Immunoexpression of Macroh2a in Uveal Melanoma

Abstract

MacroH2A is a histone variant whose expression has been studied in several neoplasms, including cutaneous melanomas (CMs). In the literature, it has been demonstrated that macroH2A.1 levels gradually decrease during CM progression, and a high expression of macroH2A.1 in CM cells relates to a better prognosis. Although both uveal and cutaneous melanomas arise from melanocytes, uveal melanoma (UM) is biologically and genetically distinct from the more common cutaneous melanoma. Metastasis to the liver is a frequent occurrence in UM, and about 40%–50% of patients die of metastatic disease, even with early diagnosis, proper treatment, and close follow-up. We wanted to investigate macroH2A.1 immunohistochemical expression in UM. Our results demonstrated that mH2A.1 expression was higher in metastatic UM (21/23, 91.4%), while only 18/32 (56.3%). UMs without metastases showed mH2A.1 staining. These data could suggest a possible prognostic role for mH2A.1 and could form a basis for developing new pharmacological strategies for UM treatment.

1. Introduction

Uveal melanoma (UM) is the most frequent primitive intraocular neoplasm in middle age [1]: it occurs mainly in the choroid and ciliary bodies and less frequently in the iris, and some authors have suggested that these melanomas arise from previous benign nevi [2]. Histologically, three forms of UMs can be identified: (a) the spindle cell variant; (b) the epithelioid cell variant; and (c) the mixed cell variant, showing both epithelioid and spindle cells [3]. The prognosis of UM is poor because about 50% of patients will develop hepatic metastasis even 10–15 years after surgery [4]. Because of the strange behavior of this tumor, researchers have tried to determine what could be the mechanisms underlying the late development of liver metastases. Histone variants are chromatin components that replace replication-coupled histones in a fraction of nucleosomes and confer unique biological functions to chromatin [5]. MacroH2A (mH2A) is a histone variant whose expression has been studied in cutaneous melanomas (CMs). It has been shown that the loss of mH2A isoforms in cutaneous melanomas is correlated with increasing malignant phenotypes: this mechanism would seem to be mediated by the upregulation of CDK8, which inhibits the proliferation of melanoma cells. During CM progression, tumor cells show a low expression of mH2A, and conversely, high levels of mH2A expression correlate with a better prognosis [6,7].

In the present study, we studied the immunohistochemical expression of mH2A.1 in 55 primitive UMs, both with and without metastases, to understand whether expression may be correlated with a greater risk of metastasis in order to identify a marker able to predict the behavior of UM.

2. Materials and Methods

2.1. Patients and Tissue Samples

A retrospective study was performed on 55 primitive choroid and/or ciliary body melanomas after surgical treatment consisting of enucleation in cases not eligible for radiotherapy, such as plaque brachytherapy or proton beam radiotherapy [8], at the Eye Clinic, University of Catania, from October 2009 to October 2017.

No written informed consent was necessary because of the retrospective nature of the study.

The research protocols were conformed to the ethical guidelines of the Declaration of Helsinki.

The patients were 28 males and 27 females at an average age of 67 years (range 29–85). In particular, the patients with metastatic UM were 11 males and 12 females at an average age of 72 years (range 50–85): disease progression caused death in 13 of the 23 patients. The patients with nonmetastatic UM were 17 males and 15 females at an average age of 64 years (range 29–84) (

Table 1. Demographics, tumor parameters, disease-free time, follow-up, and macroH2A expression in primary uveal melanomas (UMs) without metastasis (n = 32).

