Abstract
There is a correlation between DNA methylation and the diseased stage and poor survival. 5-methylcytosine (5-mC) is one of the epigenetic modifications of bases that researchers focus on. Staining with 5-mC immunohistochemistry was used to examine pathological samples taken from individuals diagnosed with cutaneous melanoma. Between Breslow levels 2 and 4, there was a significant difference in the H-score of 5-mC expression (p = 0.046). A significant reduction in 5-mC expression H-scores was seen in patients who were diagnosed with ulcers (p = 0.039). It was shown that patients with low 5-mC had a significantly worse overall survival rate (p = 0.027).
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Introduction
Cutaneous melanoma is an aggressive skin cancer with rapid metastatic potential and high mortality. Although it represents only 0.6% of all cancer cases, it is disproportionately responsible for an estimated 65% of skin cancer-related mortalities1. Unfortunately, the incidence of this cancer is increasing. Data from 2020 indicated that approximately 100,350 new cases were diagnosed and 6,850 deaths were attributed to cutaneous melanoma in the U.S., with predictions suggesting a continual rise1. At the cellular level, melanomas originate from unchecked melanocyte proliferation within the basal layer of the skin. These melanocytes are critical for melanin production and shield the skin from the damaging effects of ultraviolet (UV) rays2. However, when exposed to excessive UV light, the DNA within skin cells becomes vulnerable, leading to potential mutations. The pronounced genetic variability observed in cutaneous melanoma highlights its virulence and the need for effective therapeutic interventions3.
Genetic variability can be significantly influenced by epigenetics. Epigenetics is a process that can have a substantial impact on genetic diversity. It involves reversible alterations in gene expression, such as acetylation, methylation, and histone modification. These changes modify the phenotype without altering the genotype. This emphasises the significance of epigenetic mechanisms in influencing the range of observable traits and the development of diseases without altering the DNA sequence4. The addition of a methyl group to the 5th carbon position of cytosine, resulting in the formation of 5-methylcytosine (5-mC), is one epigenetic type of DNA methylation, which plays a central role as a negative regulator of transcription initiation at CpG islands found in approximately 60% of genes and is involved in the maintenance of a constitutively inactivated, heterochromic genomic region by conferring genomic stability and integrity4. Global DNA hypomethylation, also known as genome-wide hypomethylation, can result in chromosomal abnormalities, proto-oncogene expression, and loss of transcriptional repression of the genome5,6,7.
Cancer genomes often exhibit global hypomethylation, leading to genomic instability, along with simultaneous hypermethylation of the promoter regions of specific tumour suppressor genes, resulting in their silencing8,9. This duality in methylation patterns presents both a challenge and an opportunity. The complexity of these patterns, intertwined with other epigenetic marks, adds layers of intricacy to the cancer epigenomic landscape10,11. These distinctive methylation signatures hold promise not only as diagnostic and prognostic markers but also as potential therapeutic targets.
Current research investigates how variations in DNA methylation in normal tissues may be used to create cancer biomarkers. Recent studies conducted at several research organizations have shown that human malignancies of the breast, liver, lung, pancreas, colon, prostate, and brain exhibit global hypomethylation, which is characterized by significantly decreased levels of 5-mC12,13,14. Despite the growing understanding that aberrant DNA methylation is an essential factor in the progression of melanoma, the epigenome of cutaneous melanoma is more hypomethylated than that of benign nevi15. This results in significantly reduced 5-mC levels, which is an epigenetic hallmark of melanoma. This process may be crucial for the epigenetic control of melanoma cell proliferation, growth, and advancement16. Such epigenetic alterations in melanoma can drive disease progression, affect metastatic potential, and modulate treatment responses. Global hypomethylation, a feature of many cancers, can lead to chromosomal instability and tumour progression, whereas hypermethylation of specific promoter regions can silence tumour suppressor genes and other protective pathways8,9,17. In melanoma, these methylation dynamics further interact with UV exposure, genetic mutations, and other epigenetic modifications, adding layers of complexity to the epigenomic landscape10.
