 1. Domain structure of human HIF- and HIF-1.

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ing to the HRE DNA sequence (Crews, 1998). Two

HIF-1, A New Target for Therapy

(Bruick and McKnight, 2001; Masson et al., 2001). Mutation

Human HIF- dioxygenase was termed prolyl hydroxylase

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Downloaded from molpharm.aspetjournals.org by guest on February 15, 2012

Huang et al., 2002). The biochemical characteristics of the

HIF-1, A New Target for Therapy

oxygen as a substrate allows FIH-1 to serve as a second

The Target Gene of HIF-1

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D, has also been shown to increase HIF-1 levels under

proangiogenic factors leads to an increase in the vascular

Decreases cellular Fe level

Wang and Semenza, 1993

Richard et al., 2000

Kasuno et al., 2004

Davidson et al., 2005

Gao et al., 2004

Callapina et al., 2005

Haddad and Land, 2001

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HIF-1, A New Target for Therapy

(Volm and Koomagi, 2000). Moreover, hypoxia depressed the

The Role of HIF-1 in Development and

Erythropoiesis/ iron metabolism

Semenza et al., 1991

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The Implication of HIF-1 in Therapy

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HIF-1, A New Target for Therapy

HIF-2 and HIF-3), the link between HIF-1 activation and

Downloaded from molpharm.aspetjournals.org by guest on February 15, 2012

Downloaded from molpharm.aspetjournals.org by guest on February 15, 2012

Crews ST (1998) Control of cell lineage-specific development and transcription by

HIF-1, A New Target for Therapy

ization is associated with increased myocardial expression of vascular endothelial

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Ruas JL, Poellinger L, and Pereira T (2002) Functional analysis of hypoxia-inducible

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