The regulatory role of AP-2β in monoaminergic neurotransmitter systems: insights on its signalling pathway, linked disorders and theragnostic potential

Monoaminergic neurotransmitter systems play a central role in neuronal function and behaviour. Dysregulation of these systems gives rise to neuropsychiatric and neurodegenerative disorders with high prevalence and societal burden, collectively termed monoamine neurotransmitter disorders (MNDs). Despite extensive research, the transcriptional regulation of monoaminergic neurotransmitter systems is not fully explored. Interestingly, certain drugs that act on these systems have been shown to modulate central levels of the transcription factor AP-2 beta (AP-2β, gene: TFAP2Β). AP-2β regulates multiple key genes within these systems and thereby its levels correlate with monoamine neurotransmitters measures; yet, its signalling pathways are not well understood. Moreover, although dysregulation of TFAP2Β has been associated with MNDs, the underlying mechanisms for these associations remain elusive. In this context, this review addresses AP-2β, considering its basic structural aspects, regulation and signalling pathways in the controlling of monoaminergic neurotransmitter systems, and possible mechanisms underpinning associated MNDS. It also underscores the significance of AP-2β as a potential diagnostic biomarker and its potential and limitations as a therapeutic target for specific MNDs as well as possible pharmaceutical interventions for targeting it. In essence, this review emphasizes the role of AP-2β as a key regulator of the monoaminergic neurotransmitter systems and its importance for understanding the pathogenesis and improving the management of MNDs.

Despite extensive studies on AP-2β crucial role in monoaminergic neurotransmitter systems, little is known about its signalling pathways in controlling these systems, making the underlying mechanisms for associated MNDs rather ambiguous. Thus, we review studies on the AP-2β basic structure, its overarching signalling pathways in the control of monoaminergic neurotransmitters and its polymorphisms associated with MNDs. Also, we discuss possible underlying mechanisms for these associations. Most importantly, we explore its usefulness as a diagnostic biomarker for specific MNDs and underline key opportunities and challenges for targeting it.

The AP-2 transcription factor family, structure and transduction mechanisms
The transcription factor activating protein 2 (AP-2) was first cloned in 1987 [40]. At present, five members of the transcription factor AP-2 have been identified: AP-2α, AP-2β, AP-2γ, AP-2δ and AP-2ε, which are encoded by TFAP2A/α, TFAP2Β/β, TFAP2C/γ, TFAP2D/δ, TFAP2E/ε respectively [41]. The AP-2 proteins are highly conserved across species [42] and have differential expression and functions, thereby their mutations give rise to diverse disorders, see Table 1. Structurally, they can form either hetero-or homodimers with a molecular weight of around 50 kDa. They share three regions: a highly conserved C-terminal helix-span-helix homodimerization motif, which starts with a glutamine amino acid; followed by a central basic region, both regions constitute the DNA binding domain; and a less conserved N-terminal proline-and glutamine-rich transactivation region responsible for protein binding domain [42][43][44][45] (Fig. 1).
There are two DNA binding sites for AP-2: 2 cis-acting DNA sequences 5′-(G/C)CCCA(G/C)(G/C)(G/C)-3′ and the palindromic sequence 5′-GCCNNNGGC-3′ [27,46,47]. Except for AP-2δ, the transactivation domain of AP-2 proteins is characterized by a PY motif (XPPXY) and other highly conserved residues in the protein binding domain [48]. Despite structure similarities (76% homology) between AP-2α & AP-2β [49], their gene mutations give rise to different phenotypes (Table 1). Moreover, AP-2α-null mice exhibit severe craniofacial defects while AP-2β KO mice display massive apoptosis of renal cells and terminal renal failure [49][50][51][52]. This might indicate that they are involved in differential signalling pathways. Although the crystal structure of each AP-2 protein has not yet been established, a highly accurate prediction of their protein structures has been produced by AlphaFold [53] and is available at Uniprot (Q92481).

