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Article ; Online: A case of hereditary hemorrhagic telangiectasia treated with cryotherapy.

Wen, Su-Ying / Huang, Ya-Yun

2024 Volume 23, Issue 5, Page(s) 1929–1930

MeSH term(s)	Humans ; Telangiectasia, Hereditary Hemorrhagic/complications ; Telangiectasia, Hereditary Hemorrhagic/therapy ; Cryotherapy ; Female ; Treatment Outcome ; Male ; Adult ; Middle Aged
Language	English
Publishing date	2024-01-31
Publishing country	England
Document type	Case Reports ; Letter
ZDB-ID	2280551-5
ISSN	1473-2165 ; 1473-2130
ISSN (online)	1473-2165
ISSN	1473-2130
DOI	10.1111/jocd.16202
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Article ; Online: Impact of Type 1 Versus Type 2 Diabetes on Developing Herpes Zoster and Post-herpetic Neuralgia: A Population-based Cohort Study.

Wen, Su-Ying / Ou-Yang, Chao / Chang, Catherine / Chen, Chu-Chieh / Chang, Hung-Yu

Acta dermato-venereologica

2023 Volume 103, Page(s) adv9400

Abstract: Type 2 diabetes is associated with an increased risk of herpes zoster and postherpetic neuralgia. However, the association of type 1 diabetes with herpes zoster or postherpetic neuralgia remains unclear. This retrospective cohort study using Taiwan's ... ...

Abstract	Type 2 diabetes is associated with an increased risk of herpes zoster and postherpetic neuralgia. However, the association of type 1 diabetes with herpes zoster or postherpetic neuralgia remains unclear. This retrospective cohort study using Taiwan's Health Insurance Research Database included 199,566 patients with type 1 diabetes and 1,458,331 with type 2 diabetes, identified during the period 2000 to 2012. Patients with type 1 diabetes had a significantly higher risk of developing herpes zoster than those with type 2 diabetes (p < 0.001). Across all age groups, the impact of diabetes on herpes zoster was greater in type 1 than in type 2 diabetes. Patients with both type 1 and type 2 diabetes had a 1.45-fold higher risk of post-herpetic neuralgia than those without diabetes (hazard ratio 1.45, 95% confidence interval 1.28-1.65; hazard ratio 1.45, 95% confidence interval 1.37-1.52, respectively), and there was no difference between the 2 types of diabetes (hazard ratio 1.06; 95% confidence interval 0.93-1.21). The results recommend consideration of herpes zoster vaccination at an earlier age in patients with type 1 diabetes.
MeSH term(s)	Humans ; Neuralgia, Postherpetic/diagnosis ; Neuralgia, Postherpetic/epidemiology ; Neuralgia, Postherpetic/complications ; Cohort Studies ; Diabetes Mellitus, Type 2/diagnosis ; Diabetes Mellitus, Type 2/epidemiology ; Retrospective Studies ; Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 1/diagnosis ; Diabetes Mellitus, Type 1/epidemiology ; Herpes Zoster/epidemiology ; Herpesvirus 3, Human
Language	English
Publishing date	2023-10-03
Publishing country	Sweden
Document type	Journal Article
ZDB-ID	80007-7
ISSN	1651-2057 ; 0001-5555
ISSN (online)	1651-2057
ISSN	0001-5555
DOI	10.2340/actadv.v103.9400
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Article ; Online: Reversion of glucocorticoid-induced senescence and collagen synthesis decrease by LY294002 is mediated through p38 in skin.

Le, Quoc-Vu / Wen, Su-Ying / Chen, Chih-Jung / Huang, Chih-Yang / Kuo, Wei-Wen

International journal of biological sciences

2022 Volume 18, Issue 16, Page(s) 6102–6113

Abstract: Glucocorticoids (GCs) are the most common treatment for inflammatory skin disorders; however, they show several adverse side effects, including atrophy and collagen decrease following chronic treatment. In particular, transcription factors and p38 ... ...

