|Home | About | Journals | Submit | Contact Us | Français|
The hypoxia inducible factor, HIF-1 is a central regulator of the response to low oxygen or inflammatory stress and plays an essential role in the survival and function of immune cells. However, the mechanisms regulating non-hypoxic induction of HIF-1 remain unclear. Here, we assess the impact of germline heterozygosity of a novel, oxygen independent ubiquitin ligase for HIF-1α; the hypoxia associated factor, HAF (encoded by SART1). SART1−/− mice were embryonic lethal, whereas male SART1+/− mice spontaneously recapitulated key features of non-alcoholic steatohepatitis (NASH) driven HCC including steatosis, fibrosis and inflammatory cytokine production. Male but not female SART1+/− mice showed significant upregulation of HIF-1α in circulating and liver-infiltrating immune cells but not in hepatocytes prior to the development of malignancy. Additionally, Kupffer cells derived from male but not female SART1+/− mice produced increased levels of the HIF-1 dependent chemokine, RANTES, compared to wild-type. This was associated with increased liver-neutrophilic infiltration whereas infiltration of lymphocytes and macrophages were not significantly different. Neutralization of circulating RANTES decreased liver neutrophilic infiltration, and attenuated HCC tumor initiation/growth in SART1+/− mice. Conclusion: We establish a new tumor suppressor role for HAF in immune cell function by preventing inappropriate HIF-1 activation in male mice, and identify RANTES as a novel therapeutic target for NASH and NASH-driven HCC.
Hypoxia is a state of reduced oxygen pressure below its physiological threshold, which impacts both normal and disease processes (1, 2). Hypoxia characterizes virtually every site of inflammation, thus requiring infiltrating immune cells to undergo a metabolic switch towards anerobic pathways to maintain energy requirements. The hypoxia inducible factor (HIF) transcription factors are central regulators of the hypoxic response. The HIFs are heterodimers comprising one of three major oxygen labile HIF-α subunits (HIF-1α, HIF-2α and HIF-3α), and a constitutive HIF-1β subunit, which together form the HIF-1, HIF-2 and HIF-3 transcriptional complexes respectively (3). HIF-1 plays an essential role in the survival and function of immune cells, by facilitating energy generation through anerobic glycolysis (4). Under aerobic conditions, HIF-α is hydroxylated by oxygen-dependent prolyl-hydroxylases, promoting ubiquitination by the von Hippel-Lindau protein (pVHL) E3 ligase complex resulting in HIF-α proteasomal degradation (5). Under hypoxic conditions, pVHL binding is abrogated, HIF-α is stabilized and heterodimerizes with HIF-1β to transactivate a variety of hypoxia-responsive genes (6). HIF-1α can also be induced under non-hypoxic conditions by pro-inflammatory cytokines, which allow the initiation of an inflammatory response before tissues become hypoxic (4, 7). In addition to pVHL, the hypoxia associated factor, HAF (encoded by SART1), is an isoform specific E3 ubiquitin ligase that specifically degrades HIF-1α (but not HIF-2α), in an oxygen-independent manner (8). Also known as SART1, HAF is expressed in both normal and malignant proliferating tissue (9, 10), is important for spliceosome assembly (11), and cell division (12). Here, we address the physiological role of HAF.
The SART1+/− mice were derived from the Texas Institute for Genomic Medicine gene trap C57BL/6 SART1−/− ES cell line (Clone IST11321E11). Genotyping was performed using allele-specific PCR (Supplemental methods). All animal procedures were performed in accordance with institutional animal care and use protocols.
Differential gene expression profiling of SART1+/− versus wild-type livers (3 replicates each) were performed using the GeneChip® Mouse Genome 430 2.0 Array and the 3′ IVT PLUS Reagent Kit (Affymetrix, P/N 902416, Santa Clara CA); GEO Accession GSE71057. Data analysis was performed using Transcriptome Analysis Console 2.0, which generated the heatmaps, and Ingenuity Pathway Analysis (Qiagen Inc., Valencia CA). Hit validation was performed by Taqman custom arrays (Life Technologies, Carlsbad CA).
Human HCC (of unknown etiology, Fig 8A) was purchased from US Biomax Inc (Rockville, MD). Sections in Fig 8B-D were from formalin fixed paraffin-embedded non-alcoholic steatohepatitis (NASH) associated HCC tumors collected during surgical resections and liver transplants (normal liver samples) at the Mayo Clinic between 1997 and 2013. Sections were examined by pathologist, graded histologically and classified by etiology. The study was approved by the Mayo Clinic Institutional Review Board.
