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Dermatology Research and Practice
Volume 2011 (2011), Article ID 463184, 9 pages
http://dx.doi.org/10.1155/2011/463184
Review Article

Molecular Nevogenesis

Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL 33136, USA

Received 28 October 2010; Accepted 12 February 2011

Academic Editor: Takashi Hashimoto

Copyright © 2011 Andrew L. Ross et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Despite recent advances, the biology underlying nevogenesis remains unclear. Activating mutations in NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi. Their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively. These mutations are likely to play a critical role in driving nevogenesis. While each mutation is able to activate the MAP kinase pathway, they also interact with a host of different proteins in other pathways. The different melanocytic developmental pathways activated by each mutation cause the cells to migrate, proliferate, and differentiate to different extents within the skin. This causes each mutation to give rise to a characteristic growth pattern. The exact location and differentiation state of the cell of origin for benign moles remains to be discovered. Further research is necessary to fully understand nevus development given that most of the same developmental pathways are also present in melanoma.

1. Introduction

Nevogenesis is a multifactorial process that involves a complex interplay of genetic and environmental factors. Although we are only just beginning to understand this process, it is already clear that certain molecular pathways within nevocytes need to be activated in order for nevogenesis to occur. This paper will focus on the relevant identified pathways that promote the development of the different nevus phenotypes.

2. Nevus Life Cycle

Benign melanocytic lesions follow an archetypal life cycle that consists of four stages: initiation, promotion, senescence, and involution. Initiation occurs when a nevus progenitor cell acquires a mutation that will permit future growth. Promotion occurs when the mutated cell is activated and proliferation begins. This proliferation is likely instigated by a change in local environmental factors that promotes melanocytic growth and then sustained by the previously acquired mutation. After a period of growth, nevi stop proliferating through the activation of senescence pathways. This allows them to remain stable for extended periods of time before undergoing involution.

3. Models for Nevogenesis

Current models of nevogenesis propose that melanocytic neoplasms arise from a single cell of origin [1, 2]. However, the differentiation state of this cell has not been clearly established. It is also uncertain if the progenitor cell is located in the dermis, epidermis, or both.

One possibility is that an immature melanocytic stem cell serves as the nevus progenitor cell. Although this progenitor cell most likely resides in the dermis, its presence in the epidermis can not be excluded. In this model, the immature cell remains in a quiescent state in the skin and acquires mutations secondary to UV light exposure or other mutagenic processes. When environmental signals activate this cell to produce melanocytes, an abnormal proliferation occurs due to the genetic alterations. The specific underlying mutation and local environmental conditions alter the daughter cells’ normal melanocytic differentiation and migratory pathways in a characteristic manner. This causes the nevus to assume a discrete phenotypic pattern.

One of the advantages of this immature progenitor cell model is that the mutated cells can remain quiescent until activated. This readily explains the association of childhood sun exposure with the development of nevi and melanoma later in life. It would also explain the phenomenon of eruptive nevi simultaneously growing in response to a cytokine or an immunoregulatory medication. Consequently, this model seems to fit best with clinical findings.

It has also been suggested that a differentiated melanocyte serves as the cell of origin for melanocytic neoplasms. In this model, the nevogenic mutation occurs in a differentiated melanocyte. The mutation causes the cell to regain proliferative capacity. However, this genetic event would also have to promote dedifferentiation and the development of invasive properties in order to allow the cell to migrate to greater depths in the dermis. In this model, nevus growth would occur immediately after the initial mutagenic event in either a fast or slow manner. This is somewhat more difficult to reconcile with the clinical behavior of nevi.

