1. Introduction

Skin represents the primary line of defense against environmental stressors, including chemical stimuli, microbial insults, allergens, and ultraviolet (UV) radiation. Protection from UV rays is essentially based on melanogenesis, the process leading to the synthesis of pigments called melanin, the main substance that influences skin color. Melanin protects the skin from harmful UV rays, as it can absorb UV and visible light and shows antioxidative and radical scavenging abilities, limiting UV-induced effects on cellular macromolecules, mainly DNA, thus protecting cells from genotoxic damage ^[1]. Therefore, reduced melanogenesis is also a major risk factor for melanoma and other skin cancers ^[2][3]. Nevertheless, increased melanogenesis and melanin accumulation is associated with hyperpigmentation disorders ^[4][5]. Skin hyperpigmentation, often associated with aging, hormonal changes, and UVB, is very common in clinical dermatology and includes dermal conditions such as melasma, chloasma, freckles, age spots, and sunspots ^[5]. In addition, both hyperpigmentation and hypopigmentation, as observed in vitiligo lesions, are frequently the consequence of inflammation, induced by skin stressors ^[6]. Indeed, the modulation of skin pigmentation still represents a challenge in treating dermatological disorders, despite several studies having investigated potential cures ^[7][8]. Melanin is produced by highly specialized cells called melanocytes that are in strict contact with other skin cells, especially keratinocytes. The process of skin coloration consists of melanin biosynthesis and the translocation of melanosomes, small organelles containing melanin, from melanocytes into epidermal keratinocytes ^[6][7][9].

Melanogenesis is a very complex process which includes the development, survival, and differentiation of melanocytes. It involves more than 150 genes and several signaling pathways that operate both at transcriptional and post-transcriptional levels in regulating the main melanogenic molecular players. These include transcription factors, enzymes, and regulatory molecules produced by melanocytes, as well as other skin cells including keratinocytes, dermal fibroblasts, and inflammatory and endocrine cells ^{[6][7][10][11]}.

Altered gene expression and melanogenic regulatory factor activities are involved in melanogenesis dysfunction ^[4][11]. Increasingly, studies indicate that gene expression is also influenced by several epigenetic events, including chromatin modification, DNA methylation, and non-coding RNA classes such as long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) ^{[12][13][14][15]}. Indeed, the role of miRNAs in melanogenesis has been widely investigated.

2. Melanin Biosynthesis

Melanin synthesis occurs in highly specialized cells called melanocytes, localized in the basal layer of the epidermis and hair follicles ^[16][17]. Melanocytes consist of several ramifications called dendrites that end in keratinocytes, and each melanocyte is strictly connected to more than 30 keratinocytes, constituting the melanogenic unit ^[18]. During melanogenesis, a series of sequential reactions synthesize melanin, which is translocated into neighboring keratinocytes by means of melanosomes ^[6][7][9].

Melanin synthesis occurs in highly specialized cells called melanocytes, localized in the basal layer of the epidermis and hair follicles [17,18]. Melanocytes consist of several ramifications called dendrites that end in keratinocytes, and each melanocyte is strictly connected to more than 30 keratinocytes, constituting the melanogenic unit [19]. During melanogenesis, a series of sequential reactions synthesize melanin, which is translocated into neighboring keratinocytes by means of melanosomes [6,7,9].

Melanin production is controlled by several enzymes including tyrosinase (TYR), tyrosine hydroxylase I (THI), and phenylalanine hydroxylase (PAH) in the initiation phase of melanin synthesis. Tyrosinase-associated protein 1 (TYRP-1) and tyrosinase-associated protein 2 (TYRP-2), also called dopachrome tautomerase (DCT), operate in the later phase ^[4][19]. TYR is a membrane-bound glycoprotein which plays a key role in the process, as it is considered the rate-limiting enzyme for melanin biosynthesis (

Melanin production is controlled by several enzymes including tyrosinase (TYR), tyrosine hydroxylase I (THI), and phenylalanine hydroxylase (PAH) in the initiation phase of melanin synthesis. Tyrosinase-associated protein 1 (TYRP-1) and tyrosinase-associated protein 2 (TYRP-2), also called dopachrome tautomerase (DCT), operate in the later phase [4,20]. TYR is a membrane-bound glycoprotein which plays a key role in the process, as it is considered the rate-limiting enzyme for melanin biosynthesis (

Figure 1

).

Figure 1.

 Representation of the melanogenic unit and melanin synthesis in melanosomes (

left

). Schematic representation of eumelanin and pheomelanin biosynthetic pathways (

right

).

The reaction catalyzed by TYR leads to L-tyrosine being transformed into dopaquinone by oxidation ^[20]. Dopaquinone is highly reactive and can follow two reaction chains from which eumelanin and pheomelanin originate:

The reaction catalyzed by TYR leads to L-tyrosine being transformed into dopaquinone by oxidation [21]. Dopaquinone is highly reactive and can follow two reaction chains from which eumelanin and pheomelanin originate:

(1)

(1) In reactions leading to eumelanin production, dopaquinone undergoes intramolecular cyclization to produce leukodopachrome (cyclodopa). Cyclodopa undergoes redox exchange with another molecule of dopaquinone to form dopachrome and DOPA ^[20][21]. The dopachrome downstream process is branched in two ways. The first leads to the formation of 5,6-dihydroxyindole-2-carboxylic acid (DHICA) through TYRP-2 intervention and then into eumelanin by TYRP-1 conversion. The second leads to the conversion of dopachrome into 5,6-dihydroxyindole (DHI) and then into eumelanin involving TYR. At the end of this reaction, black-brownish eumelanin is formed.

