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Review Article - (2010) Volume 1, Issue 1
The complex multifactorial pathogenesis of acne vulgaris, the most common skin disease, may be explained at the level of genomic regulation. A recent hypothesis suggested that a relative nuclear defi ciency of the metabolic sensor and nuclear transcription factor FoxO1 appears to play a key role in the pathogenesis of acne vulgaris. FoxO1 has been identified as an important regulator of androgen receptor, cell proliferation, apoptosis, lipogenesis, oxidative stress regulation, innate and acquired immunity, all important aspects involved in the pathogenesis of acne. It is the intention of this review article to provide further evidence for the potential function of the PI3K/Akt/FoxO1 signaling pathway for other types of acne and acne-like eruptions. Apparently unrelated acneigenic stimuli like hyperglycemic food, insulinotropic milk and dairy product consumption, smoking, psychological stress, fibroblast growth factor receptor-2 mutations in Apert syndrome and acneiform nevus, chloracne, and antidepressant-induced acne are all associated with upregulated PI3K/Akt-signaling known to result in a nuclear deficiency of FoxO1. Reduced nuclear levels of FoxO1 may increase the expression of important acne target genes and derepress nuclear receptors, suggested to be involved in the clinical manifestation of acne. Accumulating indirect evidence supports the role of growth factor- and growth factorlike acneigenic stimuli in posttranslational modifi cation of nuclear FoxO1 and strenghtens the hypothesis of a nuclear FoxO1 deficiency as the possible underlying cause of acne vulgaris and clinical acne variants. This review intends to stimulate future research activities on the promising PI3K/Akt/FoxO1 signaling pathway which may be most helpful to unravel the pathogenesis of acne.
<Keywords: Acne; Acne variants; Acneigenic stimuli; Phosphoinositol-3 kinase/Akt; FoxO1
It is the purpose of this review to support the hypothetical concept that the nuclear transcription factor FoxO1, a member of the class O subfamily of forkhead box (FoxO) transcription factors may be involved in the pathogenesis of acne vulgaris and other acne variants. It has been suggested that FoxO1 is the key to understand the relationship between genetic, metabolic and environmental factors leading to acne [1]. It will be shown that various growth factor- and growth factor-like signals like insulin and insulin-like growth factor-1 (IGF-1) which are perceived by distinct cell membrane receptors are intergrated at the level of phosphoinositol-3 kinase (PI3K)/Akt activation (Figure 1). The activated kinase Akt (protein kinase B) translocates into the nucleus where Akt phosphorylates the nuclear FoxO1 protein. Phosphorylated FoxO1 is exported from the nucleus into the cytoplasm thereby derepressing target genes and activating nuclear receptors involved in acne pathogenesis (Figure 1) [1-3].
Figure 1: Various growth factors and acneigenic stimuli activate PI3K/Akt signal transduction. Phosphorylated (black hexagons) FoxO1 is exported out of the nucleus into the cytoplasm. The resulting derepression and activation of acne target genes as well as the derepression of inhibitory nuclear receptors induce androgen receptor (AR) transactivation, comedogenesis, lipogenesis and follicular infl ammation and T-cell proliferation. PI3K: Phosphoinositol-3 kinase; Akt: Akt kinase; IR: Insulin Receptor; IGF1R: IGF1-Receptor; FGFR2: Fibroblast Growth Factor Receptor-2; CRHR: Corticotropin Releasing Hormone Receptor; MC5R: Melanocortin-5-Receptor; IL1R: Interleukin-1 Receptor; PGs: Peptidoglykanes; TLR2: Toll-like-Receptor-2; 5HTR: Serotonin Receptor; nAChR: Nicotine Receptor; APN: Aminopeptidase N, DP IV: Dipeptidylpeptidase IV; AhR/ARNT: Arylhydrocarbon Receptor/aryl Hydrocarbon Nuclear Translocator.