As previously mentioned, both of these models are based on nevi arising from a single cell of origin. The concept of monoclonal origination is supported by the fact that NRAS and BRAF mutations are almost always mutually exclusive. However, recent studies on BRAF (reviewed below) have documented mutation heterogeneity within nevi. There exist at least two explanations for this phenomenon. First, an unidentified primary mutation that impacts DNA synthesis and repair machinery could make melanocytes more susceptible to developing BRAF mutations. Alternatively, local environmental conditions could lead to the recruitment of cells with different mutations to the lesion (hamartoma). Although a hamartoma can not be excluded, it seems likely that there are unidentified processes occurring within these cells that drive the heterogeneity of BRAF mutations.

4. NRAS and Congenital Nevi

NRAS is one of the three major isoforms of the RAS family of GTPase proteins that are involved in cell growth, differentiation, and survival. NRAS activates four major signaling pathways: (1) RAF-MEK-ERK, (2) RalGDS, (3) PI3K-AKT/PDK1, and (4) PLC/PKC (see Figure 1). Activation of these pathways results in a variety of different outcomes that include cell cycle progression, upregulated transcription, upregulated translation, nuclear transport, and calcium signaling. All reported NRAS gene mutations occur in exon 2 and exon 3 (known before as exon 1 and exon 2). Approximately 65% of the mutations occur at codon 61 in exon 3, where the most frequent amino acids substitutions are Q61K and Q61R [14]. The replacement of the glutamine residue (Q61) with lysine (K) or arginine (R) results in an aberrant protein that is unable to cleave GTP, and thus the protein remains constitutively active. Although NRAS mutations have been reported in other melanocytic nevi, the mutation seems to be most closely associated with congenital melanocytic neoplasms (see Table 1) [11, 1517].

tab1
Table 1: Congenital melanocytic nevi.
463184.fig.001
Figure 1: Relative position of RAS, RAF, and GNAQ in intracellular signaling. Mutations in NRAS, HRAS<BRAF, and GNAQ lead to alterations in transcription factor expression (MIT-F and Brn2 not shown). This in turn drives a number of processes like cell cycle progression. The contribution of the transcription factor Myc to cell cycle progression and its relationship to tumor suppressors are shown downstream of the aforementioned mutations.

In 1994, Carr and Mackie provided the first report documenting the presence of an activating NRAS mutation in 28% (12 of 43) of congenital melanocytic nevi (CMN) [3]. This finding was confirmed by subsequent studies [4, 5]. Following this discovery, BRAF mutations were also reported in CMN with incidences ranging between 39 and 86% [68]. However, it is important to note that all of the aforementioned studies relied solely on histological appearance to classify the lesions as CMN. As such, there was no evidence that these lesions had been present at birth. Thus, many of the specimens likely represented acquired nevi with histological features of congenital nevi. Bauer et al. demonstrated that using nevi with histological features of CMN but no documentation of presence at birth introduces a selection bias that artificially increases the incidence of BRAF mutations in CMN [11]. Reaves et al. addressed this issue by selecting CMN specimens whose presence were documented in medical records at birth. None of the 36 medium and large CMN in this series possessed BRAF mutations [9].

The following year Ichii-Nakato et al. found that 79% (33 of 42) of small CMN and 30% (6 of 20) of medium CMN present at birth by records or parents testimony were BRAF positive [10]. This study demonstrated a statistically significant difference in the BRAF mutation rate between small- and medium- sized CMN. The recent studies that document CMN presence at birth have reported NRAS mutations in 81% (26 of 32) [11] and 70% (19 of 27) [11, 13] of the CMN. BRAF mutations were found in 0% (0 of 32) [11] and 22% (6 of 27) [13] of the nevi. One report noted that 76% (26 of 34) [12] of CMN had BRAF mutations; however, the study contained a disproportionately high number of small CMN.

Overall, NRAS mutations were found to exist in 55% (77 of 141) of the CMN specimens specifically assayed for genetic NRAS abnormalities, making it the most common mutation in CMN. BRAF mutations are also common, occurring in 39.3% (90 of 229) of the CMN specifically assayed for genetic BRAF abnormalities. NRAS mutations clustered in medium and large CMN (66%; 62 of 94 specimens studied) while BRAF mutations clustered more frequently in the small CMN (79%; 53 of 67 specimens documented as <1.5 cm). The latter association may be due to the inclusion of acquired nevi with histological features of congenital nevi and/or a difference in the growth potential between the two genes.