Sex	Age (years)	Location	Thickness (mm)	Largest Diameter (mm)	Cell Type	Pathological T Stage	DFS (Months)	Follow-Up (Months)	MacroH2A
									IS	ES	IRS
F	29	Ch	14.2	16.2	Mc	pT2a	138	138	3	4	12	H
F	83	Ch/CB	14.84	16.8	Mc	pT2b	123	123	0	0	0	L
F	55	Ch	9.8	13.9	Sc	pT2a	122	122	0	0	0	L
F	30	Ch/CB	12.05	9.2	Sc	pT2b	122	122	2	1	2	L
M	74	Ch/CB	10.04	16.1	Sc	pT2b	121	121	3	4	12	H
M	64	Ch	7.7	11.5	Sc	pT1a	112	112	3	4	12	H
F	36	Ch	5.81	12.7	Sc	pT1a	109	109	3	1	3	L
F	59	Ch	8.4	16.7	Mc	pT2a	108	108	2	2	4	L
M	36	Ch	6.47	9.8	Mc	pT1a	108	108	0	0	0	L
M	84	Ch/CB	11.9	14.8	Mc	pT2b	106	106	0	0	0	L
F	67	Ch	10.42	13.02	Mc	pT3a	105	105	0	0	0	L
M	73	Ch	9.7	11.3	Mc	pT2a	102	102	0	0	0	L
F	45	Ch	13.7	10.2	Mc	pT2a	96	96	0	0	0	L
M	58	Ch	13.1	14.3	Mc	pT2a	96	96	2	1	2	L
M	63	Ch	3.3	11.7	Sc	pT2a	85	85	2	3	6	L
M	54	Ch	6.32	10	Sc	pT2a	83	83	3	4	12	H
F	84	Ch	11.7	17.4	Mc	pT3a	78	78	3	4	12	H
M	73	Ch	9.24	17.7	Ec	pT2a	72	72	2	1	2	L
M	83	Ch	10.62	9.4	Ec	pT3a	72	72	3	4	12	H
F	71	Ch	3.68	6.4	Ec	pT1a	71	71	0	0	0	L
M	55	Ch/CB	7.5	8.9	Ec	pT2b	61	61	3	4	12	H
M	52	Ch	9.2	12.1	Sc	pT2b	60	60	3	4	12	H
M	46	Ch	8.76	11.3	Sc	pT2a	54	54	0	0	0	L
F	76	Ch	8.02	10.7	Mc	pT1a	48	48	3	2	6	L
F	63	Ch	10.3	13.7	Mc	pT2a	42	42	0	0	0	L
F	41	Ch	5.85	10.3	Mc	pT1a	42	42	0	0	0	L
F	55	Ch	3.2	7.6	Mc	pT2a	24	24	2	4	8	L
F	74	Ch	8.6	10.2	Mc	pT4b	24	24	2	1	2	L
M	68	Ch/CB	10.1	10.1	Ec	pT1b	24	24	0	0	0	L
M	74	Ch/CB	14.45	17.5	Ec	pT4b	18	18	2	1	2	L
M	70	Ch/CB	16.27	20.8	Sc	pT4b	12	12	0	0	0	L
M	66	Ch	9.2	14.1	Mc	pT3a	12	12	1	1	1	L

Abbreviations: DFS, disease-free survival; Ch, choroid; CB, ciliary body; Mc, mixed cell; Sc, spindle cell; Ec, epithelioid cell.

and

Table 2. Demographics, tumor parameters, disease-free time, follow-up, and macroH2A expression in primary UMs with metastasis (n = 23).