AP-2β transcription factor
AP-2β was first characterized in 1995 [41]. Two splice variants for AP-2βhave been identified, both can exert transcriptional regulatory activity but have a little different in tissue expressions: one short at 198 aa (22.1 kDa) (UniProt ID X6R4Y8), which is not well studied, and one long at 460 aa (50.5 kDa) (UniProt Q92481) that has been thoroughly investigated [58,59]. AP-2β is highly expressed in the brain and peripheral neurons, eyes, smooth muscles of ductus arteriosus, skin, bone marrow, adipose and lymphoid tissues, proximal digestive tract, the adrenal medulla of the kidney and across the urogenital system [36,58,60]. In addition to its function in monoaminergic neurons, TFAP2Β is also involved in specification of glycinergic and GABAergic interneurons [61][62][63]. TFAP2Β mutations lead to the development of severe disorders such as craniosynostosis, Char Syndrome, dental anomalies, defects in patent ductus arteriosus, terminal renal failure and others [64][65][66][67] ( Table 1).

Regulation of AP-2β activity
To better understand its associated MNDs, the mechanisms regulating AP-2β activity should be first articulated. Two key mechanisms have been shown to modulate the DNA-binding and/or transcriptional activities of AP-2β: protein-protein interactions through the protein-binding domain and post-translational modifications employing the DNA-binding domain ( Figs. 1 and 2).

Protein-protein interactions
AP-2β has a specific protein-binding domain, also known as a transactivation domain [44,45,67]. Binding to this domain modulates the DNA-binding ability of AP-2β at the adjacent DNA-binding domain [67]. A study by Ding et al. has shown, for example, that the potassium channel tetramerization domain 1 (KCTD1) binds to the N-terminal protein-binding domain of AP-2β and inhibits its transcriptional activity in human DNA binding domain is comprised of helix-span-helix and a central basic region, whereas the protein binding domain, also known as the transactivation region, has a special PY motif that is highly conserved. X denotes any amino acid. The picture was influenced by [42,44,45,54], and SwissProt ID: Q92481 & Q61313 and created with Biorender. com cell lines [68]. Another study by Zarelli et al. has reported that in zebrafish, potassium channel tetramerization domain 15 (KCTD15) inhibits the expression of AP-2 [69]. Interestingly, KCTD1 and KCTD15 have remarkably similar amino acid sequences [70], which may explain the similarity of their effects on AP-2β. Additional inhibitors of AP-2β transcriptional activity are the protein kinase D (PKD) [71], which, by phosphorylating AP-2β, inhibits its DNA binding activity, as well as the hypoxia-inducible factor-2alpha (HIF-2α), which negatively regulates the expression AP-2β [72]. The dynamics of protein-protein interaction can also lead to enhanced AP-2β activities. Cpb/p300-interacting transactivator 2 & 4 (CITED2 & CITED4), are coactivators and enhancers of AP-2β-induced transcriptional activation [73,74]. Additionally, YEATS domain-containing protein 4 (YEATS4, also known as GAS41) augments both, the DNA-binding and the transcriptional activity of AP-2β [75]. For more information about other protein interactions with AP-2β, see Fig. 2.

Post-translational modifications
Post-translational modification is another mechanism that can modulate the transcriptional or DNA-binding activity of AP-2β. For example, the sumoylation of AP-2β by ubiquitin carrier protein 9 (UBC9) has been shown to decrease its transcriptional activity [77]. KCTD15 mentioned earlier can also enhance the activity of AP-2β through sumoylation [78,79]. Accordingly, KCTD15 can modulate the activity of AP-2β directly (blocking) and post-translationally (activating) ( Table 2).
In summary, different modulators have been shown to regulate the activity of the AP-2β by two mechanisms: the protein-protein interaction through the transactivation domain and post-transcriptional modification through the DNA-binding domain. These two mechanisms could be utilized to pharmacologically modulate AP-2β activity, possibily by targeting these modulators.

