Energy metabolism and cancer -
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Funding: This work was supported by grant funding from the Canadian Institutes of Health Research CIHR. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist. Over 50 years ago, Otto Warburg first proposed that mitochondrial injury that leads to depressed electron transport chain function and respiratory defects is an important step in the development and progression of carcinogenesis [1] , [2].
Over the past two decades, many studies have shown that tumours preferentially use glycolysis for energy production over oxidative phosphorylation, a characteristic that has become a hallmark of tumour pathophysiology [3] — [5].
Known as the Warburg effect, cancer cells predominantly utilize glycolysis for ATP production even in the presence of abundant oxygen, an environment that would normally result in energy production through oxidative phosphorylation [2] , [6].
Alterations in mitochondrial DNA correspond to increased production of ROS and impaired oxidative phosphorylation, resulting in decreased ATP production and increased glycolytic dependence [5] , [7].
The increased production of reactive oxygen species, particularly H 2 O 2 , by cancer cells is likely the result of mitochondrial dysfunction, as mitochondria are considered to be the predominant cellular source of reactive oxygen species [8]. Four to five percent of the O 2 consumed by oxidative phosphorylation in the mitochondria is normally converted to reactive oxygen species; therefore defects to the electron transport chain system in cancer cells would result in excessive reactive oxygen species formation [8] — [10].
Excessively produced, H 2 O 2 can act as a signaling molecule by oxidizing cysteine molecules on proteins, activating several signaling pathways including MAPK, as well as several transcription factors including AP-1, p53, NF-κB, and Ets-1 [11] — [15].
Ets-1, a member of the Ets protein family of transcription factors, regulates the expression of a diverse set of proteins through its interaction with specific consensus sequences upstream of target genes [16].
The over-expression of Ets-1 has been associated with a multitude of different cancers, specifically with regards to tumour progression and invasion [16] — [19].
Additionally, over-expression of Ets-1 has also been associated with poor prognosis in breast [20] , ovarian [21] , and cervical carcinomas [22]. Traditionally, Ets-1 is thought to function as a transcriptional activator and its high expression in endothelial and stromal cells correlates with tumour cell invasiveness and unfavourable outcome in ovarian and breast cancer [23] — [25].
Our laboratory and that of others have highlighted the importance of Ets-1 in the regulation of different aspects of cancer cell behaviour, including extracellular matrix remodeling, invasion, angiogenesis [26] , and drug resistance [27].
The link between Ets-1 and cancer invasiveness can potentially be explained by the list of known target genes regulated by this transcription factor. Several MMPs and integrin genes, as well as urokinase plasminogen activator uPA , which are all known mediators of extracellular matrix degradation and cell migration, are known targets for Ets-1 [28] — [31].
Many genes crucial to angiogenesis and extracellular matrix remodeling, such as matrix metalloproteinases MMP-1, MMP-3, MMP-9 , uPA and Integrinβ3, are under the direct regulation of Ets-1 [26].
This transcription factor is thus considered to be an important mediator of cancer cell development and tumour progression. In this study we have demonstrated that Ets-1 plays a role in the regulation of energy metabolism in ovarian cancer cells.
Using high throughput genomic analysis, we have found that Ets-1 regulates, either directly or indirectly, several important genes involved in mitochondrial metabolic and antioxidant defense pathways in our Ets-1 over-expression ovarian cancer cell model.
Functionally, we have shown that glycolysis, oxidative phosphorylation, and cellular respiratory systems are altered in response to changes in Ets-1 expression. Taken together, our findings indicate that Ets-1 is a key transcription factor involved in regulating metabolic and oxidative stress in cancer cells.
Ets-1 was over-expressed in ovarian cancer cells using a tetracycline-inducible system, generating Ets1 cells.
Ets-1 protein expression in tetracycline-treated and Ets1 was examined via Western blotting Figure 1. Ets-1 protein expression was not detectable in whole cell lysates, but was readily detected in the induced Ets1 lysate. Increased Ets-1 expression was found to be a specific effect as the protein levels of two similar Ets family members, Ets-2 and PEA3 were not altered in this model of Ets-1 over-expression Figure 2.