Sex	Age (years)	Location	Thickness (mm)	Largest Diameter (mm)	Cell Type	Pathological T Stage	DFS (Months)	Follow-Up (Months)	MacroH2A
									IS	ES	IRS
F	58	Ch	6.04	17.8	Mc	pT2a	63	64 (†)	3	3	9	L
M	69	Ch	7.21	15.8	Mc	pT2a	54	81 (†)	3	4	12	H
F	75	Ch/CB	15.5	15.3	Mc	pT3b	44	62 (†)	3	4	12	H
F	50	Ch	7.36	15.6	Ec	pT2a	41	81	3	4	12	H
M	62	Ch	13.68	16	Mc	pT3a	38	51 (†)	3	4	12	H
F	51	Ch/CB	11.4	18.5	Mc	pT3b	38	61	3	4	12	H
M	71	Ch	13.14	17.1	Ec	pT3a	33	34 (†)	3	4	12	H
M	76	Ch/CB	11.6	6.5	Mc	pT1a	31	39	0	0	0	L
M	72	Ch	10.3	15.4	Mc	pT3b	27	35 (†)	3	4	12	H
F	85	Ch/CB	7.3	14.7	Sc	pT2d (EE)	26	49 (†)	3	4	12	H
M	73	Ch	5.73	11.7	Ec	pT2a	26	42 (†)	3	4	12	H
F	51	Ch	9.42	19	Mc	pT3a	25	39	1	1	1	L
F	74	Ch	5.7	12.1	Sc	pT2a	24	37 (†)	3	4	12	H
F	67	Ch	3.49	20	Mc	pT4a	24	31 (†)	3	4	12	H
M	74	Ch	11.35	10.5	Ec	pT3a	19	47	3	4	12	H
M	82	Ch	9.7	11	Ec	pT2a	19	42	3	4	12	H
F	72	Ch	6.7	15.2	Ec	pT2a	14	28 (†)	3	4	12	H
M	76	Ch	13.7	17.1	Mc	pT2a	14	70	3	4	12	H
M	79	Ch	13.91	16.1	Ec	pT3b	13	38	3	4	12	H
F	66	Ch/CB	8.95	12.5	Mc	pT2b	12	37 (†)	3	4	12	H
F	60	Ch	8.25	16.5	Ec	pT2a	11	37 (†)	3	4	12	H
F	57	Ch/CB	13.6	19	Ec	pT2b	6	55	3	4	12	H
M	72	Ch/CB	13.3	15.4	Mc	pT3b	0	51	3	4	12	H

Abbreviations: DFS, disease-free survival; Ch, choroid; CB, ciliary body; Mc, mixed cell; Sc, spindle cell; Ec, epithelioid cell; EE, extrascleral extension; (†) death.

).

The size and site of tumor onset were studied by ophthalmoscopy and A and B scan ultrasonography, while the study of metastases was performed by physical examination, hepatic ultrasound, and computerized tomography. The median follow-up period was 60 months (range 8–138 months). Forty melanomas were localized only in the choroid, while 15 involved both the choroid and the ciliary body: only in one case was an extrascleral extension found. As concerns histotypes, 15 cases were classified as epithelioid cells and 12 as spindle cells, and 28 cases were diagnosed as mixed type.

Based on the eighth TNM classification, 23 metastatic UMs were distributed as follows: pT1a (1 case, 4.3%), pT2a (9 cases, 39.1%), pT2b (2 cases, 8.7%), pT2d (1 case, 4.3%), pT3a (4 cases, 17.4%), pT3b (5 cases, 21.7%) and pT4a (1 case, 4.3%). TNM staging in 32 patients with metastatic UMs included pT1a (6 cases, 18.7%), pT1b (1 case, 3.1%), pT2a (12 cases, 37.5%), pT2b (6 cases, 18.7%), pT3a (4 cases, 12.5%), and pT4b (3 cases, 9.4%). We also tested mH2A in two cases of metastasis from uveal melanoma.

The cases were collected from the files of the Anatomic Pathology Department of Medical, Surgical, and Advanced Technologies, Gian Filippo Ingrassia, University of Catania. Some cases were excluded from the study for the following reasons: (1) if it was not possible to obtain sections from paraffin blocks for immunohistochemical staining, (2) the absence of representative tumor tissue, (3) the presence of exclusively necrotic material, and (4) preoperatively treated UMs.

Five sections were cut from each paraffin block. Briefly, the deparaffinized slides were pretreated with 10 mg/mL of ovalbumin in phosphate-buffered saline (PBS) followed by 0.2% biotin+ in PBS, each for 15 min at room temperature, and they were rinsed for 20 min with PBS (Bio-Optica, Milan, Italy) in order to reduce the usually seen nonspecific immunoreactivity due to endogenous biotin. Microwave pretreatment was performed to unmask antigenic sites. Then the slides were incubated overnight at 4 °C with rabbit polyclonal anti-macroH2A.1 antibody (ab37264; Abcam, Cambridge, UK) diluted 1:200 in PBS (Sigma, Milan, Italy). Sections were counterstained with hematoxylin, dehydrated, mounted (Zymed Laboratories, San Francisco, CA, USA), and observed with a light microscope (Carl Zeiss, Oberkochen, Germany).