AP-2β signalling regulation of monoaminergic neurotransmitter systems
AP-2β is a vital transcription factor for the proper development and function of the monoaminergic neurotransmitter systems [24,62,80]. It plays an essential role in the maturation of chromaffin cells, sympathetic neuronal differentiation, and regulation of monoaminergic transmission, including adrenergic, noradrenergic and dopaminergic, and serotonergic transmission, during both development and adulthood [24,46,62,[80][81][82]. Several key genes regulating the monoaminergic neurotransmitters' biosynthesis, degradation and synaptic activity have a recognition site for AP-2β in their promoter regions [21-23, 27, 83, 84]. Since AP-2β enhances both monoaminergic transmissions, AP-2β levels correlate with monoamine neurotransmitter transmission in the brainstem [24,25,62]. This might explain why the central level of AP-2β has been changed after treatment with certain drugs that act on monoaminergic neurotransmitters, such as phenelzine (MAOI) and citalopram (SNRI) [24,38,85].
Furthermore, AP-2β represses the Dopamine receptor D 1A (DRD 1A ) receptor through binding to the D 1A silencer 1 (D1AS1) [94]. Blocking this receptor leads to decreased adenylyl cyclase (AC) activity and lowered cyclic adenosine monophosphate (cAMP), resulting in dopamine-related behavioural changes such as reward, cognition and learning [94][95][96] (Fig. 3). DRD1 A plays a significant role in the modulation of memory and cognition [97][98][99]; hence, it would be interesting to explore the association of TFAP2B polymorphisms with cognitive functions.
The effect of AP-2β on dopamine turnover is under debate. Damberg et al. have reported that AP-2β is Table 2 The coactivators and suppressors of AP-2β KCTD1: the potassium channel tetramerization domain 1; KCTD15: potassium channel tetramerization domain 15; PKD: protein kinase D; HIF-2α: inducible factor-2alpha; CITED2: Cpb/p300-interacting transactivator 2; CITED4: Cpb/p300interacting transactivator 4: YEATS4; YEATS domain-containing protein 4; UBC: ubiquitin carrier protein 9; UBE2I: ubiquitin-conjugating enzyme E2 I positively correlated with the indices of dopamine metabolites, namely homovanillic acid (HAV) and 3-methoxy-4-hydroxy-phenylgly (MGPG) in rat forebrain [24] but not in CSF of humans [25]. Moreover, DBH enzyme is responsible for converting dopamine into norepinephrine in catecholaminergic neurons [100]; thus, given its transcriptional activation effect on DBH [33,46,82,89,90], AP-2β might enhance the turnover of dopamine by boosting its conversion into norepinephrine. On the other hand, Schabram et al. have suggested that AP-2β enhances dopamine availability and decreases its turnover through its repressing effect on MAO-A and COMT [92]. In total, it is difficult to conclude the influence of AP-2β on dopamine levels and hence, more investigations in this area are recommended, especially in the AP-2β-associated MNDs where dopamine is a key player, e.g. obesity and anxiety.

AP-2β regulation of serotonergic transmission
AP-2β controls multiple key genes in the serotonergic (5-HT) pathway (Fig. 4) and has been shown to enhance serotonergic turnover and transmission in the brain [24], perhaps by increasing serotonin availability in the synaptic cleft. Two key genes in the serotonergic system have been shown to be negatively regulated by AP-2β: MAO-A [28,[91][92][93] and 5-HTT [19,20,101]. 5-HTT transports 5-HT into presynaptic where it is degraded by MAO. Thus, inhibiting 5-HTT and MAO genes by AP-2β may result in increased serotonin levels in the synaptic cleft and serotonergic transmission [24,25]. In addition, AP-2β has a binding site on tryptophan hydroxylase (TPH), aromatic l-Amino acid decarboxylase (AADC) as well as rat 5-Htr2 and human 5HT3R [62,[102][103][104][105][106][107]]; yet, its regulatory effect on these genes is still unknown. Given the positive correlation between AP-2β and serotonergic activity in the brainstem [24,25], it is reasonable to suggest that AP-2β may enhance the expression of TPH and AADC as well, although studies are needed to confirm this suggestion.
Taken together, AP-2β can modulate both arms of monoaminergic neurotransmitter systems, by controlling the key genes in catecholaminergic and serotonergic transmission, indicating its role as a key regulator of monoaminergic neurotransmitter systems and its importance for better understanding and management of MNDS.