MRI was performed by operators blinded to study design using a Bruker 11.7T MRI system (Supplemental methods). After initial imaging, tumor-bearing mice were stratified into 2 groups and injected IP with 400μg RANTES neutralizing antibody (MAB478, R&D systems, Minneapolis MN) or saline twice per week for 5 weeks, after which mice were re-imaged and tumor volumes were recalculated.
These were performed using Student’s T-tests using Graphpad Prism 6 or Microsoft Excel. p<0.05 were considered significant with *p < 0.05, **p < 0.01.
All other methods are listed in Supplemental methods.
HAF heterozygous mice (SART1+/−) were generated using C57BL/6 embryonic stem cells produced by the gene trap method (Fig. 1A-B). Tissue-wide profiling of male wild-type and SART1+/− mice confirmed expression of HAF in multiple organs including skin, lung, heart, liver, kidney, spleen and colon, with highest expression within the spleen (Fig. 1C). HAF heterozygosity was associated with significant decreases of HAF in heart, liver and kidney, and caused more subtle decreases in other tissues in which HAF could be detected (Fig. 1C-D).
Out of a total of 99 pups resulting from pairings with heterozygous parents, 70 were het, whereas 29 were wild-type, close to the expected ratio of 2:1:1 for het: wild-type: knockout, consistent with embryonic lethality. By genotyping embryos at various developmental stages, knockouts were only identified at E11.5, and SART1−/− embryos showed diminished size and vascularization compared to their heterozygous or wild-type littermates (Fig. 1E). Thus, knockout of SART1 results in embryonic lethality at approximately E11.5.
Despite the embryonic lethality ofHAF knockout mice, mice heterozygous for HAF (SART1+/−) appeared to develop normally, and displayed no anatomically observable defects. However, at >14 months, male SART1+/ mice were significantly smaller, and had ruffled fur compared to their wild-type counterparts (Fig. 2A and Supplemental Data S1A). Necropsy revealed multifocal large liver tumors (histologically confirmed as HCC) in ~83% (5/6) of male SART1+/− mice, which were absent from their wild-type littermates (Fig. 2A), whereas both wild-type and SART1+/− male mice exhibited severe hepatic steatosis. The livers of the SART1+/− mice displayed hallmarks of non-alcoholic steatohepatitis (NASH)-driven HCC including hepatic steatosis (confirmed by Oil Red O staining), fibrosis (confirmed by Sirius Red staining) and foci of immune cell infiltration (Fig. 2B, Fig.4E-F). Visual analysis of additional male SART1+/− mice confirmed grossly visible tumors in an additional 90% (9/10) of mice. By contrast, the livers of age-matched SART1+/− females showed minimal steatosis, and no malignant tumors were detected either grossly or histologically (0/4, not shown). At age 10 months, HCC was detected in 42% (5/12) of mice, whereas pre-neoplastic foci of hepatocellular alterations and/or adenomas were present in 83% (10/12) of mice. By contrast, none were observed in wild-type littermates (Fig. 2A). Consistent with enlarged livers and decreased overall body weight, the average liver weights/body weight ratios in SART1+/− mice were also significantly higher than their wild-type counterparts (Fig. 2C, RHS). Liver tumors were detected by MRI in a further 57% (4/7) of male SART1 +/− mice aged 16-18 months (S1B), but were not detected in male mice under the 10 months (0/21), nor in female SART1+/− mice aged 16-19 months (0/3). The rapid growth of the liver tumors was apparent when we monitored tumor growth in one 1616-18 month old mouse, where we found multiple large liver tumor nodules (S1C) confirmed histologically as HCC. No other obvious abnormalities were observed in the blood or any of the other major organs apart from age-related changes. Hence, germline haploinsufficiency of HAF promotes spontaneous HCC development only in male mice > age 10 months.