(2)

(2) In reactions leading to pheomelanin production, in the presence of cystein or glutathione, dopaquinone can be converted into 5-S-cysteinyldopa, or glutathionyldopa, which is then converted into quinoline and finally polymerized into red-yellow pheomelanin.

In the skin, both eumelanin and pheomelanin form complex heteropolymers. The total amount of melanin, as well as the ratio between eumelanin to pheomelanin, are considered to determine skin color. Indeed, the role of the ratio between eumelanin and pheomelanin is still under debate, as many authors indicate that it remains unchanged in various phototypes of 

human skin and, thus, skin color is dependent on total melanin amount ^[4][21]. Synthesized melanin is collected into melanosomes, which follow a complex maturation process and are transported to keratinocytes along actin filaments in association with motor proteins ^[4][22].

 skin and, thus, skin color is dependent on total melanin amount [4,22]. Synthesized melanin is collected into melanosomes, which follow a complex maturation process and are transported to keratinocytes along actin filaments in association with motor proteins [4,23].

3. Melanogenesis Regulation

Several stimuli control melanogenesis, including external factors such as UV rays or environmental pollution ^[11]. Furthermore, a series of endogenous molecules released by melanocytes, keratinocytes, dermal fibroblasts, and immune cells modulate the process paracrinally and autocrinally. These are mainly the α-melanocyte stimulating hormone (α-MSH) and the adrenocorticotropic hormone (ACTH), derived from the cleavage of pro-opiomelanocortin (POMC), from both melanocytes and keratinocytes ^[11][23]. In addition, stem cell factor (SCF), peptide endothelin 1 (ET-1), hepatocyte growth factor (HGF), keratinocyte growth factor (KGF), basic fibroblast growth factor (bFGF), and inflammatory mediators such as cytokines, prostaglandin E2 (PGE2), and nitric oxide (NO) significantly regulate melanogenesis ^[24][25]. All these stimuli operate with the activation of several signaling pathways ^[9][26]. Detailed descriptions of the multiple pathways in melanogenesis have been recently reported by others ^{[6][7][9][11]}. Here, the main signaling pathways are briefly summarized (

Several stimuli control melanogenesis, including external factors such as UV rays or environmental pollution [11]. Furthermore, a series of endogenous molecules released by melanocytes, keratinocytes, dermal fibroblasts, and immune cells modulate the process paracrinally and autocrinally. These are mainly the α-melanocyte stimulating hormone (α-MSH) and the adrenocorticotropic hormone (ACTH), derived from the cleavage of pro-opiomelanocortin (POMC), from both melanocytes and keratinocytes [11,24]. In addition, stem cell factor (SCF), peptide endothelin 1 (ET-1), hepatocyte growth factor (HGF), keratinocyte growth factor (KGF), basic fibroblast growth factor (bFGF), and inflammatory mediators such as cytokines, prostaglandin E2 (PGE2), and nitric oxide (NO) significantly regulate melanogenesis [25,26]. All these stimuli operate with the activation of several signaling pathways [9,27]. Detailed descriptions of the multiple pathways in melanogenesis have been recently reported by others [6,7,9,11]. Here, the main signaling pathways are briefly summarized (

Figure 2

).

Figure 2.

 Main signaling pathways involved in melanogenesis regulation. α-melanocyte stimulating hormone (α-MSH) binds to melanocortin 1 receptor (MC1R), which increases cAMP levels, activating PKA and PI3K/AKT pathway. The former phosphorylates CREB protein, promoting 

MITF

 transcription; the latter interplays with Wnt/β-catenin pathway by phosphorylating GSK-3β, which, in turn, releases β-catenin to promote 

MITF

 transcription. Stem cell factor (SCF) binds to c-KIT receptor, activating MAPK pathway and phosphorylating CREB. Peptide endothelin 1 (ET-1) binds to its receptor, ETRB, activating PKC and stimulating 

MITF

 transcription. 

MITF

 is phosphorylated at the post-transcriptional level to promote transcription of the melanogenic enzymes.

In melanocytes, signaling pathways regulating melanogenesis operate through membrane receptors with different molecular activities. These receptors include G protein-coupled receptors (GPCRs) such as the melanocortin-1 receptor (MC1R), which is mainly expressed in melanocytes ^[27], adrenergic receptors, endothelin type B receptor (ETRB), frizzled receptor (FZD), and tyrosine kinase receptors such as tyrosine kinase receptor KIT, bFGF, and HGF receptors ^[7][28]. Most signaling pathways lead to the regulation of microphthalmia-associated transcription factor (

In melanocytes, signaling pathways regulating melanogenesis operate through membrane receptors with different molecular activities. These receptors include G protein-coupled receptors (GPCRs) such as the melanocortin-1 receptor (MC1R), which is mainly expressed in melanocytes [28], adrenergic receptors, endothelin type B receptor (ETRB), frizzled receptor (FZD), and tyrosine kinase receptors such as tyrosine kinase receptor KIT, bFGF, and HGF receptors [7,29]. Most signaling pathways lead to the regulation of microphthalmia-associated transcription factor (

MITF

), a basic helix–loop–helix leucine zipper (bHLH-ZIP) transcription factor. 

