Hexiao Wang

Hexiao Wang


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 May 2020 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
YLYan-Song Lu
Yan-Song Lu
YJYuan Jiang
Yuan Jiang
JYJin-Ping Yuan
Jin-Ping Yuan
SJShi-Bin Jiang
Shi-Bin Jiang
YYYang Yang
Yang Yang
HCHong-Duo Chen
Hong-Duo Chen
Photodamages caused by UVA radiation induced oxidative injuries are closely related to photoaging and skin cancer. Paeoniflorin (PF), extracted from the root of Paeonia lactiflora, has been reported to be an effective antioxidant. PLIN2, known as adipose differentiation-related protein, has been previously involved in the regulation of oxidative stress. In this study, we were sought to investigate the photo-protective property of PF and PLIN2 in UVA-radiated human dermal fibroblasts (HDFs). HDFs were pre-treated with PF (800 μM) followed by UVA radiation (22.5 J/cm2). MTS activity, cell apoptosis, ROS, MDA, and SOD were detected, respectively. The expressions of Nrf2, HO-1, NQ-O1, and PLIN2 were determined using RT-qPCR or western blot. Nrf2 was silenced by siRNA, and PLIN2 was overexpressed via lentiviral transduction. Comparing to the UVA radiation, PF pre-treatment could prominently increase the MTS activity, decrease cell apoptosis, reduce the generations of ROS and MDA, increase the activity of SOD and increase the expression of Nrf2 and its target genes HO-1 and NQ-O1. When Nrf2 was knocked down, PF lost above protective properties. In addition, UVA induced oxidative stress led to upregulation of PLIN2 and the latter could be decreased by PF. Overexpression of PLIN2 improved MTS activity and reduced MDA level in HDFs. The combination of PLIN2 overexpression and PF pre-treatment corporately inhibited UVA-induced injury. Besides, we also found that PF and PLIN2 had a compensatory protection against UVA induced oxidative stress. In conclusion, our study demonstrated that UVA induced photodamages could be inhibited by PF via Nrf2/HO-1/NQ-O1 signaling pathway or by PLIN2, and the combination of PLIN2 overexpression and PF played additive effects against UVA-related oxidative stress.

4 August 2022 in Journal of Investigative Dermatology
Verified
Journal Article
Closed access
LZLiming Zhang
Liming Zhang
LQLi Qiu
Li Qiu
JWJian Wu
Jian Wu
YQYumeng Qi
Yumeng Qi
XGXinghua Gao
Xinghua Gao
TXTing Xiao
Ting Xiao

1 January 2022 in Allergy, Asthma & Immunology Research
Verified
Journal Article
Open access
PDF file
LZLiming Zhang
Liming Zhang
LQLi Qiu
Li Qiu
JWJian Wu
Jian Wu
YQYumeng Qi
Yumeng Qi
HWHexiao Wang
Hexiao Wang
TXTing Xiao
Ting Xiao
Zhang L, et al. Allergy Asthma Immunol Res. 2022 Jan;14(1):131-142. https://doi.org/10.4168/aair.2022.14.1.131

13 August 2020 in Journal of Cellular and Molecular Medicine
Verified
Journal Article
Open access
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SJShi‐Bin Jiang
Shi‐Bin Jiang
YLYan‐Song Lu
Yan‐Song Lu
TLTao Liu
Tao Liu
LLLiang‐Man Li
Liang‐Man Li
HWHexiao Wang
Hexiao Wang
HCHong‐Duo Chen
Hong‐Duo Chen
Both SIRT1 and UVA radiation are involved in cellular damage processes such as apoptosis, senescence and ageing. MicroRNAs (miRNAs) have been reported to be closely related to UV radiation, as well as to SIRT1. In this study, we investigated the connections among SIRT1, UVA and miRNA in human skin primary fibroblasts. Our results showed that UVA altered the protein level of SIRT1 in a time point–dependent manner. Using miRNA microarray, bioinformatics analysis, we found that knocking down SIRT1 could cause up‐regulation of miR‐27a‐5p and the latter could down‐regulate SMAD2, and these results were verified by qRT‐PCR or Western blot. Furthermore, UVA radiation (5 J/cm2), knocking down SIRT1 or overexpression of miR‐27a‐5p led to increased expression of MMP1, and decreased expressions of COL1 and BCL2. We also found additive impacts on MMP1, COL1 and BCL2 under the combination of UVA radiation + Sirtinol (SIRT1 inhibitor), or UVA radiation + miR‐27a‐5p mimic. SIRT1 activator resveratrol could reverse damage changes caused by UVA radiation. Besides, absent of SIRT1 or overexpression of miR‐27a‐5p increased cell apoptosis and induced cell arrest in G2/M phase. Taken together, these results demonstrated that UVA could influence a novel SIRT1‐miR‐27a‐5p‐SMAD2‐MMP1/COL1/BCL2 axis in skin primary fibroblasts, and may provide potential therapeutic targets for UVA‐induced skin damage.

31 December 2019 in Evidence-Based Complementary and Alternative Medicine
Verified
Journal Article
Open access
PDF file
SJS. B. Jiang
S. B. Jiang
YLY. S. Lu
Y. S. Lu
YZY. H. Zhang
Y. H. Zhang
YWYan Wu
Yan Wu
HWHexiao Wang
Hexiao Wang
HCH. D. Chen
H. D. Chen
Background. There are many possible ways to treat verruca, but no one is the single perfect treatment. YIKEER is a kind of compound preparation of Chinese traditional medicine, which has been used in the treatment of verruca for several years. Aim. To confirm the effects of YIKEER for verruca. Method. Patients with verruca vulgaris, verruca plantaris, or verruca plana were instructed to apply YIKEER stock solution or diluent to the lesions once or twice daily for 5–7 days. Then, the YIKEER was ceased for 3–4 days, and sea buckthorn oil was used for wound repairing. The total procession was defined as one session. Result. Respective 88.05% verruca vulgaris patients, 86.03% verruca plantaris patients, and 82.42% verruca plana patients achieved complete response. Most patients gained complete or partial responses after 4 treatment sessions. The percentage of patients who achieved at least 50% improvement was 90.34% for verruca vulgaris, 90.60% for verruca plantaris, and 80.91% for verruca plana after 4-session treatment. The efficacy of verruca vulgaris or verruca plantaris was better than that of verruca plana. Conclusion. YIKEER is an effective, safe, and well-tolerated agent for treating verruca including verruca vulgaris, verruca plantaris, and verruca plana.

28 May 2025 in Journal of Photochemistry and Photobiology B: Biology
Verified
Journal Article
Closed access
DSDongxin Shi
Dongxin Shi
HCHaitao Chu
Haitao Chu
YSYijun Sun
Yijun Sun
HHHailun He
Hailun He
WHWenyue Huang
Wenyue Huang
YWYan Wu
Yan Wu