State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.
Institute of Chinese Medicine and State Key Laboratory of Research on Bioactivities and Clinical Applications of Medicinal Plants, The Chinese University of Hong Kong, Hong Kong SAR, China.
Phytother Res. 2022 Jun;36(6):2641-2659. doi: 10.1002/ptr.7482. Epub 2022 May 10.
Colorectal cancer (CRC), the third most common cancer globally, is associated with intestinal inflammation that leads to poor prognosis. RA-XII, a natural cyclopeptide, has previously been reported to possess anti-tumor activities. Here, the anti-inflammatory activities of RA-XII were investigated in colitis-associated colon cancer mice and a co-culture in vitro model, in which colon cancer cells HCT116 and macrophages RAW264.7 were grown together to mimic the inflammatory microenvironment of CRC. Changes of inflammatory-related molecules and protein expressions in cells were evaluated after RA-XII incubation. Besides, azoxymethane and dextran sulfate sodium-induced colitis-associated colon cancer mice were treated with RA-XII for 24 days, inflammatory parameters and gut microbiome alterations were studied. Our results showed that RA-XII reversed the inflammatory responses of RAW264.7 cells induced by LPS and modulated the protein expressions of AKT, STAT3/p-STAT3, P70S6K, NF-κB and GSK3β and suppressed the expression of LC3A/B in HCT116 cells in co-culture system. RA-XII treatment restored the colitis damage in colon, reduced colon tumors numbers and decreased inflammatory factors (IL-6, IL-10 and TNF-α). The role of RA-XII on regulating gut microbiome was also demonstrated for the first time. In conclusion, our findings provided new scientific evidence for developing RA-XII as a potent anti-inflammatory agent for CRC.
结直肠癌(CRC)是全球第三大常见癌症,与导致预后不良的肠道炎症有关。RA-XII 是一种天然环肽,先前已被报道具有抗肿瘤活性。本研究旨在探讨 RA-XII 在结肠炎相关结直肠癌小鼠和体外共培养模型中的抗炎活性,其中结肠癌细胞 HCT116 和巨噬细胞 RAW264.7 共同培养以模拟 CRC 的炎症微环境。在 RA-XII 孵育后,评估细胞中炎症相关分子和蛋白表达的变化。此外,用 RA-XII 治疗 24 天的氧化偶氮甲烷和葡聚糖硫酸钠诱导的结肠炎相关结直肠癌小鼠,研究炎症参数和肠道微生物组的变化。结果表明,RA-XII 逆转了 LPS 诱导的 RAW264.7 细胞的炎症反应,并调节了 AKT、STAT3/p-STAT3、P70S6K、NF-κB 和 GSK3β 的蛋白表达,抑制了共培养系统中 HCT116 细胞中 LC3A/B 的表达。RA-XII 治疗恢复了结肠的结肠炎损伤,减少了结肠肿瘤数量,并降低了炎症因子(IL-6、IL-10 和 TNF-α)。这是首次证明 RA-XII 对调节肠道微生物组的作用。总之,我们的研究结果为开发 RA-XII 作为治疗 CRC 的有效抗炎剂提供了新的科学依据。