MITF is the dominant transcription factor in melanogenesis as it controls melanocyte development, survival, and proliferation, as well as the steps involved in melanin synthesis ^[29][30]. 

 is the dominant transcription factor in melanogenesis as it controls melanocyte development, survival, and proliferation, as well as the steps involved in melanin synthesis [30,31]. 

MITF

 induces the transcription of the melanogenic genes, including 

TYR

, 

TYRP-1

, and 

TYRP-2, by binding to the conserved consensus elements of the promoter regions ^[30]. Moreover, 

, by binding to the conserved consensus elements of the promoter regions [31]. Moreover, 

MITF regulates several other genes involved in melanogenesis, including those required to control melanosome maturation, traffic, and distribution to keratinocytes ^[31]. Due to the prominent role of 

 regulates several other genes involved in melanogenesis, including those required to control melanosome maturation, traffic, and distribution to keratinocytes [32]. Due to the prominent role of 

MITF

, regulation of its expression and activity represents a key event in melanogenesis. At the transcriptional level, 

MITF

 expression is regulated by several transcriptional factors that bind the 

MITF promoter, including cyclic adenosine monophosphate (cAMP)-response element binding protein (CREB), paired box family of transcription factor 3 (PAX3), sex determining region Y-box 9 and 10 (Sox9, Sox10), and Wnt/β-catenin pathway effector lymphoid enhancer-binding factor 1 (LEF-1) ^[7][30].

 promoter, including cyclic adenosine monophosphate (cAMP)-response element binding protein (CREB), paired box family of transcription factor 3 (PAX3), sex determining region Y-box 9 and 10 (Sox9, Sox10), and Wnt/β-catenin pathway effector lymphoid enhancer-binding factor 1 (LEF-1) [7,31].

Furthermore, 

MITF activity is regulated at the post-transcriptional level mainly by phosphorylation ^[32]. 

 activity is regulated at the post-transcriptional level mainly by phosphorylation [33]. 

MITF may be phosphorylated by several kinases such as MAPK, p38, ribosomal S6 kinase (RSK), and GSK3β ^{[7][11][33][34]}. 

 may be phosphorylated by several kinases such as MAPK, p38, ribosomal S6 kinase (RSK), and GSK3β [7,11,34,35]. 

MITF phosphorylation can favor the recruitment of transcriptional coactivator CBP/P300 of CREB, thus increasing the transcription of TYR, TYRP-1, and TYRP-2 melanogenic enzymes ^[30]. The MAPK signaling pathway can be activated by several extracellular factors, which operate through tyrosine kinase receptors including SCF, a relevant signal produced by keratinocytes and fibroblasts, and HGF and bFGF, mainly produced by keratinocytes ^[35]. Notably, melanogenesis-related signaling pathways may be positively or negatively modulated by several inflammatory factors that finally regulate skin pigmentation. This regulation is very complex as some molecules have a stimulatory effect on melanogenesis, while others show inhibitory effects. In addition, the production of these inflammatory mediators depends on the communication between several epidermal and dermal cells, as well as specific stimuli inducing inflammation ^[6].

 phosphorylation can favor the recruitment of transcriptional coactivator CBP/P300 of CREB, thus increasing the transcription of TYR, TYRP-1, and TYRP-2 melanogenic enzymes [31]. The MAPK signaling pathway can be activated by several extracellular factors, which operate through tyrosine kinase receptors including SCF, a relevant signal produced by keratinocytes and fibroblasts, and HGF and bFGF, mainly produced by keratinocytes [36]. Notably, melanogenesis-related signaling pathways may be positively or negatively modulated by several inflammatory factors that finally regulate skin pigmentation. This regulation is very complex as some molecules have a stimulatory effect on melanogenesis, while others show inhibitory effects. In addition, the production of these inflammatory mediators depends on the communication between several epidermal and dermal cells, as well as specific stimuli inducing inflammation [6].

As mentioned above, UV rays represent external stimuli with significant effects on melanogenic signaling pathways, resulting in increased melanin production. Several cellular and molecular processes are involved in the UV–skin reaction. Indeed, UV irradiation induces 

MITF expression and consequently melanogenic gene expression ^[3][30]. Acquired knowledge shows that UV irradiation influences different skin cell types, including melanocytes, keratinocytes, and dermal fibroblasts. UV-induced melanogenesis has been associated with the release of several molecules, including α-MSH, ACTH, SCF, and ET-1, which regulate the signaling pathways described above ^{[24][35][36][37]}.

 expression and consequently melanogenic gene expression [3,31]. Acquired knowledge shows that UV irradiation influences different skin cell types, including melanocytes, keratinocytes, and dermal fibroblasts. UV-induced melanogenesis has been associated with the release of several molecules, including α-MSH, ACTH, SCF, and ET-1, which regulate the signaling pathways described above [25,36,37,38].

