Protective effects of Andrographolide sodium bisulfate on UV-induced skin carcinogenesis in mice model

Although the mortality of skin cancer patients is relatively low, there are still a large number of patients died of these tumors at high incidence rate. Chronic exposure to solar UV irradiation is the most common cause of nonmelanoma skin tumors. Our research aimed to explore the effects of androgr...

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Veröffentlicht in:European journal of pharmaceutical sciences 2022-09, Vol.176, p.106232-106232, Article 106232
Hauptverfasser: Zhong, Qing-Yuan, Luo, Qi-Hong, Lin, Bing, Lin, Bao-Qin, Su, Zi-Ren, Zhan, Janis Ya-Xian
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container_title European journal of pharmaceutical sciences
container_volume 176
creator Zhong, Qing-Yuan
Luo, Qi-Hong
Lin, Bing
Lin, Bao-Qin
Su, Zi-Ren
Zhan, Janis Ya-Xian
description Although the mortality of skin cancer patients is relatively low, there are still a large number of patients died of these tumors at high incidence rate. Chronic exposure to solar UV irradiation is the most common cause of nonmelanoma skin tumors. Our research aimed to explore the effects of andrographolide sodium bisulfate (ASB) on UV-induced skin cancer and to reveal the underlying molecular mechanism. In the present study, histopathology changes, immunohistochemical analysis, ELISA analysis and western blot analysis were mainly used in vivo. The results indicated that ASB significantly inhibited increase of skin epidermal thickness, inflammatory cells infiltration and fibers damage in dermis, oxidative stress injury and skin carcinogenesis. Moreover, the western blot analysis showed that protein expressions of NF-κB, Nrf2, p62, LC3 II/I and p-p62 (Ser 349) in mouse skin induced by UV were dramatically suppressed in the ASB-pretreated groups. Overall, these results suggested that ASB exerted a strong preventive effect and potential therapeutic value against UV-induced skin carcinogenesis in mice through inhibiting NF-κB and Nrf2 signaling pathways and restoring autophagy. [Display omitted]
doi_str_mv 10.1016/j.ejps.2022.106232
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Chronic exposure to solar UV irradiation is the most common cause of nonmelanoma skin tumors. Our research aimed to explore the effects of andrographolide sodium bisulfate (ASB) on UV-induced skin cancer and to reveal the underlying molecular mechanism. In the present study, histopathology changes, immunohistochemical analysis, ELISA analysis and western blot analysis were mainly used in vivo. The results indicated that ASB significantly inhibited increase of skin epidermal thickness, inflammatory cells infiltration and fibers damage in dermis, oxidative stress injury and skin carcinogenesis. Moreover, the western blot analysis showed that protein expressions of NF-κB, Nrf2, p62, LC3 II/I and p-p62 (Ser 349) in mouse skin induced by UV were dramatically suppressed in the ASB-pretreated groups. 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Overall, these results suggested that ASB exerted a strong preventive effect and potential therapeutic value against UV-induced skin carcinogenesis in mice through inhibiting NF-κB and Nrf2 signaling pathways and restoring autophagy. 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subjects Andrographolide sodium bisulfate
NF-κB
Nrf2
p62
skin carcinogenesis
title Protective effects of Andrographolide sodium bisulfate on UV-induced skin carcinogenesis in mice model
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