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Association Study to Evaluate FoxO1 and FoxO3 Gene in CHD in Han Chinese

  • Ying Zhao ,

    Contributed equally to this work with: Ying Zhao, Yanbo Yu

    Affiliation Department of Geriatrics, Jinan Military General Hospital, Jinan, China

  • Yanbo Yu ,

    Contributed equally to this work with: Ying Zhao, Yanbo Yu

    Affiliation Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, China

  • Xiaoli Tian,

    Affiliation Department of Human Population Genetics, Institute of Molecular Medicine, Peking University, Beijing, China

  • Xi Yang,

    Affiliation Department of Human Population Genetics, Institute of Molecular Medicine, Peking University, Beijing, China

  • Xueqi Li,

    Affiliation Department of Cardiology, the Fourth Affiliated Hospital of Harbin Medical University, Harbin, China

  • Feng Jiang,

    Affiliation Department of Cardiology, the Fourth Affiliated Hospital of Harbin Medical University, Harbin, China

  • Yundai Chen ,

    ydchen301@163.com (YC); jnshimw@163.com (MS)

    Affiliation Department of Cardiology, Chinese PLA General Hospital, Beijing, China

  • Maowei Shi

    ydchen301@163.com (YC); jnshimw@163.com (MS)

    Affiliation Department of Geriatrics, Jinan Military General Hospital, Jinan, China

Association Study to Evaluate FoxO1 and FoxO3 Gene in CHD in Han Chinese

  • Ying Zhao, 
  • Yanbo Yu, 
  • Xiaoli Tian, 
  • Xi Yang, 
  • Xueqi Li, 
  • Feng Jiang, 
  • Yundai Chen, 
  • Maowei Shi
PLOS
x

Abstract

Background

Coronary heart disease (CHD) is one of the leading causes of mortality and morbidity in China. Genetic factors that predispose individuals to CHD are unclear. In the present study, we aimed to determine whether the variation of FoxOs, a novel genetic factor associated with longevity, was associated with CHD in Han Chinese populations.

Methods

1271 CHD patients and 1287 age-and sex-matched controls from Beijing and Harbin were included. We selected four tagging single nucleotide polymorphisms (SNPs) of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and two tagging SNPs of FoxO3 (rs768023 and rs1268165). And the genotypes of these SNPs were determined in both CHD patients and non-CHD controls.

Results

For population from Beijing, four SNPs of FoxO1 and two SNPs of FoxO3 were found not to be associated with CHD (p>0.05). And this was validated in the other population from Harbin (p>0.05). After combining the two geographically isolated case-control populations, the results showed that the six SNPs did not necessarily predispose to CHD in Han Chinese(p>0.05). In stratified analysis according to gender, the history of smoking, hypertension, diabetes mellitus, hyperlipidemia and the metabolic syndrome, we further explored that neither the variants of FoxO1 nor the variants of FoxO3 might be associated with CHD (p>0.05).

Conclusion

The variants of FoxO1 and FoxO3 may not increase the prevalence of CHD in Han Chinese population.

Introduction

Coronary heart disease (CHD) is the most common cause of death in China and accounts for approximately one third of all deaths around the world. Multiple risk factors are involved in the cause of CHD, including modifiable factors (life styles, smoking, hypertension, hyperlipidemia, diabetes), and fixed factors (aging, gender, genetic predisposition) [1]. Over decades, the mechanisms of oxidative stress and inflammation in association with endothelial dysfunction and vascular smooth muscle proliferation have been investigated by numerous studies, with reactive oxygen species (ROS) being the common mechanism by which different CHD risk factors trigger atherosclerosis [2], [3]. All these events can be regulated by transcription factors which control the expression of genes associated with the progression of CHD. Therefore, identification of possible transcription factors related with the CHD process may help in efforts to decrease the risk of the disease.

Forkhead transcription factors of the O class (FoxOs), primarily identified as downstream targets of insulin/IGF-1 signaling pathway, consist of four members, FoxO1, FoxO3, FoxO4 and FoxO6 [4]. These transcription factors have been identified as important regulators involved in cellular differentiation, apoptosis, oxidative stress, glucose metabolism and other cellular functions [5], [6]. Furthermore, FoxOs are increasingly considered as potential clinical targets for multiple disorders since they modulate the expression of genes associated with metabolic disease [7], [8], cardiovascular injury [9], neurodegeneration [10], tumorigenesis [11] and cell longevity [12].

