6-Gingerol as an arginase inhibitor prevents urethane-induced lung carcinogenesis by reprogramming tumor supporting M2 macrophages to M1 phenotype. Issue 9 (28th August 2018)

• Record Type: Journal Article
• Authors: Yao, Jingjing; Du, Zhenhua; Li, Zibo; Zhang, Shuhui; Lin, Yukun; Li, Haiyun; Zhou, Lin; Wang, Yuehua; Yan, Guixi; Wu, Xianchuang; Duan, Yongjian; Du, Gangjun
• Is Part Of: Food & function. Volume 9:Issue 9(2018)
• Page Start: 4611
• Page End: 4620
• Publication Date: 2018-08-28
• Subjects: Food -- Analysis -- Periodicals; Food -- Composition -- Periodicals; Nutrition -- Periodicals; 664.07
• DOI: 10.1039/c8fo01147h
• Languages: English
• ISSNs: 2042-6496

Abstract

Abstract : 6-Gingerol (6-G) is the main bioactive component in Ginger (Zingiber officinale Roscoe). Abstract : 6-Gingerol (6-G) is the main bioactive component in Ginger (Zingiber officinale Roscoe). The aim of this study was to explore the contribution of macrophage polarization in 6-G-associated anti-cancer effects. In a urethane-induced lung carcinogenic model, lung carcinogenesis was positively correlated with macrophage (F4/80 + ) infiltration in lung interstitial in the control group. Furthermore, higher numbers of arginase + /F4/80 + M2 cells than iNOS + /F4/80 + M1 cells were observed in interstitial macrophages. Moreover, macrophage depletion by liposome-encapsulated clodronate (LEC) could significantly prevent lung carcinogenesis, whereas pexidartinib promoted lung carcinogenesis. After 6-G treatment, lung carcinogenesis was ameliorated with increased M1 macrophages and decreased M2 macrophages in the lung interstitial. ELISA showed that the levels of IFN-γ and IL-12 increased and the levels of IL-10 and TGF-β1 decreased in the alveolar cavity compared to those in the control group. Unexpectedly, the carcinogenesis-preventing efficacy of 6-G was promoted in LEC-treated mice, but completely aborted in pexidartinib-treated mice. In the in vitro experiment, 6-G reset the IL-4-induced arginase + M2 cells toward iNOS + M1 cells and exhibited reduced levels of arginase 1 and ROS and elevated levels of L-arginine and NO. LEC and nor-NOHA selectively suppressed M2 macrophages but had a negligible effect on M1 macrophages, whereas pexidartinib decreased both M2 and M1 macrophages. The iNOS + macrophage-promoting efficacy of 6-G was increased by LEC, but was completely eliminated by pretreatment with pexidartinib or nor-NOHA. M2 macrophage-resetting efficacy of 6-G was confirmed in a Lewis lung cancer allograft model. This study indicated a reprogramming effect of 6-G as an arginase inhibitor on tumor supporting macrophages.