TFAP2Β polymorphisms
The TFAP2Β gene is located on chromosome 6p12-p21, and it has eleven axons with a size of 29,910 bases [115,116]. TFAP2B has many polymorphic regions that affect mostly its transcriptional activity rather than its protein structure [29,34,117]. This in turn influences the expression of its target genes in the monoaminergic neurotransmitter systems. Consequently, TFAP2Β functional polymorphisms have been associated with different MNDs. To date, three functional polymorphisms of TFAP2Β are known to be associated with MNDs. One is located in intron 1, in which polymorphic regions (SNP at intron 1 + 774T/G and a nearby variable number tandem repeat, VNTR, allele), have been shown to postively regulate TFAP2B transcriptional activity, enhancing its expression. Subjects who carry the disease-related alleles (S-allele: T-nucleotide for SNP, nine repeats for VNTR) show higher expression of TFAP2Β, which is associated with a higher risk for T2D and a lower risk for depression [34,36,102,118].
The second polymorphism is located in intron 2 in a polymorphic region [CAAA] close to the 3`-splice site of exon 2 between nucleotides 12593 and 12612 [27,51]. Repeats of this sequence in variable regions suggest its important role in functional polymorphisms [25,27,60]. Interestingly, the 5-repeat alleles of indel intron 2 of TFAP2B have been shown to increase the expression of TFAP2Β [19]. The intron 2 polymorphism is associated with adiposity, neonatal temperament and anxietyrelated personality traits [19,26,27,29]. Strikingly, there is significant linkage disequilibrium between the polymorphisms of intron 1 and intron 2 [27,29,119], indicating that their association is not by chance. This suggests that the associations observed with intron 2 polymorphisms are most likely a result of the functional polymorphism in intron 1 [28].
The third TFAP2Β polymorphism, rs987237, is located in intron 3 and has three different genotypes, AA, AG and GG that are associated with obesity, BMI, waist circumference and differential effects on weight loss [120][121][122][123]. Stocks et al. have suggested that the TFAP2Β rs987237 variant may be linked to enhanced activity of this transcription factor since it is also in complete linkage disequilibrium with intron 1 [120].
Overall, three TFAP2Β polymorphisms have been shown to mostly enhance its transcription activity. This in turn affects the expression of the key genes in the monoaminergic neurotransmitter systems that have putative binding sites for AP-2β.
The mechanisms underlying AP-2β-induced insulin resistance and adiposity are rather unclear. Several studies have attributed the role of AP-2β in insulin resistance and adiposity to its regulatory effect on genes that encode adipocytokines, which have AP-2β binding sites in their promoters. For instance, TFAP2Β overexpression has been shown to inhibit the expression of adiponectin and leptin but also enhance the expression of interleukin 6 (IL-6), monocyte chemoattractant protein-1 (MCP) and tumour necrosis factor-alpha (TNF-alpha) [34,124,[132][133][134][135]. However, Tsukada et al. have demonstrated that overexpressed TFAP2Β has no effect on most adipocytokines like adiponectin, leptin and IL-6 [34]. Additionally, a study by Nordquist et al. have shown no association of adiponectin levels to insulin resistance or to the TFAP2Β polymorphism [29]. Furthermore, AP-2β has been reported to enhance glucose uptake (enhancing the translocation of the glucose transport 4, GLUT4) but also reduce insulin sensitivity through both, repressing the expression of insulin receptor substrate 1 (IRS-I) and lipid accumulation [29,31,36,133,134]. The enhanced glucose uptake effect, however, is not in line with the inhibitory effect of AP-2β on adiponectin and leptin mentioned above since higher adiponectin and leptin have been shown to enhance glucose uptake [136,137]. Given such discrepancies, it is reasonable to suggest another pathway by which AP-2β contributes to obesity and T2D, possibly through monoaminergic neurotransmitter systems.
The association of TFAP2Β with obesity-related disorders might also be linked to its repression effect on 5-HTT. First, 5-HTT re-uptakes 5-HT from the synaptic cleft into the presynaptic neurons. As we mentioned previously, AP-2β represses the expression of 5-HTT [19,20,101] and 5-HTT gene promotor methylation is associated with reward and eating behaviour as well as human obesity [147] and suppression of 5-HTT, by hypermethylation, in humans is associated with a high prevalence of obesity [148].
The genetic interaction between TFAP2Β and KCTD15, an obesity-linked gene, is also likely to positively contribute to AP-2β-induced obesity and metabolic dysfunction. In this regard, our group has recently shown that in Drosophila, the homologue of KCTD15, Twz, genetically interacts with Drosophila TfAP-2 to regulate octopaminergic (human noradrenergic) signalling. We have further demonstrated that mouse TFAP2β and Kctd15 directly interact with Ube2i, a mouse sumoylation enzyme, to induce consummatory behaviour [79]. Strikingly, consistent with these findings is a recent study by Gamero-Villarroel et al. that has identified the genetic interaction between KCTD15 and TFAP2Β in individuals with eating disorders [78]. The same study has suggested that after sumoylation of TFAP2Β by KCTD15, a post-translational effect is initiated by E1-3 enzymes and ATP, resulting in elevated catecholamine levels and induction of feeding behaviour [78].

