Yi Yang, Zheng Zhao, Lulu Lu, Na Gao, Jiangang Hu, Gangwen Han, Xiaolei Ma
{"title":"中国女性黄褐斑皮肤病变的条带蛋白质组学分析。","authors":"Yi Yang, Zheng Zhao, Lulu Lu, Na Gao, Jiangang Hu, Gangwen Han, Xiaolei Ma","doi":"10.2147/CCID.S538073","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Melasma is a common, chronic, and recurring disorder of hyperpigmentation arising from hyperfunctional melanocytes that deposit excessive amounts of melanin in the epidermis and dermis. The pathophysiology of melasma remains unclear and the treatment is challenging. Proteomic Analysis may contribute to understand the pathogenesis of melasma.</p><p><strong>Patients and methods: </strong>In this study, transepidermal water loss(TWEL) was evaluated to assess skin barrier function. Melasma area and severity index score was used to measure the severity of melasma. Data independent acquisition mass spectrometry was used to perform a comparative analysis of protein expression in female skin samples(cheeks) from 8 healthy controls and 8 melasma subjects. The hospital anxiety and depression scale were used to assess the anxiety and depression levels of the melasma patients.</p><p><strong>Results: </strong>The results showed that the melasma patients had higher TEWL values than the controls (12.95 ± 2.44 versus 6.86 ± 2.19, p < 0.01). Quantitative proteomic analysis identified a total of 230 differentially expressed proteins, including 193 upregulated and 37 downregulated. Enrichment analysis of these proteins based on GO, KEGG databases and protein-protein interaction analysis revealed that functional cluster associated with skin barrier (which included ALB, ANXA5, HSPB1, IQGAP1, S100A7), immunity and inflammation (which included YWHAZ, YWHAE, HSPA5, CSNK2B), melanogenesis (which included ALDH1A1, YWHAH, NDRG2, PMEL, APOE), psychoneurosis (which included YWHAE,YWHAH, PFN1, C3) and hormone (which included ARPC2, HSC70 and HSP70).</p><p><strong>Conclusion: </strong>Our non-invasive proteomics analysis of human epidermal proteins may guide future research on female melasma and help in the development of treatments for melasma.</p>","PeriodicalId":10447,"journal":{"name":"Clinical, Cosmetic and Investigational Dermatology","volume":"18 ","pages":"2341-2357"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439839/pdf/","citationCount":"0","resultStr":"{\"title\":\"Tape-Strip Proteomic Analysis of Female Melasma Skin Lesions in a Chinese Population.\",\"authors\":\"Yi Yang, Zheng Zhao, Lulu Lu, Na Gao, Jiangang Hu, Gangwen Han, Xiaolei Ma\",\"doi\":\"10.2147/CCID.S538073\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Melasma is a common, chronic, and recurring disorder of hyperpigmentation arising from hyperfunctional melanocytes that deposit excessive amounts of melanin in the epidermis and dermis. The pathophysiology of melasma remains unclear and the treatment is challenging. Proteomic Analysis may contribute to understand the pathogenesis of melasma.</p><p><strong>Patients and methods: </strong>In this study, transepidermal water loss(TWEL) was evaluated to assess skin barrier function. Melasma area and severity index score was used to measure the severity of melasma. Data independent acquisition mass spectrometry was used to perform a comparative analysis of protein expression in female skin samples(cheeks) from 8 healthy controls and 8 melasma subjects. The hospital anxiety and depression scale were used to assess the anxiety and depression levels of the melasma patients.</p><p><strong>Results: </strong>The results showed that the melasma patients had higher TEWL values than the controls (12.95 ± 2.44 versus 6.86 ± 2.19, p < 0.01). Quantitative proteomic analysis identified a total of 230 differentially expressed proteins, including 193 upregulated and 37 downregulated. Enrichment analysis of these proteins based on GO, KEGG databases and protein-protein interaction analysis revealed that functional cluster associated with skin barrier (which included ALB, ANXA5, HSPB1, IQGAP1, S100A7), immunity and inflammation (which included YWHAZ, YWHAE, HSPA5, CSNK2B), melanogenesis (which included ALDH1A1, YWHAH, NDRG2, PMEL, APOE), psychoneurosis (which included YWHAE,YWHAH, PFN1, C3) and hormone (which included ARPC2, HSC70 and HSP70).</p><p><strong>Conclusion: </strong>Our non-invasive proteomics analysis of human epidermal proteins may guide future research on female melasma and help in the development of treatments for melasma.</p>\",\"PeriodicalId\":10447,\"journal\":{\"name\":\"Clinical, Cosmetic and Investigational Dermatology\",\"volume\":\"18 \",\"pages\":\"2341-2357\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12439839/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical, Cosmetic and Investigational Dermatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2147/CCID.S538073\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical, Cosmetic and Investigational Dermatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/CCID.S538073","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
Tape-Strip Proteomic Analysis of Female Melasma Skin Lesions in a Chinese Population.
Purpose: Melasma is a common, chronic, and recurring disorder of hyperpigmentation arising from hyperfunctional melanocytes that deposit excessive amounts of melanin in the epidermis and dermis. The pathophysiology of melasma remains unclear and the treatment is challenging. Proteomic Analysis may contribute to understand the pathogenesis of melasma.
Patients and methods: In this study, transepidermal water loss(TWEL) was evaluated to assess skin barrier function. Melasma area and severity index score was used to measure the severity of melasma. Data independent acquisition mass spectrometry was used to perform a comparative analysis of protein expression in female skin samples(cheeks) from 8 healthy controls and 8 melasma subjects. The hospital anxiety and depression scale were used to assess the anxiety and depression levels of the melasma patients.
Results: The results showed that the melasma patients had higher TEWL values than the controls (12.95 ± 2.44 versus 6.86 ± 2.19, p < 0.01). Quantitative proteomic analysis identified a total of 230 differentially expressed proteins, including 193 upregulated and 37 downregulated. Enrichment analysis of these proteins based on GO, KEGG databases and protein-protein interaction analysis revealed that functional cluster associated with skin barrier (which included ALB, ANXA5, HSPB1, IQGAP1, S100A7), immunity and inflammation (which included YWHAZ, YWHAE, HSPA5, CSNK2B), melanogenesis (which included ALDH1A1, YWHAH, NDRG2, PMEL, APOE), psychoneurosis (which included YWHAE,YWHAH, PFN1, C3) and hormone (which included ARPC2, HSC70 and HSP70).
Conclusion: Our non-invasive proteomics analysis of human epidermal proteins may guide future research on female melasma and help in the development of treatments for melasma.
期刊介绍:
Clinical, Cosmetic and Investigational Dermatology is an international, peer-reviewed, open access journal that focuses on the latest clinical and experimental research in all aspects of skin disease and cosmetic interventions. Normal and pathological processes in skin development and aging, their modification and treatment, as well as basic research into histology of dermal and dermal structures that provide clinical insights and potential treatment options are key topics for the journal.
Patient satisfaction, preference, quality of life, compliance, persistence and their role in developing new management options to optimize outcomes for target conditions constitute major areas of interest.
The journal is characterized by the rapid reporting of clinical studies, reviews and original research in skin research and skin care.
All areas of dermatology will be covered; contributions will be welcomed from all clinicians and basic science researchers globally.