The immunohistochemical expression of mH2A.1 was evaluated as positive if brown chromogen was observed in the nucleus. Normal skin was tested as a positive control, while the negative control was obtained through omission of the primary antibody.

Immunoreaction intensity and the percentage of stained cells were evaluated by light microscopy. Four levels (0–3) of the intensity of staining (IS) were identified: no evidence of immunoreactivity = 0, mild immunoreactivity = 1, intermediate immunoreactivity = 2, and intense immunoreactivity = 3, as described previously [9]. The extent score (ES), understood as the proportion of mH2A.1 immunopositive cells, included five levels: <5% (0), 5%–30% (+), 31%–50% (++), 51%–75% (+++), and >75% (++++). Counting was performed at 200× magnification. The intensity reactivity score (IRS) was obtained by multiplication of the intensity of staining (IS) and the percentage of positive cells: when the IRS was ≤6, mH2A.1 expression was considered to be “low” (L-IRS), while an IRS >6 was considered to be “high” expression (H-IRS).

The evaluation of immunohistochemical expression of mH2A was performed separately by three specialists in anatomic pathology (R.C., L.P., and L.S.), who were blind to the patient’s identity, clinical data, and group identification.

2.2. Statistical Analysis

We compared the rate of high and low levels of mH2A.1 expression in melanoma of patients with and without metastasis using a chi-square test. The agreement among observations was assessed by Cohen’s kappa coefficient.

We performed a univariate analysis based on a Cox proportional hazards regression model to test factors related to time free from metastasis. The parameters investigated were gender, age, melanoma location (choroid or ciliary body), temporal or nasal location, cell type (epithelioid, spindle cells, or mixed), echographic parameters (height, greatest diameter), and mH2A.1 expression (low and high).

Factors with a p-value <0.15 were included in the multivariate analysis.

We performed a survival analysis based on high and low mH2A.1 expression using the Kaplan–Meier test: survival rates were compared using a log-rank (Mantel–Cox) test, and p-values lower than 0.05 were considered to be statistically significant.

3. Results

3.1. Clinicopathological Characteristics of UMs

Comparing patients without metastasis and with metastasis, no significant difference was observed in median age, site (choroid or choroid/ciliary body), thickness, cell type, extrascleral extension, and pTNM: patients with metastatic melanoma showed a greater median largest diameter (15.6 mm vs 11.9 mm, p = 0.007) and higher median mH2A.1 expression (12 vs 2, p < 0.001). They also had lower median disease-free survival (25 months vs 81 months, p < 0.001) (

Table 3. Medians (range) of demographics, tumor parameters, disease-free time, follow-up, and macroH2A expression in primary UMs without and with systemic metastasis.

	Sex	Age	Location	Thickness	Largest Diameter	Cell Type	Extrascleral	Pathological	DFS (Months)	Follow-Up (Months)	Macro H2A
	m–f	(Years)					Extension	T Stage
All	28–27	67	Ch 40	9.7	14.1	Ec: 15	No: 54	pT1a: 7	42	60	12
(n = 55)		(29–85)	Ch/CB 15	(3.2–16.3)	(6.4–20.8)	Sc: 12	Yes: 1	pT1b:1	(0–138)	(8–138)	(0–12)
						Mc: 28		pT2a: 21
								pT2b: 8
								pT2d: 1
								pT3a: 8
								pT3b: 5
								pT4a: 1
								pT4b: 3
Metastasis-free	17–15	64	Ch24	9.5	11.9	Ec: 6	No: 32	pT1a: 6	81	81	2
(n = 32)		(29–84)	Ch/CB 8	(3.2–16.3)	(6.4–20.8)	Sc: 10		pT1b: 1	(12–138)	(8–138)	(0–12)
						Mc: 16		pT2a: 12
								pT2b: 6
								pT3a: 4
								pT4b: 3
Metastasis	11–12	72	Ch 16	9.7	15.6	Ec: 9	No: 22	pT1a: 1	25	42	12
(n = 23)		(50–85)	Ch/CB 7	(3.5–15.5)	(6.5–20)	Sc: 2	Yes: 1	pT2a: 9	(0–63)	13 deaths	(0–12)
						Mc: 12		pT2b: 2		(28–81)
								pT2d: 1
								pT3a: 4
								pT3b: 5
								Pt4b: 1
p (metastasis-free vs metastasis)		0.400 *	0.762 °	0.911 *	0.007 *	0.400 *	0.418°	0.560 *	<0.001 *	0.001 *	<0.001 *