Exploring the genetic contribution to the pathogenesis of CHD has been considered important step for the medical intervention of the disease. With regard to the research on the genetics of FoxOs, it was firstly reported in human soft tissue tumors and leukemias [13], [14]. Recent genome-wide association study in the Framingham population indicated that FoxO1 was strongly associated with the age of death [15]. In addition, several association studies on human longevity highlighted the role of FoxO3 in Japanese, German and Southern Italian [16][18]. It is probable that FoxO1 and FoxO3 affect longevity through multiple mechanisms, such as insulin resistance, stress responses or proneness to disease. In the cardiovascular system, FoxOs regulate multiple aspects of cellular function in vascular tissues. And FoxO1 and/or FoxO3 are/is considered as apoptosis-regulating gene for the onset of diabetic cardiomyopathy [19], cardiac hypertrophy [20] and ischemic heart disease [21]. It has been reported that the upregulation of FoxO1 and FoxO3 appears to disrupt cardiac hypertrophy [22], [23]. In a balloon carotid arterial injury rat model, gene transfer of FoxO3 can inhibit vascular smooth muscle cell proliferation and neointimal hyperplasia [24]. The expression of FoxO1 can be stimulated by α1-adrenergic agonists and ultimately lead to apoptotic endothelial cell injury [25]. Considering the possible role of FoxO1 and FoxO3 in the maintenance of vascular homeostasis, in the present study we aimed to investigate the intrinsic association of FoxO1 and FoxO3 with CHD phenotype in Han Chinese. We selected four tagging SNPs of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and two tagging SNPs of FoxO3 (rs768023, rs1268165). The frequencies of FoxO1 and FoxO3 were testified in Chinese CHD patients from two different regions.

Materials and Methods

1. Subjects

The cases of this study were all hospitalized patients recruited from two medical centers in Beijing and Harbin. All the CHD patients were diagnosed by one of the following standards: (1) based on World Health Organization criteria in terms of elevations of cardiac enzymes, electrocardiography and clinical symptoms; (2) angiographic evidence of more than 50% stenosis in one or more major coronary arteries; (3) previous history of PCI (percutaneous coronary intervention) or CABG (coronary artery bypass graft). The control subjects matched with the patients for age and sex. And they were recruited from the two medical centers meeting the following criteria: (1) with no family history of CHD in first-degree relatives before the age of 60 in male and the age of 55 in female; (2) no clinical symptoms for CHD; (3) resting electrocardiography(ECG) showed normal results. The participants with no less than 2 risk factors of CHD (age>45 for man and >55 for woman, hypertension, diabetes, overweight, hyperlipidemia) were subjected to treadmill stress test and selected as controls if their ECG were normal without clinical symptoms. Those with history of cardiomyopathy, valvular disease, peripheral vascular disease, stroke, severe hepatic and kidney deficiency were ruled out.

Smokers were defined as individuals who were smoking or who had stopped<1 years before they were enrolled in this study based on self-reports.

Hypertension was diagnosed by the following criteria: (1) at present receiving antihypertensive therapy; (2)blood pressure≥140/90 mmHg confirmed at least three times of different days.

Diabetes mellitus was defined by: (1) taking hypoglycemic agents; (2) fasting serum glucose≥7.0 mmol/L, 2 h postprandial glucose level≥11.1 mmol/L in two measurements; (3) oral glucose tolerance test confirmed.

Hyperlipidemia was defined by: (1) taking lipid-reducing treatment (2) total cholesterol ≥200 mg/dL or low density lipoprotein cholesterol≥130 mg/dL.

Body mass index (BMI) was calculated by the formula: body weight (Kg)/height2 (m2).

The metabolic syndrome (MetS) was diagnosed by three or more of the following criteria: elevated WC (waist circumference) (for Chinese, the cut points for WC were ≥85 cm in men and ≥80 cm in women); TG≥1.7 mmol/l; HDL-C<1.0 mmol/l in men and <1.3 mmol/l in women; BP≥130/85 mmHg or on antihypertensive drug treatment in a patient with a history of hypertension; or FPG≥5.6 mmol/l.

Written informed consent was obtained from all individuals, and the study protocol was approved by the Ethics Committee of the PLA General Hospital and the Ethics Committee of Harbin Medical University. The study conformed to the principles outlined in the Declaration of Helsinki.

