Expression of Androgen, Estrogen, and Progesterone Receptors in the Skin of Patients with Severe Acne and the Assessment of Their Predictive Potential Using Artificial Intelligence Methods

Olga M. Demina

 
For citation: Demina OM. Expression of Androgen, Estrogen, and Progesterone Receptors in the Skin of Patients with Severe Acne and the Assessment of Their Predictive Potential Using Artificial Intelligence Methods. International Journal of Biomedicine. 2024;14(4):595-601. doi:10.21103/Article14(4)_OA10
 
Originally published December 5, 2024
 

Abstract: 

Background: In recent years, the study of acne pathogenesis has continued, and genetic regulation, innate and adaptive immune responses, and the contribution of several endocrinologic mechanisms have been reported. A sebaceous-hair follicle (SHF) is known to be regulated by sex hormones, including androgens, estrogens, and progesterone. At present, there is evidence of the involvement of sex hormones in the pathogenesis of acne. Still, there is no data on immunohistochemical (IHC) analysis of sex hormone receptor expression in the skin of severe acne (SA) in the available literature. There is also no IHC analysis of predictors of acne development. The present study aimed to determine and analyze the immunohistochemical expression of androgen, estrogen, and progesterone receptors in the skin of SA patients and to evaluate their predictive potential using artificial intelligence methods.
Methods and Results: This prospective, open, non-randomized, single-center comparative study was conducted between 2019 and 2023. The study included 53 patients (the main group [MG]) with SA and 21 apparently healthy individuals (the comparison group [CG]). Participants were between 15 and 46 years old (the median age was 22.0 years).  
An IHC study was performed in the Pathomorphological Department at the NMRC PHOI, named after Dmitry Rogachev (Moscow, Russia). Skin samples from patients were collected by punch biopsy. To perform the IHC study, we used the mouse monoclonal anti-androgen receptor (AR) antibody (Clone AR441, diluted 1:50; DAKO, Denmark), mouse monoclonal anti-estrogen receptor (ER) antibody (Clone 1D5, RTU; DAKO, Denmark), and mouse monoclonal anti-progesterone receptor (PR) antibody (Clone PgR636, RTU; DAKO, Denmark). For each marker under study, positivity was determined in three compartments: epidermal keratinocytes, dermal fibroblasts, and sebocytes of sebaceous glands.
Quantitative AR, ER, and PR expression assessment was performed using QuPath image analysis software according to the manufacturer's protocol. Statistical analysis was performed using Python 3.11. The predictive potential of the studied IHC markers was assessed using mathematical modeling methods and artificial intelligence.
Our study revealed for the first time a significant increase in the AR expression in epidermal keratinocytes and dermal fibroblasts in SA patients compared to healthy individuals, with no significant difference in the AR expression in sebocytes of sebaceous glands and overall positivity. A significant ER overexpression in dermal fibroblasts of SA patients with no significant differences for other studied compartments and overall positivity was also found. Moreover, the studied compartments had no statistically significant differences in progesterone receptor expression.
Conclusion: Mathematical modeling methods using artificial intelligence have made it possible to establish for the first time that the AR expression in dermal fibroblasts is a significant predictor of severe acne.

Keywords: 
acne • immunohistochemical study • androgen • estrogen • progesterone • receptor
References: 
  1. Greydanus DE, Azmeh R, Cabral MD, Dickson CA, Patel DR. Acne in the first three decades of life: An update of a disorder with profound implications for all decades of life. Dis Mon. 2021 Apr;67(4):101103. doi: 10.1016/j.disamonth.2020.101103. Epub 2020 Oct 9. PMID: 33041056.
  2. Williams HC, Dellavalle RP, Garner S. Acne vulgaris. Lancet. 2012 Jan 28;379(9813):361-72. doi: 10.1016/S0140-6736(11)60321-8. Epub 2011 Aug 29. Erratum in: Lancet. 2012 Jan 28;379(9813):314. PMID: 21880356.
  3. Navarini AA, Simpson MA, Weale M, Knight J, Carlavan I, Reiniche P, et al.; Acne Genetic Study Group; Willis C, Déret S, Voegel JJ, Spector T, Smith CH, Trembath RC, Barker JN. Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. Nat Commun. 2014 Jun 13;5:4020. doi: 10.1038/ncomms5020.
  4. He L, Wu WJ, Yang JK, Cheng H, Zuo XB, Lai W, et al. Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne. Nat Commun. 2014;5:2870. doi: 10.1038/ncomms3870. 
  5. Zhang M, Qureshi AA, Hunter DJ, Han J. A genome-wide association study of severe teenage acne in European Americans. Hum Genet. 2014 Mar;133(3):259-64. doi: 10.1007/s00439-013-1374-4. 
  6. Rumyantsev AG, Dеmina OM. The Impact of Single-Nucleotide Polymorphisms in Regulatory Genes on the Development of Severe Acne. International Journal of Biomedicine. 2023;13(1):134-140. doi:10.21103/Article13(1)_OA19
  7. Azzi L, El-Alfy M, Labrie F. Gender differences and effects of sex steroids and dehydroepiandrosterone on androgen and oestrogen alpha receptors in mouse sebaceous glands. Br J Dermatol. 2006 Jan;154(1):21-7. doi: 10.1111/j.1365-2133.2005.06847.x. PMID: 16403089.
  8. Clayton RW, Göbel K, Niessen CM, Paus R, van Steensel MAM, Lim X. Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis. Br J Dermatol. 2019 Oct;181(4):677-690. doi: 10.1111/bjd.17981. Epub 2019 May 6. PMID: 31056753.
  9. Fritsch M, Orfanos CE, Zouboulis CC. Sebocytes are the key regulators of androgen homeostasis in human skin. J Invest Dermatol. 2001 May;116(5):793-800. doi: 10.1046/j.1523-1747.2001.01312.x. PMID: 11348472.
  10. Hazarika N. Acne vulgaris: new evidence in pathogenesis and future modalities of treatment. J Dermatolog Treat. 2021 May;32(3):277-285. doi: 10.1080/09546634.2019.1654075. Epub 2019 Aug 29. PMID: 31393195.
  11. Kurokawa I, Nakase K. Recent advances in understanding and managing acne. F1000Res. 2020 Jul 29;9:F1000 Faculty Rev-792. doi: 10.12688/f1000research.25588.1. PMID: 32765835; PMCID: PMC7391011.
  12. Miller WL, Auchus RJ. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocr Rev. 2011 Feb;32(1):81-151. doi: 10.1210/er.2010-0013. Epub 2010 Nov 4. Erratum in: Endocr Rev. 2011 Aug;32(4):579. PMID: 21051590; PMCID: PMC3365799.
  13. Schulster M, Bernie AM, Ramasamy R. The role of estradiol in male reproductive function. Asian J Androl. 2016 May-Jun;18(3):435-40. doi: 10.4103/1008-682X.173932. PMID: 26908066; PMCID: PMC4854098.
  14. Tang HY, Xiao B, Liu X, Yang GL. [Signaling Pathways in the Pathogenesis of Acne Vulgaris]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2020 Aug 30;42(4):559-561. Chinese. doi: 10.3881/j.issn.1000-503X.11470. PMID: 32895111.
  15. Del Rosso JQ, Kircik LH, Stein Gold L, Thiboutot D. Androgens, Androgen Receptors, and the Skin: From the Laboratory to the Clinic With Emphasis on Clinical and Therapeutic Implications. J Drugs Dermatol. 2020 Mar 1;19(3):30-35. PMID: 32550699.

Download Article
Received October 13, 2024.
Accepted November 13, 2024.
©2024 International Medical Research and Development Corporation.