The protein expression of ETS family transcription factors A Ets-2 and B PEA3 were compared in and Ets1 ovarian cancer cells to determine the specificity of our Ets-1 expression model.
Western blot analysis showed that neither of these transcription factors was affected by Ets-1 expression in cells. Microarray analysis of and Ets1 cells revealed that 3, genes of the 28, genes probed were up-regulated or down-regulated in response to Ets-1 over-expression by at least 1.
For this study, we have chosen to report and examine changes in selected mRNAs whose functions are relevant to mitochondrial activity, cellular metabolism, and oxidative stress.
Real time qRT-PCR validation was conducted using 10 target genes representing various fold change values, and results were normalized to 4 separate housekeeping genes. Although both PPARG and SDHB gene expression in Ets1 cells were not significantly different from cells, the fold changes determined from real time qRT-PCR were associated with the microarray fold changes by a correlation coefficient of 0.
Therefore, fold changes greater than 1. The expression of G6PD, PDHA, HK, and CYC were examined by Western blotting to determine whether the gene expression differences observed were also present at the protein level.
We did not find any significant differences in protein expression between and Ets1 cells for any of the enzymes examined data not shown.
Microarray analysis of Ets1 ovarian cancer cells revealed that Ets-1 is involved in the regulation of mitochondrial stress and dysfunction as metabolic genes, including those involved in glycolysis, glycolytic feeder pathways, the TCA cycle, and lipid metabolism Table 2 , and genes involved in antioxidant defense Table 3 were altered in Ets-1 over-expressing cells.
To evaluate whether cells with stable over-expression of Ets-1 favour glycolysis over oxidative phosphorylation for energy, as predicted by our microarray analysis, cells were grown in glucose-free media supplemented with the glycolytic inhibitor 2-DG, an analog of glucose.
Cells were grown in the presence of varying amounts of 2-DG, and representative growth curves were generated for each cell line. The growth of cells in media containing 2-DG was inhibited to a greater extent in cells with a higher Ets-1 expression than in parental cells Figure 3A.
Our results indicated that Ets1 cells induced with tetracycline were the most sensitive to 2-DG, with an IC 50 of 0. To discount any treatment effect, parental cells were treated with tetracycline, and showed no significant growth inhibition by 2-DG with an IC 50 of 3.
Growth of cells in normal or glucose-free media supplemented with sodium pyruvate was compared over 96 hrs, after which it was observed that the proliferation of cells with increased expression of Ets-1 was notably slower compared to parental cells Figure 3B.
Treatment with glucose-free media resulted in a decreased proliferation rate for all cells tested in comparison to normally supplemented media data not shown.
B and Ets1 cells were grown in the absence of glucose, and proliferation assays were conducted at 24 hour intervals. Our microarray analyses suggest that Ets-1 over-expression resulted in an overall down-regulation of genes that encode electron transport chain components, suggesting that these cell lines would likely display decreased O 2 consumption Table 4.
This assumption was evaluated using high-resolution respirometry, where basal oxygen consumption was measured following the addition of cells to an oxygraph. Basal oxygen consumption was significantly lower in induced Ets1 cells No significant tetracycline treatment effect on basal oxygen consumption was found following induction of cells, confirming that tetracycline did not affect oxygen consumption in our model data not shown.
Basal oxygen consumption was determined for and Ets1 ovarian cancer cells. Ets-1 expression was associated with a significant decrease in basal oxygen consumption suggesting a decreased reliance on oxidative phosphorylation in Ets1 cells. Mitochondrial reactive oxygen species activate several key signaling pathways involved in tumourigenesis and up-regulate the expression of important oncogenic transcription factors including Ets-1 [32].