We hypothesized that a reduction in 5-mC levels related to global methylation could be used to predict the prognosis and survival associated with the pathological characteristics of cutaneous melanoma and that this reduction might serve as a future targeted therapy option and prognostic marker.
Results
Clinicopathological characteristics
As shown in Table 1, a total of 48 patients with cutaneous melanoma were included in this study; 22 were males (45%), and 26 were females (55%). With a median age of 65, the patients' ages ranged from 28 to 94. Histological subtype analysis showed that 10.5% (five cases) of diagnoses were superficial spreading, 52% (25 cases) were nodular, and 37.5% (18 cases) were acral lentiginous. Most cases were at Breslow level 4, while Breslow levels 3, 2, and 1 made up 58%, 19%, 17%, and 6% of cases, respectively.
According to the AJCC Cancer Staging Manual, Eighth Edition, 27 out of 48 patients (56%) were diagnosed in the advanced stage (III–IV) and 21 (44%) were in the early stage (I–II). Out of the total, 30 individuals (62.5%) had ulcers, while 18 individuals (37.5%) did not.
Regarding the nodal stage, most patients were at stage 0 (46%), with a minority at stage 1 (27%), 2 (12.5%), and 3 (14.5%). The median duration for disease-free survival (DFS) follow-up was 13 months (range: 3–52 months), while the median period for overall survival (OS) follow-up was 25 months (range: 4–95 months). The calculated H scores ranged from 1.11 to 162.05, with a median score of 68.68.
5-mC H score and clinicopathological correlation
The Kruskal‒Wallis test with post hoc pairwise comparison was used to analyse the correlation of the H score of 5-mC expression with each clinicopathological characteristic. The results revealed that the H score of 5-mC expression was significantly different between patients with Breslow levels 2 and 4 (p = 0.046; Fig. 1a), while the other scores were not significantly different. Patients who presented with ulcers had significantly lower H scores for 5-mC expression (p = 0.039; Fig. 1b) than those without ulcers (Table 1). The metastatic lymph nodes in patients with stages 2 and 3 disease had decreased 5-mC H scores than those in patients with stages 0 and 1 disease; however, this difference was not significant (Fig. 1c). In addition, there was no association between the H score of 5-mC expression and other factors, including recurrence (p = 0.322) and death (p = 0.949).
5-mC H score and outcome analysis
The median DFS and OS in this study were 17 months (range 3–62 months) and 30 months (range 5–96 months), respectively. We used the median H score (68.68) as the cut-off, as shown in Fig. 2a and c. Patients with 5-mC expression scores of ˂ 68.68 had shorter DFS than patients with 5-mC expression scores of ≥ 68.68; however, the difference was not significant (p = 0.123; Table 2 and Fig. 2b). In contrast, mortality outcomes were significantly predicted by 5-mC H scores of ≥ 68.68 (p = 0.037) and Breslow levels 3 (p = 0.040) and 4 (p = 0.037; Table 3). Multivariate analysis also demonstrated that a 5-mC expression score of ≥ 68.68 was an independent variable for OS (HR = 0.293, p = 0.025; Table 3 and Fig. 2d) in patients with cutaneous melanoma.
Discussion
Global hypomethylation in cutaneous melanoma has been reported to be associated with genomic instability, activation of oncogenes, and altered immune responses. This extensive reduction in methyl groups, primarily from repetitive sequences, can lead to chromosomal abnormalities, contributing to tumour progression18,19.
In this study, the severity of cutaneous melanoma correlated with the H score. For example, the Breslow level and ulceration were significantly associated with the H score (p values of 0.024 and 0.039, respectively). Based on these findings, we conclude that hypomethylation is associated with the aggressiveness of cutaneous melanoma. The recurrence and death rates in this study were 60.4% and 56.3%, respectively (Tables 2 and 3), and there was no correlation between any of the other factors, including sex, age, histological subtype, Breslow level, tumour stage, ulcer status, or staging node, except for the H score, which indicated a trend towards a higher recurrence rate for H scores < 68.68 than for H scores > 68.68. The recurrence rate can be predicted based on global hypomethylation by evaluating 5-mC levels and H scores.
