Glucagon Enhances Chemotherapy Efficacy By Inhibition of Tumor Vessels in Colorectal Cancer

Abstract: Chemotherapy is widely used to treat colorectal cancer (CRC). Despite its substantial benefits, the development of drug resistance and adverse effects remain challenging. This study aimed to elucidate a novel role of glucagon in anti‐cancer therapy. In a series of in vitro experiments, glucagon inhibited cell migration and tube formation in both endothelial and tumor cells. In vivo studies demonstrated decreased tumor blood vessels and fewer pseudo‐vessels in mice treated with glucagon. The combination of glucagon and chemotherapy exhibited enhanced tumor inhibition. Mechanistic studies demonstrated that glucagon increased the permeability of blood vessels, leading to a pronounced disruption of vessel morphology. Signaling pathway analysis identified a VEGF/VEGFR‐dependent mechanism whereby glucagon attenuated angiogenesis through its receptor. Clinical data analysis revealed a positive correlation between elevated glucagon expression and chemotherapy response. This is the first study to reveal a role for glucagon in inhibiting angiogenesis and vascular mimicry. Additionally, the delivery of glucagon‐encapsulated PEGylated liposomes to tumor‐bearing mice amplified the inhibition of angiogenesis and vascular mimicry, consequently reinforcing chemotherapy efficacy. Collectively, the findings demonstrate the role of glucagon in inhibiting tumor vessel network and suggest the potential utility of glucagon as a promising predictive marker for patients with CRC receiving chemotherapy.

Object Details

• Location: Deutsche Nationalbibliothek Frankfurt am Main
• Extent: Online-Ressource
• Language: Englisch

References and Relationships

• Bibliographic citation: Glucagon Enhances Chemotherapy Efficacy By Inhibition of Tumor Vessels in Colorectal Cancer ; day:10 ; month:12 ; year:2023 ; extent:18 ; Advanced science ; (10.12.2023) (gesamt 18)

Contributors, Places and Time

• Creator: Xu, Yuxue ; Ni, Feixue ; Sun, Daxi ; Peng, Yue ; Zhao, Yaxuan ; Wu, Xiaojun ; Li, Shasha ; Qi, Xiangyu ; He, Xinkang ; Li, Min ; Zhou, Yizi ; Zhang, Chao ; Yan, Miao ; Yao, Cuifang ; Zhu, Shuaishuai ; Yang, Yang ; An, Baijiao ; Yang, Chunhua ; Zhang, Guilong ; Jiang, Wenguo ; Mi, Jia ; Chen, Xinju ; Wei, Pengfei ; Tian, Geng ; Zhang, Yin

Further information

• DOI: 10.1002/advs.202307271
• URN: urn:nbn:de:101:1-2023121114135479802386
• Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Last update: 15.08.2025, 7:21 AM CEST