When examined histologically, livers of 1-month-old SART1+/− mice were indistinguishable from those of their wild-type littermates (Fig. 2D). However, at age 6 months, SART1+/− liverslivers showed moderate to marked microvesicular hepatic steatosis with increased severity in the centrilobular/periacinar and midzonal regions, and also showed multiple foci of altered hepatocytes with atypical nuclei (Fig. 2E, ,3A).3A). These foci were composed of hypertrophic or cytomegalic hepatocytes and showed increased proliferation supported by the increased number of mitotic and binucleated hepatocytes. Although these foci are considered pre-neoplastic lesions predisposing to tumor development, no neoplastic lesions were observed at this age. By contrast, livers of wild-type littermates showed only very mild steatosis, and no pre-neoplastic lesions. Consistent with the age-related progression to HCC, the elevation of the serum transaminases alanine aminotransferase (ALT), aspartate aminotransferase (AST), or alkaline phosphatase (ALP) in the SART1 +/− mice versus wild type become apparent from 6 months of age (S1D). The age-associated liver phenotypes of the SART1+/− mice are summarized in Fig. 3B and S1E. Intriguingly, although HAF levels in SART1+/− versus wild-type livers were not significantly different at age 1 month, HAF levels decreased with increasing age, which reflected the development of liver pathology in the SART1 +/− mice (Fig. 3C-D). Hence, although initially normal, the livers of SART1+/− mice first manifest foci of pre-neoplastic hepatocellular alteration, coinciding with the development of hepatic steatosis, which then progress to HCC.
To evaluate global changes in gene expression associated with HCC in the SART1 +/− mice, we performed microarray analysis comparing a SART1 +/−liver tumor (T) to an age-matched wild-type liver (N). Using a fold change cut-off of 2.0 fold up-or-down regulated, and p<0.05, 2290 genes were differentially expressed in T vs N groups out of 20185 total genes probed by the array (Fig. 3E). Intriguingly, the top differentially expressed gene was alpha fetoprotein (Afp, 441 fold induction versus normal), which encodes a blood serum marker typically used for diagnosis of HCC in humans (S2A). Using Ingenuity Pathway Analysis (IPA), the top biological functions associated with these differentially expressed genes were those involved in the inflammatory response, cancer, and lipid metabolism (S2B). We also observed highly significant changes in genes associated with hepatocyte hyperplasia/proliferation, steatosis and HCC. All these expression changes were consistent with the observed steatosis/steatohepatitis/HCC phenotype in the SART1+/− livers.
To investigate the molecular pathogenesis of hepatic steatosis in the SART1+/− mice, we examined the expression of subsets of genes known to be involved in the various aspects of lipid metabolism. According to IPA, 39 out of 45 genes involved in fatty acid metabolism were significantly decreased (p=6.86E-13; Fig. 3E, S3A). This included Acyl-CoA synthase long-chain family member 1 (Acsl1), which catalyzes one of the first steps of fatty acid oxidation; and a large number of cytochrome P450 (CYP) genes, which have diverse roles in liver metabolism (13). By contrast, levels of the major transcription factors that promote lipogenesis and lipid uptake, sterol regulatory element–binding protein-1c (SREBP-1c, SREBF1), carbohydrate response element binding protein (ChREBP, MLXIPL), and peroxisome proliferator-activated receptor gamma (PPAR-γ, PPARG), were not significantly altered in our dataset, nor were their downstream gene expression profiles significantly altered. The trend of decreased expression of genes involved in fatty acid oxidation was validated using 3 additional SART1+/− livers normalized to livers from 3 wild-type littermates, and was also confirmed at the protein level for Acsl1 and CYP2b10 (Fig. 3F).
To determine whether fatty acid oxidation was indeed dysfunctional in the SART1+/− mice, hepatocytes from 4 month old SART1+/− mice and their wild-type littermates were subjected to metabolic analysis using the Seahorse XF Extracellular Flux analyzer. Using oxygen consumption rate, OCR, as an indicator of mitochondrial respiration, we found that SART1+/− hepatocytes showed a lower basal level of respiration compared to wild-type (Fig. 4A). When treated with the mitochondrial uncoupler FCCP, which induces maximal respiration, SART1+/− hepatocytes showed an almost 4-fold decrease in the ability to utilize exogenous palmitate compared to wild-type hepatocytes (Fig. 4A-B). Similar results were obtained using Huh7 human hepatoma cells transiently transfected with control or HAF (SART1) siRNA (Fig. 4C-D). Thus, the enhanced hepatic steatosis observed in the SART1 +/− livers is likely due to defective fatty acid oxidation. .