Nuclear FoxO1 export has an effect on the activity of androgen receptor (AR), peroxisome proliferator-activated receptors (PPARs), liver X receptors (LXRs), the expression of key genes of cell cycle control (cyclin D1, D2, p21, p27), matrix modulation by matrix metalloproteinases (MMPs), the promoter activity of sterol regulatory element binding proteins (SREBPs) as the most important transcription factors of lipogenesis, the insulin sensitivity regulating glucose transporter protein-4 (GLUT4), the innate and acquired immune responses regulating antimicrobial peptide synthesis, tolllike receptor-2 (TLR2) expression and T cell proliferation. It has also been demonstrated that retinoids are potent inducers of FoxO proteins, and FoxO1 mediates retinoid-induced adverse effects like isotretinoin-induced hypertriglyceridemia [1]. The similar clinical appearance of acne vulgaris and acne variants and isotretinoin´s mode of action on all pathogenical aspects of acne implies the existence of a common signaling pathway. In this paper, the effect of acneigenic stimuli on the PI3K/Akt/FoxO1 signal transduction pathway and its contribution to the pathogenesis of clinical acne variants is dissected in further detail.
FoxO1 and aggravation of acne by milk consumption
After nearly half a century, the role of diet in the pathogenesis of acne has regained recent scientific interest [4-10].Western diet has been associated with a high prevalence of acne [4-10]. Western life style nutrition in industrialized countries is associated with increased insulin/ IGF-1 signaling, which is superimposed on the physiological growth factor signaling of puberty, a mechanism which may well explain the high and increasing prevalence of acne in industrialized countries. Milk consumption induces high serum levels of IGF-1 [11- 15]. Milk consumption has been associated with linear growth and the manifestation of acne [16-18]. It is the biologic principle of milk to promote growth by increased insulin/IGF-1 signaling and induction of insulin resistance [11,12,15,19-23]. The relation between milkinduced insulin/IGF-1 signaling and the pathogenesis of acne and chronic diseases of Western civilization has recently been presented [7,10,24-27]. The insulinotropic effect of milk resides within the hydrophilic whey protein fraction [28]. Both insulin and IGF-1 reduce nulear levels of FoxO1 [2,3].
FoxO1 and aggravation of acne by hyperglycemic carbohydrates
Nutrients rich in carbohydrates with a high glycemic index (GI) induce hyperglycemia, reactive hyperinsulinemia, and increased IGF- 1 serum levels. In contrast, a diet with a low glycemic load decreased serum IGF-1 levels and significantly improved acne following a 12- week diet [29]. A diet with a low glycemic load versus a diet with a high glycemic load in 12 male acne patients showed a significant increase of IGF binding protein-1 (IGFBP-1) and IGFBP-3 in the low glycemic load group, suggesting that a diet with a low glycemic load reduces free IGF-1 activity and bioavailablity [30]. Intriguingly, the genes of IGFBP-1 and IGFBP-3 are FoxO-controled [3]. Improvement of acne has also been reported during the carbohydrate-restricted South Beach Florida diet [31,32]. A population-based cross-sectional study in Oslo of 3775 late adolescents (age 18 and 19 years) revealed a statistically significant association between acne and frequent consumption of chocolate, sweets and potato chips [33]. Restriction of carbohydrates and consumption of carbohydrates with a low GI will reduce insulin secretion of pancreatic β-cells and lowers basal insulin levels thereby improving the nuclear content of the nutritional sensor and transcription factor FoxO1.
FoxO1 and acne-related endocrine disorders
The polycystic ovary syndrome (PCOS) is a common endocrine disorder affecting 5-20 % of women depending on their ethical background [34]. Hyperandrogenemia, altered gonadotropin secretion as well as insulin resistance are involved in the pathogenesis of PCOS. PCOS is frequently associated with acne and hirsutism. Insulin resistance of adipose tissue and muscle in PCOS leads to increased insulin/IGF-1 signaling to epithelial targets like the pilosebaceous units which are not insulin resistant [34-36]. Other endocrine disorders with increased levels of insulin and/ or IGF-1 and insulin resistance are often associated with acne like HAIR-AN (hyperandrogenism, insulin resistance, acanthosis nigricans) syndrome [37]. An increased incidence of acne is observed in acromegaly [38], Laron syndrome overdosed with recombinant IGF-1 [39,40], premature adrenarche and precocious pubarche [41-44]. All these endocrine disorders with increased insulin/IGF-1 levels are expected to be associated with reduced nuclear concentrations of FoxO1, thus promoting the development of acne.