No correlations were found between factors such as sex, age, histologic subtype, tumour stage, ulcer status, or nodal stage and mortality. However, the H score and Breslow level indicated a higher death rate when the H score was less than 68.68 (HR 0.391, p = 0.037). In addition, multivariate analysis revealed that the mortality rate was significantly associated with the H score at the cut-off point of 68.68 (p = 0.025). We also discovered that hypomethylation was associated with high Breslow levels, with Breslow levels 3 and 4 having HRs of 0.07 and 0.076, respectively, and p values of 0.04 and 0.037, respectively. In essence, global hypomethylation measured by the H score from 5-mC IHC offers a promising avenue for predicting both recurrence and mortality in patients with cutaneous melanoma. Our study robustly established that 5-mC IHC can serve as a powerful tool for mortality prediction, potentially refining patient prognosis and enhancing personalized treatment strategies.
The evolving understanding of cutaneous melanoma severity and its intricate association with hypomethylation has taken centre stage in oncology research. In this study, elucidation of the H score as an instrumental predictive marker has established a compelling avenue for further exploration. Melanoma exhibits global hypomethylation, which plays an important role in predicting patient prognosis15,20,21.
Our findings are consistent with those of Ehrlich22, who emphasized the connection between hypomethylation and various types of cancer. This finding suggested a broad and significant role of epigenetic modulation in tumorigenesis22. Furthermore, while Cohen et al.23 proposed the initial concept of the H score, its application was limited to breast cancer, highlighting the innovative nature of our melanoma-centric focus. In contrast, Hyams et al.24 emphasized that age, sex, and histological subtype were potential prognostic factors. The discrepancy between our results and theirs emphasizes the complex character of melanoma and thus begs for a more nuanced understanding, perhaps by merging different datasets.
The utility of the Breslow level, as emphasized by both Atique et al.25 and Rashed et al.26, has universal acceptance in determining the prognosis of melanoma. Interestingly, Ecsedi et al.27 suggested a correlation between the Breslow depth and hypomethylation, and our investigation thoroughly confirmed this hypothesis. Micevic et al.16 provided basic knowledge on the potential of the 5-mC score among molecular markers. Our research extends this narrative by emphasizing the predictive process of the H score. Similarly, the preliminary work of Yang et al.28 on molecular markers laid the groundwork for our research. Fath et al.29 suggested that epigenetic factors may have a greater influence on melanoma than genetic alterations, and our data indirectly support this view. This evolving understanding is reinforced by the work of Van Doorn et al.30, who revealed an association between DNA methylation and the aggressiveness of tumours in various skin cancers. Constrained promoter hypermethylation and global hypomethylation are epigenetic characteristics of melanoma, and both have an impact on tumour behaviour31.
There are many DNA methylation analysis techniques, including methylation-specific polymerase chain reaction (PCR), pyrosequencing, and bisulfite genome sequencing32,33. IHC is unique and provides contextual awareness. The use of IHC in this study was crucial for studying methylation in tissue architecture34. IHC is enhanced by spatial resolution and is different from other methods because it shows both "what" and "where." This localization capacity is useful for studying methylation during tissue- and cell-specific events35,36. Determining whether tumour cells exhibit methylation alterations can reveal disease progression and guide targeted therapy37. This technique is simple and affordable, making it a suitable choice for many laboratories. This practicality and fast turnaround enable prompt clinical testing. The versatility of IHC for evaluating paraffin-embedded and frozen tissue slices allows important historical materials to be studied in addition to new samples38,39. This study is limited by the small number of patients who were analysed. A multicenter study, or one that includes a greater number of participants, will produce more data and have better value. Furthermore, investigating the molecular mechanisms related to the connections between 5-mC and melanoma is essential. For confounding factors such as age, tumour location, and treatment history. Given that the studies were carried out at an average age of 65, the patients' ages varied from 28 to 94 years. Some research implies that ageing can affect methylation levels40,41. In this study, there was no significant difference in age groups among the majority of patients. According to the literature review, there is no difference in methylation between methylation level and location31,42,43. Some papers found that previous therapy had no effect on methylation levels31,44, and in our analysis, we recruited a melanoma patient who had not previously received treatment. Finally, the study's results were unaffected by age, tumour location, or treatment experience.