Alcoholism
That dysregulation of monoamine neurotransmitters contributes to the development of alcoholism is well known. Reports have indicated that TFAP2Β polymorphism in the intron 1, which can enhance AP-2β transcription, is associated with severe alcoholism in women [28]. This association has been linked to the effect of AP-2β on several targets in the monoaminergic system. AP-2β lowers the levels of MAO and lowered levels of MAO are linked to alcoholism [28,[149][150][151]. AP-2β activation of dopamine-beta-hydroxylase (DBH) [82] may also contribute to alcoholism, since in alcohol-dependent persons, DBH is hypomethylated and its enzyme is more active, resulting in a reduction of dopamine levels [152,153]. However, inhibition of DRD1 or DRD1 KO mice has been shown to reduce alcohol-seeking behaviour [154][155][156][157], suggesting that AP-2β-induced alcohol intake might be independent of its repressing effect on DRD1 [94].
Moreover, AP-2β-enhanced serotonergic transmission may also contribute to alcohol abuse, perhaps through inhibition of 5-HTT [19,20,101] and lowering MAO [28,[91][92][93]. In agreement with this notion, increased serotonin levels or 5-HTT KO mice have been found to trigger alcoholism [158][159][160], and MAO-A methylation is associated with alcoholism in women [161]. Furthermore, alcoholics have higher levels of both, the transcript and protein of tryptophan hydroxylase, TPH [162], the rateliming enzyme in serotonin synthesis, which has a binding site for AP-2β in its promotor [107]. Increased levels of TPH have been reported to enhance serotonin levels [163].

Anxiety and depression
TFAP2Β intron 2 polymorphisms are associated with low anxiety [26,27,93], and its intron 1 polymorphism, which enhances its expression, protects against the risk of depression in patients with attention deficit hyperactivity disorder [102]. However, when psychosocial adversity is considered, individuals with TFAP2Β intron 2 polymorphisms who are homozygous for the short TFAP2Β allele exhibited higher depression scores [117].
This association might be ascribed to the AP-2β regulatory effect on the monoaminergic neurotransmitters in the brain. Mechanistically, AP-2β inhibits 5-HTT expression [19,20,101] and inhibition of 5-HTT, by SSRIs for instance, leads to increased serotonin, which alleviates anxiety and depression [164]. Moreover, AP-2β reduces MAO levels [28,[91][92][93], which may also contribute to reduced anxiety and depression. In agreement with this possibility, deficiency of MAO-A or MAO-B leads to reduced anxiety-like behaviour in mice, as well as inhibition of MAO-A reduces depression in mice, and likewise, drugs that inhibit MAO-B reduce depression as well [165,166]. Interestingly, MAO inhibitors enhance the levels of noradrenaline and serotonin levels in the brain to alleviate anxiety [167] and depression [168]. In consonance with these effects, AP-2β enhances noradrenaline and serotonin transmission [24], both of which have been reported to exert anxiolytic and antidepressant effects [9,[169][170][171].
Since certain antidepressant/anxiolytic drugs, e.g. citalopram (SSRI) and imipramine (TCA), have been reported to modulate the levels of AP-2β in the brainstem of the rat [24,38,84], probably due to its transcriptional regulation of the key targets in monoaminergic neurotransmitter systems, future clinical anxiolytic/antidepressant drug development should monitor the level of AP-2β for better management and/or prevention of depression and anxiety.

Antisocial behaviour
Antisocial behaviour in children and adolescents refers to a heterogeneous set of actions outside the norms of society, including aggression, impulsive behaviour and criminal acts, which are linked to monoaminergic neurotransmitter systems [172][173][174][175]. TFAP2Β has been associated with aggression in fruit flies and humans, as well as with general antisocial behaviour in humans [27,28,81,176]. However, the TFAP2Β signalling mechanisms that underlie such association have not been fully elucidated. The repressing effect of AP-2β on monoamine-degrading enzymes, such as COMT and MAO might explain such an association since several reports have revealed that lowered expression of MAO-A, or MAO-A KO mice, as well as lower activity of COMT or COMT-deficiency in mice are associated with higher aggression [177][178][179][180][181][182]. Furthermore, activation of DBH expression by AP-2β may also play a part in provoking high aggression. Activation of DBH enhances the conversion of dopamine to adrenaline and it has been reported that higher adrenergic signalling provokes aggression [183], and DBH KO mice have lower levels of aggression [184], all linking AP-2β-mediated higher aggression to enhanced adrenergic signalling.
Nevertheless, the AP-2β association with higher aggression might be independent of its enhancement effect on serotonergic signalling, specifically, its repressing effect on 5-HTT. This is because several preclinical and clinical studies have indicated that high levels of serotonin and lower expression or blocking of 5-HTT or knocking out 5-HTT in mice lead to reduced aggression outbursts and violent behaviour [185][186][187][188], an effect opposite to that of AP-2β. It would be interesting to investigate the association of TFAP2Β polymorphisms and their interaction with key monoamine neurotransmitter genes to aggression and antisocial behaviour.

