Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar 608002, Tamil Nadu, India.
Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar 608002, Tamil Nadu, India.
Toxicol Appl Pharmacol. 2018 Aug 1;352:87-96. doi: 10.1016/j.taap.2018.05.030. Epub 2018 May 23.
Previously, we proved that caffeic acid (CA), a major dietary phenolic acid, prevents skin carcinogenesis by modulating inflammatory signaling in mouse skin. However, the actual mechanisms of CA against UVB (280-320 nm) induced photocarcinogenesis remains unclear. The present results confirms that CA significantly inhibits single UVB-induced CPDs formation, oxidative DNA damage, ROS generation and frequency of apoptotic cell death in human dermal fibroblasts (HDFa). Furthermore, CA prevents UVB-induced expression of PI3K and AKT kinases through activation of PTEN which subsequently promotes XPC dependant NER proteins such as XPC, XPE, TFIIH (p44) and ERCC1 in HDFa cells and mouse skin tissue. Further, CA directly activates PTEN through hydrogen bond and hydrophobic interactions. Taken together, these findings suggest that CA prevents UVB-induced photodamage through the activation of PTEN expression in human dermal fibroblasts and mouse skin.
先前,我们证明了咖啡酸(CA),一种主要的膳食酚酸,通过调节小鼠皮肤中的炎症信号来预防皮肤癌发生。然而,CA 对 UVB(280-320nm)诱导的光致癌作用的实际机制尚不清楚。本研究结果证实,CA 可显著抑制人真皮成纤维细胞(HDFa)中单 UVB 诱导的 CPDs 形成、氧化 DNA 损伤、ROS 生成和凋亡细胞死亡频率。此外,CA 通过激活 PTEN 来抑制 UVB 诱导的 PI3K 和 AKT 激酶的表达,从而促进 XPC 依赖的 NER 蛋白,如 XPC、XPE、TFIIH(p44)和 ERCC1 在 HDFa 细胞和小鼠皮肤组织中的表达。此外,CA 通过氢键和疏水相互作用直接激活 PTEN。综上所述,这些发现表明 CA 通过在人真皮成纤维细胞和小鼠皮肤中激活 PTEN 的表达来预防 UVB 诱导的光损伤。