The initiating event that causes the NRAS mutation is not yet known. Nevertheless, it is clear that UV radiation does not play a role in initiation given that the mutation occurs in utero. It is also uncertain which type of cell undergoes initiation, though it likely occurs in a neural crest stem cell. The resultant disregulation of the neural crest stem cell during development then leads to a massive deposition of nevocytes along its native migration pathways to the epidermis. The presence of NRAS mutant cells in the dermis also appears to alter local environmental conditions as evidenced by the presence of longer and darker hair than the surrounding skin. BRAF mutations may also give rise to congenital nevi, though these lesions tend to be smaller. This may be due to the way the mutations function. NRAS mutations favor upregulation of the CRAF isoform of RAF over the BRAF isoform [30]. Although CRAF and BRAF exhibit a significant amount of functional redundancy, they have been shown to possess some unique functions [31]. One important example of this is CRAF’s ability to inhibit apoptosis [32]. Theoretically, inhibition of apoptosis could allow for a greater expansion of melanocytes and thus account for the association of NRAS mutations with larger CMN.

In summary, activating NRAS mutations appear to be most closely associated with the development of congenital melanocytic nevi. This association is accentuated in the larger lesions. BRAF mutations may also be associated with the development of CMN. Lastly, it is likely that there remain other unidentified mutations that contribute to the development of CMN.

5. HRAS and Spitz Nevi

HRAS is another member of the RAS protein family that is involved in signal transduction from the cell surface to the nucleus. Like NRAS, HRAS is able to activate all of the same aforementioned pathways (see Figure 1). HRAS mutations in exon 2 and exon 3 have previously been reported in melanocytic lesions [17, 19]. The most frequently reported mutation involves the replacement of a glutamine at residue 61 (Q61) of exon 3 with a lysine(K) residue [17]. This leads to the production of an aberrant protein that can not be deactivated and thus stimulates cell growth and differentiation.

Genetic anomalies in HRAS occur almost exclusively in Spitz nevi (see Table 2). To date, no studies have been able to demonstrate the presence of genetic HRAS abnormalities in common acquired nevi, congenital nevi, or dysplastic nevi [38, 39]. Bastian et al. first noted HRAS copy number amplifications in 24% (4 of 17) of unequivocally diagnosed Spitz nevi in 1999 using comparative genomic hybridization analysis [18]. A second larger study by Bastian et al. not only demonstrated the presence of increased HRAS copy numbers in 12% (12 of 102) of Spitz nevi but also established the presence of HRAS mutations in 67% (8 of 12) of the Spitz nevi with increased copy numbers [19].

tab2
Table 2: Spitz nevi.

In 2003, while trying to ascertain the specificity of the archetypal V600E BRAF mutation as a marker for melanoma, Yazdi et al. demonstrated the absence of BRAF mutations in the 69 Spitz nevi studied [7]. This finding was confirmed in multiple studies over the next two years [17, 2024]. In the 220 Spitz nevi analyzed in these experiments, not one harbored a BRAF mutation (see Table 2). All but one of the studies [22] utilized microdissection techniques of melanocytes from histological samples to decrease the rate of false negative results. However, only one study went as far to differentiate and include atypical Spitz nevi in the analysis [17].