* Kolmogorov–Smirnov test. ° Fisher’s exact test. Abbreviations: Mc, mixed cell; Sc, spindle cell; Ec, epithelioid cell.

).

3.2. mH2A.1 Expression and Clinicopathological Features in UMs

Immunohistochemistry showed only mH2A.1 nuclear staining: no immunohistochemical expression of mH2A.1 was observed in non-neoplastic ocular tissue. Interobserver agreement was excellent (kappa = 0.943).

Considering the whole group (n = 55), the median mH2A.1 value was 12: H-IRS was observed in 28 (50.9%) melanomas and L-IRS in 27 (49.1%).

In 32 nonmetastatic primary UMs, mH2A.1 IS was intense/intermediate in 18 cases (56.3%) and mild in only one case (3.1%), while in 13 (40.6%) cases no immunoreactivity was observed (Figure 1). ES was >50% in 10 cases (31.3%) and 5%–30% in 9 cases (28.1%). Only 8/32 cases (25%) showed H-IRS, while 24 cases (75%) showed L-IRS (Table 1) (Fisher’s exact test, p < 0.001,

Table 4. Number of UMs (with and without metastasis) with low and high macroH2A.

mH2A	Metastasis (n = 23)	Metastasis-Free (n = 32)
Low	3 (13%) *	24 (75%)
High	20 (87%)	8 (25%)

Abbreviations: mH2A, macroH2A. p (Fisher’s exact test). * p < 0.0001.

).

In 23 metastatic primary UMs, mH2A.1 IS was intense/intermediate in 21 cases (91.4%) and mild in 1 case (4.3%). Only 1 case (4.3%) showed an absence of immunoreactivity (Figure 2). ES was >75% in 20 cases (87%), 50%–75% in 1 case (4.3%), and 5%–30% in 1 case (4.3%). Here, 20/23 cases (87%) showed H-IRS, while only 3 cases (13%) had L-IRS (Table 2) (Fisher’s exact test, p < 0.001, Table 4).

In two cases of metastasis from uveal melanoma, mH2A.1 showed diffuse and intense immunoreactivity with H-IRS (Figure 3).

Univariate analysis based on a Cox proportional hazards regression model revealed that factors related to the presence of metastasis were age (p = 0.053), greater tumor size (p = 0.009), pT (pathological Tumor) stage (p = 0.016), the epithelioid variant (p = 0.011), and mH2A.1 expression (p < 0.001). Factors significantly related to the presence of metastasis in the multivariate analysis were mH2A.1 expression (p = 0.002), greater tumor size (p = 0.026), and the epithelioid variant (p = 0.019).

Here, mH2A.1 expression was not related to histological type (Spearman’s rho, p = 0.173). A Kaplan–Meier survival analysis showed that the estimated survival times free from metastasis were greater in patients with low mH2A.1 expression in UMs: mean values (SE (Standard error), with 95% CI (confidential interval)) were 110.3 (6.80) (CI: 97.0 to 123.7) in patients with low mH2A.1 expression and 56.7 (10.0) (CI: 37.2 to 76.2) in patients with high mH2A.1 expression (p < 0.001, log-rank (Mantel–Cox) test, Figure 4).