FoxO1 and smoker´s acne
Recent evidence supports the association between smoking and persistence of postpubertal acne [45,46]. There is evidence that smokers are insulin resistant and hyperinsulinemic, as compared with non-smokers [47]. Hyperinsulinemia, dyslipidemia and exaggerated adrenal androgen response to ACTH have been observed in male smokers [48]. Smoking is associated with increased free testosterone and fasting insulin levels in women with PCOS, resulting in aggravated insulin resistance [49]. Thus, smoking is associated with increased insulin/PI3K/Akt signaling of the pilosebaceous unit which may drive FoxO1 out of the nucleus.
Nicotine binds to acetylcholine receptors (AChRs). Undifferentiated sebocytes expressed α3, α9, β4, m3-m5 AChRs, whereas α7, β2, β4, m2, and m4 were found in mature sebocytes [50]. Presence of AChRs and nicotinic activity are also found in the infundibulum of the pilosebaceous unit and can promote infundibular epithelial hyperplasia and follicular plugging, suggesting an important role for the cholinergic system in acne vulgaris and acne inversa (hidradenitis suppurativa) [51]. Activation of Akt in human airway epithelial cells by nicotine and a tobacco-specific carcinogen (NNK) has been shown [52]. Activation of Akt by nicotine or NNK occurred within minutes at concentrations achievable by smokers and depended upon α3-/ α4-containing or α7-containing nicotinic AChRs, respectively [52]. In neuronal cells, α7 nicotinic AchRs have been shown to activate the PI3K/Akt pathway [53]. A time-dependent increase in phosphorylated Akt in oral keratinocytes and other epithelial cell lines has been observed with 100 µM nicotine treatment [54]. Thus, insulin, nicotine and other components of tobacco smoke may converge in the activation of the PI3K/Akt pathway as demonstrated in various cell systems. Activation of PI3K/Akt by smoking acts like growth factor signaling which most likely reduces the nuclear content of FoxO1.
FoxO1 and stress-induced acne
The sebaceous gland is not only a passive endocrine target organ that reacts to sex hormones but also plays an active part of various neuroendocrine/ neuromediator axes involving corticotropin releasing hormone (CRH) and melanocortin peptides [55,56].
Most growth factors signal via tyrosine kinase receptors which activate the PI3K/Akt pathway. A further mechanism of PI3K activation by G-protein coupled receptors (GPCRs) involves a direct binding of Gβα subunits and the GTPase Ras [57]. The human sebaceous gland has been shown to express GPCRs for neuropeptides, such as CRH and melanocortins, β-endorphin, vasoactive intestinal polypeptide, NP Y and calcitonin gene-related peptide. These receptors modulate the production of inflammatory cytokines, proliferation, differentiation, lipogenesis and androgen metabolism in human sebocytes [58-61].
The hypothalamic-pituitary-adrenal (HPA) axis mediates neuroendocrine responses of sebaceous glands to stress [62]. CRH is the principal neuroregulator of the HPA-axis and plays an important role in coordinating the endocrine, autonomic and immune responses to stress [63]. The presence of CRH and its receptors CRHR1 and CRHR2 have been demonstrated in human sebaceous glands and SZ95 sebocytes [60,64-66]. CRH can induce synthesis of neutral lipids in SZ95 sebocytes, whereas antalarmin, a CRHR1 specific inhibitor, reduced sebaceous neutral lipid synthesis [66]. A significant increase in CRHR expression has been observed in sebaceous glands in acneinvolved skin compared with sebaceous glands not involved with acne [60]. Thus, substantial evidence points to the important role of CRH/ CRHR signaling in the induction of lipogenesis and inflammation in acne [67]. In human monocytic cells, CRH has been demonstrated to activate the PI3K/Akt pathway [68]. These data imply that acneigenic effects of stress might reduce nuclear levels of FoxO1 via CRH/CRHRinduced upregulation of PI3K/Akt in sebaceous glands (Figure 1).
The proopiomelanocortin system also plays an important role as a neuromediator system in controling the sebaceous gland. The α-melanocyte-stimulating hormone (α-MSH) can stimulate sebocyte differentiation and lipogenesis [69,70]. Human sebocytes express melanocortin-1 receptor (MC1R) and MC5R [67,71,72]. MC1R was expressed in both undifferentiated and differentiated sebocytes. In acne-involved sebaceous glands a higher expression of MC1R could be detected in comparison with sebocytes of normal skin [73].