4. miRNA Activities and Identification

MicroRNAs (miRNAs) represent a class of non-coding RNAs of approximately 21–23 nucleotides in length. Since their discovery in 1993 ^[38], miRNAs have been largely studied as essential regulators of gene expression. miRNAs are highly conserved among species and are found in different cell types and organisms, including plants, animals, and viruses ^[39][40]. It is now estimated that miRNAs target approximately 60% of genes in 

MicroRNAs (miRNAs) represent a class of non-coding RNAs of approximately 21–23 nucleotides in length. Since their discovery in 1993 [39], miRNAs have been largely studied as essential regulators of gene expression. miRNAs are highly conserved among species and are found in different cell types and organisms, including plants, animals, and viruses [40,41]. It is now estimated that miRNAs target approximately 60% of genes in 

humans and other mammals ^[41]. Due to their role in mRNA expression regulation, miRNAs are involved in all cellular activities, including proliferation, differentiation, migration, apoptosis, and immune responses, both in normal and pathological conditions ^{[42][43][44][45]}. Several mechanisms ensure high stability in miRNAs. Since they can be easily detected in almost all bodily fluids, miRNAs are now considered important biological markers and potential therapeutic molecules ^[46]. Inside cells, miRNAs derive from long precursor transcripts which give rise to mature miRNAs through a multi-step process and are then incorporated into an RNA–protein complex known as the RNA-Induced Silencing Complex (RISC) ^[47]. miRNA activity mainly induces gene expression reduction by binding to sequences in the 3′ untranslated region (3′-UTR) of target genes. This can lead to mRNA target degradation, or inhibition of translation and reduction in protein levels ^[44]. However, miRNA activities show higher complexity as each miRNA can target different genes and several miRNAs can regulate the same gene’s expression. Moreover, the strict interplay between long non-coding RNAs (lncRNAs) and miRNAs contributes to gene expression regulation ^[39][44][48].

 and other mammals [42]. Due to their role in mRNA expression regulation, miRNAs are involved in all cellular activities, including proliferation, differentiation, migration, apoptosis, and immune responses, both in normal and pathological conditions [43,44,45,46]. Several mechanisms ensure high stability in miRNAs. Since they can be easily detected in almost all bodily fluids, miRNAs are now considered important biological markers and potential therapeutic molecules [47]. Inside cells, miRNAs derive from long precursor transcripts which give rise to mature miRNAs through a multi-step process and are then incorporated into an RNA–protein complex known as the RNA-Induced Silencing Complex (RISC) [48]. miRNA activity mainly induces gene expression reduction by binding to sequences in the 3′ untranslated region (3′-UTR) of target genes. This can lead to mRNA target degradation, or inhibition of translation and reduction in protein levels [45]. However, miRNA activities show higher complexity as each miRNA can target different genes and several miRNAs can regulate the same gene’s expression. Moreover, the strict interplay between long non-coding RNAs (lncRNAs) and miRNAs contributes to gene expression regulation [40,45,49].

In general, from a methodological point of view, investigations into miRNA functions and roles in a selected process include a preliminary phase of miRNA identification using high-throughput methods such as microarray, followed by target gene identification with a bioinformatics approach. Finally, target genes need to be validated by 3′-UTR reporter assays and analysis conducted on induced cellular effects following transfection experiments with miRNA mimics and antagomiRs ^[49]. miRNAs are involved in skin development and functions both in normal and pathological conditions ^[50]. Furthermore, increasing evidence shows that selected miRNAs regulate specific events occurring in the skin, such as melanogenesis, as detailed below ^[51][52].

In general, from a methodological point of view, investigations into miRNA functions and roles in a selected process include a preliminary phase of miRNA identification using high-throughput methods such as microarray, followed by target gene identification with a bioinformatics approach. Finally, target genes need to be validated by 3′-UTR reporter assays and analysis conducted on induced cellular effects following transfection experiments with miRNA mimics and antagomiRs [50]. miRNAs are involved in skin development and functions both in normal and pathological conditions [16]. Furthermore, increasing evidence shows that selected miRNAs regulate specific events occurring in the skin, such as melanogenesis, as detailed below [51,52].