2. genotyping

Venous blood was collected by standard vein puncture in fasting condition and without intake of any medication either at the time of acute coronary event onset or at most for 2 weeks. Human genomic DNA was extracted from EDTA-anticoagulated blood using the proteinase K methods described previously [26]. Based on the hapmap(CHB+JPT), the four tagging SNPs of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and the two tagging SNPs of FoxO3 (rs768023, rs1268165) were selected. The selections of the SNPs were based on the following criteria: (1) tag SNPs based on r2≥0.8; (2) functional position; (3)minor allele frequency>10%. DNA fragments of 120–180 bp containing SNPs were amplified by PCR from 10 ng of genomic DNA from each participant, with the primers listed (Table 1). The amplified DNA fragments were purified and used for genotyping by direct-sequencing with a BigDye v3.1 kit and running on ABI 3130XL.

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Table 1. The pairs of PCR primers for amplifications of SNPs for FoxO1 and FoxO3.

http://dx.doi.org/10.1371/journal.pone.0086252.t001

3. Statistical analysis

Continuous data was expressed as mean±standard deviation. The differences in general characteristics between case and control were compared by student t test for quantitative variables and chi-square test for categorical variables. Chi-square test was also used to test for deviation of genotype distribution from Hardy-Weinberg equilibrium. All statistical analysis was performed with SPSS 17.0. HaploView 4.2 was used to analyze linkage disequilibrium (LD), and LD was demonstrated by r2 value. r2≥0.8 indicated the SNPs were in a same natural haplotype block. A P-value<0.05 was considered statistically significant.

Results

1. Characteristics of population

Baseline characteristics of all subjects were presented in Table 2. CHD patients and non-CHD controls were collected from two medical centers in north-eastern and northern China. All participants were Han Chinese. Population 1 was from Beijing consisting of 808 cases and 829 age- and sex-matched non-CHD controls. Population 2 was from Harbin comprising 463 cases and 458 age- and sex-matched non-CHD controls. Significant differences were found between cases and controls in Population 1 and 2 in terms of BMI, smoking, hypertension, diabetes mellitus, hyperlipidemia and MetS.

2. Genotype distribution and allelic frequencies

In both two groups from different regions, there was no significant deviation for four tagging SNPs of FoxO1 and two tagging SNPs of FoxO3 by the Hardy-Weinberg equilibrium test. To test the genotype association between FoxO1/FoxO3 and CHD, we performed Chi-square test (table 3). For population from Beijing, six SNPs of FoxO1 and FoxO3 were found not to be associated with CHD (p>0.05). And this was validated in the other population from Harbin (p>0.05). After combining the two geographically isolated case-control populations, the results showed that the six SNPs did not necessarily predispose to CHD in Han Chinese(p>0.05). We further conducted stratification analysis according to gender, smoking, medical history of hypertension, diabetes mellitus, hyperlipidemia and MetS, and no obvious association between genotype distribution and CHD was observed in CHD patients and non-CHD controls (Table S1, Table S2, Table S3, Table S4, Table S5 and Table S6).

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Table 3. Frequency of FoxO1 and FoxO3 polymorphism in CHD from two different populations.

http://dx.doi.org/10.1371/journal.pone.0086252.t003

Discussion

In the present study, we identified four tagging SNPs of FoxO1 and two tagging SNPs of FoxO3 with CHD in two geographically isolated Han Chinese populations. And our data showed that these six investigated SNPs of FoxO1/FoxO3 might not be distributed differently between CHD patients and non-CHD controls in population from Beijing and Harbin. Stratification analysis was carried out to understand the interaction between genetic and other risk factors, and the addition of other risk factors seemed not influencing the susceptibility for CHD. These results indicated for the first time that the association of FoxO1/FoxO3 with the risk of CHD was not statistically significant in Han Chinese.

How the genetic determinants contribute to CHD has provoked great interest in recent years. These population-based genome-wide association studies (GWAS) were trying to identify specific genotypes and alleles responsible for CHD. As is known, FoxOs, acting as important heredity factors in aging, are important regulators involved in the process of oxidative stress, immune surveillance, vascular tone and cardiovascular development. Besides, FoxOs can modulate the metabolic environment by regulating the expressions of specific enzyme and energy-dependant proteins [27]. Several lines of evidence demonstrated that FoxO1 and FoxO3 were expressed in murine heart and coronary arteries [28][30]. Altered FoxO1 function in vascular endothelial cells was reported to be responsible for the observed worsening of lesions [31]. FoxO3 can regulate the expression of certain factors in cardiac fibroblasts, such as peroxiredoxin III-a cardioprotectant [32]. Furthermore, FoxO3 is also expressed in endothelial cells, and it can modulate endothelial cell migration and sprouting during vascular development. However, in our genotyping research, neither FoxO1 nor FoxO3 was testified to be associated with CHD. It may be explained with considerations as follows.