MC5R, only expressed in differentiated sebocytes and apparently stimulates lipogenesis [72]. MC5R function also seems to be related to stress response. Upregulation of MC5R was detected in the rat adrenal cortex as a consequence of a chronic stress [74]. MC5R has a preferential affinity for α-MSH, followed by ACTH and β-MSH [75]. By this mechanism stress-induced ACTH release may stimulate sebaceous glands via MC5R. Targeted deletion of MC5R resulted in deficient secretion of sebaceous glands [76]. MC5R stimulation by á-MSH induced a 10- or 16-fold rise of cAMP levels and activated ERK1/2 which was abolished by PI3K inhibiton. These data demonstrate that MC5R signals through a PI3K-regulated pathway [77]. In analogy to other GPCR-signals, MC5R-mediate activation of the PI3K/Akt pathway may contribute to further downregulation of the nuclear content of FoxO1, thereby promoting sebaceous lipogenesis.
FoxO1 and ectopeptidase inhibitor-mediated effects on acne and immune function
Ectopeptidases are important functional transmembrane proteins which are able to modulate bioactive peptide responses and influence growth, apoptosis and differentiation, as well as adhesion and motility of cells [78]. Ectopeptidase-mediated signal transduction frequently involves tyrosine phosphorylation [78]. Ectopeptidases possess a short intracytoplasmic domain with no obvious motifs [78]. Recently, the ectopeptidases dipeptidylpeptidase IV (DP IV) and aminopeptidase N (APN) have been associated with the initiation of acne [79]. It could be demonstrated that inhibitors of DP IV and APN have potent immunosuppressive and anti-inflammatory effects in various disease models [79]. Interleukin-1 (IL-1) is a known cytokine involved in the initation of acne [80]. Intriguingly, inhibitors of DP IV and APN have been demonstrated to stimulate the expression of IL-1 receptor antagonist which may counteract the acne-promoting effect of IL-1 [79]. In SZ95 sebocytes, DP IV- and APN-inhibitors suppressed proliferation, enhanced terminal differentiation and slightly decreased total neutral lipid production [79]. Thus, inhibitors of DP IV and APN may be able to reduce comedogenesis, lipogenesis and inflammation [79].
It has recently been shown in Drosophila that the induction of antimicrobial peptides (AMPs) can be achieved independently of tolllike receptor (TLR) pathways by FoxO-dependent gene regulation [81]. AMP genes are activated in response to nuclear FoxO activity [81]. Increased growth factor signaling of puberty and insulinotropic Western diet may reduce nuclear levels of FoxO1 and AMP activity thus promoting P. acnes growth and biofilm formation. P. acnes mediated TLR2-stimulation may then initiate T-cell infiltration as observed in early acne lesions [80]. Indeed, around uninvolved follicles of early acne lesions large numbers of CD4+ T cells over and above the constitutive level of surveillance T cells in normal skin have been detected. Within the CD4+ T cell population, the majority were memory/effectors, with a similar proportion exhibiting a skin homing phenotype suggesting the start of a specific inflammatory response from the adaptive immune system [80].
DP IV and DP IV-like enzymes, such as dipeptidyl peptidase II, dipeptidyl peptidase VIII, and dipeptidyl peptidase IX, have been recognized to regulate T lymphocyte activation [82,83], whereas DP IV- and APN-inhibitors suppressed proliferation of P. acnes-stimulated T cells ex vivo and induced an anti-inflammatory cytokine profile [84]. Remarkably, FoxO1 plays not only a role in the regulation of innate immunity but is of great importance in the regulation of T-cell function and T-cell homeostasis [85]. In resting T-cells, FoxO proteins reside in the nucleus. Akt activation via the stimulation of the T-cell receptor (TcR), CD28, and cytokine signaling pathways inactivates nuclear FoxO proteins which is associated with the induction of T cell proliferation [85-87]. Indeed, ectopic expression of an Akt-insensitive FoxO1 mutant suppresses T-cell proliferation, suggesting that inactivation of FoxO1,i.e.muclear extrusion of FoxO1, is an obligatory step for T-cells to enter the cell cycle [87].