4.1. miRNA Regulating MITF

Due to the key role of 

MITF

 as an essential regulator of the melanogenic process, several studies have investigated miRNAs with potential effects on 

MITF expression and consequent regulation of mRNA levels in melanogenic enzymes ^{[3][29][30][53]} (

 expression and consequent regulation of mRNA levels in melanogenic enzymes [3,30,31,53] (

Table 1

). Some preliminary studies concerning melanogenesis regulation by miRNAs have been performed in fiber-producing animals, such as 

alpaca

, due to the contribution of melanin synthesis to coat color and the specific interest of 

alpaca

 breeders in animal color coat modulation. Differences in miRNA profiles from 

alpaca skins with different colored coats were identified and most differentially expressed miRNAs showed predicted targets involved in pigmentation ^[54][55]. These results led to further investigation concerning the functional role of selected miRNAs. Data obtained by Zhu Z et al. (2010) demonstrated the functional role of miR-25 in reducing 

 skins with different colored coats were identified and most differentially expressed miRNAs showed predicted targets involved in pigmentation [54,55]. These results led to further investigation concerning the functional role of selected miRNAs. Data obtained by Zhu Z et al. (2010) demonstrated the functional role of miR-25 in reducing 

MITF

 mRNA and protein, 

TYR

, and 

TYRP-1

 expression in cultured melanocytes. In addition, an inverse relationship was observed between miR-25 level and coat color. Similarly, in 

alpaca

 melanocytes, miR508-3p also directly targets 

MITF

, binding to the 3′-UTR of the gene. miR508-3p overexpression downregulated 

MITF

 expression, resulting in a decrease in TYR, TYRP-2, and melanin production [56]. Interestingly, in 2012, Dong C. et al. investigated the role of miR-137, another miR-targeting 

MITF

, in a transgenic mice model [57]. Initially investigating melanoma cells lines, where its overexpression downregulated 

MITF

 [58], it was found that miR-137 also decreased the expression of the MITF protein and its downstream genes in transgenic mice. Notably, miR-137 had an impact on coat color, demonstrating that modulating a specific miR may significantly regulate melanogenesis, at least in animal models [57].

Table 1.

 microRNAs regulating MITF in melanogenesis.

miRNA	Cell Model	Target Gene	Effect on Melanogenesis	Ref.

miR-25	Alpaca melanocytes	MITF	Negative	[56]
miR508-3p	Alpaca melanocytes	MITF	Negative	[56]
miR-137	Alpaca melanocytes	MITF	Negative	[58]
miR-675	Melanocytes of melasma patients, keratinocytes of melasma	MITF	Negative	[5][59][60][5,59,60]
miR-218

 [64], has been also investigated in immortalized 

human

 epidermal melanocytes (Pig-1), where it downregulates 

MITF

 expression and melanin synthesis [63]. Recently, miR-141-3p and miR-200a-3p have been identified as 

MITF

 regulators [52]. In this study, comparing miRNA expression profiles in B16-4A5 

mouse

 melanoma cells which were treated or untreated with α-MSH led to 13 miRNAs being identified as differentially expressed through miRNA array analysis. miR-141-3p, miR-200a-3p, and miR-148a-3p, which target 

MITF

, were downregulated in α-MSH-stimulated cells when compared to untreated cells. Furthermore, miR-141-3p and miR-200a-3p overexpression suppressed 

MITF

 expression and 

TYR

 activity in B16-4A5 cells. Notably, the inhibitory effect on melanin synthesis was confirmed in a three-dimensional tissue culture model of the 

human

 epidermis (3D-MHE model) [52].

4.2. miRNAs Regulating Other Genes in Melanogenesis

Besides the abovementioned studied group of miRNAs, with significant regulatory roles in 

MITF

, other miRNAs are involved in melanogenesis by regulating the expression of other molecular targets, including melanogenic enzymes, transcription factors, or components of the signaling pathways which regulate melanogenesis (

Table 2

).

Several miRNAs, including miR-450b-5p, miR-1208, miR-326, miR-434-5p, miR330-5p, miR-125, miR-145, and miR-203, have been predicted as targeting 

TYR

 and most also target other genes, including 

MITF ^[65][66].

 [65,66].

Table 2.

 Other microRNAs involved in melanogenesis.

miRNA	Cell Model	Target Gene	Effect on Melanogenesis	Ref.

miR-434-5p	Mouse skin, human skin cell cultures	TYR	Negative	[65]
miR-330-5p	Melanoma cells, normal human melanocytes	TYR	Negative	[56][67][56,67]
miR-203	Keratinocytes exposed to UV	Kinesin Superfamily Protein 5b	Positive	[67]
miR-3196	Keratinocytes exposed to UV	Unknown target gene	Positive	[67]
Melan-a murine melanocytes,	human skin OTC	MITF	Negative	[61]
miR-21a-5p	Human melanocytes	SOX5	Positive	[68]	miR-183	B16 melanoma cells	MITF	Negative	[62]
miR-340	Human epidermal melanocytes (Pig-I)	MITF	Negative	[63][64][63,64]
miR-200a-3p	B16-4A5 melanoma cells	MITF	Negative	[52]
miR-148a-3p	B16-4A5 melanoma cells	MITF	Negative	[52]
miR-141-3p	B16-4A5 melanoma cells	MITF	Negative	[52]

Other studies have identified miRNAs regulating skin pigmentation in 

human

 melanocytes. Particular interest has been shown in miR-675, another miR which targets 