Our results confirmed the potential of hypomethylation as an indicator of cutaneous melanoma severity. Incorporating such epigenetic markers, particularly the H score, into routine clinical assessments could refine the prognostic and treatment strategies for patients, ultimately leading to more personalized and effective care. The challenges posed by these complex methylation patterns in melanomas are significant. However, distinctive methylation signatures in melanoma hold promise as diagnostic, prognostic, and therapeutic markers. The development of technologies such as whole-genome bisulfite sequencing and innovations such as CRISPR/Cas9 epigenetic editing provides new avenues for exploring, understanding, and targeting the methylation landscape in cutaneous melanoma and other cancers. Considering the potential benefits, combining the conversion of global hypomethylation to hypermethylation in melanoma with other targeted therapies like molecularly targeted tyrosine kinase inhibitors (TKIs), BRAF, MEK, etc. could enhance treatment efficacy for patients. Therefore, our results showed that 5-mC IHC can be used as an alternative prognostic marker for cutaneous melanoma. This technique is inexpensive and accurate, and errors are reduced by using automation to calculate the H score.
Summary points
-
1.
Global DNA hypomethylation, also known as genome-wide hypomethylation, can result in chromosomal abnormalities, proto-oncogene expression, and loss of transcriptional repression of the genome.
-
2.
Melanoma exhibits global hypomethylation within the whole genome, which plays an important role in predicting patient prognosis.
-
3.
Our study robustly established that 5-mC IHC can serve as a powerful tool for mortality prediction, potentially refining patient prognosis and enhancing personalized treatment strategies.
-
4.
The elucidation of the H score as an instrumental predictive marker has established a compelling avenue for further exploration.
Methods
Sample recruitment
Ethical approval for this study was granted by the Institutional Review Board of the the Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand (Med Chula COA No. 0678/2022, IRB no. 1643/2564). The retrospective study included all patients who underwent preoperative therapy at Chulalongkorn University's Division of Plastic and Reconstructive Surgery, Department of Surgery, Faculty of Medicine, Bangkok, Thailand, from 2012 to 2018. Informed consent to participate in the investigation was obtained in writing from all subjects and/or their legal guardian(s) in accordance with the Declaration of Helsinki. Prior to surgery, no patients were administered radiation therapy or chemotherapy. Inadequate pathologic tissue, absence of clinical data, and insufficient follow-up are exclusion criteria.
KR and NK confirmed the diagnosis of cutaneous melanoma and the subtype designation in all patients according to haematoxylin and eosin (H&E)-stained slides. Comprehensive clinical and follow-up data were collected, and the adequacy of the tumour tissue in the formalin-fixed paraffin-embedded tissue blocks was determined. The duration from surgery to recurrence, death, or final follow-up was documented. Ultimately, 48 participants were included in this study. Age, sex, tumour stage, and time of recurrence or death were collected from the clinical data.
Immunohistochemistry (IHC)
IHC was performed on paraffin-embedded sections of all specimens. Two-micron sections were placed on positively charged slides (SuperFrost Plus; Menzer-Glaser, Freiburg, Germany) and dewaxed with xylene and alcohol. To retrieve antigens, the sections were exposed to Tris–EDTA buffer (pH 9.0) in a microwave at 97 °C for 10 min. Subsequently, a 3.5 N HCl solution was added, and the slides were incubated for 15 min at room temperature. The slides were then subjected to 12 h incubation at 4 °C with a monoclonal antibody against 5-methylcytidine diluted 1:100 (Abcam, Cambridge, UK). A secondary antibody (DAKO EnVision+; DAKO Corp., Santa Clara, California, USA) was then applied, and the samples were incubated at 25 °C for 30 min, followed by visualization using diaminobenzidine chromogen (DAKO Corp.). The positive control was taken from the previous paper on thyroid cancer12, which tested positive for 5-mC. The negative control follows the same process but without the antibody against 5-mC.