An interaction between DP IV and IGF-2 receptor (IGF2R)- mediated T-cell activation has been described [88]. Internalization of DP IV is associated with cross-linking with IGF2R. In T-cells, triggering of DP IV by antibody is associated with calcium mobilization and activation of cellular proteins involved in TcR/CD3-mediated signal transduction [89]. At present, the mechanisms of growth factor-like signaling of ectopeptidases is not completely understood but the enzymatic activity of APN and DP IV does not appear to be essential for signal transduction [89,90]. Anti-CD3-mediated activation of human lymphocytes increased the expression of Akt. Akt activation could significantly be suppressed by a DP IV inhibitor [91]. Thus, ectopeptidase inhibitor treatment may have beneficial antiinflammatory effects on acne by downregulation of IL-1 signaling as well as downregulation of Akt-mediated T-cell proliferation by rising the nuclear levels of FoxO1 in T-cells [85,92].
FoxO1 and acne in Apert syndrome and Severe acne of early onset is a hallmark of Apert syndrome, a rare craniosynostosis syndrome [93]. Apert syndrome is associated with a gain-of-function mutation (either Ser252Trp or Pro253Arg) of fibroblast growth factor receptor-2 (FGFR2) [94-96]. Epidermal mosaicism producing an acneiform nevus has been observed in two boys exhibiting a somatic mutation of FGFR2 with a Ser252Trp substitution within the acneiform nevus [97,98 ].acneiform nevus
FGFR2, another important tyrosine kinase receptor involved in growth factor signaling, plays an important role in the regulation of pilosebaceous homeostasis and appears to be involved in the pathogenesis of acne [99,100]. Androgen-mediated mesenchymalepithelial signaling to keratinocytes and sebocytes is a fundamental process for development and homeostasis of the pilosebaceous unit and involves AR-dependent FGF/FGFR2 signaling [99,100]. Anti-acne agents have been suggested to attenuate FGFR2 signal transduction in acne [101].
Remarkably, activated FGFRs significantly contribute to PI3K/Akt signaling [102]. The mutant FGFR2s of Apert syndrome exhibited a markedly upregulated downstream signaling compared to normal FGFR2 [103]. Delayed endocytosis and proteasomal degradation of the mutant FGFR2s appear to be the cause of increased downstream signal transduction including elevated PI3K/Akt activity [103]. The gain-offunction mutations of FGFR2 with increased PI3K/Akt activity might reduce the nuclear level of FoxO1, thus explaining the development of acne in Apert syndrome and acneiform nevus. Constistent with these data is the observation that acne in Apert syndrome and acneiform nevus is responsive to oral isotretinoin treatment [98,104- 106]. Isotretinoin-induced upregulation of decreased nuclear FoxO1 levels would compensate for the signaling defect of the FGFR2 gainof- function mutations. Thus, Apert syndrome and acneiform nevus are two acne model diseases with increased growth factor signaling which result in PI3K/Akt activation with decreased nuclear levels of FoxO1.
FoxO1 and chloracne
Environmental pollutants can result in a variant of acne called chloracne by systemic exposure to certain halogenated aromatic hydrocarbons [107]. Chloracne is clinically characterized by a multitude of acne-like eruption of comedones, pustules and later on cysts, and squamous metaplasia of epithelial cells within the duct of the sebaceous gland [108]. Chloracne is regarded as a reliable indicator of dioxin exposure and is a persistent process that remains years after exposure [109,110]. The most biologically active isomer is 2,3,7,8-tetra- chlorodibenzo-p-dioxin (TCDD).
The pleiotropic effects caused by dioxins are mediated by the aryl hydrocarbon receptor (AhR), which is a ligand-activated transcription factor essential for inducing a battery of xenobiotic metabolizing enzymes [111]. AhR is considered to play not only a role in the regulation of xenobiotic metabolism but also in the regulation of growth and differentiation [112].The binding of dioxins to AhR leads to receptor dimerization with aryl hydrocarbon nuclear translocator (ARNT) followed by subsequent binding of this heterodimer to the dioxin response elements located in the promoter region of certain genes. The high level of AhR expression in epidermis, the finding that AhR was expressed in epidermal keratinocytes in a differentiationassociated manner and the essential role of many AhR/ARNTdependent genes in the maintenance of skin homeostasis supported the possible involvement of AhR/ARNT signaling in chloracne pathogenesis [113-116].