MITF and was to be found expressed at low levels in the hyperpigmented skin of melasma patients. In melanocytes or keratinocytes derived from melasma patients, miR-675 upregulation decreased TYRP-1 and TYRP-2 expression, whereas its knockdown increased their expression. Interestingly, miR-675 was also identified in exosomes released from keratinocytes into the extracellular environment ^[5][59][60]. Another miR involved in melanogenesis by binding the 3′-UTR in 

 and was to be found expressed at low levels in the hyperpigmented skin of melasma patients. In melanocytes or keratinocytes derived from melasma patients, miR-675 upregulation decreased TYRP-1 and TYRP-2 expression, whereas its knockdown increased their expression. Interestingly, miR-675 was also identified in exosomes released from keratinocytes into the extracellular environment [5,59,60]. Another miR involved in melanogenesis by binding the 3′-UTR in 

MITF

 is miR-218, which downregulated TYR, TYRP-1, and DCT mRNA and protein levels, reducing melanin content in immortalized melan-a murine melanocytes. In agreement with these data, miR-218 also suppressed melanogenesis in 

human

 pigmented skin organotypic culture (OTC) through 

MITF

 repression. Anti-miR-218 was also found to promote melanogenesis in 

human

 primary melanocytes [61].

Recently, other miRNAs, including miRNA-183 cluster, miR-340, miR-141-3p, and miR-200a-3p, have been investigated for their role in regulating 

MITF

 expression and melanogenesis [62]. Results of this research show that the miRNA-183 cluster targets the 3′-UTR of 

MITF

 in B16 

mouse

 melanoma cells. miRNA-183 cluster overexpression decreased 

MITF

, 

TYR

, 

TYRP-1

, and 

DCT

 expression and melanin production. Conversely, knockdown of the miRNA-183 cluster increased 

MITF

, 

TYR

, 

TYRP-1

, and DCT expression and, consequently, melanin levels. The miR-183 cluster was also involved in regulating the MEK/ERK signaling pathway implicated in cell proliferation and migration, by modulating mitogen-activated protein kinase 1 (MEK1), extracellular regulated protein kinases1/2 (ERK1/2), and CREB expression [62]. miR-340, which was first identified in melanoma cell lines for its ability to bind specifically to the 3′-UTR of 

MITF

miR-145
Murine melan-a melanocytes
Myo5a	Negative	[	56	]
miR-380-3p	Alpaca melanocytes	SOX6	Negative	[56]
miR-200c	Normal human epidermal keratinocytes (NHEK)	SOX1	Positive	[69]
miR-27a-3p	Alpaca and Mouse melanocytes	Wnt3a	Negative	[54][70][54,70]
miR-379	Alpaca melanocytes	IGF1R	Negative	[71]
miR-143-5p	Human melanocytes	Myo5a	Negative	[72]
miR-143-5p	Alpaca melanocytes	TAK1	Negative	[73]
miR-125b	WM266-4 human melanoma cells, MNT1 human melanoma cells	SH3BP4	Negative	[60]

Wu et al. used a miR-434-5p homologue to target 

TYR

 in cells cultured in vitro as well as in an animal model and showed efficient melanin synthesis reduction. Similarly, miR-330-5p downregulated 

TYR

 in melanoma cells and normal melanocytes, inducing depigmentation without affecting cell proliferation [66]. This miR has been also identified in exosomes derived from keratinocytes [56]. In this study, exosomes carrying miR-330-5p caused a decrease in melanin production and 

TYR

 expression in melanocytes. Similarly, miR-330-5p overexpression in melanocytes confirmed its inhibitory activity on melanogenesis. Several other miRNAs, such as miR-203, which targets 

Kinesin Superfamily Protein 5b

, involved in melanosome transfer, and miR-3196, with unknown target genes, have been identified in 

human

-derived exosomes from keratinocytes and have shown an ability to increase melanin content in melanocytes [67]. Indeed, exosomes released by Black keratinocytes, as well as Caucasian UV-irradiated keratinocytes, were able to induce increased TYR activity and melanogenic gene expression in melanocytes, at least partly as a result of miR content.

As reported above, several miRNAs which directly target 

MITF

 are involved in melanogenesis. Conversely, 

MITF

 expression may be subject to more complex regulation. For example, it has been shown that miR-21a-5p overexpression downregulated the 

SOX5

 target, as well as β-catenin and CDK2 protein expression, in normal 

human

 melanocytes. In agreement with 

SOX5

 involvement in melanogenesis, its downregulation induced an increase in 

MITF and melanogenic enzymes’ expression, with consequent stimulation of melanogenesis ^[68]. Several other miRNAs have been identified as regulators of SOX transcription factors ^[56][69][74]. miR-145, which was initially identified as a miR regulated by UV treatment and forskolin in murine melan-a melanocytes, significantly modulates several genes involved in pigmentation. miR-145 overexpression or downregulation reduced or increased the expression of several genes involved in melanin biosynthesis, such as 

 and melanogenic enzymes’ expression, with consequent stimulation of melanogenesis [68]. Several other miRNAs have been identified as regulators of SOX transcription factors [56,69,74]. miR-145, which was initially identified as a miR regulated by UV treatment and forskolin in murine melan-a melanocytes, significantly modulates several genes involved in pigmentation. miR-145 overexpression or downregulation reduced or increased the expression of several genes involved in melanin biosynthesis, such as 