In addition to metabolic dysfunction, SART1 +/− livers showed changes consistent with increased inflammatory cell activation and trafficking (Fig. 3E, S2B). Indeed, SART1+/− livers showed extensive immune cell infiltration, distributed randomly and sporadically, often in clusters, throughout the liver parenchyma (Fig. 4E). These included cells positive for F4/80 or Ly6G suggesting that these clusters contained macrophages and neutrophils respectively (Fig. 4F). Additionally, Kupffer cell hyperplasia (likely a result of phagocytosis of disrupted hepatocytes) was observed in 100% (6/6) of the SART1+/− livers but not in wild-type livers (S1E). Significantly, the liver-infiltrating immune cells were markedly HIF-1α positive in SART1+/− but not in wild-type livers (arrows, Fig. 4G). Increases in HIF-1α was manifest primarily in SART1+/− immune cells, but not in SART1+/− hepatocytes, suggesting that the HIF-1α upregulation was not due to a general hypoxic environment within the livers (Fig. 4G, S4A-B). The changes observed in SART1+/− immune cells may also reflect the distribution of HAF expression, which was detected primarily in infiltrating immune cells in wild-type livers (S4C). By contrast, HIF-2α was expressed in the immune infiltrating cells in the livers of both wild-type and SART1+/− mice (S4C).
To establish whether HIF-1α upregulation played a causal role in HCC carcinogenesis in the SART+/− mice, or occurred as a result of the HCC already present, we isolated mononuclear cells from peripheral blood (PBMCs) and spleens of 6 month old SART1+/− and wild-type mice. HIF-1α protein levels were significantly elevated in both PBMCs and splenocytes from SART1+/− versus wild type mice, but not in primary hepatocytes (Fig. 5A, S4B). We also noted that unlike the PBMCs, splenocytes did not express detectable HIF-1α unless exposed to hypoxia (only cells exposed to hypoxia are depicted), suggesting some intrinsic differences in HIF-1α expression in these cell types. These findings were associated with a reduction in HAF protein levels expected of the SART1+/− genotype (S4D). By contrast, we did not detect upregulation of HIF-1α in PBMCs or splenocytes isolated from 6 month old female SART1+/− mice, and only detected subtle decreases in HAF levels (S5A-B). Hence, the data suggest that HIF-1α upregulation in immune cells was intrinsic to the male SART1+/− mice, and occurred independently of HCC.
To determine whether HAF expression in immune cells was cell type-specific, we measured the activity of the LacZ reporter transgene used to disrupt the SART1 gene. We detected LacZ positivity in a wide variety of cell populations including spleen- and bone marrow-derived cells, and peripheral blood leukocytes (Fig 5B, S6A). To identify cell types that expressed LacZ (and therefore endogenous HAF), we stained splenocytes with surface markers: CD19 (B-Cells), TCRβ (T-Cells), Ly6G (neutrophils), F4/80 (macrophages) prior to the Lac Z activity assay. Here, we observed significant LacZ/FITC positivity in all cell types, with highest expression in B and T-cells, and macrophages, whereas no significant differences between the immune cell populations from SART1+/− and wild-type mice were observed (Fig. 5C, S6B-C). Thus, HAF is highly expressed in all immune cells, and loss of HAF in the male SART1+/− mice is associated with HIF-1α upregulation in all immune cell types.
To determine whether immune cells played a causal role in the development of HCC, we isolated Kupffer cells (KCs) from the livers of 5-month-old SART1+/− mice, and compared their secreted cytokine expression profiles to that of wild-type littermates. In general, SART1+/− KCs had higher levels of secreted cytokines than wild-type KCs (Fig. 5D, S3B). Intriguingly, levels of the chemokine Regulated on Activation, Normal T cell Expressed (RANTES) was increased by >100 fold in the SART1+/− KCs compared to wild-type KCs (Fig. 5D). RANTES plays a major role in recruiting leukocytes to sites of injury, and is transcriptionally regulated by HIF-1α by multiple functional HREs within its promoter (14, 15). Knockdown of HAF using siRNA in THP-1 cells also resulted in significant upregulation of RANTES in both normoxia and hypoxia (Fig. 5E). RANTES was significantly upregulated in the livers of SART1+/− mice over wild-type mice from 6 months of age, although increased transcription was already detected at 1 month of age (Fig. 6A). Consistent with HIF-1α upregulation, we also detected an age-dependent albeit delayed increase (compared to RANTES) in the transcription of HIF-1 target genes facilitated glucose transporter 1 (Slc2a1), Hexokinase 1 (Hk1) and pyruvate kinase (muscle) 1 (Pkm1) in the SART1+/− livers indicating a general shift towards glycolytic metabolism (Fig. 6B). By contrast, we did not observe any differences in secretion of RANTES or other cytokines by KCs from similar-aged female SART1+/− livers compared to wild-type (S5C).