Abstract	Glucocorticoids (GCs) are the most common treatment for inflammatory skin disorders; however, they show several adverse side effects, including atrophy and collagen decrease following chronic treatment. In particular, transcription factors and p38 signaling for collagen synthesis have been shown to be suppressed by the active glucocorticoid receptor (GR). LY294002 (LY), a phosphoinositide 3-kinase (PI3K) inhibitor, has been reported to protect keratinocytes in epidermis against GC-induced hypoplasia; however, its protective effect in dermis remains unclear. Furthermore, clobetasol propionate (CP) is the most used commercial synthetic GC, yet studies on how CP causes side effects in dermal fibroblasts are limited. In this study, dermal atrophy was modeled using CP in human dermal fibroblasts (HDFs) and C57BL/6 mice. CP treatment significantly upregulated FK506 binding protein 5 (FKBP51), an atrophy marker (2.4 ± 0.25 and 3.3 ± 0.3 fold in
MeSH term(s)	Mice ; Humans ; Animals ; Glucocorticoids ; Phosphatidylinositol 3-Kinases ; Mice, Inbred C57BL ; Receptors, Glucocorticoid ; Phosphoinositide-3 Kinase Inhibitors ; Atrophy
Chemical Substances	2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (31M2U1DVID) ; Glucocorticoids ; Phosphatidylinositol 3-Kinases (EC 2.7.1.-) ; Receptors, Glucocorticoid ; Phosphoinositide-3 Kinase Inhibitors
Language	English
Publishing date	2022-10-18
Publishing country	Australia
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2179208-2
ISSN	1449-2288 ; 1449-2288
ISSN (online)	1449-2288
ISSN	1449-2288
DOI	10.7150/ijbs.73915
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Article ; Online: Doxorubicin induced ROS-dependent HIF1α activation mediates blockage of IGF1R survival signaling by IGFBP3 promotes cardiac apoptosis.

Wen, Su-Ying / Ali, Ayaz / Huang, I-Chieh / Liu, Jian-Sheng / Chen, Po-Yuan / Padma Viswanadha, Vijaya / Huang, Chih-Yang / Kuo, Wei-Wen

Aging

2023 Volume 15, Issue 1, Page(s) 164–178

Abstract: Doxorubicin (Dox) causes the generation of intracellular reactive oxygen species (ROS) and inactivates insulin-like growth factor 1 (IGF1) signaling, leading to cardiomyocyte apoptosis. IGF-binding protein 3 (IGFBP3) is the most abundant circulating IGF1 ...

Abstract	Doxorubicin (Dox) causes the generation of intracellular reactive oxygen species (ROS) and inactivates insulin-like growth factor 1 (IGF1) signaling, leading to cardiomyocyte apoptosis. IGF-binding protein 3 (IGFBP3) is the most abundant circulating IGF1 carrier protein with high affinity, which has been reported to mediate ROS-induced apoptosis. Hypoxia-inducible factor 1α (HIF1A), an upstream protein of IGFBP3 is regulated by prolyl hydroxylase domain (PHD) through hydroxylation. In this study, we investigated the role of IGFBP3, HIF1A, and PHD in Dox-induced cardiac apoptosis.Cells challenged with 1 μM Dox for 24 h increased ROS generation, augmented intracellular and secreted IGFBP3 levels, and reduced IGF1 signaling. Further, we showed that Dox enhanced the extracellular association of IGF1 with IGFBP3. Moreover, echocardiography parameters, especially ejection fraction (EF) and fractional shortening (FS) were significantly reduced in ventricle tissue of Dox challenged rats. Notably, siRNA approach against IGFBP3 or an anti-IGFBP3 antibody rescued Dox-induced cardiac apoptosis, mitochondrial ROS, and the decrease in the IGF1 signaling activity. Furthermore, silencing HIF1A either using siRNA or inhibitor downregulated intracellular IGFBP3, rescued apoptosis, mitochondrial generation, and reduction in IGF1 signaling. Finally, western blot data revealed that ROS scavenger reversed Dox-induced cardiac apoptosis, increased levels of HIF1A and secreted IGFBP3, and decreased IGF1 survival signaling and PHD expression.These findings suggest that Dox-induced ROS generation suppressed PHD, which might stabilize nuclear HIF1A protein, leading to increased IGFBP3 expression and secretion. This in turn results in enhanced extracellular association of the latter with IGF1 and blocks IGF1 pro-survival signaling and may result in inducing cardiac apoptosis.
MeSH term(s)	Animals ; Rats ; Apoptosis ; Doxorubicin/pharmacology ; Insulin-Like Growth Factor Binding Protein 3/genetics ; Insulin-Like Growth Factor Binding Protein 3/metabolism ; Myocytes, Cardiac/metabolism ; Reactive Oxygen Species/metabolism ; RNA, Small Interfering/metabolism
Chemical Substances	Doxorubicin (80168379AG) ; Insulin-Like Growth Factor Binding Protein 3 ; Reactive Oxygen Species ; RNA, Small Interfering ; Hif1a protein, rat ; Igf1r protein, rat
Language	English
Publishing date	2023-01-03
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ISSN	1945-4589
ISSN (online)	1945-4589
DOI	10.18632/aging.204466
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Article ; Online: Activation of PI3K/Akt mediates the protective effect of diallyl trisulfide on doxorubicin induced cardiac apoptosis.