The following year two papers challenged the notion that Spitz nevi lack BRAF mutations, showing that 21% (10 of 48) [25] and 100% (8 of 8) [26] of the specimens studied were indeed V600E BRAF positive. However, as previously pointed out [27, 29], one study exclusively examined Reed nevi while the other included more atypical inflammatory Spitz nevi that likely represented dysplastic nevi. Consequently, it is possible that variations in histological selection criteria created the variation in V600E BRAF positivity. This underscores the notion that current histological evaluations may not be the optimal method to classify nevi. Despite the flaws with these studies, it is not easy to dismiss their findings given that Da Forno et al. and Emley et al. were able to demonstrate the presence of a V600E BRAF mutation in a total of 7% (3 of 42) of unequivocal Spitz nevi studied [28, 29]. It should also be noted that 4% (4 of 98) of Spitz nevi studied by various groups also harbored a mutation in NRAS [17, 22, 25, 2729].

In the series reviewed, HRAS mutations and gene amplification were noted to be present in 0–24% of Spitz nevi (see Table 2). However, it is likely that the reported incidence of HRAS mutations has been artificially deflated by the inclusion of certain nevi with histological classifications that are similar but likely unrelated to Spitz nevi in the literature. For example, when all of the specimens studied in Table 2 are considered, 49% (24 of 49) of genetic abnormalities identified occurred in HRAS. However, when spindle cell nevi of Reed are excluded from the specimens considered in Table 2, HRAS-associated anomalies are found to comprise 67% (24 of 36) of the genetic abnormalities identified.

The initiating events that lead to the development of HRAS mutations are unknown. It is also unknown if the progenitor cell that sustains the mutation resides in the dermis or the epidermis, though it most likely resides in the dermis. Despite our lack of knowledge regarding HRAS initiation, it is clear that this mutation is associated with a specific nevus phenotype. This is likely related to the fact that HRAS has a significantly higher affinity for the PI3K-PKB/AKT pathway when compared to other RAS isoforms [41]. It would follow that preferential PI3K-PKB/AKT activation through HRAS drives the symmetrical overgrowth of cells with an epitheliod morphology without marked activation of the melanizing pathways (since the majority Spitz nevi are largely amelanotic).

In summary, approximately 13% (24 out of 180) of unequivocal Spitz nevi studied have been shown to possess genetic HRAS anomalies. Although the majority of genetic abnormalities found in Spitz nevi involve HRAS, it is still only present in small fraction of the lesions studied. Consequently, it appears that HRAS is not the lone driving force responsible for the gross and microscopic characteristics of Spitz nevi. It is possible that unidentified mutations in other proteins such as those present in the PI3K-PKB/AKT pathway are responsible for the majority of Spitz nevi.

6. BRAF and Melanocytic Neoplasms

BRAF is a serine-threonine kinase that is activated by the RAS family of proteins. Once activated, it triggers the BRAF-MAP-ERK signaling cascade that results in the upregulation of proteins that lead to cell cycle progression, transcription, and differentiation. This in turn promotes cell growth. Although over thirty BRAF mutations are known to exist, V600E is by far the most common variant found in melanocytic neoplasms [42, 43]. In the BRAF V600E mutation, a thymine at nucleotide 1799 on exon 15 is converted into adenine, causing glutamic acid to replace valine at residue 600. While BRAF V600E mutations have been described in congenital nevi [13], Spitz nevi [17], and blue nevi [22], they have been reported to occur with greatest frequency in acquired nevi (see Table 3) [12].

tab3
Table 3: Acquired nevi.

BRAF mutations were first described in 81% (57 of 70) of acquired nevi studied by Pollock et al. in 2003 [6]. Since this initial report, hundreds of acquired nevi have been analyzed for the presence of this mutation. Overall, almost 79% (376 of 479) of the acquired nevi studied were found to possess a mutation in BRAF. Unfortunately, not all of the papers went on to subdivide the acquired nevi into their histological subtypes (junctional, dermal, compound, etc.). When the available data is compiled from the studies in Table 3, 53% (19 of 36) of compound nevi [6, 37], 66% (2 of 3) of junctional nevi [6, 37], 65% (17 of 26) of dysplastic/atypical nevi [6, 35], and 83% (40 of 48) of intradermal nevi [6, 37] were found to possess BRAF mutations. No valid conclusions can be made with regards to the relative prevalence of BRAF mutations presented in each subtype due to selection bias induced by the exclusion of studies that did not publish histological subtype. Of note, NRAS mutations were described in 4.6% (5 of 108) of acquired nevi specifically assayed for the mutation [22, 33, 34, 37]. Less than 1% (1 of 108) of the nevi studied in these series were found to possess both BRAF and NRAS mutations [22, 33, 34, 37]. This is consistent with the notion that BRAF and NRAS mutations are almost always mutually exclusive.