Atherosclerosis in CHD is often confused with vascular aging. Aged vessels show a number of characteristic pathological processes (reduced medial VSMC number, increased collagen deposition, fracture of the elastin lamellae, etc), many of which are also seen in atherosclerosis. However, by the standards of pathology, arteriosclerosis is divided into three types: atherosclerosis of large and medium-sized arteries, monckeberg medical calcific sclerosis of medium-sized arteries, and arteriolosclerosis. Thus, vascular aging is not included among the three types of arteriosclerosis. Vascular aging is a process characterized by various alternations in a physical environment of cells in vessels [33]. Oxygen free radicals and mitochondrial DNA mutations have been closely associated with vascular aging. It is of interest to note that the incidence of atherosclerosis increases with advancing age and aging is a strong risk factor for atherosclerosis [34]. However, large numbers of population-based prospective studies have shown that atherosclerosis is a complex syndrome closely associated with uncontrollable and controllable factors, such as age, gender, smoking, obesity and diabetes mellitus. Although several studies provided promising findings in the association of FoxOs gene with the aging process, due to the various risk factors and the complexity of CHD, the role of FoxOs on the pathogenesis of CHD has not been identified in our study

Oxidative stress plays an important role in the process of atherosclerosis. The dysregulated oxidant and antioxidant balance brings about the alterations in redox status, and subsequently leads to VSMC proliferation, endothelial dysfunction, inflammatory response and lipid peroxidation [35], [36]. All these detrimental events result in vessel wall thickness and vascular remodeling which induce a susceptibility to CHD. However, mounting evidence supports that chronic inflammation plays a central role in the pathogenesis of CHD, which is recognized to occur from the earliest stages of atheroma formation through to plaque rupture and thrombosis [37], [38]. Cytokines secreted by inflammatory cells (T cells, mast cells and monocytes) could contribute to the initiation, development and rupture of atherosclerotic plaque [39][41]. Therefore, the relative balance of these inflammatory processes will predict the development of CHD. Although CHD is age-associated vascular disease, the contribution of inflammatory cells and mediators in the pathogenesis of CHD should also be emphasized.

One of the major biochemical pathways playing a role in the inflammatory process is the NF-κB signaling pathway. Using apoE−/− mice, genetic suppression of NF-κB signaling led to a reduction in the size of atherosclerotic lesions [42]. Interestingly, FoxOs have been reported to suppress NF-κB signaling, providing support for the possible vasculoprotective effects of FoxOs [43]. However, we did not observe any association between FoxO1/FoxO3 variants and CHD. It should be noteworthy that atherosclerosis results from a combination of endothelial, hematopoietic, T-cell and macrophage dysfunction [44], [45]. Thereby, the modulation is very complex. Besides FoxOs, a wide range of extracellular immune stimuli, such as IL-1, IL-6, TNF-α, T-cell receptor and B-cell receptor (TCR and BCR), can mediate the regulation of NF-κB activity [45], [46]. Moreover, it has been reported that genetic polymorphisms/variations in expression of FoxO genes appear to correlate with human autoimmune disease susceptibility and or activity (such as lupus and rheumatoid arthritis) [47], [48]. Of note, the inflammation in CHD, with a special name of “metabolic inflammation”, has unique features compared to autoimmune diseases. The metabolic inflammation is mainly associated with overnutrition-induced metabolic derangements [49], . May these explain the negative indications for our association study between FoxOs and CHD.

FoxOs have been reported to play a major role in the transcriptional regulation of many proteins which are directly involved in metabolism [51][53]. Thereby, we also analyzed whether any of the selected SNPs in FoxO1/FoxO3 is associated with gender, smoking, medical history of hypertension, diabetes mellitus, hyperlipidemia and MetS in our study population. But we did not observe any significant association. However, to rule out any association of FoxO1/FoxO3 with CHD, additional studies are required in different populations with different allele frequencies.

