Wang Yijia, Wang Wenhong, Wu Xiaojing, Li Chunjun, Huang Yaping, Zhou Huiyan, Cui Yu
Laboratory of Oncologic Molecular Medicine, Tianjin Union Medical Center, Tianjin, China.
State Key Laboratory of Medicinal Chemical Biology, NanKai University, Tianjin, China.
Front Oncol. 2020 Apr 7;10:383. doi: 10.3389/fonc.2020.00383. eCollection 2020.
Cetuximab is a monoclonal antibody that acts as an anti-epidermal growth factor receptor (EGFR) agent. Cetuximab inhibits the phosphorylation and activation of EGFR and blocks downstream signal pathways of EGF/EGFR, including Ras-Raf-MAPK and PI3K-Akt pathways. Akt activation is an important factor in cetuximab resistance. It has been reported that resveratrol and connexin 43 regulate Akt in different ways based on tissue type. Since connexin 43 interacts with Akt, and resveratrol is known to upregulate connexin 43, we investigated whether resveratrol can sensitize colorectal cancer cells to cetuximab via connexin 43 upregulation. Our work confirmed that resveratrol increases the inhibition of growth by cetuximab and , upregulates connexin 43 expression and phosphorylation, increases gap junction function, and inhibits the activation of Akt and NFκB in parental or cetuximab-treated parental HCT116 and CT26 cells. Resveratrol did not exhibit these effects on connexin 43-shRNA transfected cells, so connexin 43 upregulation may contribute to Akt inhibition in these cells. Given these data, resveratrol may sensitize colorectal cancer cells to cetuximab via upregulating connexin 43 to inhibit the Akt pathway.
西妥昔单抗是一种单克隆抗体,作为一种抗表皮生长因子受体(EGFR)药物发挥作用。西妥昔单抗抑制EGFR的磷酸化和激活,并阻断EGF/EGFR的下游信号通路,包括Ras-Raf-MAPK和PI3K-Akt通路。Akt激活是西妥昔单抗耐药的一个重要因素。据报道,白藜芦醇和连接蛋白43根据组织类型以不同方式调节Akt。由于连接蛋白43与Akt相互作用,且已知白藜芦醇可上调连接蛋白43,我们研究了白藜芦醇是否可通过上调连接蛋白43使结肠癌细胞对西妥昔单抗敏感。我们的研究证实,白藜芦醇增强了西妥昔单抗对生长的抑制作用,上调了连接蛋白43的表达和磷酸化,增强了缝隙连接功能,并抑制了亲本或经西妥昔单抗处理的亲本HCT116和CT26细胞中Akt和NFκB的激活。白藜芦醇对连接蛋白43-shRNA转染细胞未表现出这些作用,因此连接蛋白43的上调可能有助于这些细胞中Akt的抑制。基于这些数据,白藜芦醇可能通过上调连接蛋白43抑制Akt通路,使结肠癌细胞对西妥昔单抗敏感。