To determine whether the immune cell sub-populations present within the SART1+/− livers were altered prior to HCC initiation, we profiled the livers of 66 month old mice. Intriguingly, we found a 6-fold increase in Ly6G+ neutrophils in SART1+/− livers relative to wild-type, also observed via immunohistochemistry, whereas levels of CD11c+ macrophages, CD4, CD8, gamma delta and NK T cells were not significantly altered (Fig. 6C-D). We also observed a 3-fold increase in Ly6G+ neutrophils within livers of 1 month old SART1+/− mice which was not observed in the spleens, suggesting that increased neutrophilic infiltration was an early event independent of hepatic steatosis, and was not due to systemic elevation of the neutrophil population (Fig. 6E-F, S7). Thus, male but not female SART1+/− KCs secrete elevated levels of cytokines/chemokines including a >100-fold increase in RANTES. This was associated with increased neutrophilic infiltration in male SART1+/− livers prior to the development of steatosis or HCC.
To determine the impact of RANTES secretion on liver neutrophilic infiltration, and HCC initiation/progression, we used a neutralizing antibody to RANTES and monitored treatment efficacy by MRI. Imaging of SART1+/− mice aged 14-18 months revealed only 4 of 15 mice bore tumors with a total volume of >100mm3 clearly detectable by MRI (Fig. 7A, S8). The mice were treated with RANTES neutralizing antibody (or saline) for 5 weeks and were re-imaged. Upon re-imaging, we observed the appearance of new nodules in the control group but not in the RANTES-treated group, suggesting that RANTES treatment prevented liver tumor initiation/promotion (Fig. 7A-C, S8). The growth of individual nodules was also markedly reduced in the RANTES-treated mice (RANTES 6.709 ± 3.872 fold, n=5, versus control 13.20 ± 6.546 fold, n=5; Fig. 7D-E). We also observed a significant decrease in Ly6G+ infiltrating neutrophils in both tumor and adjacent normal tissue of mice treated with RANTES compared to those treated with saline alone (Fig. 7F-G). Hence RANTES neutralization inhibits both the initiation/promotion and growth of liver tumors, and attenuates neutrophilic infiltration in the livers of SART1+/− mice.
Similar to the SART1+/− livers (Fig. 4G), HIF-1α positive immune infiltrating cells in the context of largely HIF-1α negative hepatocytes was also observed in human HCC including NASH-derived HCC (Fig. 8A-B). RANTES expression in both hepatocytes and immune infiltrating cells was also upregulated in NASH-derived HCC compared to normal liver (Fig. 8C). By contrast, HAF staining was detected primarily in infiltrating cells in normal human liver but was largely negative in human NASH-derived HCC (Fig. 8A, D), thus supporting a role for HAF as a tumor suppressor for HCC.
HCC is the most common primary malignancy of the liver, with more than 750,000 new patients diagnosed globally each year (16). HCC frequently develops in the context of chronic hepatitis, which may arise from infection with Hepatitis B virus (HBV) or Hepatitis C virus (HCV), and from alcoholic or non-alcoholic fatty liver disease (AFLD/NAFLD) (17). The current obesity epidemic has been associated with an increasing prevalence of NAFLD and its inflammatory component non-alcoholic steatohepatitis (NASH), which leads to HCC. The complex interplay between damaged hepatocytes and immune infiltrating cells within an inflammatory hepatic microenvironment is believed to drive HCC initiation and progression (18, 19). Hence, HCC pathogenesis has been described by the “two hit” hypothesis whereby the first “hit”-steatosis/viral infection - sensitizes the liver to a variety of second “hits”, such as oxidative stress and abnormal cytokine production, which lead to necroinflammation and fibrosis (20, 21).