In conclusion, we demonstrate that neither FoxO1 nor FoxO3 is associated with CHD in two geographically isolated Han Chinese populations. However, the number of participants in this study is relatively small, and the findings need to be cautious. A multi-center research needs to be carried out to further assess the association of FoxOs with CHD in more ethnic groups and in larger populations.

Supporting Information

Table S1.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to different genders.

doi:10.1371/journal.pone.0086252.s001

(DOC)

Table S2.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to smoking or not.

doi:10.1371/journal.pone.0086252.s002

(DOC)

Table S3.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to hypertension or not.

doi:10.1371/journal.pone.0086252.s003

(DOC)

Table S4.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to DM or not.

doi:10.1371/journal.pone.0086252.s004

(DOC)

Table S5.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to hyperlipidemia or not.

doi:10.1371/journal.pone.0086252.s005

(DOC)

Table S6.

Frequencies of FoxO1 and FoxO3 polymorphisms in two populations according to MetS or not.

doi:10.1371/journal.pone.0086252.s006

(DOC)

Acknowledgments

The authors appreciate the considerable assistance from the Department of Human Population Genetics of Peking University. We thank all participants who donated the blood samples and made the study possible.

Author Contributions

Conceived and designed the experiments: YDC MWS. Performed the experiments: YZ YBY XY. Analyzed the data: YZ YBY. Contributed reagents/materials/analysis tools: XLT XQL FJ. Wrote the paper: YZ YBY.

