Xu Cheng-Xiong, Jin Hua, Chung Youn-Sun, Shin Ji-Young, Woo Min-Ah, Lee Kee-Ho, Palmos Grace N, Choi Byeong-Dae, Cho Myung-Haing
Laboratory of Toxicology, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Cancer Lett. 2008 Jun 8;264(1):93-100. doi: 10.1016/j.canlet.2008.01.022. Epub 2008 Mar 4.
Inflammatory mediators are known to play a key role in tumorigenesis, therefore, it is a promising strategy to inhibit the inflammation for cancer prevention and/or treatment. Current study was performed to investigate the effects of chondroitin sulfate (CS) extracted from Styela clava tunic on TNF-alpha-induced inflammation and to elucidate the mechanism of CS on the regulation of inflammatory factors in JB6 cells. Our results showed that CS inhibited TNF-alpha-induced NF-kappaB activation and subsequent vascular cell adhesion molecule 1 and inducible nitric oxide synthase expressions by blocking Akt signals in JB6 cells. Our results suggest that CS may be developed as an effective anti-inflammatory agent in the future.
炎症介质在肿瘤发生过程中起着关键作用,因此,抑制炎症以预防和/或治疗癌症是一种很有前景的策略。本研究旨在探讨从柄海鞘被囊中提取的硫酸软骨素(CS)对肿瘤坏死因子-α(TNF-α)诱导的炎症的影响,并阐明CS对JB6细胞中炎症因子调控的机制。我们的结果表明,CS通过阻断JB6细胞中的Akt信号,抑制了TNF-α诱导的核因子-κB(NF-κB)激活以及随后的血管细胞黏附分子1和诱导型一氧化氮合酶的表达。我们的结果表明,CS未来可能会被开发成为一种有效的抗炎剂。