Automated digital image analysis
All slides stained with the anti-5-methylcytidine antibody were scanned digitally using an Aperio CS2 slide scanner (Leica Biosystems, Wetzlar, Germany). Subsequent image analysis was performed using the Aperio Imagescope v.10.2.2.2352 software package (Aperio Technologies, Irvine, CA, United States). For comparative analyses, both tumour and normal tissue samples from the same patient were examined. To ensure impartiality and reduce selection bias, the regions for examination were arbitrarily selected to cover the superior, inferior, left, right, and central aspects of each image field. A minimum of 5,000 nuclei were evaluated for each patient. The intensity of immunostaining was automatically assessed using the commercially available Nuclear v.9 algorithm (Aperio Technologies, Irvine, CA, United States), and the grading scale was defined in a semiquantitative manner as follows: 0 (negative staining), 1 + (weak nuclear staining), 2 + (moderate staining), and 3 + (strong staining). Simultaneously, the percentage of nuclei with each staining level was determined, as illustrated in Fig. 3. The intensity and proportion scores were averaged to generate a 5-methylcytidine immunohistochemical score, which represented the degree of methylation for each patient and was calculated by the following formula for histochemical scoring (H score) assessment; this score incorporates both the staining intensity and the percentage of stained cells at each intensity level45,46.
Statistical analysis
The data were analysed using the SPSS Windows Version 22 programme (SPSS, Inc., Chicago, IL, USA). Utilised Pearson's chi-square test and Fisher's exact test to determine a potential correlation between clinicopathological factors and 5-mC H scores. An analysis of variance (ANOVA) was conducted to compare multiple groups. Generating Kaplan–Meier curves was used to calculate disease-free survival (DFS) and overall survival (OS). The Cox regression model served as the foundation for both the univariate and multivariate survival analyses. p < 0.05 indicated statistical significance.
Ethics declarations
Ethical approval for this study was granted by the Institutional Review Board of the Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand (Med Chula COA No. 0678/2022, IRB no. 1643/2564). Patients with cutaneous melanoma requiring preoperative therapy between 2012 and 2018 were enrolled from the Division of Plastic and Reconstructive Surgery within the Department of Surgery of the Faculty of Medicine at Chulalongkorn University, Bangkok, Thailand.
Data availability
All data generated or analysed during this study are included in this published article.
References
Arnold, M. et al. Global burden of cutaneous melanoma in 2020 and projections to 2040. JAMA Dermatol. 158, 495–503 (2022).
Long, G. V., Swetter, S. M., Menzies, A. M., Gershenwald, J. E. & Scolyer, R. A. Cutaneous melanoma. Lancet 402, 485–502 (2023).
Dzwierzynski, W. W. Melanoma risk factors and prevention. Clin. Plast. Surg. 48, 543–550 (2021).
Bird, A. DNA methylation patterns and epigenetic memory. Genes Dev. 16, 6–21 (2002).
Papanicolau-Sengos, A. & Aldape, K. DNA methylation profiling: An emerging paradigm for cancer diagnosis. Annu. Rev. Pathol. Mech. Dis. 17, 295–321 (2022).
Chen, C. et al. DNA methylation: From cancer biology to clinical perspectives. Front. Biosci. Landmark. 27, 326 (2022).
Li, Y., Fan, Z., Meng, Y., Liu, S. & Zhan, H. Blood-based DNA methylation signatures in cancer: A systematic review. Biochim. Biophys. Acta Mol. Basis Dis. 1869, 166583 (2023).
Esteller, M. Cancer epigenomics: DNA methylomes and histone-modification maps. Nat. Rev. Genet. 8, 286–298 (2007).
Jones, P. A. & Baylin, S. B. The epigenomics of cancer. Cell 128, 683–692 (2007).
Feinberg, A. P. & Tycko, B. The history of cancer epigenetics. Nat. Rev. Cancer 4, 143–153 (2004).