Wen, Su-Ying / Ng, Shang-Chuan / Ho, Wen-Kun / Huang, Han-Zhe / Huang, Chih-Yang / Kuo, Wei-Wen

Current research in toxicology

2023 Volume 5, Page(s) 100136

Abstract: Diallyl trisulfide (DATS), an organosulfide compound derived from garlic, is renowned for its potent antioxidant properties, particularly in countering the generation of reactive oxygen species (ROS). It has also gained recognition as a potential agent ... ...

Abstract	Diallyl trisulfide (DATS), an organosulfide compound derived from garlic, is renowned for its potent antioxidant properties, particularly in countering the generation of reactive oxygen species (ROS). It has also gained recognition as a potential agent for preventing heart-related conditions. Doxorubicin (Dox), a commonly used chemotherapeutic drug, is known to induce severe cardiac complications by promoting ROS production. Therefore, it was imperative to investigate whether DATS possesses cardioprotective capabilities against Dox-induced cardiac apoptosis and elucidate the underlying mechanisms. In this study, we observed that the intracellular ROS levels and cardiac apoptosis were heightened in H9c2 cells exposed to Dox (1 μM). However, treatment with 10 μM DATS effectively mitigated the Dox-induced ROS generation and apoptotic signaling, concurrently activating the PI3K/Akt pathway. Notably, the anti-apoptotic effects of DATS were attenuated when PI3K siRNA and the LY294002 PI3K inhibitor were employed. Furthermore, the TUNEL assay results demonstrated a significant reduction in Dox-induced apoptosis with DATS treatment. In summary, our findings indicate that DATS can activate the PI3K/Akt pathway, reducing ROS production in cardiac cells exposed to Dox, and subsequently rescue cardiac cells from apoptosis.
Language	English
Publishing date	2023-11-11
Publishing country	Netherlands
Document type	Journal Article
ISSN	2666-027X
ISSN (online)	2666-027X
DOI	10.1016/j.crtox.2023.100136
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Article ; Online: Paeoniflorin found in Paeonia lactiflora root extract inhibits melanogenesis by regulating melanin-related signal transduction in B16F10 cells.

Wen, Su-Ying / Wu, Ya-Shian / Liu, Hsun / Ng, Shang-Chuan / Padma, Viswanadha Vijaya / Huang, Chih-Yang / Kuo, Wei-Wen

Journal of cosmetic dermatology

2023 Volume 22, Issue 10, Page(s) 2824–2830

Abstract: Background: Skin pigmentation is modulated by various processes, with melanogenesis playing a key role. Melanin is synthesized by the catalysis of melanogenesis-related enzymes, such as tyrosinase and tyrosine-related proteins TRP-1 and TRP-2. ... ...

Abstract	Background: Skin pigmentation is modulated by various processes, with melanogenesis playing a key role. Melanin is synthesized by the catalysis of melanogenesis-related enzymes, such as tyrosinase and tyrosine-related proteins TRP-1 and TRP-2. Paeoniflorin is the main bioactive component of Paeonia suffruticosa Andr., Paeonia lactiflora., or Paeonia veitchii Lynch and has been used for centuries for its anti-inflammatory, anti-oxidant, and anti-carcinogenic properties. Aims & methods: In this study, melanin biosynthesis in mouse melanoma (B16F10) cells was induced using α-melanocyte-stimulating hormone (α-MSH), and then cells were co-treated with paeoniflorin to evaluate its potential anti-melanogenic effect. Results: α-MSH stimulation increased melanin content, tyrosinase activity, and melanogenesis-related markers in a dose-dependent manner. However, treatment with paeoniflorin reversed α-MSH-induced upregulation of melanin content and tyrosinase activity. Furthermore, paeoniflorin inhibited cAMP response element-binding protein activation and TRP-1, TRP-2, and microphthalmia-associated transcription factor protein expression in α-MSH-stimulated B16F10 cells. Conclusion: Overall, these findings show the potential of paeoniflorin as a depigmenting agent for cosmetic products.
MeSH term(s)	Animals ; Mice ; Melanins ; Monophenol Monooxygenase ; Paeonia ; alpha-MSH/pharmacology ; alpha-MSH/metabolism ; Signal Transduction ; Antioxidants/pharmacology
Chemical Substances	Melanins ; Monophenol Monooxygenase (EC 1.14.18.1) ; peoniflorin (21AIQ4EV64) ; alpha-MSH (581-05-5) ; Antioxidants
Language	English
Publishing date	2023-06-08
Publishing country	England
Document type	Journal Article
ZDB-ID	2280551-5
ISSN	1473-2165 ; 1473-2130
ISSN (online)	1473-2165
ISSN	1473-2130
DOI	10.1111/jocd.15789
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Article ; Online: Epidemiology of pediatric herpes zoster after varicella infection: a population-based study.