References

  1. 1. National Cholesterol Education Program Expert Panel on Detection E, Treatment of High Blood Cholesterol in A (2002) Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation 106: 3143–3421.
  2. 2. Bachschmid MM, Schildknecht S, Matsui R, Zee R, Haeussler D, et al. (2013) Vascular aging: chronic oxidative stress and impairment of redox signaling-consequences for vascular homeostasis and disease. Ann Med 45: 17–36.
  3. 3. Hulsmans M, Van Dooren E, Holvoet P (2012) Mitochondrial reactive oxygen species and risk of atherosclerosis. Curr Atheroscler Rep 14: 264–276.
  4. 4. Eijkelenboom A, Burgering BM (2013) FOXOs: signalling integrators for homeostasis maintenance. Nat Rev Mol Cell Biol 14: 83–97.
  5. 5. Huang H, Tindall DJ (2007) Dynamic FoxO transcription factors. J Cell Sci 120: 2479–2487.
  6. 6. Maiese K, Chong ZZ, Hou J, Shang YC (2009) The “O” class: crafting clinical care with FoxO transcription factors. Adv Exp Med Biol 665: 242–260.
  7. 7. Lu T, Chai Q, Yu L, d'Uscio LV, Katusic ZS, et al. (2012) Reactive oxygen species signaling facilitates FOXO-3a/FBXO-dependent vascular BK channel beta1 subunit degradation in diabetic mice. Diabetes 61: 1860–1868.
  8. 8. Kim M, Chung H, Yoon C, Lee E, Kim T, et al. (2012) Increase of INS-1 cell apoptosis under glucose fluctuation and the involvement of FOXO-SIRT pathway. Diabetes Res Clin Pract 98: 132–139.
  9. 9. Sengupta A, Molkentin JD, Paik JH, DePinho RA, Yutzey KE (2011) FoxO transcription factors promote cardiomyocyte survival upon induction of oxidative stress. J Biol Chem 286: 7468–7478.
  10. 10. Calixto A, Jara JS, Court FA (2012) Diapause formation and downregulation of insulin-like signaling via DAF-16/FOXO delays axonal degeneration and neuronal loss. PLoS Genet 8: e1003141.
  11. 11. Katoh M, Igarashi M, Fukuda H, Nakagama H, Katoh M (2013) Cancer genetics and genomics of human FOX family genes. Cancer Lett 328: 198–206.
  12. 12. Robida-Stubbs S, Glover-Cutter K, Lamming DW, Mizunuma M, Narasimhan SD, et al. (2012) TOR signaling and rapamycin influence longevity by regulating SKN-1/Nrf and DAF-16/FoxO. Cell Metab 15: 713–724.
  13. 13. Parry P, Wei Y, Evans G (1994) Cloning and characterization of the t(X;11) breakpoint from a leukemic cell line identify a new member of the forkhead gene family. Genes Chromosomes Cancer 11: 79–84.
  14. 14. Galili N, Davis RJ, Fredericks WJ, Mukhopadhyay S, Rauscher FJ 3rd, et al. (1993) Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma. Nat Genet 5: 230–235.
  15. 15. Lunetta KL, D'Agostino RB Sr, Karasik D, Benjamin EJ, Guo CY, et al. (2007) Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. BMC Med Genet 8 Suppl 1: S13.
  16. 16. Willcox BJ, Donlon TA, He Q, Chen R, Grove JS, et al. (2008) FOXO3A genotype is strongly associated with human longevity. Proc Natl Acad Sci U S A 105: 13987–13992.
  17. 17. Flachsbart F, Caliebe A, Kleindorp R, Blanche H, von Eller-Eberstein H, et al. (2009) Association of FOXO3A variation with human longevity confirmed in German centenarians. Proc Natl Acad Sci U S A 106: 2700–2705.
  18. 18. Anselmi CV, Malovini A, Roncarati R, Novelli V, Villa F, et al. (2009) Association of the FOXO3A locus with extreme longevity in a southern Italian centenarian study. Rejuvenation Res 12: 95–104.
  19. 19. Relling DP, Esberg LB, Fang CX, Johnson WT, Murphy EJ, et al. (2006) High-fat diet-induced juvenile obesity leads to cardiomyocyte dysfunction and upregulation of Foxo3a transcription factor independent of lipotoxicity and apoptosis. J Hypertens 24: 549–561.
  20. 20. Ni YG, Berenji K, Wang N, Oh M, Sachan N, et al. (2006) Foxo transcription factors blunt cardiac hypertrophy by inhibiting calcineurin signaling. Circulation 114: 1159–1168.
  21. 21. Dabek J, Owczarek A, Gasior Z, Ulczok R, Skowerski M, et al. (2008) Oligonucleotide microarray analysis of genes regulating apoptosis in chronically ischemic and postinfarction myocardium. Biochem Genet 46: 241–247.
  22. 22. Evans-Anderson HJ, Alfieri CM, Yutzey KE (2008) Regulation of cardiomyocyte proliferation and myocardial growth during development by FOXO transcription factors. Circ Res 102: 686–694.
  23. 23. Li HH, Willis MS, Lockyer P, Miller N, McDonough H, et al. (2007) Atrogin-1 inhibits Akt-dependent cardiac hypertrophy in mice via ubiquitin-dependent coactivation of Forkhead proteins. J Clin Invest 117: 3211–3223.
  24. 24. Abid MR, Yano K, Guo S, Patel VI, Shrikhande G, et al. (2005) Forkhead transcription factors inhibit vascular smooth muscle cell proliferation and neointimal hyperplasia. J Biol Chem 280: 29864–29873.
  25. 25. Morris JB, Kenney B, Huynh H, Woodcock EA (2005) Regulation of the proapoptotic factor FOXO1 (FKHR) in cardiomyocytes by growth factors and alpha1-adrenergic agonists. Endocrinology 146: 4370–4376.