Benzo[a]pyrene (BaP) and TCDD modulate signal transduction pathways in various cells. BaP produced a mitogenic signal in human mammary epithelial cells. Both BaP and TCDD activated IGF-1 signaling pathways in a human mammary epithelial cell line under insulin-deficient conditions [117]. Increased signaling through IGF1R activated PI3K [117]. In contrast, the PI3K inhibitor LY294002 was found to inhibit the growth-promoting effects of TCDD seen under insulin-deficient conditions. Thus, aromatic hydrocarbons like TCDD and BaP activate IGF1R signaling and increase the activity of PI3K which will reduce nulear concentrations of FoxO1, a mechanism most likely involved in the pathogenesis of chloracne.
BaP is a component found in tobacco smoke and tar and has been shown to activate Akt in osteoblasts [118]. Activation of the PI3K/ Akt oncogenic pathway is known to inhibit apoptosis. In a mammary epithelial cell line, TCDD stimulated PI3K and inhibited growth factor withdrawal-induced apoptosis [119]. Intriguingly, ozone, one of the main components of photochemical smog of urban environment, has been shown to activate the PI3K in epidermal keratinocytes [120]. Thus, PI3K/Akt activation by environmental acneigens like polyaromatic hydrocarbons and ozone might be involved in the pathogenesis of tar acne, smoker´s acne, pollutant-induced acne and chloracne.
FoxO1, antidepressant-induced acne and isotretinoin-induced depression
Severe acne and acneiform eruptions have been observed with high doses of tricyclic antidepressants like amineptine and lithium therapy [121-124]. In brain of mice, lithium significantly decreased the transcriptional activity and protein levels of FoxO3 [125], the most important activator of the FoxO1 promoter [126]. In mice, elevated serotonergic activity due to D-fenfluramine administration increased PI3K/Akt-mediated phosphorylation of FoxO1 and FoxO3a in various regions of the brain resulting in nuclear deficieny of FoxO1 and FoxO3a content [127]. Long-term treatment with imipramine increased phosphorylation of FoxO1 and FoxO3 as well [127]. FoxOs in neuronal cells of rodents have been shown to be of functional importance in the regulation of behavioral manifestation [127,128]. Various cells of the skin express functionally active membrane-bound receptors for serotonin (5-hydroxytryptamine) [129]. It has been observed that ligand binding to serotonin receptors resulted in Akt activation [130-133]. Upregulated serotonin levels by antidepressants reduce nuclear concentrations of FoxO1 and FoxO3 in neuronal cells, mechanisms which appears to be associated with improved mood and reduced anxiety. Indeed, FoxO3-deficient mice presented with a significant anti-depressant-like behavior [127]. A nuclear increase of FoxO1 by oral isotretinoin treatment could be associated with mood disturbances and depression reported during isotretinoin therapy [134].
Modification of serotonin receptor signaling by antidepressants might thus be associated with PI3K/Akt activation and reduced nuclear levels of FoxO1 which may mediate antidepressant-induced acne.
All major factors in acne pathogenesis, i.e., AR-mediated signal transduction, increased proliferation of keratinocytes, augmented lipogenesis, upregulation of TLR2 signaling with local activation of innate and adaptive immune responses has been linked to a nuclear deficiency of FoxO1 [1]. By means of translational medicine, all studied acneigenic stimuli and their receptor-mediated signal transductions appear to converge at the integration level of PI3K/Akt. The net activation of PI3K/Akt could finally determine the nuclear content of FoxO1 and its gene regulatory impact. Acnegenic stimuli which have to be regarded as growth factor- or growth factor-like signals appear to focus on a common convergence point, the nuclear content of transcription factor FoxO1.
The hypothetical concept of a nuclear FoxO1 deficiency in acne vulgaris and related acne variants for the first time offers a unified explanation for the acne-aggravating consumption of insulinotropic dairy products, carbohydrates with high GI, acne-promoting effects of smoking, psychological stress, acneigenic effects of polyaromatic hydrocarbons, the effect of mutant FGFR2s in Apert syndrome and acneiform nevus and IL-1á-induced acne in PAPA syndrome. Furthermore, the presented hypothesis sheds a new light on the therapeutic and adverse effects of oral isotretinoin. Increased nuclear FoxO1 concentrations by systemic isotretinoin treatment have been proposed as isotretinoin´s major mode of action (Figure 2) [135].