The initiating events that lead to the acquisition of the BRAF V600E mutation are not known. Despite this, there is compelling evidence that the incidence of BRAF V600E mutations is not associated with the cumulative dose of UV exposure. Supporting evidence includes (1) studies that have shown that BRAF mutations occur more frequently in areas of intermittent sun exposure than areas of chronic sun exposure [34, 44]; (2) the fact that the V600E mutant lacks a classic UV signature [42]; and (3) reports that have characterized V600E mutations in CMN that developed in utero [12]. Nevertheless, these observations do not preclude UV exposure from contributing to the development of the V600E mutation. This is supported by the fact that BRAF mutations have been associated with UV exposure at a young age [45].

Thomas et al. have proposed an alternative mechanism for UV-induced BRAF mutations. It involves UVA radiation generating reactive oxygen species (ROS) that lead to the formation of cyclobutane pyrimidine dimers adjacent to nucleotide 1799. When replicative polymerase delta gets stuck at the adjacent cyclobutane pyrimidine dimer, error-prone polymerase eta assumes polymerase delta’s replicative duties. This in turn would result in the commonly found T1799A substitution [45]. If this hypothesis is true, then the generation of ROS through any mechanism should produce BRAF V600E mutations. It is thus interesting to note an association between certain melanocortin-1 receptor (MC1R) polymorphisms and the incidence of BRAF V600E mutations [46]. This is because certain MC1R polymorphisms lead to increased pheomelanin production [47, 48], and pheomelanin is known to trigger ROS production [49].

It would be convenient to ascribe the molecular nevogenesis of acquired nevi to a single clonal population that developed from an oncogenic BRAF V600E-mutation in a single precursor cell. Unfortunately, current evidence argues against this. It has been shown that the percentage of total mutant alleles in BRAF V600E positive nevi varies from 5 and 40% [37]. This is much less than the 50% value that would be seen in a population of cells derived from a single heterozygous clone. Additionally, Lin et al. demonstrated that BRAF V600E mutations within single nevi were often heterozygous for a nearby single nucleotide polymorphism [50]. This suggests that the mutation must have occurred at least twice, once on each sister chromosome. Taken together, the data indicates that BRAF mutations do not represent an initiating event of nevogenesis. Instead, it is more likely that the mutation develops as part of a secondary process and may drive the promotion stage of nevogenesis. The presence of polyclonal BRAF V600E mutations also favors the supposition that an error-prone polymerase may be responsible for inserting an adenosine at nucelotide 1799 when it is invoked by oxidative stress. It is also possible that a different initiating mutation will be identified that creates a pro-BRAF V600E mutagenic environment in the acquired nevi. This would allow for a single clonal population especially prone to V600E mutations to be responsible for nevogenesis.

In summary, approximately 79% (376 of 479) of acquired nevi harbor BRAF mutations. The polyclonal nature of these BRAF mutations suggests that they represent a secondary event driving the promotion phase of nevogenesis. As such, the underlying initiating events that drive nevogenesis in acquired nevi remain to be identified.

7. GNAQ and Blue Nevi

GNAQ encodes an alpha subunit of the heterotrimeric G-protein responsible for transducing signals between G-protein couples receptors (GPCRS) and their downstream effectors. These effectors include but are not limited to the PLC/PKC and RAF-MEK-ERK pathways that also sit downstream of RAS [51]. GNAQ mutations almost exclusively involve the replacement of a glutamine residue at codon 209 of exon 5 by either leucine (51%) or proline (47%) residues [40, 5254]. The affected residue is present in the ras-like domain of GNAQ and corresponds to the Q61 mutation found in NRAS and HRAS [40].