Wen, Su-Ying / Liu, Wen-Liang

Pediatrics

2015 Volume 135, Issue 3, Page(s) e565–71

Abstract: Background: There are limited population-based data regarding pediatric herpes zoster (HZ).: Methods: Children aged <12 years with varicella infections between 2000 and 2006 were identified from a national population-based database and followed-up ... ...

Abstract	Background: There are limited population-based data regarding pediatric herpes zoster (HZ). Methods: Children aged <12 years with varicella infections between 2000 and 2006 were identified from a national population-based database and followed-up for a diagnosis of HZ until December 2008. Since a routine varicella vaccination program was started in 2004, vaccinated children without medically attended varicella were identified between 2004 and 2006, and followed-up for a diagnosis of HZ until December 2008. Results: Of 27 517 children with medically attended varicella, 428 developed HZ. The incidence of HZ was 262.1 per 100 000 person-years. Of 25 132 vaccinated children without medically attended varicella, 106 developed HZ. The incidence of HZ was 93.3 per 100 000 person-years. The mean duration from varicella to HZ was 4.12 years. Children diagnosed with varicella at aged <2 years had a higher incidence (P < .001) and shorter duration (P = .04) than those diagnosed aged ≧2 years. Children diagnosed with varicella aged ≥2 but <8 years had a significantly increased incidence of HZ after than before the vaccination program (relative risk = 1.85 at 3 years of follow-up, P = .03). Children with varicella infections had a significantly greater risk of HZ than vaccinated children without a history of varicella (relative risk = 2.31 at 4 years of follow-up, P < .001). Conclusions: This study demonstrates the population-based epidemiologic characteristics of pediatric HZ among those who contracted varicella. In the early postvaricella vaccination period, an increased HZ incidence was observed among children with varicella infection aged ≥2 years.
MeSH term(s)	Chickenpox/epidemiology ; Chickenpox/prevention & control ; Chickenpox Vaccine/therapeutic use ; Child ; Child, Preschool ; Female ; Follow-Up Studies ; Herpes Zoster/epidemiology ; Herpes Zoster/prevention & control ; Herpesvirus 3, Human/immunology ; Herpesvirus Vaccines/therapeutic use ; Humans ; Immunization Programs ; Incidence ; Infant ; Male ; Population Surveillance ; Retrospective Studies ; Taiwan/epidemiology ; Vaccination/methods
Chemical Substances	Chickenpox Vaccine ; Herpesvirus Vaccines
Language	English
Publishing date	2015-03
Publishing country	United States
Document type	Journal Article ; Multicenter Study
ZDB-ID	207677-9
ISSN	1098-4275 ; 0031-4005
ISSN (online)	1098-4275
ISSN	0031-4005
DOI	10.1542/peds.2013-4037
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Article ; Online: Quantitative and rapid estimations of human sub-surface skin mass using ultra-high-resolution spectral domain optical coherence tomography.

Kuo, Wen-Chuan / Kuo, Yue-Ming / Wen, Su-Ying

Journal of biophotonics

2016 Volume 9, Issue 4, Page(s) 343–350

Abstract: Non-invasive and quantitative estimations for the delineation of sub-surface tumor margins could greatly aid in the early detection and monitoring of the morphological appearances of tumor growth, ensure complete tumor excision without the unnecessary ... ...

Abstract	Non-invasive and quantitative estimations for the delineation of sub-surface tumor margins could greatly aid in the early detection and monitoring of the morphological appearances of tumor growth, ensure complete tumor excision without the unnecessary sacrifice of healthy tissue, and facilitate post-operative follow-up for recurrence. In this study, a high-speed, non-invasive, and ultra-high-resolution spectral domain optical coherence tomography (UHR-SDOCT) imaging platform was developed for the quantitative measurement of human sub-surface skin mass. With a proposed robust, semi-automatic analysis, the system can rapidly quantify lesion area and shape regularity by an en-face-oriented algorithm. Various sizes of nylon sutures embedded in pork skin were used first as a phantom to verify the accuracy of our algorithm, and then in vivo, feasibility was proven using benign human angiomas and pigmented nevi. Clinically, this is the first step towards an automated skin lesion measurement system. In vivo optical coherence tomography (OCT) image of angioma (A). Thin red arrows point to a blood vessel (BV).
MeSH term(s)	Animals ; Humans ; Imaging, Three-Dimensional ; Nevus, Pigmented/diagnostic imaging ; Skin Diseases/diagnostic imaging ; Swine ; Time Factors ; Tomography, Optical Coherence/methods
Language	English
Publishing date	2016-04
Publishing country	Germany
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2390063-5
ISSN	1864-0648 ; 1864-063X
ISSN (online)	1864-0648
ISSN	1864-063X
DOI	10.1002/jbio.201400153
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Article: Protective effects of galangin against H2O2‐induced aging via the IGF‐1 signaling pathway in human dermal fibroblasts