Subsequent treatment of these cells with H 2 O 2 increased Ets-1 expression in a dose-dependent manner, suggesting that this transcription factor is highly responsive to tumour-derived signals. Our previous analysis of the Ets-1 promoter led to the identification of an antioxidant response element ARE that proved to be pivotal in regulating the expression of Ets-1 under both basal and H 2 O 2 -induced conditions [15].
Traditionally, the functional importance of Ets-1 over-expression in cancer has been associated with the regulation of matrix-degrading proteases and angiogenic factors [26] , [34]. However, our recent findings that mitochondrial reactive oxygen species potently affects Ets-1 expression at the transcriptional level [15] suggest that the importance of this transcription factor in cancer initiation and progression extends beyond angiogenesis and metastasis alone.
We hypothesized that Ets-1 may be involved in the regulation of mitochondrial metabolism in cancer cells because mitochondrial stress from both increased reactive oxygen species production and electron transport chain malfunction result in increased Ets-1 mRNA and protein [15].
In order to determine the functional importance of Ets-1 expression in cancer cell metabolism, we generated the tetracycline-inducible Ets-1 over-expressing ovarian cancer cell line Ets1.
Parental cells do not express detectable levels of Ets-1 protein endogenously. To analyze the genomic consequences of Ets-1 over-expression in these ovarian cancer cells, we conducted a human gene microarray.
Our findings indicate that Ets-1 is either directly or indirectly involved in regulating the expression of more than 3, of the over 28, human genes examined. Interestingly, our findings suggest that Ets-1 could act as a transcriptional repressor of more than half 1, of these genes in ovarian carcinoma cells.
Although Ets-1 has been studied extensively in both physiological and pathological processes [17] , it is rarely referred to as a transcriptional repressor.
In the context of mitochondrial dysfunction and metabolism, Ets-1 was found to at least partially down-regulate several components of the electron transport chain. Complex I, the most prominent site for electron leakage leading to excessive reactive oxygen species production in the electron transport chain, is composed of 39 nuclear encoded subunit genes, of which Ets-1 down-regulates Another important site for electron leakage and reactive oxygen species production is Complex III, which is composed of 10 subunits, of which Ets-1 down-regulates 3.
Ets-1 also represses components of Complex IV, Complex V ATP synthases, as well as some electron transport associated factors. Taken together, these repressive functions suggest that Ets-1 is prominently involved in the decreased reliance on oxidative phosphorylation frequently associated with cancer cells.
Consequently, genes encoding mitochondrial proteins involved in oxidative phosphorylation would be down-regulated, and cells would require alternate methods of ATP production including glycolysis and fatty acid oxidation.
Given that components of almost every complex of the electron transport chain, several key enzymes of the TCA cycle, and ultimately the reducing equivalents needed for electron transport were similarly down-regulated, Ets-1 over-expressing cells appear to have a decreased capacity to generate ATP via oxidative phosphorylation at the gene expression level.
Cancer cells commonly have a decreased reliance on oxidative phosphorylation for energy generation, and they likewise have an increased dependence on glycolysis and fat metabolism for cellular energy [35].
In further support that Ets-1 is involved in the regulation of altered cancer metabolism, Ets-1 is associated with the increased expression of many genes involved in glycolysis, glycolytic feeder pathways, and the pentose phosphate pathway.
Additionally, the expression of Ets-1 is also correlated with increases in the expression of many genes involved with lipid metabolism and biosynthesis. Taken together, these trends suggest that Ets-1 is an important transcriptional regulator not only in the catabolic, but also anabolic metabolic transitions of cancer cells that ultimately promote tumourigenesis [35].
It was almost half a century ago when the up-regulation of fatty acid synthase FASN was first described in cancer [36] , which is now known to be over-expressed in the majority of cancers. Interestingly, Ets-1 was also found to be involved in the regulation of increased FASN gene expression in our ovarian cancer model.
Thus, our gene expression findings suggest that Ets-1 is a key transcription factor involved in the metabolism of cancer cells, and particularly important in the metabolic shift towards glycolysis and anabolic means of energy production.