Robertson, K. D. DNA methylation and human disease. Nat. Rev. Genet. 6, 597–610 (2005).
Keelawat, S. et al. Detection of global hypermethylation in well-differentiated thyroid neoplasms by immunohistochemical (5-methylcytidine) analysis. J. Endocrinol. Investig. 38, 725–732 (2015).
Taryma-Lesniak, O., Sokolowska, K. E. & Wojdacz, T. K. Short history of 5-methylcytosine: from discovery to clinical applications. J. Clin. Pathol. 74, 692–696 (2021).
Barciszewska, A.-M. Global DNA demethylation as an epigenetic marker of human brain metastases. Biosci. Rep. 38, 20180731 (2018).
Conway, K. et al. DNA-methylation profiling distinguishes malignant melanomas from benign nevi. Pigm. Cell Melanom. Res. 24, 352–360 (2011).
Micevic, G., Theodosakis, N., Taube, J. M., Bosenberg, M. W. & Rodić, N. Attenuation of genome-wide 5-methylcytosine level is an epigenetic feature of cutaneous malignant melanomas. Melanom. Res. 27, 85–96 (2017).
Baylin, S. B. & Jones, P. A. A decade of exploring the cancer epigenome: Biological and translational implications. Nat. Rev. Cancer 11, 726–734 (2011).
Shen, J. et al. Global methylation of blood leukocyte DNA and risk of melanoma. Int. J. Cancer 140, 1503–1509 (2017).
Ecsedi, S. I. et al. Transposable hypomethylation is associated with metastatic capacity of primary melanomas. Int. J. Clin. Exp. Pathol. 6, 2943–2948 (2013).
Lian, C. G. et al. Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma. Cell 150, 1135–1146 (2012).
Chatterjee, A. et al. Marked global DNA hypomethylation is associated with constitutive PD-L1 expression in melanoma. Science 4, 312–325 (2018).
Ehrlich, M. DNA hypomethylation in cancer cells. Epigenomics 1, 239–259 (2009).
Cohen, D. A. et al. Interobserver agreement among pathologists for semiquantitative hormone receptor scoring in breast carcinoma. Am. J. Clin. Pathol. 138, 796–802 (2012).
Hyams, D. M., Cook, R. W. & Buzaid, A. C. Identification of risk in cutaneous melanoma patients: prognostic and predictive markers. J. Surg. Oncol. 119, 175–186 (2019).
Atique, U., Mushtaq, S., Rana, I. A. & Hassan, U. Clinicopathologic features of cutaneous malignant melanoma and their impact on prognosis. Cureus 12, e10450 (2020).
Rashed, H., Flatman, K., Bamford, M., Teo, K. W. & Saldanha, G. Breslow density is a novel prognostic feature in cutaneous malignant melanoma. Histopathology 70, 264–272 (2017).
Ecsedi, S. et al. DNA methylation characteristics of primary melanomas with distinct biological behaviour. PLoS ONE 9, e96612 (2014).
Yang, K., Oak, A. S. W., Slominski, R. M., Brożyna, A. A. & Slominski, A. T. Current molecular markers of melanoma and treatment targets. Int. J. Mol. Sci. 21, 3535 (2020).
Fath, M. K. et al. Current understanding of epigenetics role in melanoma treatment and resistance. Cancer Cell Int. 22, 313 (2022).
Van Doorn, R., Gruis, N. A., Willemze, R., van der Velden, P. A. & Tensen, C. P. Aberrant DNA methylation in cutaneous malignancies. Semin. Oncol. 32, 479–487 (2005).
Micevic, G., Theodosakis, N. & Bosenberg, M. Aberrant DNA methylation in melanoma: biomarker and therapeutic opportunities. Clin. Epigenet. 9, 34 (2017).
Li, Y. & Tollefsbol, T. O. DNA methylation detection: Bisulfite genomic sequencing analysis. Methods Mol. Biol. 791, 11–21 (2011).
Kurdyukov, S. & Bullock, M. DNA methylation analysis: Choosing the right method. Biology 5, 3 (2016).