Alzheimer's disease (AD)
While genetic variants of TFAP2Β have been suggested to play a role in resilience to AD [189], increased AP-2β has been shown to bestow a neuroprotective effect in AD due to the AP-2β-enhancing effect on the expression of apolipoprotein E (apoE), an important protective protein in AD pathogenesis [32,190]. The effects of AP-2β on catecholamines might also contribute to its protective effect in AD. Firstly, lowered catecholamine levels contribute to the development and pathogenesis of AD [191][192][193] and, by the same token, AP-2β has been shown to increase catecholamine signalling in the brain [24,46,[86][87][88]. AD is also associated with lower levels of DBH and PNMT [194][195][196][197][198], which both are activated by AP-2β [46,[86][87][88]. In addition, COMT and MAO-B levels are higher in AD [192,[199][200][201], and both are lowered by AP-2β [21,92,93]. Supporting this notion, COMT and MAO inhibitors have been repurposed for the treatment of AD [202][203][204]. Secondly, AP-2β enhances serotonin activity in the brain which might add further protective effects in AD. Consistent with this extrapolation is the observation that reduced serotonin levels in the brain can enhance the risk for AD [205], providing the rationale for SSRI use to delay the onset of AD [206]. Taken together, it might be suggested that, through its enhancing catecholaminergic and serotonergic activities, AP-2β may exert a protective role in AD. Thus, elucidating the association of TFAP2Β polymorphisms and their interactions with COMT, MAO, to AD could unveil a potential biomarker for early diagnosis and management of AD.

Neuroblastoma
Transcription factors serve as essential regulators of cell development, proliferation and differentiation; consequently, dysregulation of them brings about oncogenic transformation and cancers [207,208]. Neuroblastoma is an embryonal pediatric malignant tumour originating from the sympathetic nervous system and characterized by extremely low noradrenergic neuronal differentiation [33]. However, the molecular mechanisms underlying lowered neuronal differentiation in neuroblastoma are still under investigation.
Recent studies have revealed an important role of AP-2β in the pathogenesis and progression of neuroblastoma [33,37,209,210]. Thorell et al. have identified TFAP2Β as a potential tumour suppressor gene in neuroblastoma [210]. Ikram et al. have also indicated that low AP-2β expression results in lower noradrenergic neuronal differentiation and is thereby significantly associated with poor prognostic markers and unfavourable patient outcomes [33]. In contrast, induction of AP-2β expression has been found to impair tumour cell proliferation and slow tumour progression by enhancing both differentiation of noradrenergic neurons as well as noradrenergic signalling through increased expression of TH and DBH [33]. In addition to its effects on sympathetic neurons, AP-2β has been demonstrated to enhance retinoic acid (RA) responsiveness, which potentiates neuronal differentiation and therefore is used in neuroblastoma therapy [33].
Altogether, AP-2β is associated with certain MNDS, although the underlying mechanisms are not fully elucidated. As we mentioned above, the underlying mechanisms for this association might be linked to AP-2β regulatory effects on key genes of monoaminergic neurotransmitters. However, further preclinical studies investigating the molecular mechanisms underlying AP-2β associated MNDs, e.g. manipulating the expression of TFAP2B in neuronal cell culture or rats' models of MNDs and examining the levels of the key enzymes of monoaminergic neurotransmission, are warranted.