Although it is important to note that Etsmediated metabolic regulation is likely achieved by a large consortium of different transcription factors, a more complex regulatory network of transcription factors influenced by mitochondrial dysfunction have yet to be elucidated.
We have demonstrated that the over-expression of Ets-1 in our ovarian cancer model did not affect protein levels of two closely related ETS family members; however, it is possible that other ETS transcription factors from this very large family also influence cancer metabolism.
Considering that these transcription factors recognize almost identical consensus sequences, the repetition of the experiments within this study following the over-expression of other ETS family members could yield similar results. In addition, such experiments would further characterize the potentially large transcriptional network involved in the specialized metabolism of cancer cells.
To determine the functional relevance of our genomic results, we have examined the glycolytic capability of our Ets-1 over-expression model.
We have indirectly evaluated the oxidative phosphorylation capacity of these cells through treatment with the glycolytic inhibitor 2-DG. Additionally, the Ets-1 over-expressing ovarian cancer cells displayed significantly decreased growth following glucose deprivation, further emphasizing their glycolytic reliance.
The growth rate of all cell types in glucose-free media was decreased as compared to normally supplemented media, particularly after 48 hrs when a distinct divergence in cell growth was consistently observed, likely due to decreased glucose availability.
Over-expression of Ets-1 potently exacerbated this divergence as the growth of induced Ets1 cells drastically decreased after 48 hrs. However at the protein level, we did not find any significant differences in the expression of glucosephosphate dehydrogenase, pyruvate dehydrogenase, cytochrome c , or hexokinase, which are all enzymes involved in glycolysis or oxidative phosphorylation.
Importantly, we did see repeatable and significant differences in glycolytic dependence associated with Ets-1 expression, and the lack of changes in protein expression could therefore be due to post-translational modifications mediated by Ets For example, differences within the catalytic region of an enzyme would result in functional differences, but would not necessarily be detectable via Western blot, as this technique is dependent on the specific epitope targeted by the antibody used.
Thus, we plan to examine the enzyme activity of these metabolic enzymes in future studies to determine if any differences exist between and Ets1 cells that could account for the functional differences we have demonstrated in this study. The evaluation of O 2 consumption of a population of cells is a functional evaluation of oxidative capacity, as it represents a good estimate of the rate at which electrons are passing along the electron transport chain and being reduced to H 2 O 2.
The polarographic system used in this study to measure O 2 consumption includes sensors that yield a current proportional to the partial pressure of O 2 in cell containing media by consuming O 2 in a cathode half reaction, thus the signal responds exponentially to changes in O 2 pressure within the sample.
In the absence of specific complex substrates and ADP, thereby simulating respiration, the basal rate of O 2 consumption can be measured. We have observed significant decreases in O 2 consumption in cells with increased Ets-1 expression.
Our results indicate that Ets-1 is directly involved in the regulation of cellular oxidative capacity, where Ets-1 over-expression led to significantly decreased O 2 consumption, and Ets-1 down-regulated cells displayed a very prominent increase in O 2 consumption.
These results suggest that up-regulated Ets-1 expression promotes a decreased dependence on oxidative phosphorylation for energy, and provides further evidence towards the functional importance of Ets-1 in cancer cell metabolism.
High levels of oxidative stress are typically observed in the tumour microenvironment as a result of imbalances in antioxidant defense factors, and impaired DNA repair mechanisms [37] — [39]. In breast cancer cells lines, increased malignancy is associated with high levels of reactive oxygen species-producing superoxide dismutase activity, in combination with decreased levels of reactive oxygen species-detoxifying glutathione peroxidases and the H 2 O 2 -detoxifying enzyme catalase [40].
Similar antioxidant enzyme imbalances have been found in melanoma [41] , as well as lung [42] , prostate [43] , and thyroid cancers [44]. Our microarray analysis determined that Ets-1 is a regulator of antioxidant gene expression in ovarian cancer cells, particularly glutathione peroxidases, which preferentially target H 2 O 2 and lipid hydroperoxides for detoxification.