SOX9

, 

MITF

, 

TYR

, and 

TYRP-1 ^[74][75], and in melanosome transfer, such as 

 [74,75], and in melanosome transfer, such as 

Myosin Va

 (

Myo5a

), 

Rab27a

, and 

fascin1

 (

Fscn1

), respectively [76]. Notably, miR-145 targeted the 3′-UTR binding site of 

Myo5a

, a molecular motor involved in the intracellular trafficking of vesicles and organelles. A further miR that binds an SOX family component is miR-380-3p, which targets 

SOX6

 by binding to the 3′-UTR region. In 

alpaca

 melanocytes, miR-380-3p overexpression downregulated 

SOX6

 and increased β-catenin. Differently from studies indicating that β-catenin induces 

MITF

 transcription, in this study, miR-380-3p overexpression caused decreased mRNA levels of melanin-related genes including 

MITF

, 

TYR

, 

TYRP-1

, and 

DCT

, suggesting other 

SOX6

 activities in 

MITF

 regulation [56].

Recently, miR-200c has been identified as a 

SOX1

 regulator. Specifically, miR-200c induced 

SOX1

 downregulation by direct binding to the 

SOX1

 3′-UTR, leading to intranuclear β-catenin upregulation and increased expression of 

MITF

-dependent gene expression as well as melanogenesis. These effects were induced in normal 

human

 epidermal melanocytes (NHEM) treated with exosomes containing miR-200c, produced by normal 

human

 epidermal keratinocytes (NHEK). Notably, miR-200c was found at low levels in exosomes derived from keratinocytes in vitiligo lesions compared to exosomes from NHEK, with a consequent inhibition in melanin production [69]. Some miRNAs have also been involved in modulating the extracellular ligands which regulate melanogenic signaling pathways. An example is miR-27a-3p, which directly targets 

Wnt3a

, a component of the Wnt signaling pathway. miR-27a-3p was found to be expressed at higher levels in 

alpaca

 white skin compared to brown skin [54] and was similarly related to skin color in mice [70]. Furthermore, its functional role in downregulating 

Wnt3a

, and thus inhibiting β-catenin and melanogenesis, was confirmed in 

mouse

 melanocytes transfected with miR-27a-3p [70]. In addition, miR-379 was shown to modulate 

insulin-like growth factor receptor I

 (

IGFR1

) in 

alpaca

 melanocytes. Insulin-like growth factor 1 (IGF1), mainly produced in dermal cells, has been shown to improve melanogenesis through the cAMP pathway. Likewise, miR-379 overexpression reduced melanogenesis by inhibiting the cAMP response element (CRE)-binding protein (CREB)/(

MITF

) pathway in 

alpaca

 melanocytes [71].

Finally, miRNAs involved in the regulation of melanosome processing and transfer have been also identified. Among them, miR-143-5p targets 

Myo5a

, which belongs to the complex 

Rab27a/MLPH/Myo5a

 that connects melanosomes to the actin cytoskeleton in 

human

 melanocytes [72]. In a more recent study, Qi S. et al. inhibited miR-143-5p expression using Short Tandem Target Mimics (STTMs) in order to evaluate the functional role of miR-143-5p. As a consequence, increased melanogenic gene expression, including 

MITF

, TYR, and TYRP-1, MLPH, and Rab27, and melanin production were observed [77]. This result indicates the effective possibility of modulating melanin biosynthesis by a miRNA-regulating approach. In addition, miR-143-5p overexpression induces a decrease in 

TGF-β-activated kinase 1

 (

TAK1

) expression with consequent effects on melanocyte migration and proliferation and 

MITF

 downregulation in 

alpaca

 melanocytes. Therefore, miR-143-5p may regulate melanogenesis by modulating different gene targets [73]. By means of a bioinformatic approach, followed by experimental validation, miR-125b has also been shown to directly target 

SRC homology 3 domain-binding protein 4

 (

SH3BP4

), a gene regulated by 

MITF

, which may act by controlling melanogenic enzymes’ distribution to melanosomes or the mTOR signaling pathway. Indeed, when miR-125b was overexpressed in WM266-4 and MNT1 

human

 melanoma cells, decreased levels of the melanogenic enzymes TYR and DCT were observed, although these genes are not direct miR-125b targets [78].

4.3. miRNA Regulated by UV Rays

UV rays can modify intracellular functions in different ways: by directly or indirectly damaging DNA through reactive oxygen species (ROS), inducing apoptosis, cell cycle arrest, and carcinogenesis. The expression profiles of the miRNAs involved in these events are modified by UV irradiation ^[79][80][81]. Among the UV-induced effects, it is well known that there is a correlation between UVB irradiation and melanogenesis stimulation ^[1]. miRNA profiling in irradiated 

UV rays can modify intracellular functions in different ways: by directly or indirectly damaging DNA through reactive oxygen species (ROS), inducing apoptosis, cell cycle arrest, and carcinogenesis. The expression profiles of the miRNAs involved in these events are modified by UV irradiation [79,80,81]. Among the UV-induced effects, it is well known that there is a correlation between UVB irradiation and melanogenesis stimulation [1]. miRNA profiling in irradiated 

mouse melanocytes has been helpful in identifying miRNAs involved in melanogenesis, such as miR-145 ^[74]. Furthermore, several miRNAs targeting different pigmentation genes have been involved in UV ray effects, including miR-145, miR-137, miR-148, and miR-25 ^[57][82][83].