  26. 26. Tian XL, Wang QK (2006) Generation of transgenic mice for cardiovascular research. Methods Mol Med 129: 69–81.
  27. 27. Nakae J, Oki M, Cao Y (2008) The FoxO transcription factors and metabolic regulation. FEBS Lett 582: 54–67.
  28. 28. Sengupta A, Kalinichenko VV, Yutzey KE (2013) FoxO1 and FoxM1 transcription factors have antagonistic functions in neonatal cardiomyocyte cell-cycle withdrawal and IGF1 gene regulation. Circ Res 112: 267–277.
  29. 29. Battiprolu PK, Hojayev B, Jiang N, Wang ZV, Luo X, et al. (2012) Metabolic stress-induced activation of FoxO1 triggers diabetic cardiomyopathy in mice. J Clin Invest 122: 1109–1118.
  30. 30. Geng T, Li P, Yin X, Yan Z (2011) PGC-1alpha promotes nitric oxide antioxidant defenses and inhibits FOXO signaling against cardiac cachexia in mice. Am J Pathol 178: 1738–1748.
  31. 31. Qiang L, Tsuchiya K, Kim-Muller JY, Lin HV, Welch C, et al. (2012) Increased atherosclerosis and endothelial dysfunction in mice bearing constitutively deacetylated alleles of Foxo1 gene. J Biol Chem 287: 13944–13951.
  32. 32. Chiribau CB, Cheng L, Cucoranu IC, Yu YS, Clempus RE, et al. (2008) FOXO3A regulates peroxiredoxin III expression in human cardiac fibroblasts. J Biol Chem 283: 8211–8217.
  33. 33. O'Rourke MF (2007) Arterial aging: pathophysiological principles. Vasc Med 12: 329–341.
  34. 34. Wang JC, Bennett M (2012) Aging and atherosclerosis: mechanisms, functional consequences, and potential therapeutics for cellular senescence. Circ Res 111: 245–259.
  35. 35. Madamanchi NR, Runge MS (2007) Mitochondrial dysfunction in atherosclerosis. Circ Res 100: 460–473.
  36. 36. Wassmann S, Wassmann K, Nickenig G (2004) Modulation of oxidant and antioxidant enzyme expression and function in vascular cells. Hypertension 44: 381–386.
  37. 37. Lytvyn OI, Kopitsa MP, Petyunina OV (2004) Interaction between inflammation and thrombosis in acute coronary syndrome. Kardiol Pol 61: 110–116 discussion 114–116.
  38. 38. Rossouw JE, Cushman M, Greenland P, Lloyd-Jones DM, Bray P, et al. (2008) Inflammatory, lipid, thrombotic, and genetic markers of coronary heart disease risk in the women's health initiative trials of hormone therapy. Arch Intern Med 168: 2245–2253.
  39. 39. Iwata H, Nagai R (2012) Novel immune signals and atherosclerosis. Curr Atheroscler Rep 14: 484–490.
  40. 40. Frieri M (2012) Accelerated atherosclerosis in systemic lupus erythematosus: role of proinflammatory cytokines and therapeutic approaches. Curr Allergy Asthma Rep 12: 25–32.
  41. 41. Weber C, Noels H (2011) Atherosclerosis: current pathogenesis and therapeutic options. Nat Med 17: 1410–1422.
  42. 42. Cuaz-Perolin C, Billiet L, Bauge E, Copin C, Scott-Algara D, et al. (2008) Antiinflammatory and antiatherogenic effects of the NF-kappaB inhibitor acetyl-11-keto-beta-boswellic acid in LPS-challenged ApoE−/− mice. Arterioscler Thromb Vasc Biol 28: 272–277.
  43. 43. Peng SL (2007) Immune regulation by Foxo transcription factors. Autoimmunity 40: 462–469.
  44. 44. Carter AM (2005) Inflammation, thrombosis and acute coronary syndromes. Diab Vasc Dis Res 2: 113–121.
  45. 45. Tilstra JS, Clauson CL, Niedernhofer LJ, Robbins PD (2011) NF-kappaB in Aging and Disease. Aging Dis 2: 449–465.
  46. 46. Hayden MS, Ghosh S (2008) Shared principles in NF-kappaB signaling. Cell 132: 344–362.
  47. 47. Kuo CC, Lin SC (2007) Altered FOXO1 transcript levels in peripheral blood mononuclear cells of systemic lupus erythematosus and rheumatoid arthritis patients. Mol Med 13: 561–566.
  48. 48. Maiese K, Chong ZZ, Shang YC, Hou J (2009) FoxO proteins: cunning concepts and considerations for the cardiovascular system. Clin Sci (Lond) 116: 191–203.
  49. 49. Gregor MF, Hotamisligil GS (2011) Inflammatory mechanisms in obesity. Annu Rev Immunol 29: 415–445.
  50. 50. Cai D (2009) NFkappaB-mediated metabolic inflammation in peripheral tissues versus central nervous system. Cell Cycle 8: 2542–2548.
  51. 51. Nakae J, Kitamura T, Silver DL, Accili D (2001) The forkhead transcription factor Foxo1 (Fkhr) confers insulin sensitivity onto glucose-6-phosphatase expression. J Clin Invest 108: 1359–1367.
  52. 52. Schmoll D, Walker KS, Alessi DR, Grempler R, Burchell A, et al. (2000) Regulation of glucose-6-phosphatase gene expression by protein kinase Balpha and the forkhead transcription factor FKHR. Evidence for insulin response unit-dependent and -independent effects of insulin on promoter activity. J Biol Chem 275: 36324–36333.
  53. 53. Yeagley D, Guo S, Unterman T, Quinn PG (2001) Gene- and activation-specific mechanisms for insulin inhibition of basal and glucocorticoid-induced insulin-like growth factor binding protein-1 and phosphoenolpyruvate carboxykinase transcription. Roles of forkhead and insulin response sequences. J Biol Chem 276: 33705–33710.