AP-2β as a biomarker
Transcription factors are currently widely used as diagnostic biomarkers for the early detection of several diseases [211][212][213]. A wide range of brain-related disorders and cancers are accompanied by alterations in the levels and activity of TFAP2Β/AP-2β, which underscores its diagnostic importance for such diseases. TFAP2Β overexpression, for instance, has been implicated not only as a protective or favourable prognostic factor in several cancers like breast, renal cell, cervical and endometrial cancers but also as a poor prognostic factor in thyroid cancer and lung adenocarcinoma [214][215][216][217][218][219][220][221][222][223][224][225] (See Table 1).
Along the same line, AP-2β might also constitute a diagnostic biomarker for other MNDs. For example, while TFAP2Β/AP-2β overexpression has already been suggested as a favourable prognostic marker in neuroblastoma [33,210], it might further be considered as a biomarker for other MNDs where TFAP2Β/AP-2β overexpression is implicated, such as alcoholism, obesity, T2D and aggression. Nevertheless, clinical studies are needed to address its specificity and characterize its validity as a biomarker for the early diagnosis of these disorders.

AP-2β as a potential therapeutic target
In the last decade, targeting transcription factors with selective therapeutic agents has gained growing interest because transcription factors act as on/off switches of gene expression, a process that leads to neurological disorders and cancers when disrupted. In this context, clinical reports have highlighted the potential of AP-2β as a therapeutic target for specific cancers such as lung adenocarcinoma [216], renal cell tumorigenesis [220], and breast [221] and endometrial cancers [217].
TFAP2Β/AP-2β might also be considered an interesting therapeutic target for the management of specific MNDs, where its synergistic effects on multiple targets may be beneficial for the treatment or prevention of complex diseases. This concerns specifically the neurometabolic disorders, such as obesity and type 2 diabetes, that are characterised by widespread systemic alterations through diverse factors including, behavioural, neural, hormonal, adipose and intestinal along with the involvement of different mediators such as monoamine neurotransmitters, insulin and adipocytokines. In this regard, researchers have emphasized the importance of AP-2β as a promising drug target for the prevention and treatment of obesity and T2D [34][35][36]. AP-2β can target multiple features of obesity and T2D centrally and peripherally by modulating key-obesity linked genes such as IRS-1, GLUT4, adipocytokines related genes, as well as catecholaminergic and serotonergic genes involved in reward, consummatory behaviour and insulin resistance ( Table 3). Some of these genes are, intriguingly, recognized as therapeutic targets of several drugs used for obesity-linked diseases.

Inhibition of AP-2β Peptide inhibitors
Neuroblastoma Suppression TH (+) [33,82,89] DBH (+) [33,46,82,89,90] PNMT (+) [46,[86][87][88] Norepinephrine (+) Epinephrine (+) Dopamine Activation of AP-2β AP-2β analogue or activators Tetracycline [33] localized drug delivery, which could minimize peripheral undesired effects. This is supported by the fact that Trichostatin A, a potential drug used for neuroblastoma, has been shown to augment monoamine pools by inhibiting COMT and MAO-A genes [226], a mechanism similar to that of AP-2β. Like other drug targets at the transcription level, offtarget effects could pose a substantial challenge. AP-2β has been reported to modulate multiple key genes within and outside the monoaminergic neurotransmitter systems, suggesting off-target effects. Consequently, such ubiquitous off-target effects might limit its potential as a therapeutic target due to the lack of specificity and the risk of adverse effects.