Few investigators have studied the genetic profiles of blue nevi. Combined data from these studies indicates that GNAQ is by far the most common genetic anomaly (82.8%); BRAF V600E mutations are rare (6.7%); NRAS mutations have not been have not yet been identified (see Table 4) [7, 22, 40]. Van Raamsdonk et al. have also reported one GNAQ mutation in seventeen nevi of Ota studied [40]. No studies have identified the presence of GNAQ mutations in other benign melanocytic tumors [39].

tab4
Table 4: Blue nevi.

The initiating events that lead to the acquisition of GNAQ mutations are unknown. Although this mutation does not bear a classic UV signature, oxidative stress, possibly from UVA exposure, could play a role. The GNAQ mutation most likely occurs in a dermal melanocytic precursor as no epidermal component is present in the majority of lesions. This is consistent with what is known to occur in mice where the GNAQ mutation has been shown to lead to the accumulation of dermal melanin [51].

8. Conclusion

All of the previously discussed activating mutations occur in proteins that are components of complex cellular transduction pathways that exhibit a fair amount of overlap and redundancy (see Figure 1). As a result, NRAS, HRAS, BRAF, and GNAQ are all able to alter expression patterns of multiple transcription factors like Jun, Fos, Myc, NFκB, Brn2, and MITF. These transcription factors in turn drive proliferation, differentiation, and senescence [5557]. Despite the fact that NRAS, HRAS, BRAF, and GNAQ are involved in convergent pathways, mutations in these genes result in different cellular effects. This can be attributed to the various positions of each gene product in the pathways and different specificities for downstream effector molecules [41, 58]. This in turn results in each specific mutation generating its own characteristic growth pattern. The growth patterns may be further influenced by the location and the developmental stage of the cell of origin.

The role of each of these mutations in nevus initiation and promotion has yet to be fully elucidated. It is likely that the acquisition of NRAS, HRAS, and GNAQ mutations represents the initiating event that primes a nevus progenitor cell to respond abnormally to normal melanocyte recruitment signals. Mutations in BRAF are more likely to represent secondary events in nevogenesis given their polyclonal nature. As such, BRAF mutations probably play a major role in acquired nevus growth promotion.

NRAS, HRAS, and BRAF are all components of the mitogenic RAS-RAF-MEK-ERK pathway known to promote cellular proliferation [55]. GNAQ is also able to upregulate the RAF-MEK-ERK pathway via PKC [52]. Consequently, mutations in all of the respective gene products have the potential to promote melanocytic proliferation. However, it is also possible these mutations function to sustain growth promotion once another, earlier event, such as a change in extracellular signaling, induces the recruitment of the mutated melanocyte.

All of these mutations have also been described in melanoma. The discriminating feature that distinguishes these benign nevi from melanoma is the induction of senescence pathways that signal growth arrests. This terminates the promotion phase and prevents indefinite proliferation.

In conclusion, NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi, and their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively, (Table 5). In the future, dermoscopy and other noninvasive invivo imaging technologies may allow us to better predict which lesions harbor a specific mutation. There is still much to be learned about how these mutations occur, as well as the developmental stage and location of the progenitor cell. Since these mutations can also be found in melanoma, a further understanding of nevogenesis will have a direct impact on melanoma research efforts.

tab5
Table 5: Summary of common mutations found in congenital, spitz, acquired, and blue nevi.

Disclosures

Dr. Grichnik is a major share holder of DigitalDerm Inc., consults and has received past grants from Spectral Image Inc., is a consultant for Genentech, and is the skINsight section editor for the Archives of Dermatology. The other authors have no disclosures.

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