 melanocytes has been helpful in identifying miRNAs involved in melanogenesis, such as miR-145 [74]. Furthermore, several miRNAs targeting different pigmentation genes have been involved in UV ray effects, including miR-145, miR-137, miR-148, and miR-25 [57,82,83].

miR-340 upregulation was identified in pigmented cells treated with UVB irradiation among miRNAs related to UV irradiation. Studies have shown that miR-340 significantly represses RhoA protein expression and stimulates melanosome transport [81]. Recently, the functional role of miR-340 has been further investigated in immortalized 

human

 epidermal melanocytes (Pig-1), confirming that its expression is modulated by UV and that it downregulates 

MITF

 expression and melanin synthesis. Notably, miR-340 mimics decreased melanin content in irradiated cells [63]. A further example of a miR potentially being involved in UV-induced pigmentation modulation is miR-21. The latter has been largely investigated in melanoma and shown to be increased by UV radiation in melanocytes, keratinocytes, and fibroblasts [84]. In 

mouse

 skin melanocytes, miR-21 has been shown to enhance 

MITF

 expression by targeting 

SOX5

 [85]. Inversely, miR-21a-5p has been observed with different levels of activity in UV-irradiated A375.S2 

human

 melanoma and B16F10 melanoma 

mouse cells. Indeed, in these UV-treated cells, increased melanin content was associated with an increase in α-MSH expression and reduced EGFR and Akt phosphorylation. miR-21 overexpression negatively modulated these UV-induced effects ^[86]. Interestingly, this miR has been also involved in communication between melanocytes and keratinocytes. Extracellular vesicles derived from UVA-exposed melanocytes modified keratinocyte behavior by inducing miR-21 upregulation and TGF-β and IL-6/STAT3 signaling pathway activation ^[87]. UVA and UVB rays also induce changes in miRNA produced by keratinocytes ^[88][89]. Accumulating evidence indicates that exosomes and exosomal miRNAs represent an effective means of communication for melanocytes and keratinocytes ^[56]. Notably, in Caucasian 

 cells. Indeed, in these UV-treated cells, increased melanin content was associated with an increase in α-MSH expression and reduced EGFR and Akt phosphorylation. miR-21 overexpression negatively modulated these UV-induced effects [86]. Interestingly, this miR has been also involved in communication between melanocytes and keratinocytes. Extracellular vesicles derived from UVA-exposed melanocytes modified keratinocyte behavior by inducing miR-21 upregulation and TGF-β and IL-6/STAT3 signaling pathway activation [87]. UVA and UVB rays also induce changes in miRNA produced by keratinocytes [88,89]. Accumulating evidence indicates that exosomes and exosomal miRNAs represent an effective means of communication for melanocytes and keratinocytes [56]. Notably, in Caucasian 

human

 keratinocytes, UV rays induce the release of miR, such as hsa-miR-3196, which may stimulate melanin synthesis in melanocytes [67]. Recently, miR-675 production by 

human

 keratinocytes has been shown and its role as a paracrine regulator of melanogenesis has been confirmed in vitro, indicating increased exosomal miR-675 in cells irradiated with a 585 nm light emitting diode (LED) and its ability to attenuate melanogenesis in melanocytes [90].

4.4. Common miRNAs in Melanogenesis and Melanomagenesis

Several miRNAs regulating melanogenesis play an important role in melanoma [91]. For instance, miR-340, miR-218, and miR-137, which inhibit melanogenesis, have a tumor suppressor role during melanomagenesis by negatively regulating 

MITF expression ^{[58][61][64][92]}. Other miRNAs which regulate melanogenesis, including miR-379, -200c, -203, -200a-3p, -125b, -183, -508-3p, -675, -143-5p, -141-3p, -145, and -330-5p, can act as tumor suppressors in melanomagenesis, although the target genes may differ from those identified in melanogenesis. On the contrary, miR-21a-5p, -25, and -27a-3p have shown an oncogenic role, being upregulated in metastatic melanoma and during tumor progression ^[93][94].

 expression [58,61,64,92]. Other miRNAs which regulate melanogenesis, including miR-379, -200c, -203, -200a-3p, -125b, -183, -508-3p, -675, -143-5p, -141-3p, -145, and -330-5p, can act as tumor suppressors in melanomagenesis, although the target genes may differ from those identified in melanogenesis. On the contrary, miR-21a-5p, -25, and -27a-3p have shown an oncogenic role, being upregulated in metastatic melanoma and during tumor progression [93,94].

Interestingly, some miRNAs involved in both melanogenesis and melanomagenesis, such as miR-21a-3p, -25, -3196, -145, -137, -148, and -675 are induced by UV rays, the main environmental risk factor for melanoma ^{[79][80][81][95]}.

Interestingly, some miRNAs involved in both melanogenesis and melanomagenesis, such as miR-21a-3p, -25, -3196, -145, -137, -148, and -675 are induced by UV rays, the main environmental risk factor for melanoma [79,80,81,95].