Here, we show that germline haploinsufficiency of SART1 induces HCC in the context of NASH only in male mice. This is to our knowledge, the only genetic model where haploinsufficency promotes HCC without requiring any further manipulation. The livers of the SART1+/− mice showed decreased fatty acid oxidation, providing a likely mechanism for the hepatic steatosis (or first ‘hit’), and also showed constitutive stabilization of HIF-1α specifically in immune cells, elevated cytokine secretion by KCs, and increased neutrophilic infiltration prior to HCC development (together constituting the second ‘hit’). The activation of these immune cells likely promotes oxidative damage and inflammation, driving progression to HCC. Although infiltrating immune cells are known to be involved in HCC initiation and progression, the plethora of inflammatory cytokines upregulated in human HCC have confounded the identification of individual key cytokines to target for therapy (22-25). The robust timeline for HCC development in the male SART1+/− mice enabled the identification of RANTES as an early, non-redundant event driving HCC initiation and progression, likely by promoting neutrophil infiltration. Intriguingly, increased circulating RANTES has been associated with obesity in humans, and is upregulated in patients with NAFLD/NASH, suggesting that RANTES might be involved in the progression to NASH-driven HCC (26, 27). The evaluation of the relevance of HIF-1/RANTES to NASH-driven HCC is currently being investigated in a larger patient set. Intriguingly, RANTES elevation has also been observed in patients with alcoholic and viral hepatitis, whereas RANTES polymorphisms correlate to susceptibility to HCC suggesting that RANTES may be a valid therapeutic target for HCC regardless of etiology (28, 29).
An intriguing observation in our studies was that HCC did not occur in female SART1+/− mice. This male predominance also occurs in human HCC, and in chemically-induced HCC in mice (with the hepatic procarcinogen N-nitrosodiethylamine, DEN) (30, 31). The male bias for DEN-induced HCC has been attributed to the suppressive effect of estrogen on IL-6 production, aa driving factor for DEN-induced HCC (30). Whether the male bias observed in our model is related to IL-6 production is unclear, but it does appear to be associated with an intrinsic resistance of both wild-type and SART1+/− female mice to hepatic steatosis, an initiating factor for HCC in the male SART1+/− mice. Female SART1+/− and wild-type mice even at >16 months of age develop only mild hepatic steatosis, if at all, and do not become obese like their male counterparts (our unpublished observations). The age-dependent decrease in HAF levels in male SART1+/− mice, which was accompanied by immune cell specific upregulation of HIF-1α, was not observed in female mice suggesting that the predisposition to steatosis in males may drive further decreases in HAF, hence exacerbating the development of liver pathology (Fig 3C, ,5A,5A, S5). Additional factors driving the male bias may be the sex-dependent production of RANTES (Fig 5D, S5C), which has been previously reported in obese mice (26). Nevertheless, steatosis per se is insufficient to induce HCC as germline VHL+/− mice, or mice bearing hepatocyte-specific VHL deletion, develop severe hepatic steatosis but not HCC (32, 33). Since VHL is unable to degrade HIF-1α under hypoxic conditions, it is possible that HAF, as an oxygen-independent ubiquitin ligase, may play a more central role in attenuating inappropriate HIF-1α upregulation under hypoxic, inflammatory conditions. Indeed, the high expression levels of endogenous HAF within the mouse spleen and in immune infiltrating cells (Fig. 1C, ,8A,8A, D) supports an immune-specific physiological role of HAF as a suppressor of HIF-1α.
In view of the systemic activation of immune mediators in male SART1+/− mice, we also observed increased lymphohistiocytic infiltration in the lungs, gastro-intestinal tract, and lymph nodes of SART1+/− mice compared to wild-type (our unpublished observations). Hence, it is likely that other organ-specific stresses may lead to inflammation-induced cancer in these organs, and this is currently under investigation. In addition to its role as a ubiquitin ligase for HIF-1α, HAF has also been known to play a role in pre-mRNA splicing (11), and to inhibit Hepatitis C virus (HCV) replication in hepatoma cells via changes in splicing (34). Hence, splicing changes in the SART1+/− mouse are also currently being explored.
In conclusion, this study identifies a novel tumor suppressor function of HAF by maintaining regular hepatic metabolism, and in preventing inappropriate immune cell activation, possibly by suppressing HIF-1α. Additionally, we described a novel mouse model of NASH-derived HCC, which closely recapitulates the human disease. Our findings highlight a central role of the HIF-1/RANTES axis in HCC initiation and progression, thus identifying a novel target for therapy.
The authors would like to thank Catherine D. Moser and Nasra H. Giama from Mayo Clinic for liver tissue preparation and curation.
Financial support: R01CA181106 (MYK), R01CA098920 (GP), R01CA164679 and P01CA177322 (CW), P30DK084567 and Mayo Clinic Cancer Center grant CA15083 (LRR) , and the SBP NCI Cancer Center Support Grant P30 CA030199. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
No conflict of interest is declared.