The presented hypothesis offers new therapeutic and dietary treatment strategies for acne. These include especially the reduction of insulinotropic and IGF-1 rising dairy products, the restriction of carbohydrates with high GI, cessation of smoking, avoidance of occupational exposition with acneigenic polyaromatic hydrocarbons, the consideration of drug-induced imbalances of nuclear content of FoxO1 and the control of psychological stress factors. As most of these factors are associated with Western life style [24-26], acne could be regarded as a condition with up-regulated growth factor signaling primarily due to environmental effectors. Various apparently unrelatated acneigenic stimuli either environmental (smoking, aromatic hydrocarbons, ozone), dietary (hyperglycemic carbohydrates and hyperinsulinotropic milk and dairy products), drug-induced (antidepressants, lithium) or genetic (FGFR2-mutations, AR polymorphism with short N-terminal CAG repeats) appear to be integrated at the level of PI3K/Akt activation. These promote the nuclear extrusion of the transcription factor FoxO1. Thus, evidence from translational medicine supports the potential function of the PI3K/Akt/FoxO1 signaling pathway in acne and its variants. Future studies in acne research should focus on growth factor signaling, especially on the role of nutrigenomic regulation of insulinotropic Western diet, to understand acne pathogenesis at the level of gene regulation and the precise role of FoxO transcription factors in the clinical manifestation of the most common skin disease of industrialized countries (Table 1).
Research target | Research question | Predicted results |
---|---|---|
Sebocyte | Regulatory role of FoxO1 in sebaceous lipogenesis; FoxO1-mediated co-regulation of androgen receptor, PPARγ, LXR, RAR, RXR; mechanism of isotretinoin-induced sebocyte apoptosis | Decreased levels of nuclear FoxO1 in sebocytes in acne may stimulate sebaceous lipogenesis; isotretinoin may induce sebocyte apoptosis by upregulation of nuclear FoxO1 and FoxO1-dependent apoptosis genes like IGFBP-3 and neutrophil gelatinase-associated lipocalin |
Keratinocyte | Investigation of the role of FoxO1 in keratincyte proliferation in the pilosebaceous unit (PSU) | Decreased nuclear levels of FoxO1 in acro-infundibular keratinocytes in acne may be associated with decreased cyclin D1, D2 and increased p21 and p27 |
Oxidative stress | Clarification of the role of FoxO1 in oxidative stress responses of the PSU; antioxidative mechanisms of isotretinoin action | Downregulated nuclear FoxO1 in acne may result in increased oxidative stress with suppressed expression of FoxO1-regulated catalase and superoxide dismutase |
Innate immunity | Role of FoxO1 in the regulation of innate immunity of the PSU | Downregulated nuclear FoxO1 in acne may decrease local innate immunity of the sebaceous follicle allowing P. acnes overgrowth and biofilm formation |
Acquired immunity | Influence of FoxO1 in T-cell regulation of the PSU; Influence of isotretinoin on FoxO1-mediated T-cell regulation | Reduced levels of nuclear FoxO1 in T-cells in PSU of acne patients; anti-inflammatory effect of isotretinoin or ectopeptidase inhibitors by upregulation of nuclear FoxO1 in T-cells |
Dermal response | Role of FoxO1 in matrix metalloproteinase (MMP) regulation and dermal remodeling | Downregulated nuclear FoxO1 in acne may increase the activity of MMPs promoting increased dermal tissue destruction |
Mode of retinoid action Adverse drug effects of isotretinoin | Clarification of the role of FoxO1 in isotretinoin´s mode of action; Role of retinoids in FoxO-regulation; isotretinoin-induced hypertriglyceridemia, FoxO-1-mediated impairment of glucose metabolism, role of FoxOs in neurological adverse effects of isotretinoin | Isotretinoin´s primary mode of action appears to be an increase of nuclear levels of FoxO1; high levels of nuclear FoxO1 may be associated with increased hepatic VLDL secretion, decreased apo-CIII-mediated VLDL hydrolysis by apo-CIII-dependent lipoprotein lipase, increased hepatic gluconeogenesis and increased neuronal levels of nuclear FoxO1with neurological alterations (mood disturbances) |
Table 1: Proposed FoxO1-related topics for future acne research.
The author declares that he has no competing interest.