This increased expression of antioxidants is in response to mitochondrial oxidative stress in the form of excessive reactive oxygen species production, and we have previously shown that Ets-1 gene expression increases in response to H 2 O 2 [15].
However, it is important to note that Ets-1 also down-regulated genes encoding certain H 2 O 2 -detoxifying enzymes, suggesting that these cancer cells likely require and maintain a certain level of H 2 O 2 to encourage the high growth rates inherent to tumour progression.
A novel function for Ets-1 was elucidated in this study following genomic and functional analysis of an ovarian cancer Ets-1 expression model. To our knowledge, this is the first study to show a role for this transcription factor in metabolism.
Numerous down-regulated genes were identified in Ets-1 over-expressing cells including those encoding several mitochondrial proteins involved in oxidative phosphorylation, as well as important metabolic enzymes that are responsible for the generation of required substrates of the electron transport chain.
Functional assays confirmed that Ets-1 over-expressing cancer cells displayed reduced oxidative phosphorylation capabilities, as well as enhanced reliance on glycolysis for cellular energy. Additionally, Ets-1 was shown to be important in the regulation of cellular O 2 consumption further suggesting a reduced usage of oxidative phosphorylation in cancer cells expressing Ets Therefore, damage to the mitochondria results in increased production of H 2 O 2 and consequent up-regulation of Ets-1, which then participates in an active regulatory network that encourages reliance on glycolysis and lipid metabolism for cellular energy requirements.
Thus, Ets-1 may be grouped with other transcription factors that have been observed to up-regulate the expression of mitochondrial proteins NRFs or genes involved in glycolysis HIF-1 in response to specific stresses [45] , [46].
In summary, our findings demonstrate a novel role for Ets-1 in the regulation of cellular metabolism in response to mitochondrial stress. Paul Andrews Georgetown University, Rockville MD [33].
Media and supplements were purchased from Invitrogen Life Technologies Burlington, ON, Canada , and FBS from Fisher Scientific Ottawa, ON, Canada.
All reagents were purchased from Sigma Oakville, ON, Canada. Membranes were incubated overnight with primary antibody in 0. Proteins were detected using ECL chemiluminescence reagent Amersham , and exposed to film. Total RNA was isolated using Trizol reagent as indicated by the manufacturer Invitrogen.
Quantitative real-time PCR was conducted using a DNA Engine® thermal cycler Bio-Rad and Platinum SYBR Green qPCR SuperMix UDG Invitrogen with primer sequences listed in Table 5. Target gene expression was normalized to the pooled gene expression values of β-actin ACTB , B-2 macroglobulin B2M , glyceraldehydephosphdate dehydrogenate GAPDH , and RNA polymerase II RPII as housekeeping controls.
Data was normalized to housekeeper gene expression and efficiency corrected using the ΔΔCt method of relative quantification, where statistical significance and standard error were determined from ΔCt values.
Total RNA was isolated from tetracycline-induced and Ets1 cells as described, purified using the RNeasy purification kit Qiagen , and hybridized to the GeneChip® Human Gene 1. RNA quality analysis via bioanalyzer, microarray preparation, hybridization, and detection were performed by The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.
All low-level analyses, calculation of differential expression, and statistical adjustments were computed using R version 2. Background correction and normalization was performed using the robust multi-array average RMA algorithm. Reported q-values represent the minimum FDR at which a particular test can be considered significant.
Fold change expression values of 10 random target genes of varying fold change magnitude were validated using real time PCR. Corresponding relative fold changes were determined using the ΔΔCT method of relative quantification, and correlation coefficients were calculated to determine the relationship between real time PCR and microarray findings.
Cellular growth rate and the inhibition of proliferation were evaluated by assessing total cell numbers, where 2×10 3 cells were plated onto well tissue culture plates and allowed to adhere.
Cells were treated with 2-deoxy-D-glucose 2-DG; Sigma administered at concentrations ranging from 1—7. Fluorescence was evaluated using a Cytofluor series multiwell plate reader excitation nm, emission nm PerSeptive Biosystems, Framingham, MA. Cell number was standardized to fluorescence for each cell type by comparison with a standard curve of known cell numbers.