Targeting AP-2β (druggability), challenges and future insights
Until recently, transcription factors had been considered very challenging targets (undruggable) since transcription factors lack obvious druggable pockets and the transcription process is carried out in the nucleus; therefore, the therapeutic agent should have the appropriate physicochemical properties to cross many biological barriers and reach the nucleus with sufficient concentration. Moreover, many crucial components involved in the transcription process do not have the enzymatic activity adequate for pharmaco-chemical interventions [227,228].
So far, manipulation of transcription factor activity at protein-protein interaction levels has been successfully implemented and a few drugs have been approved for various disorders [227,229]. As mentioned previously, several proteins have been reported to modulate the levels and activity of AP-2β (see Table 2). Such modulator proteins can be targeted to regulate TFAP2Β/AP-2β at different levels: at transcription, post-translation or the DNA-binding site (Fig. 5). Yet, potency and selectivity may pose a substantial issue because targeting these proteins can elicit a chain of inadvertent adverse effects since they are also involved in diverse biological processes and regulate other AP-2 transcription factors [42]. Possible sites and targets that can be potentially exploited to modulate AP-2β activities and/or levels. One proposal for modulating AP-2β is through protein-protein interactions whereby co-activators/suppressors bind to the transactivation domain and modify AP-2β transcription activity and DNA-binding activities, as indicated within the yellow square. Inducing degradation of AP-2β could be achieved through designing peptide inhibitors binding selectively to its transactivation domain to form a non-functional complex or by enhancing PKD phosphorylation of AP-2β [71] or by developing specific monoclonal antibodies that can bind and inactivate AP-2β. By contrast, enhancing AP-2β activity could be feasible by designing artificial transcription factor analogues (TFA) that can act as AP-2β agonists. Some monoaminergic drugs, such as phenelzine and citalopram, also have been shown to alter the brain levels of AP-2β [38,39]] while tetracycline induces its gene expression [33]. Despite these challenges, in the last decade, advances in pharmacological interventions have facilitated the druggability of transcription factors by specifically modulating their DNA-binding and transcription regulation activities at specific pockets. Interestingly, such pharmacological strategies have been successfully applied preclinically [228,[230][231][232][233][234] and clinically [235,236], and at least 10% of drugs obtained FDA approval [208,228,237,238]. Moreover, a recent article in Nature Reviews Drug Discovery by Henley et al. has discussed the renewed interest in the advent of pharmacological interventions for targeting transcription factors [208]. Currently, about ten drugs acting on transcription factors are in clinical trials [208], indicating a driving trend toward targeting transcription factors.
For example, inducing protein degradation of the transcription factor can be driven by exploiting its transactivation domain. Binding to this part with a specific peptide can form a non-functional complex for degradation. Such technology has facilitated abolishing of transcription factor activity by designing peptide inhibitors, also known as peptide therapeutics [233] that binds to the transactivation domain of the transcription factor and thereby hinder its interactions with other proteins and ultimately induce its degradation (Fig. 5). An interesting example in this context is YK-4-279, which peptide inhibitor that binds to the oncogenic transcription factor EWS-FLI1 to inhibit its activities. YK-4-279 is used to treat Ewing sarcomas [231,239].
In parallel, providing the basic knowledge of its domain structure and binding sites, direct inhibition of AP-2β, by peptide inhibitors capable of selectively binding to its transactivation domain and inducing its degradation could be attractively applicable. Such specific peptide inhibitors could interfere with the dynamic of AP-2β protein-protein interactions and subsequently block its transcriptional activity on the target genes. This represents an interesting therapeutic approach for the management of obesity and related neurometabolic disorders where higher AP-2β levels are implicated.
On the other hand, mimicking transcription factor activity has been made feasible, especially in cancer and neurometabolic disorders. Many artificial transcription factors, also called transcription factor analogues (TFAs), have been successfully developed for several cancers and loss-of-function mutations to restore the overall functions of the transcription factors [231]. Dimethyl fumarate (DMF), for example, is an NRF2 activator, which is FDA-approved for multiple sclerosis (MS) [237]. In a similar vein, induction of AP-2β-related transcriptional effects on its target genes could be achieved by designing an AP-2β analogue with sufficient selectivity and potency (Fig. 5). Such AP-2β agonists could mediate effects similar to that of AP-2β and thereby be used in disorders where higher AP-2β is therapeutically advantageous such as in neuroblastoma. Nevertheless, full characterization of the protein crystal structure of AP-2β is a prerequisite for developing such therapeutic agents.

Concluding remarks
AP-2β is a central regulator of monoamine neurotransmitters and its dysregulation is associated with MNDs. The underlying mechanisms for its associated MNDs could be linked to its regulatory role in monoaminergic transmission, yet more studies are recommended. For example, knockout/overexpression of TFAP2B in rat models of MNDs and examining the expression of the key monoaminergic genes can help clarify the molecular pathogenesis of the associated MNDs. Moreover, the molecular functions of AP-2β within the monoaminergic systems underline its importance as a promising biomarker for the early diagnosis of relevant MNDs. Given its effect on multiple targets within and outside monoaminergic systems, AP-2β could be considered a dirty drug target due to the odds of having adverse effects. Nevertheless, several dirty drugs that aim for multiple targets at once are clinically effective in the treatment of complex diseases [240,241], which might also underscore the therapeutic potential of the AP-2β for complex MNDs like obesity and neuroblastoma. Future drug development targeting monoaminergic systems could take advantage of monitoring the AP-2β levels during clinical studies for better management and treatment of MNDs.