Wen, Su‐Ying / Chen, Jia‐Yi / Chen, Chih‐Jung / Huang, Chih‐Yang / Kuo, Wei‐Wen

Environmental toxicology. 2020 Feb., v. 35, no. 2

2020

Abstract: Galangin, a natural flavonol, has anti‐inflammatory and antioxidative potential. However, the cytoprotective effects of galangin against oxidative‐induced aging in human fibroblasts have not been well studied. IGF‐1 signaling pathway is associated with ... ...

Abstract	Galangin, a natural flavonol, has anti‐inflammatory and antioxidative potential. However, the cytoprotective effects of galangin against oxidative‐induced aging in human fibroblasts have not been well studied. IGF‐1 signaling pathway is associated with the control of aging and longevity in human. The goal of this study was to investigate the effects of galangin on human skin fibroblast HS68 cells under H2O2 exposure to induce aging. In this study, we demonstrate that galangin could decrease the levels of pro‐inflammatory proteins and enhanced collagen formation through promoting the IGF‐1R pathway. Furthermore, aging markers such as senescence‐associated β‐galactosidase p53, p21Cip1/WAF1, and p16INK4A were upregulated under H2O2 exposure and galangin could reverse its effects. Taken together, these data indicated that anti‐inflammatory and antiaging activities of galangin may be mediated through the IGF‐1R signaling pathway. These findings may provide the evidence for galangin to develop as an antiwrinkle product on human skin.
Keywords	anti-aging properties ; antioxidant activity ; beta-galactosidase ; collagen ; fibroblasts ; flavonols ; hydrogen peroxide ; insulin-like growth factor I ; insulin-like growth factor I receptor ; longevity ; protective effect ; signal transduction ; skin (animal)
Language	English
Dates of publication	2020-02
Size	p. 115-123.
Publishing place	John Wiley & Sons, Inc.
Document type	Article
Note	JOURNAL ARTICLE
ZDB-ID	1463449-1
ISSN	1522-7278 ; 1520-4081
ISSN (online)	1522-7278
ISSN	1520-4081
DOI	10.1002/tox.22847
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Article ; Online: Protective effects of galangin against H

Wen, Su-Ying / Chen, Jia-Yi / Chen, Chih-Jung / Huang, Chih-Yang / Kuo, Wei-Wen

Environmental toxicology

2019 Volume 35, Issue 2, Page(s) 115–123

Abstract: Galangin, a natural flavonol, has anti-inflammatory and antioxidative potential. However, the cytoprotective effects of galangin against oxidative-induced aging in human fibroblasts have not been well studied. IGF-1 signaling pathway is associated with ... ...

Abstract	Galangin, a natural flavonol, has anti-inflammatory and antioxidative potential. However, the cytoprotective effects of galangin against oxidative-induced aging in human fibroblasts have not been well studied. IGF-1 signaling pathway is associated with the control of aging and longevity in human. The goal of this study was to investigate the effects of galangin on human skin fibroblast HS68 cells under H
MeSH term(s)	Aging/drug effects ; Aging/metabolism ; Anti-Inflammatory Agents/pharmacology ; Biomarkers/metabolism ; Cell Line ; Collagen/biosynthesis ; Fibroblasts/drug effects ; Flavonoids/pharmacology ; Humans ; Hydrogen Peroxide/toxicity ; Insulin-Like Growth Factor I/metabolism ; Oxidation-Reduction ; Signal Transduction ; Skin/drug effects ; Skin/metabolism
Chemical Substances	Anti-Inflammatory Agents ; Biomarkers ; Flavonoids ; IGF1 protein, human ; galangin (142FWE6ECS) ; Insulin-Like Growth Factor I (67763-96-6) ; Collagen (9007-34-5) ; Hydrogen Peroxide (BBX060AN9V)
Language	English
Publishing date	2019-09-30
Publishing country	United States
Document type	Journal Article
ZDB-ID	1463449-1
ISSN	1522-7278 ; 1520-4081
ISSN (online)	1522-7278
ISSN	1520-4081
DOI	10.1002/tox.22847
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