Martisova, A. et al. DNA methylation in solid tumors: Functions and methods of detection. Int. J. Mol. Sci. 22, 4247 (2021).
Sahara, N. et al. Diagnostic accuracy of immunohistochemistry in detecting MGMT methylation status in patients with glioma. Asian Pac. J. Cancer Prev. 22, 3803–3808 (2021).
Zluvova, J., Janousek, B. & Vyskot, B. Immunohistochemical study of DNA methylation dynamics during plant development. J. Exp. Bot. 52, 2265–2273 (2001).
Fujiwara, S. et al. Gene expression and methylation analysis in melanomas and melanocytes from the same patient: Loss of NPM2 expression is a potential immunohistochemical marker for melanoma. Front. Oncol. 8, 675 (2018).
Koopmans, A. E. et al. Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma. Mod. Pathol. 27, 1321–1330 (2014).
Wang, M. et al. Differential gene expression and methylation analysis of melanoma in TCGA database to further study the expression pattern of KYNU in melanoma. J. Pers. Med. 12, 1209 (2022).
Johnson, A. A. et al. The role of DNA methylation in aging, rejuvenation, and age-related disease. Rejuven. Res 15, 483–494 (2012).
Salameh, Y., Bejaoui, Y. & El Hajj, N. DNA methylation biomarkers in aging and age-related diseases. Front. Genet. 11, 171 (2020).
Aleotti, V. et al. Methylation markers in cutaneous melanoma: Unravelling the potential utility of their tracking by liquid biopsy. Cancers 13, 6217 (2021).
Jin, S.-G., Xiong, W., Wu, X., Yang, L. & Pfeifer, G. P. The DNA methylation landscape of human melanoma. Genomics 106, 322–330 (2015).
Kraft, T. et al. Patient-specific identification of genome-wide DNA-methylation differences between intracranial and extracranial melanoma metastases. Sci. Rep. 13, 444 (2023).
Nicholson, R. I. et al. Hormone sensitivity in breast cancer: influence of heterogeneity of oestrogen receptor expression and cell proliferation. Eur. J. Cancer Clin. Oncol. 27, 908–913 (1991).
McCarty, K. S. Jr. et al. Use of a monoclonal anti-estrogen receptor antibody in the immunohistochemical evaluation of human tumors. Cancer Res. 46, 4244–4248 (1986).
Acknowledgements
The present study was supported by the Ratchadapiseksompotch Fund (Grant No. RA67/022; Faculty of Medicine, Chulalongkorn University).
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Conceptualization: Jiraroch Meevassana, Shananya Varophas, Piyawan Prabsattru, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. Formal analysis: Jiraroch Meevassana, Shananya Varophas, Nakarin Kitkumthorn. Funding acquisition: Jiraroch Meevassana, Shananya Varophas, Piyawan Prabsattru, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. Methodology: Jiraroch Meevassana, Shananya Varophas, Nakarin Kitkumthorn. Project administration: Jiraroch Meevassana. Resources: Jiraroch Meevassana. Software: Jiraroch Meevassana, Nakarin Kitkumthorn. Supervision: Jiraroch Meevassana, Nakarin Kitkumthorn. Validation: Nakarin Kitkumthorn Jiraroch Meevassana. Visualization: Jiraroch Meevassana, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. Writing—original draft: Jiraroch Meevassana, Shananya Varophas, Piyawan Prabsattru, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. Investigation: Jiraroch Meevassana, Shananya Varophas, Piyawan Prabsattru, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. Writing—review & editing: Jiraroch Meevassana, Shananya Varophas, Piyawan Prabsattru, Supitcha Kamolratanakul, Komkrit Ruangritchankul, Nakarin Kitkumthorn. All the authors have approved the final article.
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Meevassana, J., Varophas, S., Prabsattru, P. et al. 5-Methylcytosine immunohistochemistry for predicting cutaneous melanoma prognosis. Sci Rep 14, 7554 (2024). https://doi.org/10.1038/s41598-024-58011-z
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DOI: https://doi.org/10.1038/s41598-024-58011-z
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