4. Discussion

UM is an ambiguous neoplasia because regardless of the histological subtype and initial stage, it can metastasize to the liver, even after 10–15 years [4]. From the diagnosis of hepatic metastasis, death usually occurs within one year, and there is a lack of effective treatment. Asymptomatic patients with an early detection of metastasis seem to have an apparent benefit, while adjuvant therapies and screening do not seem to provide a significant survival benefit [10,11]. The prognosis of UM depends on multiple clinical data points: adult/senile age, male gender, large tumor, tumor thickness, ciliary body site, eye or skin melanocytosis, extraocular involvement at presentation, and advanced stage. Histopathological parameters (epithelioid cell variant, numerous mitoses, microvascular proliferation, microvascular loops and patterns, intratumoral lymphocytes, intratumoral macrophages, strong expression of IGF-1R (insulin-like growth factor-1 receptor) and HLA (Human Leucocyte Antigen) class I and II), cytogenetic factors (monosomy 3, chromosome 8q-gain or 8p-loss, chromosome 1p-loss, chromosome 6q-loss), and transcriptomic factors (gene expression profile class 2) [10,11] play a role as prognostic factors.

However, much remains to be understood to limit the onset of metastases or to identify effective treatments in metastatic patients.

Indeed, research is being focused on factors that can identify tumors with aggressive behavior and find new therapeutic targets. Our research group has tried to determine the unusual behavior of UM by testing different molecules and factors such as ADAM10, RKIP, pRKIP, ABCB5, and SPANX-C [9,12,13].

Recent studies have reported the inactivation of somatic mutations in gene-encoding BRCA-1-associated protein 1 (BAP1) in about 84% of metastasizing UMs [14]: the high frequency of BAP1 mutations in metastatic UMs encouraged us to search for new therapeutic strategies with the target molecule BAP1, which have deubiquitinase activity on histone H2A [15,16]. In different tumors, including skin melanoma, mH2A and its variants, which are widely distributed along chromatin [17,18,19], have been regarded as a potential prognostic marker [20,21].

Previously, Kapoor et al. [6] reported that the histone variant mH2A suppressed the tumor progression of malignant cutaneous melanoma and that the loss of mH2A isoforms was positively correlated with increasing malignant phenotypes of cutaneous melanoma cells in culture and human tissue samples. In addition, they suggested that the tumor-promoting function of mH2A loss was mediated, at least in part, through direct transcriptional upregulation of CDK8.

Lei et al. [7] showed that high expression of mH2A suppressed melanoma cell progression and arrested cells in the G2/M phase. Thus, we hypothesized that an alteration in mH2A expression could contribute to a change in the phenotype of UMs, promoting tumor progression. Therefore, mH2A would be the basis for this mechanism, whose final effect would be stabilizing the cell cycle, which is frequently observed in malignant neoplasms, in particular in tumor lesions with a low proliferative index. Furthermore, the arrest of the cell cycle would make the cell not very sensitive to chemotherapy, suggesting a further predictive role in the response to therapy. In the present study, we showed that an elevated increased expression of mH2A correlated with tumor progression: indeed, metastasizing UMs showed the highest expression of mH2A. This assay might prove that a high expression of histone protein correlates with an advanced tumor phase.

In this study, we saw that mH2A overexpression was a prognostic factor for the risk of metastasis. In our series of UMs, mH2A was strongly expressed in more than 75% of neoplastic cells, with a median IRS value of 12. In patients with H-IRS, we observed an increased incidence of metastasis after surgical treatment. These data were also confirmed by the high expression of mH2A in metastases, although this was limited to only two cases. Conversely, the cases with L-IRS showed a decreased risk of metastasis. In addition, a Kaplan–Meier survival analysis showed that patients with UMs and H-IRS had lower metastasis-free survival times.

In conclusion, our results highlight the important role played by mH2A in UM progression. The immunohistochemical expression of mH2A could be a suitable and easily detectable marker in the primary tumor, predicting the risk of UM metastasis and thus directing strategies for monitoring and therapy.