Plates of cells were frozen every 24 hrs up to and including the 96 hr time point and Hoechst assays were performed at each time point. All oxygen consumption assays were performed on the OROBOROS oxygraph Oroboros, Innsbruck, Austria at 37°C. Freshly harvested cells were added to the oxygraph chambers containing 1.
The total O 2 concentration and flux were recorded at 1 sec intervals throughout the experiment. Once the oxygen concentration stabilized, the basal O 2 consumption was determined for each cell line and condition, where OROBOROS software was used for data acquisition and analysis.
We thank Stephanie Marra and Darren Hamelinck for their excellent technical assistance in the generation of stable cell lines.
Conceived and designed the experiments: MLV LAW GS. Performed the experiments: MLV LAW. Analyzed the data: MLV LAW CPV. Wrote the paper: MLV. Browse Subject Areas?
Cancer cells have been thought to largely forgo the mitochondrial phase of energy production. The observation that cancer cells, which are growing and dividing rapidly, would rely only on the less-efficient phase of glucose metabolism has long been a puzzle to researchers.
Lactate is produced when glucose is metabolized rapidly in the cytoplasm. The new work suggests that the lactate produced by the revved-up anaerobic metabolism can be further metabolized following transport into the mitochondria rather than being excreted, as happens in noncancerous cells, noted Michael Espey, Ph.
For the test, the investigators selected lactate, assuming that it would not be as widely distributed in cells as other compounds. The results were surprising—nearly every lipid in the cell ended up being tagged as a metabolic product of lactate. To confirm the findings, the researchers conducted additional experiments with individual mitochondria in cancer cells.
These experiments showed that lactate can be transported into mitochondria and used to generate nutrients for the cell. The results have raised many new questions. Patti said. A broader question, Dr.
Espey added, is: What mechanisms govern how cells use their resources to meet their needs? He and his colleagues published a recent study showing that lactate is an energy source for human lung tumors in mice. The new study shows that mitochondria can contain one of the enzymes associated with lactate metabolism, Dr.
DeBerardinis continued. In his study of lung tumors, Dr. DeBerardinis had assumed that lactate would be metabolized in the cytoplasm rather than the mitochondria.
DeBerardinis noted. Future studies will address the generality of the new findings for other types of cancer, Dr. Espey predicted. January 3, , by Elia Ben-Ari. December 15, , by Edward Winstead. November 30, , by Shana Spindler.
Metabolomics Study Reveals another Energy Source for Cancer Cells Subscribe. October 20, , by NCI Staff Enlarge.
Anr more information about PLOS Subject Areas, click here. Energu cells predominantly utilize glycolysis for ATP Low-glycemic weight control even in Joint and bone health supplements presence ,etabolism abundant oxygen, an environment that would normally an in energy production through oxidative phosphorylation. Metabolisj the molecular canncer Energy metabolism and cancer metsbolism metabolic switch to aerobic glycolysis jetabolism Energy metabolism and cancer been fully elucidated, it is likely that mitochondrial damage to the electron transport chain and the resulting increased production of reactive oxygen species are significant driving forces. In this study, we have investigated the role of the transcription factor Ets-1 in the regulation of mitochondrial function and metabolism. Ets-1 was over-expressed using a stably-incorporated tetracycline-inducible expression vector in the ovarian cancer cell linewhich does not express detectable basal levels of Ets-1 protein. Microarray analysis of the effects of Ets-1 over-expression in these ovarian cancer cells shows that Ets-1 up-regulates key enzymes involved in glycolysis and associated feeder pathways, fatty acid metabolism, and antioxidant defense. The Hallmarks of Cancer are ten Energy metabolism and cancer principles shared metwbolism all cancers. You can read metabolizm first eight Hallmarks of Cancer articles here. Uncontrolled growth defines cancer. Of course, this process requires energy. Cancer cells must adjust their metabolism accordingly to enable this frenzied growth.
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